WO2011019413A1 - Pharmaceutical composition and administrations thereof - Google Patents

Pharmaceutical composition and administrations thereof Download PDF

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Publication number
WO2011019413A1
WO2011019413A1 PCT/US2010/024609 US2010024609W WO2011019413A1 WO 2011019413 A1 WO2011019413 A1 WO 2011019413A1 US 2010024609 W US2010024609 W US 2010024609W WO 2011019413 A1 WO2011019413 A1 WO 2011019413A1
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WIPO (PCT)
Prior art keywords
weight
composition
solid dispersion
pharmaceutical composition
amorphous compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US2010/024609
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English (en)
French (fr)
Inventor
William Rowe
Patricia Hurter
Christopher R. Young
Kirk Dinehart
Marinus Jacobus Verwijs
Kirk Overhoff
Peter D. J. Grootenhuis
Martyn Botfield
Alfredo Grossi
Gregor Zlokarnik
Fredrick F. Van Goor
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Vertex Pharmaceuticals Inc
Original Assignee
Vertex Pharmaceuticals Inc
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Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=43587043&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2011019413(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from PCT/US2009/004629 external-priority patent/WO2010019239A2/en
Priority to JP2012524706A priority Critical patent/JP2013501787A/ja
Priority to MEP-2019-101A priority patent/ME03356B/me
Priority to EP10708442.8A priority patent/EP2464337B2/en
Priority to LTEP10708442.8T priority patent/LT2464337T/lt
Priority to RS20190432A priority patent/RS58604B2/sr
Priority to DK10708442.8T priority patent/DK2464337T4/da
Priority to NZ597823A priority patent/NZ597823A/en
Priority to ES10708442T priority patent/ES2718273T5/es
Priority to CN2010800415071A priority patent/CN102497859A/zh
Priority to PL10708442.8T priority patent/PL2464337T5/pl
Priority to MX2012001939A priority patent/MX2012001939A/es
Priority to SG2012009080A priority patent/SG178337A1/en
Priority to AU2010282986A priority patent/AU2010282986A1/en
Priority to FIEP10708442.8T priority patent/FI2464337T4/fi
Priority to BR112012008082A priority patent/BR112012008082A2/pt
Priority to SI201031871T priority patent/SI2464337T2/sl
Priority to RU2012109390/15A priority patent/RU2012109390A/ru
Priority to KR1020127006386A priority patent/KR20120061875A/ko
Priority to SM20190210T priority patent/SMT201900210T1/it
Application filed by Vertex Pharmaceuticals Inc filed Critical Vertex Pharmaceuticals Inc
Priority to CA2769695A priority patent/CA2769695A1/en
Priority to HRP20190660TT priority patent/HRP20190660T4/hr
Publication of WO2011019413A1 publication Critical patent/WO2011019413A1/en
Priority to ZA2012/00722A priority patent/ZA201200722B/en
Priority to IL218057A priority patent/IL218057A0/en
Anticipated expiration legal-status Critical
Priority to CY20191100385T priority patent/CY1121572T1/el
Ceased legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1629—Organic macromolecular compounds
    • A61K9/1635—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1629—Organic macromolecular compounds
    • A61K9/1652—Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2009—Inorganic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2013—Organic compounds, e.g. phospholipids, fats
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2013—Organic compounds, e.g. phospholipids, fats
    • A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2022—Organic macromolecular compounds
    • A61K9/2027—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2022—Organic macromolecular compounds
    • A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • A—HUMAN NECESSITIES
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    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
    • A61K9/2806—Coating materials
    • A61K9/282—Organic compounds, e.g. fats
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    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
    • A61K9/2806—Coating materials
    • A61K9/2833—Organic macromolecular compounds
    • A61K9/284—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/08—Bronchodilators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Definitions

  • the present invention relates to pharmaceutical compositions comprising a solid dispersion of N-[2,4-Bis(l, l-dimethylethyl)-5-hydroxyphenyl]-l,4-dihydro-4-oxoquinoline- 3-carboxamide, and methods of manufacturing and administering pharmaceutical
  • compositions comprising N-[2,4-Bis(l,l-dimethylethyl)-5-hydroxyphenyl]-l,4-dihydro-4- oxoquinoline-3-carboxamide.
  • Cystic fibrosis is a recessive genetic disease that affects approximately 30,000 children and adults in the United States and approximately 30,000 children and adults in Europe. Despite progress in the treatment of CF, there is no cure.
  • CF is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene that encodes an epithelial chloride ion channel responsible for aiding in the regulation of salt and water absorption and secretion in various tissues.
  • CFTR cystic fibrosis transmembrane conductance regulator
  • Small molecule drugs known as potentiators that increase the probability of CFTR channel opening represent one potential therapeutic strategy to treat CF.
  • CFTR is a cAMP/ATP-mediated anion channel that is expressed in a variety of cells types, including absorptive and secretory epithelia cells, where it regulates anion flux across the membrane, as well as the activity of other ion channels and proteins.
  • epithelia cells normal functioning of CFTR is critical for the maintenance of electrolyte transport throughout the body, including respiratory and digestive tissue.
  • CFTR is composed of approximately 1480 amino acids that encode a protein made up of a tandem repeat of transmembrane domains, each containing six transmembrane helices and a nucleotide binding domain. The two transmembrane domains are linked by a large, polar, regulatory (R)-domain with multiple phosphorylation sites that regulate channel activity and cellular trafficking.
  • CFTR cystic fibrosis
  • a defect in this gene causes mutations in CFTR resulting in cystic fibrosis ("CF"), the most common fatal genetic disease in humans. Cystic fibrosis affects approximately one in every 2,500 infants in the United States. Within the general United States population, up to 10 million people carry a single copy of the defective gene without apparent ill effects. In contrast, individuals with two copies of the CF associated gene suffer from the debilitating and fatal effects of CF, including chronic lung disease.
  • the most prevalent mutation is a deletion of phenylalanine at position 508 of the CFTR amino acid sequence, and is commonly referred to as ⁇ F508-CFTR. This mutation occurs in approximately 70% of the cases of cystic fibrosis and is associated with a severe disease.
  • CFTR transports a variety of molecules in addition to anions
  • this role represents one element in an important mechanism of transporting ions and water across the epithelium.
  • the other elements include the epithelial Na+ channel, ENaC, Na+/2C1-/K+ co-transporter, Na+-K+-ATPase pump and the basolateral membrane K+ channels, that are responsible for the uptake of chloride into the cell.
  • N-[2,4-bis(l,l-dimethylethyl)-5-hydroxyphenyl]-l,4-dihydro-4-oxoquinoline-3- carboxamide is a potent and selective CFTR potentiator of wild-type and mutant (including e.g., ⁇ F508, R117H, and G551D) forms of human CFTR.
  • N-[2,4-bis(l,l-dimethylethyl)-5- hydroxyphenyl]-l,4-dihydro-4-oxoquinoline-3-carboxamide is useful for treatment of adult patients with cystic fibrosis and at least one G55 ID-CFTR allele.
  • the invention relates to pharmaceutical compositions comprising a solid dispersion of N-[2,4-bis( 1 , 1 -dimethylethyl)-5-hydroxyphenyl]- 1 ,4-dihydro-4-oxoquinoline-3- carboxamide ("Compound 1").
  • the pharmaceutical compositions may also include one or more of the following excipients: a filler, a disintegrant, a glidant, a lubricant, a binder, and a surfactant.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises about 15 mg of amorphous Compound 1. In certain embodiments, the solid dispersion comprises about 15 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises about 25 mg of amorphous Compound 1. In certain embodiments, the solid dispersion comprises about 25 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises about 50 mg of amorphous Compound 1. In certain embodiments, the solid dispersion comprises about 50 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises about 75 mg of amorphous Compound 1. In certain embodiments, the solid dispersion comprises about 75 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises about 100 mg of amorphous Compound 1. In certain embodiments, the solid dispersion comprises about 100 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises about 150 mg of amorphous Compound 1. In certain embodiments, the solid dispersion comprises about 150 mg of substantially amorphous Compound 1. [0022] In one embodiment, the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises about 250 mg of amorphous Compound 1. In certain embodiments, the solid dispersion comprises about 250 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises up to about 5 mg of amorphous Compound 1. In certain embodiments, the solid dispersion comprises to about 5 mg of substantially amorphous Compound 1. For instance, the solid dispersion comprises 0.5 mg, 0.75 mg, 1 mg, 2 mg, 3 mg, 4 mg, or 5 mg of amorphous or substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises up to about 1 mg of amorphous Compound 1.
  • the solid dispersion comprises to about 1 mg of substantially amorphous Compound 1.
  • the solid dispersion comprises 0.5 mg, 0.75 mg, or 1 mg of amorphous or substantially amorphous Compound 1.
  • the solid form of Compound 1 in the pharmaceutical composition is a solid dispersion comprising substantially amorphous or amorphous Compound 1 and a polymer, such as hydroxypropylmethylcellulose (HPMC), hydroxypropylmethylcellulose acetate succinate (HPMCAS), vinylpyrrolidone/vinyl acetate copolymer (PVP/VA), polyvinylpyrrolidone (PVP), methacrylic acid/methacrylate copolymers, hydroxypropyl cellulose (HPC), or any combination thereof.
  • a polymer such as hydroxypropylmethylcellulose (HPMC), hydroxypropylmethylcellulose acetate succinate (HPMCAS), vinylpyrrolidone/vinyl acetate copolymer (PVP/VA), polyvinylpyrrolidone (PVP), methacrylic acid/methacrylate copolymers, hydroxypropyl cellulose (HPC), or any combination thereof.
  • HPMC hydroxypropylmethylcellulose
  • the solid dispersion has a concentration of at least 20 wt% of Compound 1, by weight of the solid dispersion. In other instances, the solid dispersion comprises 80 wt% or less of HPMCAS or PVP/VA. Some solid dispersions comprise from about 40 wt% to about 60 wt% of substantially amorphous or amorphous Compound 1 by weight of the solid dispersion and from about 60 wt% to about 40 wt% of polymer by weight of the solid dispersion.
  • Solid dispersions comprise from about 65 wt% to about 95 wt% of substantially amorphous or amorphous Compound 1 by weight of the solid dispersion and from about 45 wt% to about 5 wt% of polymer by weight of the solid dispersion.
  • Solid dispersions can also optionally comprise additives such as a surfactant (e.g., sodium lauryl sulfate (SLS)), which can be present in a concentration of less than 10 wt% of surfactant by weight of solid dispersion.
  • a surfactant e.g., sodium lauryl sulfate (SLS)
  • Still other solid dispersions comprise from about 45 wt% to about 85 wt% of substantially amorphous or amorphous Compound 1, from about 0.45 wt% to about 0.55 wt% of SLS, and from about 14.45 wt% to about 55.55 wt% of HPMCAS or PVP/VA by weight of the solid dispersion.
  • the pharmaceutical compositions also comprise a filler (e.g., lactose, sorbitol, celluloses, calcium phosphates, starches, sugars (e.g., mannitol, sucrose, or the like) or any combination thereof) in concentrations of at least about 10 wt% by weight of the composition; a disintegrant (e.g., sodium croscarmellose, sodium starch glycolate, or a combination thereof) in concentrations of about 10 wt% or less by weight of the composition; a surfactant (e.g., sodium lauryl sulfate, sodium stearyl fumarate (SSF), polyoxyethylene 20 sorbitan mono-oleate, or any combination thereof) in concentrations of about 10 wt% or less by weight of the composition; a binder (e.g., microcrystalline cellulose, dibasic calcium phosphate, sucrose, corn (maize) starch, modified cellulose (e.g.,
  • hydroxymethyl cellulose in concentrations of at least about 1 wt% by weight of the composition; a glidant (e.g., colloidal silicon dioxide, talc, or a combination thereof) in concentrations of about 2 wt% or less by weight of the composition; and a lubricant (e.g., magnesium stearate, stearic acid, hydrogenated oil, sodium stearyl fumarate, or any combination thereof) in concentrations of about 2 wt% or less by weight of the composition.
  • a glidant e.g., colloidal silicon dioxide, talc, or a combination thereof
  • a lubricant e.g., magnesium stearate, stearic acid, hydrogenated oil, sodium stearyl fumarate, or any combination thereof
  • Such pharmaceutical compositions can optionally comprise one or more colorants, fragrances, and/or flavors to enhance its visual appeal, taste, and scent.
  • Another aspect of the present invention provides a pharmaceutical composition consisting of a tablet that comprises a solid dispersion, a filler, a disintegrant, a surfactant, a binder, a glidant, and a lubricant, wherein the tablet has a dissolution of at least about 50% in about 30 minutes, and the solid dispersion comprises substantially amorphous Compound 1.
  • dissolution is measured with a standard USP Type II apparatus that employs a dissolution media of 0.6% sodium lauryl sulfate dissolved in 900 mL of DI water (or a volume of media having the same ratio of SLS to DI water) at a temperature of about 37 0 C. A single experimental tablet is tested in each test vessel of the apparatus.
  • Dissolution can also be measured with a standard USP Type II apparatus that employs a dissolution media of 0.7% sodium lauryl sulfate dissolved in 900 mL of 50 mM sodium phosphate buffer (pH 6.8) at a temperature of about 37 0 C. Dissolution can also be measured with a standard USP Type II apparatus that employs a dissolution media of 0.5% sodium lauryl sulfate dissolved in 900 mL of 50 mM sodium phosphate buffer (pH 6.8) at a temperature of about 37 0 C. A single experimental tablet is tested in each test vessel of the apparatus.
  • Another aspect of the present invention provides a pharmaceutical composition consisting of a tablet that comprises a solid dispersion comprising amorphous or substantially amorphous Compound 1 and HPMCAS or PVP/VA; and, a filler, a disintegrant, a surfactant, a binder, a glidant, and a lubricant, wherein the tablet has a hardness of at least about 5 Kp.
  • the tablets described herein are coated.
  • coated tablets described herein are colored.
  • the colored, coated tablets include text or images.
  • the text or images can be printed on the colored, coated tablet.
  • the colored, coated tablets include about 3 wt% of a film coating comprising a blue colorant, such as OPADR Y® II.
  • the colored tablets can be labeled with a logo and text indicating the strength of the active ingredient in the tablet using a black ink, such as Opacode® WB or Opacode® S-l-17823.
  • the colored, coated tablets are coated with a colorant, waxed, and then labeled with a logo, other image, and/or text using a suitable ink.
  • the tablets are coated with about 3 wt% of colorant, and waxed with Carnauba wax powder weighed out in the amount of about 0.01% w/w of the starting tablet core weight.
  • the waxed tablets can be labeled with a logo and text indicating the strength of the active ingredient in the tablet using a suitable ink.
  • Another aspect of the present invention provides a method of producing a pharmaceutical composition
  • a method of producing a pharmaceutical composition comprising the steps of providing an admixture of a solid dispersion of amorphous Compound 1 , a binder, a glidant, a surfactant, a lubricant, a disintegrant, and a filler, and compressing the admixture into a tablet having a dissolution of at least about 50% in about 30 minutes.
  • the admixture is compressed to a hardness of at least about 5 Kp.
  • Another aspect of the present invention provides a method of producing a pharmaceutical composition comprising the steps of providing an admixture of a solid dispersion of amorphous Compound 1, a binder, a glidant, a surfactant, a lubricant, a disintegrant, and a filler, and compressing the admixture into a tablet having a dissolution of at least about 70% in about 30 minutes.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient at least once per day at least one tablet comprising a solid dispersion of substantially amorphous or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, in which the solid dispersion comprises at least about 25 mg of substantially amorphous or amorphous
  • the tablet is orally administered to the patient once per day.
  • Other tablets useful in this method comprise a solid dispersion containing at least about 50 mg of substantially amorphous or amorphous Compound 1.
  • Some tablets useful in this method comprise a solid dispersion containing at least about 75 mg of substantially amorphous or amorphous Compound 1.
  • Other tablets useful in this method comprise a solid dispersion containing at least about 100 mg of substantially amorphous or amorphous Compound 1.
  • Yet other tablets useful in this method comprise a solid dispersion containing at least about 150 mg of substantially amorphous or amorphous Compound 1.
  • the administration comprises orally administering to a patient at least once per day at least one tablet comprising a solid dispersion of substantially amorphous or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, in which the solid dispersion contains at least about 250 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient at least once per day at least one tablet comprising a solid dispersion of substantially amorphous or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, in which the solid dispersion comprises up to about 5 mg of substantially amorphous or amorphous Compound 1.
  • the solid dispersion comprises 0.5 mg, 0.75 mg, 1 mg, 2 mg, 3 mg, 4 mg, or 5 mg of substantially amorphous or amorphous Compound 1.
  • the tablet is orally administered to the patient once per day.
  • the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient at least once per day at least one tablet comprising a solid dispersion of substantially amorphous or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, in which the solid dispersion comprises up to about 1 mg of substantially amorphous or amorphous Compound 1.
  • the solid dispersion comprises 0.5 mg, 0.75 mg, or 1 mg of substantially amorphous or amorphous Compound 1.
  • the tablet is orally administered to the patient once per day.
  • the present invention provides for a method of orally administering the pharmaceutical compositions described herein at least once a day. In other embodiments, the present invention provides for a method of orally administering the pharmaceutical composition described herein once a day. In some embodiments, the present invention provides for a method of orally administering the pharmaceutical composition described herein twice a day.
  • the invention also provides a method of treating or lessening the severity of a disease in a patient comprising administering to said patient one of the compositions as defined herein, and said disease is selected from cystic fibrosis, asthma, smoke induced COPD, chronic bronchitis, rhinos inusitis, constipation, pancreatitis, pancreatic insufficiency, male infertility caused by congenital bilateral absence of the vas deferens (CBAVD), mild pulmonary disease, idiopathic pancreatitis, allergic
  • bronchopulmonary aspergillosis liver disease, hereditary emphysema, hereditary hemochromatosis, coagulation-fibrinolysis deficiencies, such as protein C deficiency, Type 1 hereditary angioedema, lipid processing deficiencies, such as familial hypercholesterolemia, Type 1 chylomicronemia, abetalipoproteinemia, lysosomal storage diseases, such as I-cell disease/pseudo-Hurler, mucopolysaccharidoses, Sandhof/Tay-Sachs, Crigler-Najjar type II, polyendocrinopathy/hyperinsulemia, Diabetes mellitus, Laron dwarfism, myleoperoxidase deficiency, primary hypoparathyroidism, melanoma, glycanosis CDG type 1 , congenital hyperthyroidism, osteogenesis imperfecta, hereditary hypofibrinogenemia, ACT defic
  • Figure 1 presents a graphical illustration of the dissolution profiles of exemplary tablets according to the present invention.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of N-[2,4-bis( 1 , 1 -dimethylethyl)-5-hydroxyphenyl]- 1 ,4-dihydro-4-oxoquinoline-3- carboxamide, a method of manufacturing a pharmaceutical composition comprising N-[2,4- bisCl.l-dimethylethyO-S-hydroxyphenylj-l ⁇ -dihydro ⁇ -oxoquinoline-S-carboxamide, and a method of administering a pharmaceutical composition comprising a solid form of N-[2,4- bis(l,l-dimemylethyl)-5-hydroxyphenyl]-l,4-dihydro-4-oxoquinoline-3-carboxamide.
  • API active pharmaceutical ingredient
  • CF potentiator e.g., N-[2,4- bis( 1 ,l-dimethylethyl)-5-hydroxyphenyl]- 1 ,4-dihydro-4-oxoquinoline-3-carboxamide.
  • Compound 1 is used interchangeably with "N-[2,4- bisClJ-dimethylethyO-S-hydroxyphenyll-l ⁇ -dihydro ⁇ -oxoquinoline-S-carboxamide", which has the following structure:
  • Compound 1 also means tautomeric forms such as:
  • amorphous refers to a solid material having no long range order in the position of its molecules.
  • Amorphous solids are generally supercooled liquids in which the molecules are arranged in a random manner so that there is no well- defined arrangement, e.g., molecular packing, and no long range order.
  • Amorphous solids are generally isotropic, i.e. exhibit similar properties in all directions and do not have definite melting points.
  • an amorphous material is a solid material having no sharp characteristic crystalline peak(s) in its X-ray power diffraction (XRPD) pattern (i.e., is not crystalline as determined by XRPD). Instead, one or several broad peaks (e.g., halos) appear in its XRPD pattern. Broad peaks are characteristic of an amorphous solid. See, US
  • substantially amorphous refers to a solid material having little or no long range order in the position of its molecules.
  • substantially amorphous materials have less than about 15% crystallinity (e.g., less than about 10% crystallinity or less than about 5% crystallinity).
  • 'substantially amorphous 1 includes the descriptor, 'amorphous', which refers to materials having no (0%) crystallinity.
  • the term "dispersion” refers to a disperse system in which one substance, the dispersed phase, is distributed, in discrete units, throughout a second substance (the continuous phase or vehicle).
  • the size of the dispersed phase can vary considerably (e.g. single molecules, colloidal particles of nanometer dimension, to multiple microns in size).
  • the dispersed phases can be solids, liquids, or gases. In the case of a solid dispersion, the dispersed and continuous phases are both solids.
  • a solid dispersion can include: an amorphous drug in an amorphous polymer; an amorphous drug in crystalline polymer; a crystalline drug in an amorphous polymer; or a crystalline drug in crystalline polymer.
  • a solid dispersion can include an amorphous drug in an amorphous polymer or an amorphous drug in crystalline polymer.
  • a solid dispersion includes the polymer constituting the dispersed phase, and the drug constitutes the continuous phase.
  • a solid dispersion includes the drug constituting the dispersed phase, and the polymer constitutes the continuous phase.
  • solid dispersion generally refers to a solid dispersion of two or more components, usually one or more drugs (e.g., one drug (e.g., Compound I)) and polymer, but possibly containing other components such as surfactants or other
  • the drug(s) e.g., Compound 1
  • the drug(s) is substantially amorphous (e.g., having about 15% or less (e.g., about 10% or less, or about 5% or less)) of crystalline drug (e.g., N-[2,4-bis(l,l-dimethylethyl)-5-hydroxyphenyl]-l,4-dihydro-4-oxoquinoline-3- carboxamide) or amorphous (i.e., having no crystalline drug), and the physical stability and/or dissolution and/or solubility of the substantially amorphous or amorphous drug is enhanced by the other components.
  • crystalline drug e.g., N-[2,4-bis(l,l-dimethylethyl)-5-hydroxyphenyl]-l,4-dihydro-4-oxoquinoline-3- carboxamide
  • amorphous i.e., having no crystalline drug
  • Solid dispersions typically include a compound dispersed in an appropriate carrier medium, such as a solid state carrier.
  • a carrier comprises a polymer (e.g., a water-soluble polymer or a partially water-soluble polymer) and can include optional excipients such as functional excipients (e.g., one or more surfactants) or nonfunctional excipients (e.g., one or more fillers).
  • Another exemplary solid dispersion is a co-precipitate or a co-melt of N-[2,4-bis(l,l-dimethylethyl)-5- hydroxyphenyl]-l,4-dihydro-4-oxoquinoline-3-carboxamide with at least one polymer.
  • a "Co-precipitate” is a product after dissolving a drug and a polymer in a solvent or solvent mixture followed by the removal of the solvent or solvent mixture. Sometimes the polymer can be suspended in the solvent or solvent mixture.
  • the solvent or solvent mixture includes organic solvents and supercritical fluids.
  • a "co-melt” is a product after heating a drug and a polymer to melt, optionally in the presence of a solvent or solvent mixture, followed by mixing, removal of at least a portion of the solvent if applicable, and cooling to room temperature at a selected rate.
  • crystalstallinity refers to the degree of structural order in a solid.
  • Compound 1 which is substantially amorphous, has less than about 15%
  • crystallinity, or its solid state structure is less than about 15% crystalline.
  • Compound 1, which is amorphous, has zero (0%) crystallinity.
  • CF potentiator refers to a compound that exhibits biological activity characterized by increasing gating functionality of the mutant CFTR protein present in the cell surface to approximately wild type levels.
  • excipient is an inactive ingredient in a pharmaceutical composition.
  • excipients include fillers or diluents, surfactants, binders, glidants, lubricants, disintegrants, and the like.
  • a "disintegrant” is an excipient that hydrates a pharmaceutical composition and aids in tablet dispersion.
  • disintegrants include sodium croscarmellose and/or sodium starch glycolate.
  • a "diluent” or “filler” is an excipient that adds bulkiness to a pharmaceutical composition.
  • fillers include lactose, sorbitol, celluloses, calcium phosphates, starches, sugars (e.g., mannitol, sucrose, or the like) or any combination thereof.
  • a "surfactant” is an excipient that imparts pharmaceutical compositions with enhanced solubility and/or wetability.
  • surfactants include sodium lauryl sulfate (SLS), sodium stearyl fumarate (SSF), polyoxyethylene 20 sorbitan mono-oleate (e.g., TweenTM), or any combination thereof.
  • a "binder” is an excipient that imparts a pharmaceutical composition with enhanced cohesion or tensile strength (e.g., hardness).
  • binders include dibasic calcium phosphate, sucrose, corn (maize) starch, microcrystalline cellulose, and modified cellulose (e.g., hydroxymethyl cellulose).
  • a "glidant” is an excipient that imparts a pharmaceutical compositions with enhanced flow properties. Examples of glidants include colloidal silica and/or talc.
  • a "colorant” is an excipient that imparts a pharmaceutical composition with a desired color.
  • examples of colorants include commercially available pigments such as FD&C Blue # 1 Aluminum Lake, FD&C Blue #2, other FD&C Blue colors, titanium dioxide, iron oxide, and/or combinations thereof.
  • a "lubricant” is an excipient that is added to pharmaceutical compositions that are pressed into tablets.
  • the lubricant aids in compaction of granules into tablets and ejection of a tablet of a pharmaceutical composition from a die press.
  • examples of lubricants include magnesium stearate, stearic acid (stearin), hydrogenated oil, sodium stearyl fumarate, or any combination thereof.
  • Friability refers to the property of a tablet to remain intact and withhold its form despite an external force of pressure. Friability can be quantified using the mathematical expression presented in equation 1 :
  • Vofriabiliy 100x— f — (1)
  • Friability is measured using a standard USP testing apparatus that tumbles experimental tablets for 100 revolutions. Some tablets of the present invention have a friability of less than about 1% (e.g., less than about 0.75%, less than about 0.50%, or less than about 0.30%)
  • mean particle diameter is the average particle diameter as measured using techniques such as laser light scattering, image analysis, or sieve analysis.
  • bulk density is the mass of particles of material divided by the total volume the particles occupy. The total volume includes particle volume, inter-particle void volume and internal pore volume. Bulk density is not an intrinsic property of a material; it can change depending on how the material is processed.
  • the term "pharmaceutically acceptable salt” refers to those salts which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio.
  • a “pharmaceutically acceptable salt” means any non-toxic salt or salt of an ester of a compound of this invention that, upon administration to a recipient, is capable of providing, either directly or indirectly, a compound of this invention or an inhibitorily active metabolite or residue thereof.
  • compositions of this invention include those derived from suitable inorganic and organic acids and bases.
  • Examples of pharmaceutically acceptable, nontoxic acid addition salts are salts of an amino group formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid or with organic acids such as acetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange.
  • inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid
  • organic acids such as acetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange.
  • Other pharmaceutically acceptable salts include adipate, alginate, ascorbate, aspartate, benzenesulfonate, benzoate, bisulfate, borate, butyrate, camphorate,
  • Salts derived from appropriate bases include alkali metal, alkaline earth metal, ammonium and N+(Cl-4alkyl)4 salts.
  • This invention also envisions the quaternization of any basic nitrogen-containing groups of the compounds disclosed herein. Water or oil-soluble or dispersible products may be obtained by such quaternization.
  • Representative alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, and the like.
  • Further pharmaceutically acceptable salts include, when appropriate, nontoxic ammonium, quaternary ammonium, and amine cations formed using counterions such as halide, hydroxide, carboxylate, sulfate, phosphate, nitrate, loweralkyl sulfonate and aryl sulfonate.
  • the present invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising a CF potentiator API (e.g., a solid dispersion of Compound 1).
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1, wherein the solid dispersion comprises up to about 1 mg of substantially amorphous Compound 1.
  • the solid dispersion comprises about 0.5 mg, about 0.75, or about 1 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1, wherein the solid dispersion comprises up to about 5 mg of substantially amorphous Compound 1.
  • the solid dispersion comprises about 0.5 mg, about 0.75, about 1 mg, about 2 mg, about 3 mg, about 4 mg, or about 5 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1, wherein the solid dispersion comprises about 15 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1, wherein the solid dispersion comprises about 25 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1, wherein the solid dispersion comprises about 50 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1, wherein the solid dispersion comprises about 75 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1, wherein the solid dispersion comprises about 100 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1, wherein the solid dispersion comprises about 150 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1, wherein the solid dispersion comprises about 250 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1, wherein the solid dispersion comprises up to about 1 mg of amorphous Compound 1. For instance, the solid dispersion comprises about 0.5 mg, about 0.75, or about 1 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1, wherein the solid dispersion comprises up to about 5 mg of amorphous Compound 1.
  • the solid dispersion comprises about 0.5 mg, about 0.75, about 1 mg, about 2 mg, about 3 mg, about 4 mg, or about 5 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises about 15 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises about 25 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises about 50 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises about 75 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises about 100 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises about 150 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1, wherein the solid dispersion comprises about 250 mg of amorphous Compound 1.
  • Another aspect of the present invention provides a pharmaceutical composition comprising a solid dispersion of Compound 1 in which the solid dispersion comprises a polymer.
  • the present invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises up to about 1 mg of substantially amorphous
  • the solid dispersion comprises about 0.5 mg, about 0.75, or about
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises up to about 5 mg of substantially amorphous
  • the solid dispersion comprises about 0.5 mg, about 0.75, about 1 mg, about 2 mg, about 3 mg, about 4 mg, or about 5 mg of substantially amorphous
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises about 15 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises about 25 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises about 50 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises about 75 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises about 100 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises about 150 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises about 250 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises up to about 1 mg of substantially amorphous Compound 1.
  • the solid dispersion comprises about 0.5 mg, about 0.75, or about 1 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises up to about 5 mg of amorphous
  • the solid dispersion comprises about 0.5 mg, about 0.75, about 1 mg, about 2 mg, about 3 mg, about 4 mg, or about 5 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises about 15 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises about 25 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises about 50 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises about 75 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises about 100 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises about 150 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1 and HPMCAS, wherein the solid dispersion comprises about 250 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and PVP/VA, wherein the solid dispersion comprises about 25 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and PVP/VA, wherein the solid dispersion comprises about 50 mg of substantially amorphous
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 and
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1 and PVP/VA, wherein the solid dispersion comprises about 25 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1 and PVP/VA, wherein the solid dispersion comprises about 50 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1 and PVP/VA, wherein the solid dispersion comprises about 75 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1 and PVP/VA, wherein the solid dispersion comprises about 100 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1 and PVP/VA, wherein the solid dispersion comprises about 150 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising a solid dispersion of amorphous Compound 1 and PVP/VA, wherein the solid dispersion comprises about 250 mg of amorphous Compound 1.
  • One aspect of the present invention provides a pharmaceutical composition
  • a CF potentiator API e.g., a solid dispersion of Compound 1
  • other excipients e.g., a filler, a disintegrant, a surfactant, a binder, a glidant, a colorant, a lubricant, or any combination thereof.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises up to about 1 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises up to about 5 mg of substantially amorphous
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 15 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 25 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 50 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • a surfactant e. a binder
  • solid dispersion comprises about 75 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 100 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 150 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 250 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises up to about 1 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises up to about 5 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 25 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • the solid dispersion comprises about 50 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 75 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • the solid dispersion comprises about 100 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • the solid dispersion comprises about 150 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 250 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 25 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 50 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 75 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • a lubricant wherein the solid dispersion comprises about 100 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 150 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 250 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • the present invention provides a pharmaceutical composition comprising:
  • the solid dispersion comprises about 50 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 75 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • the solid dispersion comprises about 100 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • the solid dispersion comprises about 150 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 250 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises up to about 1 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises up to about 5 mg of substantially amorphous
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 15 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 25 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • a lubricant wherein the solid dispersion comprises about 50 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 75 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 100 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • a lubricant wherein the solid dispersion comprises about 150 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 250 mg of substantially amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises up to about 1 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 15 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 25 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • the solid dispersion comprises about 50 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 75 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • the solid dispersion comprises about 100 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • the solid dispersion comprises about 150 mg of amorphous Compound 1.
  • the present invention provides a pharmaceutical composition comprising:
  • solid dispersion comprises about 250 mg of amorphous Compound 1.
  • the pharmaceutical composition comprises a solid dispersion, a filler, a disintegrant, a surfactant, a binder, a glidant, and a lubricant, wherein the solid dispersion comprises Compound 1 and a polymer.
  • the pharmaceutical composition comprises a solid dispersion a filler, a disintegrant, a surfactant, a binder, a glidant, and a lubricant, wherein the solid dispersion comprises from about 45 wt% to about 65 wt% (e.g., about 50 wt%) of Compound 1 by weight of the dispersion and a polymer.
  • the pharmaceutical composition comprises a solid dispersion a filler, a disintegrant, a surfactant, a binder, a glidant, and a lubricant, wherein the solid dispersion comprises from about 75 wt% to about 95 wt% (e.g., about 80 wt%) of Compound 1 by weight of the dispersion and a polymer.
  • 5-hydroxyphenyl]-l,4-dihydro-4-oxoquinoline-3-carboxamide include, without limitation, those dispersions described in PCT publication no. WO 2007/079139, which is hereby incorporated by reference in its entirety.
  • the pharmaceutical composition of the present invention comprises a solid dispersion of Compound 1.
  • the solid dispersion comprises substantially amorphous Compound 1, where Compound 1 is less than about 15% (e.g., less than about 10% or less than about 5%) crystalline, and at least one polymer.
  • the solid dispersion comprises amorphous Compound 1, i.e., Compound 1 has about 0% crystallinity.
  • concentration of Compound 1 in the solid dispersion depends on several factors such as the amount of pharmaceutical composition needed to provide a desired amount of Compound 1 and the desired dissolution profile of the pharmaceutical
  • Polymers useful in these solid dispersions are inert, pharmaceutically acceptable polymers that are at least partially soluble in water or biological fluids.
  • Polymers can include homopolymers (e.g., polysaccharides) or copolymers (e.g., block copolymers).
  • the solid dispersion comprises substantially amorphous or amorphous N- [2,4-bis(l,l-dimethylethyl)-5-hydroxyphenyl]-l,4-dihydro-4-oxoquinoline-3-carboxamide and at least one polymer independently selected from hydroxypropylmethylcellulose
  • HPMC hydroxypropylmethylcellulose acetate succinate
  • the solid dispersion comprises substantially amorphous or amorphous N-[2,4-bis(l,l-dimethylethyl)-5-hydroxyphenyl]-l,4-dihydro-4- oxoquinoline-3-carboxamide and HPMCAS or PVP/VA.
  • the pharmaceutical composition comprises a solid dispersion that contains substantially amorphous Compound 1 and HPMCAS or PVP/V A, in which the solid dispersion has a mean particle diameter, measured by light scattering (e.g., using a Malvern Mastersizer available from Malvern Instruments in England) of greater than about 5 ⁇ m (e.g., greater than about 6 ⁇ m, greater than about 7 ⁇ m, greater than about 8 ⁇ m, or greater than about 10 ⁇ m).
  • a mean particle diameter measured by light scattering (e.g., using a Malvern Mastersizer available from Malvern Instruments in England) of greater than about 5 ⁇ m (e.g., greater than about 6 ⁇ m, greater than about 7 ⁇ m, greater than about 8 ⁇ m, or greater than about 10 ⁇ m).
  • the pharmaceutical composition comprises a solid dispersion that contains amorphous Compound 1 and HPMCAS or PVP/VA, in which the solid dispersion has a mean particle diameter, measured by light scattering, of greater than about 5 ⁇ m (e.g., greater than about 6 ⁇ m, greater than about 7 ⁇ m, greater than about 8 ⁇ m, or greater than about 10 ⁇ m).
  • the pharmaceutical composition comprises a solid dispersion comprising substantially amorphous Compound 1 and HPMCAS, in which the solid dispersion has a mean particle diameter, measured by light scattering, of from about 7 ⁇ m to about 25 ⁇ m.
  • the pharmaceutical composition comprises a solid dispersion comprising amorphous Compound 1 and HPMCAS, in which the solid dispersion has a mean particle diameter, measured by light scattering, of from about 7 ⁇ m to about 25 ⁇ m.
  • the pharmaceutical composition comprises a solid dispersion comprising substantially amorphous Compound 1 and HPMCAS, in which the solid dispersion has a mean particle diameter, measured by light scattering, of from about 10 ⁇ m to about 35 ⁇ m.
  • the pharmaceutical composition comprises a solid dispersion comprising amorphous Compound 1 and HPMCAS, in which the solid dispersion has a mean particle diameter, measured by light scattering, of from about 10 ⁇ m to about 35 ⁇ m.
  • the pharmaceutical composition comprises a solid dispersion comprising substantially amorphous Compound 1 and HPMCAS or PVP/VA, in which the solid dispersion has a bulk density of about 0.10 g/cc or greater (e.g., 0.15 g/cc or greater, 0.17 g/cc or greater).
  • the pharmaceutical composition comprising a solid dispersion comprising amorphous Compound 1 and HPMCAS or PVP/VA, in which the solid dispersion has a bulk density of about 0.10 g/cc or greater (e.g., 0.15 g/cc or greater, 0.17 g/cc or greater).
  • the pharmaceutical composition comprises a solid dispersion that comprises substantially amorphous Compound 1 and HPMCAS or PVP/VA, in which the solid dispersion has a bulk density of from about 0.10 g/cc to about 0.45 g/cc (e.g., from about 0.15 g/cc to about 0.42 g/cc, or from about 0.17 g/cc to about 0.40 g/cc).
  • the pharmaceutical composition comprises a solid dispersion that includes amorphous Compound 1 and HPMCAS or PVP/VA, in which the solid dispersion has a bulk density of from about 0.10 g/cc to about 0.45 g/cc (e.g., from about 0.15 g/cc to about 0.42 g/cc, or from about 0.17 g/cc to about 0.40 g/cc).
  • the pharmaceutical composition comprises a solid dispersion that comprises substantially amorphous Compound 1 and HPMCAS, in which the solid dispersion has a bulk density of from about 0.10 g/cc to about 0.45 g/cc (e.g., from about 0.15 g/cc to about 0.42 g/cc, or from about 0.17 g/cc to about 0.40 g/cc).
  • the pharmaceutical composition includes a solid dispersion that comprises amorphous Compound 1 and HPMCAS, in which the solid dispersion has a bulk density of from about 0.10 g/cc to about 0.45 g/cc (e.g., from about 0.15 g/cc to about 0.42 g/cc, or from about 0.17 g/cc to about 0.40 g/cc).
  • Alternative solid dispersions comprise substantially amorphous or amorphous
  • Compound 1 and HPMCAS or PVP/VA wherein substantially amorphous Compound 1 or amorphous Compound 1 is present in an amount of at least 20 wt% (e.g., at least 40 wt%, at least 45 wt%, at least 49 wt%, or at least 50 wt%) by weight of the solid dispersion.
  • the solid dispersion comprises HPMCAS or PVP/VA and from about 20 wt% to about 99 wt% (e.g., from about 40 wt% to about 90 wt%, from about 42 wt% to about 88 wt%, from about 45 wt% to about 85 wt%, or from about 50 wt% to about 80 wt%) of substantially amorphous or amorphous Compound 1 by weight of the solid dispersion.
  • HPMCAS or PVP/VA from about 20 wt% to about 99 wt% (e.g., from about 40 wt% to about 90 wt%, from about 42 wt% to about 88 wt%, from about 45 wt% to about 85 wt%, or from about 50 wt% to about 80 wt%) of substantially amorphous or amorphous Compound 1 by weight of the solid dispersion.
  • the solid dispersion comprises HPMCAS or PVP/VA and from about 40 wt% to about 60 wt% (e.g., from about 42 wt% to about 57 wt%, from about 45 wt% to about 55 wt%, or from about 47 wt% to about 53 wt%) of substantially amorphous or amorphous Compound 1 by weight of the solid dispersion.
  • the solid dispersion comprises HPMCAS or PVP/VA and from about 65 wt% to about 95 wt% (e.g., from about 67 wt% to about 92 wt%, from about 70 wt% to about 90 wt%, or from about 72 wt% to about 88 wt%) of substantially amorphous Compound 1 or amorphous Compound 1 by weight of the solid dispersion.
  • the solid dispersion comprises 80 wt% or less (e.g., 60 wt% or less, 55 wt% or less, or 50 wt% or less) of polymer (e.g., HPMCAS, PVP/VA, PVP, methacrylic acid/methacrylate copolymer, HPC, or any combination thereof) by weight of solid dispersion.
  • polymer e.g., HPMCAS, PVP/VA, PVP, methacrylic acid/methacrylate copolymer, HPC, or any combination thereof
  • the solid dispersion comprises from about 1 wt% to about 80 wt% (e.g., from about 10 wt% to about 60 wt%) of polymer (e.g., HPMCAS, PVP/VA, PVP, methacrylic acid/methacrylate copolymer, HPC, or any combination thereof).
  • polymer e.g., HPMCAS, PVP/VA, PVP, methacrylic acid/methacrylate copolymer, HPC, or any combination thereof.
  • Some solid dispersions comprise from about 40 wt% to about 60 wt% (e.g., from about 42 wt% to about 57 wt%, from about 45 wt% to about 55 wt%, or from about 47 wt% to about 53 wt%) of substantially amorphous Compound 1 by weight of the solid dispersion and from about 60 wt% to about 40 wt% of polymer (e.g., HPMCAS, PVP/VA, PVP, methacrylic acid/methacrylate copolymer, HPC, or any combination thereof-
  • Alternative solid dispersions comprise from about 40 wt% to about 60 wt% (e.g., from about 42 wt% to about 57 wt%, from about 45 wt% to about 55 wt%, or from about 47 wt% to about 53 wt%) of amorphous Compound 1 by weight of the solid dispersion and from about 60 wt% to about 40 wt% of
  • HPC acid/methacrylate copolymer
  • Other solid dispersions comprise from about 65 wt% to about 95 wt% (e.g., from about 67 wt% to about 92 wt%, from about 70 wt% to about 90 wt%, or from about 72 wt% to about 88 wt%) of substantially amorphous Compound 1 by weight of the solid dispersion and from about 45 wt% to about 5 wt% of polymer (e.g., HPMCAS, PVP/VA, PVP, methacrylic acid/methacrylate copolymer, HPC, or any combination thereof).
  • polymer e.g., HPMCAS, PVP/VA, PVP, methacrylic acid/methacrylate copolymer, HPC, or any combination thereof.
  • the solid dispersion comprises from about 65 wt% to about 95 wt% (e.g., from about 67 wt% to about 92 wt%, from about 70 wt% to about 90 wt%, or from about 72 wt% to about 88 wt%) of amorphous Compound 1 by weight of the solid dispersion and from about 45 wt% to about 5 wt% of polymer (e.g., HPMCAS, PVP/VA, PVP, methacrylic acid/methacrylate copolymer, HPC, or any combination thereof).
  • polymer e.g., HPMCAS, PVP/VA, PVP, methacrylic acid/methacrylate copolymer, HPC, or any combination thereof.
  • Solid dispersions useful in embodiments of the present invention can optionally comprise a surfactant.
  • Suitable surfactants include sodium lauryl sulfate (SLS), sodium stearyl fumarate (SSF), polyoxyethylene 20 sorbitan mono-oleate (e.g., TweenTM), any combination thereof, or the like.
  • the solid dispersion comprises less than 5 wt% (less than 3.0 wt%, less than 1.5 wt%, or less than 1.0 wt%) of surfactant by weight of solid dispersion.
  • the solid dispersion comprises from about 0.30 wt% to about 0.80 wt% (e.g., from about 0.35 wt% to about 0.70 wt%, from about 0.40 wt% to about 0.60 wt%, or from about 0.45 wt% to about 0.55 wt%) of surfactant by weight of solid dispersion.
  • the solid dispersion comprises from about 45 wt% to about 85 wt% of substantially amorphous or amorphous Compound 1, from about 0.45 wt% to about 0.55 wt% of SLS, and from about 14.45 wt% to about 55.55 wt% of HPMCAS or PVP/VA by weight of the solid dispersion.
  • One exemplary solid dispersion contains about 50 wt% of substantially amorphous or amorphous Compound 1, about 49.5 wt% of HPMCAS or PVP/VA, and about 0.5 wt% of SLS, by weight of the solid dispersion.
  • Another exemplary solid dispersion contains about 80 wt% of substantially amorphous or amorphous Compound 1, about 19.5 wt% of HPMCAS or PVP/VA, and about 0.5 wt% of SLS.
  • the solid dispersion comprises from about 45 wt% to about 85 wt% of substantially amorphous or amorphous Compound 1, from about 0.45 wt% to about 0.55 wt% of SLS, and from about 14.45 wt% to about 55.55 wt% of HPMCAS by weight of the solid dispersion.
  • One exemplary solid dispersion contains about 50 wt% of substantially amorphous or amorphous Compound 1, about 49.5 wt% of HPMCAS, and about 0.5 wt% of SLS, by weight of the solid dispersion.
  • Another exemplary solid dispersion contains about 80 wt% of substantially amorphous or amorphous Compound 1, about 19.5 wt% of HPMCAS or PVP/VA, and about 0.5 wt% of SLS.
  • compositions of the present invention also comprise one or more excipients such as fillers, disintegrants, surfactants, binders, glidants, lubricants, colorants, or fragrances.
  • excipients such as fillers, disintegrants, surfactants, binders, glidants, lubricants, colorants, or fragrances.
  • Fillers suitable for the present invention are compatible with the ingredients of the pharmaceutical composition, i.e., they do not substantially reduce the solubility, the hardness, the chemical stability, the physical stability, or the biological activity of the pharmaceutical composition.
  • Exemplary fillers include lactose, sorbitol, celluloses, calcium phosphates, starches, sugars (e.g., mannitol, sucrose, or the like), or any combination thereof.
  • the pharmaceutical composition comprises at least one filler in an amount of at least about 10 wt% (e.g., at least about 20 wt%, at least about 25 wt%, or at least about 27 wt%) by weight of the composition.
  • the pharmaceutical composition comprises from about 10 wt% to about 60 wt% (e.g., from about 20 wt% to about 55 wt%, from about 25 wt% to about 50 wt%, or from about 27 wt% to about 45 wt%) of filler, by weight of the composition.
  • the pharmaceutical composition comprises at least about 20 wt% (e.g., at least 25 wt% or at least 27 wt%) of lactose, by weight of the composition.
  • the pharmaceutical composition comprises from about 20 wt% to about 60 wt% (e.g., from about 25 wt% to about 55 wt% or from about 27 wt% to about 45 wt%) of lactose, by weight of the composition.
  • Disintegrants suitable for the present invention enhance the dispersal of the pharmaceutical composition and are compatible with the ingredients of the pharmaceutical composition, i.e., they do not substantially reduce the chemical stability, the physical stability, the hardness, or the biological activity of the pharmaceutical composition.
  • exemplary disintegrants include sodium croscarmellose, sodium starch glycolate, or a combination thereof.
  • the pharmaceutical composition comprises disintegrant in an amount of about 10 wt% or less (e.g., about 7 wt% or less, about 6 wt% or less, or about 5 wt% or less) by weight of the composition.
  • the pharmaceutical composition comprises from about 1 wt% to about 10 wt% (e.g., from about 1.5 wt% to about 7.5 wt% or from about 2.5 wt% to about 6 wt%) of disintegrant, by weight of the
  • the pharmaceutical composition comprises about 10 wt% or less (e.g., 7 wt% or less, 6 wt% or less, or 5 wt% or less) of sodium croscarmellose, by weight of the composition.
  • the pharmaceutical composition comprises from about 1 wt% to about 10 wt% (e.g., from about 1.5 wt% to about 7.5 wt% or from about 2.5 wt% to about 6 wt%) of sodium croscarmellose, by weight of the
  • the pharmaceutical composition comprises from about 0.1% to about 10 wt% (e.g., from about 0.5 wt% to about 7.5 wt% or from about 1.5 wt% to about 6 wt%) of disintegrant, by weight of the composition.
  • the pharmaceutical composition comprises from about 0.1% to about 10 wt% (e.g., from about 0.5 wt% to about 7.5 wt% or from about 1.5 wt% to about 6 wt%) of disintegrant, by weight of the composition.
  • composition comprises from about 0.5% to about 10 wt% (e.g., from about 1.5 wt% to about 7.5 wt% or from about 2.5 wt% to about 6 wt%) of disintegrant, by weight of the composition.
  • Surfactants suitable for the present invention enhance the solubility of the pharmaceutical composition and are compatible with the ingredients of the pharmaceutical composition, i.e., they do not substantially reduce the chemical stability, the physical stability, the hardness, or the biological activity of the pharmaceutical composition.
  • the pharmaceutical composition comprises a surfactant in an amount of about 10 wt% or less (e.g., about 5 wt% or less, about 2 wt% or less, about 1 wt% or less, about 0.8 wt% or less, or about 0.6 wt% or less) by weight of the composition.
  • the pharmaceutical composition includes from about 10 wt% to about 0.1 wt% (e.g., from about 5 wt% to about 0.2 wt% or from about 2 wt% to about 0.3 wt%) of surfactant, by weight of the composition.
  • the pharmaceutical composition comprises 10 wt% or less (e.g., about 5 wt% or less, about 2 wt% or less, about 1 wt% or less, about 0.8 wt% or less, or about 0.6 wt% or less) of sodium lauryl sulfate, by weight of the composition.
  • the pharmaceutical composition comprises from about 10 wt% to about 0.1 wt% (e.g., from about 5 wt% to about 0.2 wt% or from about 2 wt% to about 0.3 wt%) of sodium lauryl sulfate, by weight of the composition.
  • Binders suitable for the present invention enhance the tablet strength of the pharmaceutical composition and are compatible with the ingredients of the pharmaceutical composition, i.e., they do not substantially reduce the chemical stability, the physical stability, or the biological activity of the pharmaceutical composition.
  • Exemplary binders include microcrystalline cellulose, dibasic calcium phosphate, sucrose, corn (maize) starch, modified cellulose (e.g., hydroxymethyl cellulose), or any combination thereof.
  • the pharmaceutical composition comprises a binder in an amount of at least about 1 wt% (e.g., at least about 10 wt%, at least about 15 wt%, at least about 20 wt%, or at least about 22 wt%) by weight of the composition.
  • the pharmaceutical composition comprises from about 5 wt% to about 50 wt% (e.g., from about 10 wt% to about 45 wt% or from about 20 wt% to about 45 wt%) of binder, by weight of the composition.
  • the pharmaceutical composition comprises at least about 1 wt% (e.g., at least about 10 wt%, at least about 15 wt%, at least about 20 wt%, or at least about 22 wt%) of microcrystalline cellulose, by weight of the composition.
  • the pharmaceutical composition comprises from about 5 wt% to about 50 wt% (e.g., from about 10 wt% to about 45 wt% or from about 20 wt% to about 45 wt%) of microcrystalline cellulose, by weight of the composition.
  • Glidants suitable for the present invention enhance the flow properties of the pharmaceutical composition and are compatible with the ingredients of the pharmaceutical composition, i.e., they do not substantially reduce the solubility, the hardness, the chemical stability, the physical stability, or the biological activity of the pharmaceutical composition.
  • exemplary glidants include colloidal silicon dioxide, talc, or a combination thereof.
  • the pharmaceutical composition comprises a glidant in an amount of 2 wt% or less (e.g., 1.75 wt%, 1.25 wt% or less, or 1.00 wt% or less) by weight of the composition.
  • the pharmaceutical composition comprises from about 2 wt% to about 0.05 wt% (e.g., from about 1.5 wt% to about 0.07 wt% or from about 1.0 wt% to about 0.09 wt%) of glidant, by weight of the composition.
  • the pharmaceutical composition comprises 2 wt% or less (e.g., 1.75 wt%, 1.25 wt% or less, or 1.00 wt% or less) of colloidal silicon dioxide, by weight of the composition.
  • the pharmaceutical composition comprises from about 2 wt% to about 0.05 wt% (e.g., from about 1.5 wt% to about 0.07 wt% or from about 1.0 wt% to about 0.09 wt%) of colloidal silicon dioxide, by weight of the composition.
  • Lubricants suitable for the present invention improve the compression and ejection of compressed pharmaceutical compositions from a die press and are compatible with the ingredients of the pharmaceutical composition, i.e., they do not substantially reduce the solubility, the hardness, or the biological activity of the pharmaceutical composition.
  • Exemplary lubricants include magnesium stearate, stearic acid (stearin), hydrogenated oil, sodium stearyl fumarate, or any combination thereof.
  • the lubricants suitable for the present invention improve the compression and ejection of compressed pharmaceutical compositions from a die press and are compatible with the ingredients of the pharmaceutical composition, i.e., they do not substantially reduce the solubility, the hardness, or the biological activity of the pharmaceutical composition.
  • Exemplary lubricants include magnesium stearate, stearic acid (stearin), hydrogenated oil, sodium stearyl fumarate, or any combination thereof.
  • the stearin stearic acid
  • hydrogenated oil sodium stearyl fumarate
  • the pharmaceutical composition comprises a lubricant in an amount of 2 wt% or less (e.g., 1.75 wt%, 1.25 wt% or less, or 1.00 wt% or less) by weight of the composition.
  • the pharmaceutical composition comprises from about 2 wt% to about 0.10 wt% (e.g., from about 1.5 wt% to about 0.15 wt% or from about 1.3 wt% to about 0.30 wt%) of lubricant, by weight of the composition.
  • the pharmaceutical composition comprises 2 wt% or less (e.g., 1.75 wt%, 1.25 wt% or less, or 1.00 wt% or less) of magnesium stearate, by weight of the composition.
  • the pharmaceutical composition comprises from about 2 wt% to about 0.10 wt% (e.g., from about 1.5 wt% to about 0.15 wt% or from about 1.3 wt% to about 0.30 wt%) of magnesium stearate, by weight of the composition.
  • compositions of the present invention can optionally comprise one or more colorants, flavors, and/or fragrances to enhance the visual appeal, taste, and/or scent of the composition.
  • Suitable colorants, flavors, or fragrances are compatible with the ingredients of the pharmaceutical composition, i.e., they do not substantially reduce the solubility, the chemical stability, the physical stability, the hardness, or the biological activity of the pharmaceutical composition.
  • the pharmaceutical composition comprises a colorant, a flavor, and/or a fragrance.
  • the pharmaceutical composition comprises less than about 1 wt% (e.g., less than about 0.75 wt% or less than about 0.5 wt%) of each optionally ingredient, i.e., colorant, flavor and/or fragrance, by weight of the composition.
  • the pharmaceutical composition comprises less than about 1 wt% (e.g., less than about 0.75 wt% or less than about 0.5 wt%) of a colorant. In still another example, the pharmaceutical composition comprises less than about 1 wt% (e.g., less than about 0.75 wt% or less than about 0.5 wt%) of a blue colorant (e.g., FD&C Blue #1 and/or FD&C Blue #2 Aluminum Lake, commercially available from Colorcon, Inc. of West Point, PA.)
  • a blue colorant e.g., FD&C Blue #1 and/or FD&C Blue #2 Aluminum Lake, commercially available from Colorcon, Inc. of West Point, PA.
  • the pharmaceutical composition can be made into tablets and the tablets can be coated with a colorant and optionally labeled with a logo, other image and/or text using a suitable ink.
  • the pharmaceutical composition can be made into tablets and the tablets can be coated with a colorant, waxed, and optionally labeled with a logo, other image and/or text using a suitable ink.
  • Suitable colorants and inks are compatible with the ingredients of the pharmaceutical composition, i.e., they do not substantially reduce the solubility, the chemical stability, the physical stability, the hardness, or the biological activity of the pharmaceutical composition.
  • the suitable colorants and inks can be any color and are water based or solvent based.
  • tablets made from the pharmaceutical composition are coated with a colorant and then labeled with a logo, other image, and/or text using a suitable ink.
  • tablets comprising pharmaceutical composition as described herein can be coated with about 3 wt% (e.g., less than about 6 wt% or less than about 4 wt%) of film coating comprising a colorant.
  • the colored tablets can be labeled with a logo and text indicating the strength of the active ingredient in the tablet using a suitable ink.
  • tablets comprising pharmaceutical composition as described herein can be coated with about 3 wt% (e.g., less than about 6 wt% or less than about 4 wt%) of a film coating comprising a blue colorant (e.g., OPADR Y® II, commercially available from Colorcon, Inc. of West Point, PA.).
  • a blue colorant e.g., OPADR Y® II, commercially available from Colorcon, Inc. of West Point, PA.
  • the colored tablets can be labeled with a logo and text indicating the strength of the active ingredient in the tablet using a black ink (e.g., Opacode® WB, commercially available from Colorcon, Inc. of West Point, PA.).
  • tablets made from the pharmaceutical composition are coated with a colorant, waxed, and then labeled with a logo, other image, and/or text using a suitable ink.
  • tablets comprising pharmaceutical composition as described herein can be coated with about 3 wt% (e.g., less than about 6 wt% or less than about 4 wt%) of film coating comprising a colorant.
  • the colored tablets can be waxed with Carnauba wax powder weighed out in the amount of about 0.01% w/w of the starting tablet core weight.
  • the waxed tablets can be labeled with a logo and text indicating the strength of the active ingredient in the tablet using a suitable ink.
  • tablets comprising pharmaceutical composition as described herein can be coated with about 3 wt% (e.g., less than about 6 wt% or less than about 4 wt%) of a film coating comprising a blue colorant (e.g., OPADRY® II, commercially available from Colorcon, Inc. of West Point, PA.).
  • a blue colorant e.g., OPADRY® II, commercially available from Colorcon, Inc. of West Point, PA.
  • the colored tablets can be waxed with Carnauba wax powder weighed out in the amount of about 0.01% w/w of the starting tablet core weight.
  • the waxed tablets can be labeled with a logo and text indicating the strength of the active ingredient in the tablet using a black ink (e.g., Opacode® S-l-17823 - a solvent based ink, commercially available from Colorcon, Inc. of West Point, PA.).
  • a black ink e.g., Opacode® S-l
  • One exemplary pharmaceutical composition comprises from about 5 wt% to about 50 wt% (e.g., from about 5 wt% to about 25 wt%, from about 15 wt% to about 40 wt%, or from about 30 wt% to about 50 wt%) of a solid dispersion, by weight of the composition, comprising from about 40 wt% to about 60 wt% of substantially amorphous Compound 1, by weight of the dispersion, and from about 60 wt% to about 40 wt% of a polymer, by weight of the dispersion; from about 25 wt% to about 50 wt% of a filler; from about 1 wt% to about 10 wt% of a disintegrant; from about 2 wt% to about 0.3 wt% of a surfactant; from about 5 wt% to about 50 wt% of a binder; from about 2 wt% to about 0.05 wt% of a glid
  • the pharmaceutical composition comprises from about 5 wt% to about 50 wt% (e.g., from about 5 wt% to about 25 wt%, from about 15 wt% to about 40 wt%, or from about 30 wt% to about 50 wt%) of a solid dispersion, by weight of the composition, comprising from about 40 wt% to about 60 wt% of amorphous Compound 1, by weight of the dispersion, and from about 60 wt% to about 40 wt% of a polymer, by weight of the dispersion; from about 25 wt% to about 50 wt% of a filler; from about 1 wt% to about 10 wt% of a disintegrant; from about 2 wt% to about 0.3 wt% of a surfactant; from about 5 wt% to about 50 wt% of a binder; from about 2 wt% to about 0.05 wt% of a glidant; and from about 5
  • Another exemplary pharmaceutical composition comprises from about 5 wt% to about 50 wt% (e.g., from about 5 wt% to about 25 wt%, from about 15 wt% to about 40 wt%, or from about 30 wt% to about 50 wt%) of a solid dispersion, by weight of the composition, comprising from about 70 wt% to about 90 wt% of substantially amorphous Compound 1, by weight of the dispersion, and from about 30 wt% to about 10 wt% of a polymer, by weight of the dispersion; from about 25 wt% to about 50 wt% of a filler; from about 1 wt% to about 10 wt% of a disintegrant; from about 2 wt% to about 0.3 wt% of a surfactant; from about 5 wt% to about 50 wt% of a binder; from about 2 wt% to about 0.05 wt% of a glid
  • composition comprises from about 5 wt% to about 50 wt% (e.g., from about 5 wt% to about 25 wt%, from about 15 wt% to about 40 wt%, or from about 30 wt% to about 50 wt%) of a solid dispersion, by weight of the composition, comprising from about 70 wt% to about 90 wt% of amorphous Compound 1, by weight of the dispersion, and from about 30 wt% to about 10 wt% of a polymer, by weight of the dispersion; from about 25 wt% to about 50 wt% of a filler; from about 1 wt% to about 10 wt% of a disintegrant; from about 2 wt% to about 0.3 wt% of a surfactant; from about 5 wt% to about 50 wt% of a binder; from about 2 wt% to about 0.05 wt% of a glidant; and from about 2 w
  • One pharmaceutical composition of the present invention comprises about 15 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 50 wt% of substantially amorphous Compound 1 by weight of the dispersion, about 49.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 35 wt% of microcrystalline cellulose by weight of the composition; about 43 wt% of lactose by weight of the composition; about 5 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.125 wt% of colloidal silicon dioxide by weight of the composition; and about 0.5 wt% of magnesium stearate by weight of the composition.
  • the pharmaceutical composition of the present invention comprises about 15 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 50 wt% of amorphous Compound 1 by weight of the dispersion, about 49.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 35 wt% of microcrystalline cellulose by weight of the composition; about 43 wt% of lactose by weight of the composition; about 5 wt% of ssooddium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.125 wt% of colloidal silicon dioxide by weight of the composition; and about 0.5 wt% of magnesium stearate by weight of the composition.
  • Another pharmaceutical composition of the present invention comprises about
  • the dispersion comprises about 50 wt% of substantially amorphous Compound 1 by weight of the dispersion, about 49.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 25 wt% of microcrystalline cellulose by weight of the composition; about 38 wt% of lactose by weight of the composition; about 5 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.125 wt% of colloidal silicon dioxide by weight of the composition; and about 0.5 wt% of magnesium stearate by weight of the composition.
  • the pharmaceutical composition of the present invention comprises about 31 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 50 wt% of amorphous Compound 1 by weight of the dispersion, about 49.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 25 wt% of microcrystalline cellulose by weight of the composition; about 38 wt% of lactose by weight of the composition; about 5 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.125 wt% of colloidal silicon dioxide by weight of the composition; and about 0.5 wt% of magnesium stearate by weight of the composition.
  • Another pharmaceutical composition of the present invention comprises about
  • the dispersion comprises about 80 wt% of substantially amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of PVP/VA by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 27 wt% of microcrystalline cellulose by weight of the composition; about 27 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 1 wt% of colloidal silicon dioxide by weight of the composition; about 1 wt% of magnesium stearate by weight of the composition, and about 0.4 wt% of colorant by weight of the composition.
  • the pharmaceutical composition of the present invention comprises about 40 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of PVP/VA by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 27 wt% of microcrystalline cellulose by weight of the composition; about 27 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 1 wt% of colloidal silicon dioxide by weight of the composition; about 1 wt% of magnesium stearate by weight of the composition, and about 0.4 wt% of colorant by weight of the composition.
  • Another pharmaceutical composition of the present invention comprises about
  • the dispersion comprises about 80 wt% of substantially amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 27 wt% of microcrystalline cellulose by weight of the composition; about 27 wt% of lactose by weight of the composition; about 3 wt% of spdium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 1 wt% of colloidal silicon dioxide by weight of the composition; about 1 wt% of magnesium stearate by weight of the composition, and about 0.4 wt% of colorant by weight of the composition.
  • the pharmaceutical composition of the present invention comprises about 40 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 27 wt% of microcrystalline cellulose by weight of the composition; about 27 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 1 wt% of colloidal silicon dioxide by weight of the composition; about 1 wt% of magnesium stearate by weight of the composition, and about 0.4 wt% of colorant by weight of the composition.
  • composition of the present invention comprises about 34.5 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30 wt% of microcrystalline cellulose by weight of the composition; about 30 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 1 wt% of colloidal silicon dioxide by weight of the composition; about 1 wt% of magnesium stearate by weight of the composition.
  • a caplet shaped pharmaceutical tablet composition having a hardness of 9.5 Kp ⁇ 15 percent comprises about 34 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30 wt% of microcrystalline cellulose by weight of the composition; about 30 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 1 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the caplet shaped pharmaceutical tablet contains 150 mg of Compound 1.
  • the caplet shaped pharmaceutical tablet contains 150 mg of Compound 1.
  • a caplet shaped pharmaceutical tablet composition having an initial hardness of 11 Kp ⁇ 20 percent comprises about 40 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30 wt% of microcrystalline cellulose by weight of the composition; about 30 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 1 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the caplet shaped pharmaceutical tablet contains 150 mg of Compound 1.
  • a caplet shaped pharmaceutical tablet composition having an initial hardness of 11 Kp ⁇ 20 percent comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30 wt% of microcrystalline cellulose by weight of the composition; about 30.4 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 1 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the caplet shaped pharmaceutical tablet composition contains 100 mg of Compound 1. In other aspects, the caplet shaped pharmaceutical tablet composition includes a colorant coating and a printed logo or text. In some embodiments of this aspect, the caplet shaped pharmaceutical tablet composition includes a blue OPADRY® II coating and a water or solvent based ink logo or text. In certain embodiments, the caplet shaped pharmaceutical tablet contains 150 mg of Compound 1.
  • a caplet shaped pharmaceutical tablet composition having an initial hardness of between about 6 and 16 Kp comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30.5 wt% of microcrystalline cellulose by weight of the composition; about 30.4 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.5 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the caplet shaped pharmaceutical tablet composition contains 100 mg of Compound 1.
  • the caplet shaped pharmaceutical tablet composition comprises a colorant coated, a wax coating, and a printed logo or text.
  • the caplet shaped pharmaceutical tablet includes a blue OPADRY® II coating and a water or solvent based ink logo or text.
  • the colorant coating is blue OPADRY® II.
  • the wax coating comprises Carnauba wax.
  • the ink for the printed logo or text is a solvent based ink.
  • the caplet shaped pharmaceutical tablet composition contains 100 mg of Compound 1.
  • the caplet shaped pharmaceutical tablet composition comprises a colorant coated, a wax coating, and a printed logo or text.
  • the caplet shaped pharmaceutical tablet includes a blue OPADRY® II coating and a water or solvent based ink logo or text.
  • the colorant coating is blue OPADRY® II.
  • the wax coating comprises Carnauba wax.
  • the ink for the printed logo or text is a solvent based ink.
  • pharmaceutical tablet composition contains 150 mg of Compound 1.
  • a pharmaceutical tablet composition having an initial hardness of between about 9 and 21 Kp comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30.5 wt% of microcrystalline cellulose by weight of the composition; about 30.4 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.5 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the caplet shaped pharmaceutical tablet composition contains 150 mg of Compound 1.
  • the caplet shaped pharmaceutical tablet composition further comprises a colorant coated, a wax coating, and a printed logo or text.
  • the tablet includes a blue OPADR Y® II coating and a water or solvent based ink logo or text.
  • the wax coating comprises Carnauba wax.
  • the ink for the printed logo or text is a solvent based ink.
  • the caplet shaped pharmaceutical tablet composition contains 100 mg of Compound 1.
  • a pharmaceutical composition comprises about 34 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30 wt% of
  • the pharmaceutical composition contains 150 mg of Compound 1. In other embodiments, the pharmaceutical composition contains 100 mg of Compound 1.
  • a pharmaceutical composition comprises about 40 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30 wt% of
  • the pharmaceutical composition contains 150 mg of Compound 1. In other embodiments, the pharmaceutical composition contains 100 mg of Compound 1.
  • a pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0,5 wt% SLS by weight of the dispersion; about 30 wt% of
  • the pharmaceutical composition contains 100 mg of
  • the pharmaceutical composition contains 150 mg of Compound 1.
  • the pharmaceutical composition is formed as a tablet composition that includes a colorant coating and a printed logo or text.
  • the pharmaceutical tablet composition includes a blue OPADR Y® II coating and a water or solvent based ink logo or text.
  • composition comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30.5 wt% of microcrystalline cellulose by weight of the composition; about 30.4 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.5 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the pharmaceutical tablet contains 100 mg of Compound 1. In other embodiments, the pharmaceutical composition contains 150 mg of Compound 1. In some further aspects, the pharmaceutical composition is formed as a tablet and comprises a colorant coated, a wax coating, and a printed logo or text. In some embodiments of this aspect, the pharmaceutical tablet includes a blue OP ADR Y® II coating and a water or solvent based ink logo or text. In some instances, the colorant coating is blue OP ADR Y® II. In some instances, the wax coating comprises Carnauba wax. In certain aspects, the ink for the printed logo or text is a solvent based ink.
  • compositions of the present invention can be processed into a tablet form, capsule form, or suspension that is suited for oral
  • aqueous solvent e.g., DI water or saline
  • inhalation e.g., nebulizer
  • Another aspect of the present invention provides a pharmaceutical
  • composition consisting of a tablet that includes a CF potentiator API (e.g., a solid dispersion of N-[2,4-bis(l,l-dimethylethyl)-5-hydroxyphenyl]-l,4-dihydro-4-oxoquinoline-3- carboxamide) and other excipients (e.g., a filler, a disintegrant, a surfactant, a binder, a glidant, a colorant, a lubricant, or any combination thereof), each of which is described above and in the Examples below, wherein the tablet has a dissolution of at least about 50% (e.g., at least about 60%, at least about 70%, at least about 80%, at least about 90%, or at least about 99%) in about 30 minutes.
  • CF potentiator API e.g., a solid dispersion of N-[2,4-bis(l,l-dimethylethyl)-5-hydroxyphenyl]-l
  • the pharmaceutical composition consists of a tablet that includes a CF potentiator API (e.g., a solid dispersion of Compound 1) and other excipients (e.g., a filler, a disintegrant, a surfactant, a binder, a glidant, a colorant, a lubricant, or any combination thereof), each of which is described above and in the Examples below, wherein the tablet has a dissolution of from about 50% to about 100% (e.g., from about 55% to about 95% or from about 60% to about 90%) in about 30 minutes.
  • a CF potentiator API e.g., a solid dispersion of Compound 1
  • other excipients e.g., a filler, a disintegrant, a surfactant, a binder, a glidant, a colorant, a lubricant, or any combination thereof
  • the pharmaceutical composition consists of a tablet that comprises a solid dispersion comprising substantially amorphous or amorphous Compound 1 and HPMCAS or PVP/VA; and, a filler, a disintegrant, a surfactant, a binder, a glidant, and a lubricant, wherein the tablet has a dissolution of at least about 50% (e.g., at least about 60%, at least about 70%, at least about 80%, at least about 90%, or at least about 99%) in about 30 minutes.
  • a dissolution e.g., at least about 60%, at least about 70%, at least about 80%, at least about 90%, or at least about 99%
  • the pharmaceutical composition consists of a tablet that comprises a solid dispersion comprising substantially amorphous or amorphous Compound 1 and HPMCAS or PVP/VA; and, a filler, a disintegrant, a surfactant, a binder, a glidant, and a lubricant, wherein the tablet has a dissolution of from about 50% to about 100% (e.g., from about 55% to about 95% or from about 60% to about 90%) in about 30 minutes.
  • the tablet comprises a solid dispersion comprising at least about 25 mg (e.g., at least about 30 mg, at least about 40 mg, or at least about 50 mg) of substantially amorphous or amorphous Compound 1; and PVP/VA and SLS.
  • the tablet comprises a solid dispersion comprising at least about 25 mg (e.g., at least about 30 mg, at least about 40 mg, at least about 50 mg, at least about 100 mg, or at least 150 mg) of substantially amorphous or amorphous Compound 1 ; and HPMCAS and SLS.
  • Dissolution can be measured with a standard USP Type II apparatus that employs a dissolution media of 0.6% sodium lauryl sulfate dissolved in 900 mL of DI water, stirring at about 50-75 rpm at a temperature of about 37 0 C. A single experimental tablet is tested in each test vessel of the apparatus. Dissolution can also be measured with a standard USP Type II apparatus that employs a dissolution media of 0.7% sodium lauryl sulfate dissolved in 900 mL of 50 mM sodium phosphate buffer (pH 6.8), stirring at about 65 rpm at a temperature of about 37 0 C. A single experimental tablet is tested in each test vessel of the apparatus.
  • Dissolution can also be measured with a standard USP Type II apparatus that employs a dissolution media of 0.5% sodium lauryl sulfate dissolved in 900 mL of 50 mM sodium phosphate buffer (pH 6.8), stirring at about 65 rpm at a temperature of about 37 0 C. A single experimental tablet is tested in each test vessel of the apparatus.
  • Another aspect of the present invention provides a pharmaceutical
  • composition consisting of a tablet that comprises a CF potentiator API (e.g., a solid dispersion of Compound 1) and other excipients (e.g., a filler, a disintegrant, a surfactant, a binder, a glidant, a colorant, a lubricant, or any combination thereof), each of which is described above and in the Examples below, wherein the tablet has a hardness of at least about 5 Kp.
  • CF potentiator API e.g., a solid dispersion of Compound 1
  • other excipients e.g., a filler, a disintegrant, a surfactant, a binder, a glidant, a colorant, a lubricant, or any combination thereof
  • the pharmaceutical composition consists of a tablet that comprises a CF potentiator API (e.g., a solid dispersion of Compound 1) and other excipients (e.g., a filler, a disintegrant, a surfactant, a binder, a glidant, a colorant, a lubricant, or any combination thereof), each of which is described above and in the Examples below, wherein the tablet has a hardness of at least about 5 Kp (e.g., at least about 5.5, at least about 6 Kp, or at least about 7 Kp).
  • a CF potentiator API e.g., a solid dispersion of Compound 1
  • other excipients e.g., a filler, a disintegrant, a surfactant, a binder, a glidant, a colorant, a lubricant, or any combination thereof
  • Another aspect of the present invention provides a method of producing a pharmaceutical composition
  • a method of producing a pharmaceutical composition comprising providing an admixture of a solid dispersion of substantially amorphous or amorphous N-[2,4-Bis(l,l-dimethylethyl)-5-hydroxyphenyl]-l,4- dihydro-4-oxoquinoline-3-carboxamide, a binder, a glidant, a surfactant, a lubricant, a disintegrant, and a filler, and compressing the admixture into a tablet having a dissolution of at least about 50% in about 30 minutes.
  • the admixture can comprise optional additives such as one or more colorants, one or more flavors, and/or one or more fragrances as described above and in the Examples below.
  • optional additives such as one or more colorants, one or more flavors, and/or one or more fragrances as described above and in the Examples below.
  • the relative concentrations e.g., wt%) of each of these ingredients (and any optional additives) in the admixture is also presented above and in the Examples below.
  • the ingredients constituting the admixture can be provided sequentially or in any combination of additions; and, the ingredients or combination of ingredients can be provided in any order.
  • the lubricant is the last component added to the admixture.
  • the admixture comprises a solid dispersion of
  • substantially amorphous Compound 1 a binder, a glidant, a surfactant, a lubricant, a disintegrant, and a filler, wherein each of these ingredients is provided in a powder form (e.g., provided as particles having a mean diameter, measured by light scattering, of 250 ⁇ m or less (e.g., 150 ⁇ m or less, 100 ⁇ m or less, 50 ⁇ m or less, 45 ⁇ m or less, 40 ⁇ m or less, or 35 ⁇ m or less)).
  • a powder form e.g., provided as particles having a mean diameter, measured by light scattering, of 250 ⁇ m or less (e.g., 150 ⁇ m or less, 100 ⁇ m or less, 50 ⁇ m or less, 45 ⁇ m or less, 40 ⁇ m or less, or 35 ⁇ m or less)).
  • the admixture comprises a solid dispersion of amorphous Compound 1, a binder, a glidant, a surfactant, a lubricant, a disintegrant, and a filler, wherein each of these ingredients is provided in a powder form (e.g., provided as particles having a mean diameter, measured by light scattering, of 250 ⁇ m or less (e.g., 150 ⁇ m or less, 100 ⁇ m or less, 50 ⁇ m or less, 45 ⁇ m or less, 40 ⁇ m or less, or 35 ⁇ m or less)).
  • a powder form e.g., provided as particles having a mean diameter, measured by light scattering, of 250 ⁇ m or less (e.g., 150 ⁇ m or less, 100 ⁇ m or less, 50 ⁇ m or less, 45 ⁇ m or less, 40 ⁇ m or less, or 35 ⁇ m or less)).
  • the admixture comprises a solid dispersion of substantially amorphous Compound 1 , a binder, a glidant, a surfactant, a lubricant, a disintegrant, and a filler, wherein each of these ingredients is substantially free of water.
  • Each of the ingredients comprises less than 5 wt% (e.g., less than 2 wt%, less than 1 wt%, less than 0.75 wt%, less than 0.5 wt%, or less than 0.25 wt%) of water by weight of the ingredient.
  • the admixture comprises a solid dispersion of amorphous
  • Compound 1 a binder, a glidant, a surfactant, a lubricant, a disintegrant, and a filler, wherein each of these ingredients is substantially free of water.
  • Each of the ingredients comprises less than 5 wt% (e.g., less than 2 wt%, less than 1 wt%, less than 0.75 wt%, less than 0.5 wt%, or less than 0.25 wt%) of water by weight of the ingredient.
  • compressing the admixture into a tablet is
  • a form e.g., a mold
  • pressure to admixture can be accomplished using a die press or other similar apparatus.
  • the application of pressure to the admixture in the form can be repeated using the same pressure during each compression or using different pressures during the compressions.
  • the admixture is compressed using a die press that applies sufficient pressure to form a tablet having a dissolution of about 50% or more at about 30 minutes (e.g., about 55% or more at about 30 minutes or about 60% or more at about 30 minutes).
  • the admixture is compressed using a die press to produce a tablet hardness of at least about 5 Kp (at least about 5.5 Kp, at least about 6 Kp, at least about 7 Kp, at least about 11 Kp, or at least 21 Kp). In some instances, the admixture is compressed to produce a tablet hardness of between about 6 and 21 Kp.
  • tablets comprising a pharmaceutical composition as described herein can be coated with about 3.0 wt% of a film coating comprising a colorant by weight of the tablet.
  • the colorant suspension or solution used to coat the tablets comprises about 20%w/w of solids by weight of the colorant suspension or solution.
  • the coated tablets can be labeled with a logo, other image or text.
  • the method of producing a pharmaceutical composition comprises providing an admixture of a solid dispersion of substantially amorphous Compound 1, a binder, a glidant, a surfactant, a lubricant, a disintegrant, and a filler; mixing the admixture until the admixture is substantially homogenous, and
  • the method of producing a pharmaceutical composition comprises providing an admixture of a solid dispersion of amorphous Compound 1 , a binder, a glidant, a surfactant, a lubricant, a disintegrant, and a filler; mixing the admixture until the admixture is substantially
  • the admixture is mixed by stirring, blending, shaking, or the like using hand mixing, a mixer, a blender, any combination thereof, or the like.
  • mixing can occur between successive additions, continuously throughout the ingredient addition, after the addition of all of the ingredients or combinations of ingredients, or any combination thereof.
  • the admixture is mixed until it has a substantially homogenous composition.
  • the invention also provides a method of treating or lessening the severity of a disease in a patient comprising administering to said patient one of the compositions as defined herein, and said disease is selected from cystic fibrosis, asthma, smoke induced COPD, chronic bronchitis, rhinosinusitis, constipation, pancreatitis, pancreatic insufficiency, male infertility caused by congenital bilateral absence of the vas deferens (CBAVD), mild pulmonary disease, idiopathic pancreatitis, allergic
  • bronchopulmonary aspergillosis liver disease, hereditary emphysema, hereditary hemochromatosis, coagulation-fibrinolysis deficiencies, such as protein C deficiency, Type 1 hereditary angioedema, lipid processing deficiencies, such as familial hypercholesterolemia, Type 1 chylomicronemia, abetalipoproteinemia, lysosomal storage diseases, such as I-cell disease/pseudo-Hurler, mucopolysaccharidoses, Sandhof/Tay-Sachs, Crigler-Najjar type II, polyendocrinopathy/hyperinsulemia, Diabetes mellitus, Laron dwarfism, myleoperoxidase deficiency, primary hypoparathyroidism, melanoma, glycanosis CDG type 1, congenital hyperthyroidism, osteogenesis imperfecta, hereditary hypofibrinogenemia, ACT deficiency
  • the method includes treating or lessening the severity of cystic fibrosis in a patient comprising administering to said patient one of the compositions as defined herein.
  • the patient possesses mutant forms of human CFTR.
  • the patient possesses one or more of the following mutations ⁇ F5O8, Rl 17H, and G551D of human CFTR.
  • the method includes treating or lessening the severity of cystic fibrosis in a patient possessing the ⁇ F508 mutation of human CFTR comprising administering to said patient one of the compositions as defined herein.
  • the method includes treating or lessening the severity of cystic fibrosis in a patient possessing the G551D mutation of human CFTR comprising
  • the method includes treating or lessening the severity of cystic fibrosis in a patient possessing the ⁇ F508 mutation of human CFTR on at least one allele comprising administering to said patient one of the compositions as defined herein. In one embodiment, the method includes treating or lessening the severity of cystic fibrosis in a patient possessing the ⁇ F508 mutation of human CFTR on both alleles comprising administering to said patient one of the compositions as defined herein.
  • the method includes treating or lessening the severity of cystic fibrosis in a patient possessing the G551D mutation of human CFTR on at least one allele comprising administering to said patient one of the compositions as defined herein. In one embodiment, the method includes treating or lessening the severity of cystic fibrosis in a patient possessing the G551D mutation of human CFTR on both alleles comprising administering to said patient one of the compositions as defined herein.
  • the method includes treating or lessening the severity of cystic fibrosis in a patient comprising administering to said patient a pharmaceutical composition, in which the pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous or amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30.5 wt% of microcrystalline cellulose by weight of the composition; about 30.4 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.5 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the pharmaceutical composition comprises about 34.1 wt% of
  • the pharmaceutical composition contains 150 mg of Compound 1.
  • the pharmaceutical composition is formed as a tablet and comprises a colorant coated, a wax coating, and a printed logo or text.
  • the pharmaceutical tablet includes a blue OPADRY® II coating and a water or solvent based ink logo or text.
  • the colorant coating is blue OPADRY® II.
  • the wax coating comprises Carnauba wax.
  • the ink for the printed logo or text is a solvent based ink.
  • the method includes lessening the severity of cystic fibrosis in a patient comprising administering to said patient one of the compositions as defined herein.
  • the patient possesses mutant forms of human CFTR.
  • the patient possesses one or more of the following mutations ⁇ F508, Rl 17H, and G551D of human CFTR.
  • the method includes lessening the severity of cystic fibrosis in a patient possessing the ⁇ F508 mutation of human CFTR comprising administering to said patient one of the compositions as defined herein.
  • the method includes lessening the severity of cystic fibrosis in a patient possessing the G551D mutation of human CFTR comprising administering to said patient one of the compositions as defined herein. In one embodiment, the method includes lessening the severity of cystic fibrosis in a patient possessing the ⁇ F508 mutation of human CFTR on at least one allele comprising administering to said patient one of the compositions as defined herein. In one embodiment, the method includes lessening the severity of cystic fibrosis in a patient possessing the ⁇ F508 mutation of human CFTR on both alleles comprising administering to said patient one of the compositions as defined herein.
  • the method includes lessening the severity of cystic fibrosis in a patient possessing the G551D mutation of human CFTR on at least one allele comprising administering to said patient one of the compositions as defined herein. In one embodiment, the method includes lessening the severity of cystic fibrosis in a patient possessing the G551D mutation of human CFTR on both alleles comprising administering to said patient one of the compositions as defined herein.
  • the method includes lessening the severity of cystic fibrosis in a patient comprising administering to said patient a pharmaceutical composition, in which the pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous or amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30.5 wt% of microcrystalline cellulose by weight of the composition; about 30.4 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.5 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the pharmaceutical composition comprises about 34.1 wt% of a
  • the pharmaceutical composition contains 100 mg of Compound 1. In other embodiments, the pharmaceutical composition contains 150 mg of Compound 1. In some further aspects, the pharmaceutical composition is formed as a tablet and comprises a colorant coated, a wax coating, and a printed logo or text. In some embodiments of this aspect, the pharmaceutical tablet includes a blue OP ADR Y® II coating and a water or solvent based ink logo or text. In some instances, the colorant coating is blue OP ADR Y® II. In some instances, the wax coating comprises Carnauba wax. In certain aspects, the ink for the printed logo or text is a solvent based ink.
  • the invention provides a method of treating or lessening the severity of Osteoporosis in a patient comprising administering to said patient Compound 1 or a pharmaceutically acceptable salt thereof. [00231] In some embodiments, the method of treating or lessening the severity of
  • Osteoporosis in a patient comprises administering to said patient substantially amorphous Compound 1 or a pharmaceutically acceptable salt thereof.
  • Osteoporosis in a patient comprises administering to said patient amorphous Compound 1 or a pharmaceutically acceptable salt thereof.
  • Osteoporosis in a patient comprises administering to said patient a pharmaceutical composition as described herein.
  • Osteoporosis in a patient comprises administering to said patient a pharmaceutical composition, in which the pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous or amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30.5 wt% of microcrystalline cellulose by weight of the composition; about 30.4 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.5 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the pharmaceutical composition contains 100 mg of Compound 1.
  • the pharmaceutical composition contains 100 mg of Compound 1.
  • the pharmaceutical composition contains 150 mg of Compound 1.
  • the pharmaceutical composition is formed as a tablet and comprises a colorant coated, a wax coating, and a printed logo or text.
  • the pharmaceutical tablet includes a blue OPADRY® II coating and a water or solvent based ink logo or text.
  • the colorant coating is blue OPADRY® II.
  • the wax coating comprises Carnauba wax.
  • the ink for the printed logo or text is a solvent based ink.
  • the invention provides a method of treating or lessening the severity of Osteopenia in a patient comprising administering to said patient Compound 1 or a pharmaceutically acceptable salt thereof.
  • Osteopenia in a patient comprises administering to said patient substantially amorphous Compound 1 or a pharmaceutically acceptable salt thereof. [00237] In still other embodiments, the method of treating or lessening the severity of
  • Osteopenia in a patient comprises administering to said patient amorphous Compound 1.
  • Osteopenia in a patient comprises administering to said patient a pharmaceutical composition as described herein.
  • Osteopenia in a patient comprises administering to said patient a pharmaceutical composition, in which the pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous or amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30.5 wt% of microcrystalline cellulose by weight of the composition; about 30.4 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.5 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight of the composition, where
  • the pharmaceutical composition contains 100 mg of Compound 1. In other embodiments, the pharmaceutical composition contains 150 mg of Compound 1. In some further aspects, the pharmaceutical composition is formed as a tablet and comprises a colorant coated, a wax coating, and a printed logo or text. In some embodiments of this aspect, the pharmaceutical tablet includes a blue OP ADR Y® II coating and a water or solvent based ink logo or text. In some instances, the colorant coating is blue OPADRY® II. In some instances, the wax coating comprises Carnauba wax. In certain aspects, the ink for the printed logo or text is a solvent based ink.
  • the invention provides a method of bone healing and/or bone repair in a patient comprising administering to said patient Compound 1 or a
  • the method of bone healing and/or bone repair in a patient comprises administering to said patient substantially amorphous Compound 1 or a pharmaceutically acceptable salt thereof.
  • the method of bone healing and/or bone repair in a patient comprises administering to said patient amorphous Compound 1 or a
  • the method of bone healing and/or bone repair in a patient comprises administering to said patient a pharmaceutical composition as described herein.
  • the method of bone healing and/or bone repair in a patient comprises administering to said patient a pharmaceutical composition, in which the pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous or amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30.5 wt% of microcrystalline cellulose by weight of the composition; about 30.4 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.5 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight
  • the pharmaceutical composition contains 100 mg of Compound 1. In other embodiments, the pharmaceutical composition contains 150 mg of Compound 1. In some further aspects, the pharmaceutical composition is formed as a tablet and comprises a colorant coated, a wax coating, and a printed logo or text. In some embodiments of this aspect, the pharmaceutical tablet includes a blue OPADR Y® II coating and a water or solvent based ink logo or text. In some instances, the colorant coating is blue OPADRY® II. In some instances, the wax coating comprises Carnauba wax. In certain aspects, the ink for the printed logo or text is a solvent based ink.
  • the invention provides a method of reducing bone resorption in a patient comprising administering to said patient Compound 1 or a pharmaceutically acceptable salt thereof.
  • the method of reducing bone resorption in a patient comprises administering to said patient substantially amorphous Compound 1 or a
  • the method of reducing bone resorption in a patient comprises administering to said patient amorphous Compound 1 or a pharmaceutically acceptable salt thereof.
  • the method of reducing bone resorption in a patient comprises administering to said patient a pharmaceutical composition as described herein.
  • the method of reducing bone resorption in a patient comprises administering to said patient a pharmaceutical composition, in which the pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous or amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30.5 wt% of microcrystalline cellulose by weight of the composition; about 30.4 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.5 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight of
  • the pharmaceutical composition contains 100 mg of Compound 1. In other embodiments, the pharmaceutical composition contains 150 mg of Compound 1. In some further aspects, the pharmaceutical composition is formed as a tablet and comprises a colorant coated, a wax coating, and a printed logo or text. In some embodiments of this aspect, the pharmaceutical tablet includes a blue OPADR Y® II coating and a water or solvent based ink logo or text. In some instances, the colorant coating is blue OPADRY® II. In some instances, the wax coating comprises Carnauba wax. In certain aspects, the ink for the printed logo or text is a solvent based ink.
  • the invention provides a method of increasing bone deposition in a patient comprising administering to said patient Compound 1 or a
  • the method of increasing bone deposition in a patient comprises administering to said patient substantially amorphous Compound 1 or a
  • the method of increasing bone deposition in a patient comprises administering to said patient amorphous Compound 1 or a
  • the method of increasing bone deposition in a patient comprises administering to said patient a pharmaceutical composition as described herein.
  • the method of increasing bone deposition in a patient comprises administering to said patient a pharmaceutical composition, in which the pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous or amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30.5 wt% of microcrystalline cellulose by weight of the composition; about 30.4 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.5 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight of the composition
  • the pharmaceutical composition contains 100 mg of Compound 1. In other embodiments, the pharmaceutical composition contains 150 mg of Compound 1. In some further aspects, the pharmaceutical composition is formed as a tablet and comprises a colorant coated, a wax coating, and a printed logo or text. In some embodiments of this aspect, the pharmaceutical tablet includes a blue OPADRY® II coating and a water or solvent based ink logo or text. In some instances, the colorant coating is blue OPADRY® H. In some instances, the wax coating comprises Carnauba wax. In certain aspects, the ink for the printed logo or text is a solvent based ink.
  • the invention provides a method of treating or lessening the severity of COPD in a patient comprising administering to said patient Compound 1 or a pharmaceutically acceptable salt thereof.
  • COPD in a patient comprises administering to said patient substantially amorphous
  • COPD in a patient comprises administering to said patient amorphous Compound 1 or a pharmaceutically acceptable salt thereof.
  • COPD in a patient comprises administering to said patient a pharmaceutical composition as described herein.
  • COPD in a patient comprises administering to said patient a pharmaceutical composition, in which the pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous or amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30.5 wt% of microcrystalline cellulose by weight of the composition; about 30.4 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.5 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dis
  • the pharmaceutical composition contains 100 mg of Compound 1. In other embodiments, the pharmaceutical composition contains 150 mg of Compound 1. In some further aspects, the pharmaceutical composition is formed as a tablet and comprises a colorant coated, a wax coating, and a printed logo or text. In some embodiments of this aspect, the pharmaceutical tablet includes a blue OPADRY® II coating and a water or solvent based ink logo or text. In some instances, the colorant coating is blue OPADRY® II. In some instances, the wax coating comprises Carnauba wax. In certain aspects, the ink for the printed logo or text is a solvent based ink.
  • the invention provides a method of treating or lessening the severity of smoke induced COPD in a patient comprising administering to said patient Compound 1 or a pharmaceutically acceptable salt thereof.
  • the method of treating or lessening the severity of smoke induced COPD in a patient comprises administering to said patient substantially amorphous Compound 1 or a pharmaceutically acceptable salt thereof.
  • the method of treating or lessening the severity of smoke induced COPD in a patient comprises administering to said patient amorphous Compound 1 or a pharmaceutically acceptable salt thereof.
  • the method of treating or lessening the severity of smoke induced COPD in a patient comprises administering to said patient a pharmaceutical composition as described herein.
  • the method of treating or lessening the severity of smoke induced COPD in a patient comprises administering to said patient a pharmaceutical composition, in which the pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous or amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30.5 wt% of microcrystalline cellulose by weight of the composition; about 30.4 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.5 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the pharmaceutical composition contains
  • the pharmaceutical composition contains 150 mg of Compound 1.
  • the pharmaceutical composition is formed as a tablet and comprises a colorant coated, a wax coating, and a printed logo or text.
  • the pharmaceutical tablet includes a blue OP ADR Y® II coating and a water or solvent based ink logo or text.
  • the colorant coating is blue OPADR Y® II.
  • the wax coating comprises Carnauba wax.
  • the ink for the printed logo or text is a solvent based ink.
  • the invention provides a method of treating or lessening the severity of chronic bronchitis in a patient comprising administering to said patient Compound 1 or a pharmaceutically acceptable salt thereof.
  • the method of treating or lessening the severity of chronic bronchitis in a patient comprises administering to said patient substantially amorphous Compound 1 or a pharmaceutically acceptable salt thereof.
  • the method of treating or lessening the severity of chronic bronchitis in a patient comprises administering to said patient amorphous Compound 1 or a pharmaceutically acceptable salt thereof.
  • the method of treating or lessening the severity of chronic bronchitis in a patient comprises administering to said patient a pharmaceutical composition as described herein.
  • the method of treating or lessening the severity of chronic bronchitis in a patient comprises administering to said patient a pharmaceutical composition, in which the pharmaceutical composition comprises about 34.1 wt% of a solid dispersion by weight of the composition, wherein the dispersion comprises about 80 wt% of substantially amorphous or amorphous Compound 1 by weight of the dispersion, about 19.5 wt% of HPMCAS by weight of the dispersion, and about 0.5 wt% SLS by weight of the dispersion; about 30.5 wt% of microcrystalline cellulose by weight of the composition; about 30.4 wt% of lactose by weight of the composition; about 3 wt% of sodium croscarmellose by weight of the composition; about 0.5 wt% of SLS by weight of the composition; about 0.5 wt% of colloidal silicon dioxide by weight of the composition; and about 1 wt% of magnesium stearate by weight of the composition.
  • the pharmaceutical composition comprises about 34.1 wt% of
  • the pharmaceutical composition contains 150 mg of Compound 1.
  • the pharmaceutical composition is formed as a tablet and comprises a colorant coated, a wax coating, and a printed logo or text.
  • the pharmaceutical tablet includes a blue OPADR Y® II coating and a water or solvent based ink logo or text.
  • the colorant coating is blue OPADRY® II.
  • the wax coating comprises Carnauba wax.
  • the ink for the printed logo or text is a solvent based ink.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient at least once per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises up to about 1 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient at least once per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises up to about 5 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient at least once per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 15 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient at least once per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 25 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient at least once per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 50 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient at least once per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 75 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient at least once per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about lOOmg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient at least once per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 150 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient at least once per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 250 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient twice per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises up to about 1 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient twice per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises up to about 5 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient twice per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 15 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient twice per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • composition in which the solid dispersion comprises at least about 25 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient twice per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Solid dispersion comprises at least about 50 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient twice per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 75 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient twice per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 100 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient twice per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 150 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient twice per day the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 250 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient once every 12 hours.
  • the composition comprises a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises up to about 1 mg of substantially amorphous or amorphous Compound 1.
  • composition comprises a solid dispersion of substantially amorphous or amorphous Compound 1, in which the solid dispersion comprises up to about 5 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient once every 12 hours.
  • the composition comprises a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 15 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient once every 12 hours.
  • the composition comprises a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 25 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient once every 12 hours.
  • the composition comprises a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 50 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient once every 12 hours.
  • the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 75 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient once every 12 hours day.
  • composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 100 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient once every 12 hours.
  • the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 150 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient once every 12 hours.
  • the composition comprising a solid dispersion of substantially amorphous or amorphous
  • Compound 1 in which the solid dispersion comprises at least about 250 mg of substantially amorphous or amorphous Compound 1.
  • a pharmaceutical composition as described herein is orally administered to a patient once every 24 hours.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient once per day the composition comprising a solid dispersion of substantially amorphous or amorphous Compound 1, in which the solid dispersion comprises at least about 15 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient once per day the composition comprising a solid dispersion of substantially amorphous or amorphous Compound 1, in which the solid dispersion comprises at least about 25 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient once per day the composition comprising a solid dispersion of substantially amorphous or amorphous Compound 1, in which the solid dispersion comprises at least about 50 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient once per day the composition comprising a solid dispersion of substantially amorphous or amorphous Compound 1, in which the solid dispersion comprises at least about 75 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient once per day the composition comprising a solid dispersion of substantially amorphous or amorphous Compound 1 , in which the solid dispersion comprises at least about 100 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient once per day the composition comprising a solid dispersion of substantially amorphous or amorphous Compound 1, in which the solid dispersion comprises at least about 150 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient once per day the composition comprising a solid dispersion of substantially amorphous or amorphous Compound 1, in which the solid dispersion comprises at least about 250 mg of substantially amorphous or amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition
  • a method of administering a pharmaceutical composition comprising orally administering to a patient at least once per day at least one tablet comprising a pharmaceutical composition containing a solid dispersion of substantially amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, each of which is described above and in the Examples below, wherein the solid dispersion comprises up to about 1 mg (e.g., about 0.5 mg, about 0.75 mg, or about 1 mg) of substantially amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition
  • a method of administering a pharmaceutical composition comprising orally administering to a patient at least once per day at least one tablet comprising a pharmaceutical composition containing a solid dispersion of substantially amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, each of which is described above and in the Examples below, wherein the solid dispersion comprises up to about 5 mg (e.g., about 0.5 mg, about 0.75 mg, about 1 mg, about 2, mg, about 3 mg, about 4 mg, or about 5 mg) of substantially amorphous Compound 1.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition
  • a method of administering a pharmaceutical composition comprising orally administering to a patient at least once per day at least one tablet comprising a pharmaceutical composition containing a solid dispersion of substantially amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, each of which is described above and in the Examples below, wherein the solid dispersion comprises at least 15 mg (e.g., at least 25 mg, at least 35 mg, at least 40 mg, or at least 45 mg) of substantially amorphous Compound 1.
  • the present invention provides a method of
  • composition comprising orally administering to a patient at least one tablet comprising:
  • a solid dispersion comprising about 15 mg of substantially amorphous or amorphous Compound 1 ; b. a filler;
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • a solid dispersion comprising about 100 mg of substantially amorphous or amorphous Compound 1 ;
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • a solid dispersion comprising about 150 mg of substantially amorphous or amorphous Compound 1 ;
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • a solid dispersion comprising about 25 mg of substantially amorphous or amorphous Compound 1 and PVP/VA;
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • a solid dispersion comprising about 50 mg of substantially amorphous or amorphous Compound 1 and PVP/VA;
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • a solid dispersion comprising about 75 mg of substantially amorphous or amorphous Compound 1 and PVP/VA;
  • a surfactant e. a binder
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • a solid dispersion comprising about 100 mg of substantially amorphous or amorphous Compound 1 and PVP/VA;
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • a solid dispersion comprising about 150 mg of substantially amorphous or amorphous Compound 1 and PVP/VA;
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • a solid dispersion comprising about 250 mg of substantially amorphous or amorphous Compound 1 and PVP/VA;
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • a. a solid dispersion comprising about 50 mg of substantially amorphous or amorphous Compound 1 and HPMCAS;
  • a glidant f. a glidant; and g. a lubricant.
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • a. a solid dispersion comprising about 100 mg of substantially amorphous or amorphous Compound 1 and HPMCAS;
  • the present invention provides a method of administering a pharmaceutical composition comprising orally administering to a patient at least one tablet comprising:
  • a solid dispersion comprising about 150 mg of substantially amorphous or amorphous Compound 1 and HPMCAS;
  • the present invention provides a method of
  • composition comprising orally administering to a patient at least one tablet comprising:
  • a solid dispersion comprising about 250 mg of substantially amorphous or amorphous Compound 1 and HPMCAS;
  • the present invention provides for a method of orally administering the pharmaceutical composition described herein once a day. In other embodiments, the present invention provides for a method of orally administering the pharmaceutical composition described herein twice a day.
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient at least once per day at least one tablet comprising a solid dispersion of substantially amorphous or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, in which the solid dispersion comprises at least about 25 mg of substantially amorphous or amorphous
  • the tablet is orally administered to the patient once per day.
  • the administration comprises orally administering to a patient twice per day at least one tablet comprising a solid dispersion of substantially amorphous or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, in which the solid dispersion contains at least about 25 mg of substantially amorphous or amorphous Compound 1.
  • Some tablets useful in this method comprise a solid dispersion containing at least about 50 mg of substantially amorphous or amorphous
  • the administration includes orally administering to a patient twice per day at least one tablet comprising a solid dispersion of substantially amorphous or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, in which the solid dispersion contains at least about 50 mg of substantially amorphous or amorphous Compound 1.
  • Some tablets useful in this method comprise a solid dispersion containing at least about 75 mg of substantially amorphous or amorphous Compound 1.
  • the administration includes orally administering to a patient twice per day at least one tablet comprising a solid dispersion of substantially amorphous or amorphous Compound 1 , a filler, a binder, a glidant, a
  • Another aspect of the present invention provides a method of administering a pharmaceutical composition by orally administering to a patient at least once per day at least one tablet comprising a solid dispersion of substantially amorphous or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, in which the solid dispersion comprises at least about 100 mg of substantially amorphous or amorphous Compound 1.
  • the tablet is orally administered to the patient once per day.
  • the administration comprises orally administering to a patient twice per day at least one tablet comprising a solid dispersion of substantially amorphous or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, in which the solid dispersion contains at least about 100 mg of substantially amorphous or amorphous Compound 1.
  • Other tablets useful in this method comprise a solid dispersion containing at least about 150 mg of substantially amorphous or amorphous Compound 1.
  • the administration includes orally administering to a patient twice per day at least one tablet comprising a solid dispersion of substantially amorphous or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, in which the solid dispersion contains at least about 150 mg of substantially amorphous or amorphous Compound 1.
  • the administration includes orally administering to a patient at least once per day at least one tablet comprising a solid dispersion of substantially amorphous or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, in which the solid dispersion contains at least about 250 mg of substantially amorphous or amorphous
  • the administration includes orally administering to a patient once per day at least one tablet comprising a solid dispersion of substantially amorphous or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, in which the solid dispersion contains at least about 250 mg of substantially amorphous or amorphous Compound 1.
  • the administration includes orally administering to a patient twice per day at least one tablet comprising a solid dispersion of substantially amorphous or amorphous Compound 1, a filler, a binder, a glidant, a
  • the method of administering a pharmaceutical composition including orally administering to a patient at least once per day at least one tablet including a pharmaceutical composition containing a solid dispersion of amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, each of which is described above and in the Examples below, wherein the solid dispersion comprises at least 15 mg (e.g., at least 25 mg, at least 35 mg, at least 40 mg, or at least 45 mg) of substantially amorphous Compound 1.
  • composition includes orally administering to a patient at least once per day at least one tablet comprising a pharmaceutical composition containing a solid dispersion of substantially amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, wherein the solid dispersion comprises from about 30 mg to about 300 mg (e.g., from about 40 mg to about 280 mg or from about 45 mg to about 260 mg, or from about 50 mg to about 200 mg) of substantially amorphous Compound 1.
  • administering a pharmaceutical composition includes orally administering to a patient at least once per day at least one tablet comprising a pharmaceutical composition containing a solid dispersion of amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, wherein the solid dispersion comprises from about 30 mg to about 300 mg (e.g., from about 40 mg to about 280 mg or from about 45 mg to about 260 mg, or from about 50 mg to about 200 mg) of amorphous Compound 1.
  • the method of administering a pharmaceutical composition includes orally administering to a patient once per day at least one tablet comprising a pharmaceutical composition containing a solid dispersion of Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, each of which is described above and in the Examples below, wherein the solid dispersion comprises at least 15 mg (e.g., at least 25 mg, at least 35 mg, at least 40 mg, at least 45 mg, at least 75 mg, at least about 100 mg, at least about 150 mg, or at least 250 mg,) of substantially amorphous Compound 1 or amorphous Compound 1.
  • a solid dispersion comprises at least 15 mg (e.g., at least 25 mg, at least 35 mg, at least 40 mg, at least 45 mg, at least 75 mg, at least about 100 mg, at least about 150 mg, or at least 250 mg,) of substantially amorphous Compound 1 or amorphous Compound 1.
  • the method of administering a pharmaceutical composition includes orally administering to a patient once per day one tablet comprising a pharmaceutical composition containing a solid dispersion of Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, wherein the solid dispersion comprises at least 75 mg (e.g., at least 100 mg, at least 125 mg, at least 140 mg, at least 150 mg, or at least 250 mg) of substantially amorphous Compound 1 or amorphous Compound 1.
  • the method of administering a pharmaceutical composition includes orally administering to a patient once per day a plurality of tablets (e.g., two tablets, three tablets, four or five tablets), wherein each tablet comprises a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, wherein the solid dispersion comprises at least 15 mg (e.g., at least 25 mg, at least 35 mg, at least 40 mg, at least 45 mg, at least 75 mg, at least about 150 mg, or at least 250 mg,) of substantially amorphous Compound 1 or amorphous Compound 1.
  • a plurality of tablets e.g., two tablets, three tablets, four or five tablets
  • each tablet comprises a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 or amorphous Compound 1, a filler, a bin
  • the method of administering a pharmaceutical composition includes orally administering to a patient twice per day at least one tablet comprising a pharmaceutical composition containing a solid dispersion of Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, each of which is described above and in the Examples below, wherein the solid dispersion comprises at least 15 mg (e.g., at least 25 mg, at least 35 mg, at least 40 mg, at least 45 mg, at least 50 mg, at least 75 mg, at least about 150 mg, or at least 250 mg,) of substantially amorphous
  • the method of administering a pharmaceutical composition includes orally administering to a patient twice per day one tablet comprising a pharmaceutical composition containing a solid dispersion of Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, wherein the solid dispersion comprises at least 75 mg (e.g., at least 100 mg, at least 125 mg, at least 140 mg, at least 150 mg, or at least 250 mg) of substantially amorphous Compound 1 or amorphous Compound 1.
  • the method of administering a pharmaceutical composition includes orally administering to a patient twice per day one tablet comprising a pharmaceutical composition containing a solid dispersion of Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, wherein the solid dispersion comprises at least 75 mg (e.g., at least 100 mg, at least 125 mg, at least 140 mg,
  • composition includes orally administering to a patient twice per day a plurality of tablets (e.g., two tablets, three tablets, four or five tablets), wherein each tablet comprises a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, wherein the solid dispersion comprises at least 15 mg (e.g., at least 25 mg, at least 35 mg, at least 40 mg, at least 45 mg, at least 50 mg, at least 75 mg, at least about 150 mg, or at least 250 mg,) of substantially amorphous Compound 1 or amorphous Compound 1.
  • a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, where
  • the methods of administration of the present invention can optionally include orally administering a beverage (water, milk, or the like), food, and/or additional pharmaceutical compositions including additional APIs.
  • a beverage water, milk, or the like
  • food including a standard high fat high calorie CF meal or snack
  • additional pharmaceutical compositions including additional APIs the oral administration of the beverage, food, and/or additional API can occur concurrently with the oral administration of the tablet, prior to the oral administration of the tablet, and/or after the administration of the tablet.
  • the method of administering a pharmaceutical composition includes orally administering to a patient at least once per day at least one tablet comprising a pharmaceutical composition containing a solid dispersion of substantially amorphous Compound 1 or amorphous Compound 1, a filler, a binder, a glidant, a
  • the method of administering a pharmaceutical composition includes orally administering to a patient at least once per day at least one tablet comprising a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 or amorphous Compound 1, a filler, a binder, a glidant, a disintegrant, a surfactant, and a lubricant, wherein the solid dispersion comprises at least 15 mg (e.g., at least 25 mg, at least 35 mg, at least 45 mg, or at least 50 mg) of substantially amorphous Compound 1 or amorphous Compound 1, and orally administering to a patient at least once per day a second pharmaceutical composition comprising a second API.
  • the method of administering a pharmaceutical composition includes orally administering to a patient at least once per day at least one tablet comprising a pharmaceutical composition comprising a solid dispersion of substantially amorphous Compound 1 or amorphous Compound 1, a filler, a binder, a glidant,
  • pharmaceutical composition includes orally administering to a patient every 12 hours at least one tablet comprising a pharmaceutical composition as described herein, in which the tablet is administered about 30 minutes after consuming a high fat, high calorie CF meal or snack.
  • the compound and pharmaceutically acceptable compositions of the present invention can be employed in combination therapies, that is, the compound and pharmaceutically acceptable compositions can be administered concurrently with, prior to, or subsequent to, one or more other desired therapeutics or medical procedures.
  • the particular combination of therapies (therapeutics or procedures) to employ in a combination regimen will take into account compatibility of the desired therapeutics and/or procedures and the desired therapeutic effect to be achieved.
  • the therapies employed may achieve a desired effect for the same disorder (for example, an inventive compound may be administered concurrently with another agent used to treat the same disorder), or they may achieve different effects (e.g., control of any adverse effects).
  • additional therapeutic agents that are normally administered to treat or prevent a particular disease, or condition, are known as "appropriate for the disease, or condition, being treated.”
  • the additional agent is selected from a mucolytic agent, bronchodialator, an anti-biotic, an anti- infective agent, an anti-inflammatory agent, a CFTR modulator other than Compound 1 of the present invention, or a nutritional agent.
  • the additional agent is an antibiotic.
  • antibiotics useful herein include tobramycin, including tobramycin inhaled powder (TIP), azithromycin, aztreonam, including the aerosolized form of aztreonam, amikacin, including liposomal formulations thereof, ciprofloxacin, including formulations thereof suitable for administration by inhalation, levoflaxacin, including aerosolized formulations thereof, and combinations of two antibiotics, e.g., fosfomycin and tobramycin.
  • the additional agent is a mucolyte.
  • exemplary mucolytes useful herein includes Pulmozyme®.
  • the additional agent is a bronchodialator.
  • exemplary bronchodialtors include albuterol, metaprotenerol sulfate, pirbuterol acetate, salmeterol, or tetrabuline sulfate.
  • the additional agent is effective in restoring lung airway surface liquid.
  • Such agents improve the movement of salt in and out of cells, allowing mucus in the lung airway to be more hydrated and, therefore, cleared more easily.
  • exemplary such agents include hypertonic saline, denufosol tetrasodium ([[(3S,
  • bronchitol inhaled formulation of mannitol
  • the additional agent is an anti-inflammatory agent, i.e., an agent that can reduce the inflammation in the lungs.
  • agents useful herein include ibuprofen, docosahexanoic acid (DHA), sildenafil, inhaled glutathione, pioglitazone, hydroxychloroquine, or simavastatin.
  • the additional agent is a CFTR modulator other than compound 1, i.e., an agent that has the effect of modulating CFTR activity.
  • CFTR modulator other than compound 1, i.e., an agent that has the effect of modulating CFTR activity.
  • agents include ataluren ("PTC 124®"; 3-[5-(2-fluorophenyl)-l,2,4-oxadiazol-3-yl]benzoic acid), sinapultide, lancovutide, depelestat (a human recombinant neutrophil elastase inhibitor), cobiprostone (7- ⁇ (2R, 4aR, 5R, 7aR)-2-[(3S)-l,l-difluoro-3-methylpentyl]-2- hydroxy-6-oxooctahydrocyclopenta[b]pyran-5-yl ⁇ heptanoic acid), or (3-(6-(l-(2,2- difluorobenzo[d]
  • the additional agent is (3-(6-(l-(2,2- difluorobenzo[d][l,3]dioxol-5-yl) cyclopropanecarboxamido)-3-methylpyridin-2-yl)benzoic acid.
  • the additional agent is a nutritional agent.
  • exemplary such agents include pancrelipase (pancreating enzyme replacement), including Pancrease®, Pancreacarb®, Ultrase®, or Creon®, Liprotomase® (formerly Trizytek®), Aquadeks®, or glutathione inhalation.
  • the additional nutritional agent is pancrelipase.
  • a solvent system containing hypromellose acetate succinate polymer ((HPMCAS) HG grade, commercially available from Biddle Sawyer Corporation in New York, New York or Shin-Etsu Chemical Co.

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FIEP10708442.8T FI2464337T4 (fi) 2009-08-13 2010-02-18 N-[2,4-bis(1,1-dimetyylietyyli)-5-hydroksifenyyli]-1,4-dihydro-4-oksokinoliini-3-karboksamidin tablettiformulaatio käytettäväksi kystisen fibroosin hoitamisessa
CA2769695A CA2769695A1 (en) 2009-08-13 2010-02-18 Pharmaceutical composition and administrations thereof
AU2010282986A AU2010282986A1 (en) 2009-08-13 2010-02-18 Pharmaceutical composition and administrations thereof
EP10708442.8A EP2464337B2 (en) 2009-08-13 2010-02-18 Tablet formulation of N-[2,4-bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide for use in the treatment of cystic fibrosis
LTEP10708442.8T LT2464337T (lt) 2009-08-13 2010-02-18 N-[2,4-bis(1,1-dimetiletil)-5-hidroksifenil]-1,4-dihidro-4-oksochinolin-3-karboksamido tabletės forma, skirta panaudoti cistinės fibrozės gydymui
BR112012008082A BR112012008082A2 (pt) 2009-08-13 2010-02-18 composição farmacêutica e adminstrações da mesma
DK10708442.8T DK2464337T4 (da) 2009-08-13 2010-02-18 Tabletformulering af N-[2,4-bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinolin-3-carboxamid til anvendelse til behandling af cystisk fibrose
NZ597823A NZ597823A (en) 2009-08-13 2010-02-18 Pharmaceutical composition and administrations thereof
ES10708442T ES2718273T5 (en) 2009-01-23 2010-02-18 Tablet formulation of n-[2,4-bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide for use in the treatment of cystic fibrosis
CN2010800415071A CN102497859A (zh) 2009-08-13 2010-02-18 药物组合物及其施用
PL10708442.8T PL2464337T5 (pl) 2009-08-13 2010-02-18 Formulacja tabletki N-[2,4-bis(1,1-dimetyloetylo)-5-hydroksyfenylo]-1,4-dihydro-4-oksochinolino-3-karboksyamidu do użycia w leczeniu mukowiscydozy
MX2012001939A MX2012001939A (es) 2009-08-13 2010-02-18 Composicion farmaceutica y administraciones de la misma.
SG2012009080A SG178337A1 (en) 2009-08-13 2010-02-18 Pharmaceutical composition and administrations thereof
JP2012524706A JP2013501787A (ja) 2009-08-13 2010-02-18 薬学的組成物およびその投与
HRP20190660TT HRP20190660T4 (hr) 2009-08-13 2010-02-18 FORMULACIJA N-[2,4-bis(1,1-DIMETILETIL)-5-HIDROKSIFENIL]-1,4-DIHIDRO-4-OKSOHINOLIN-3-KARBOKSAMIDA U OBLIKU TABLETE ZA UPOTREBU U TRETMANU CISTIČNE FIBROZE
RS20190432A RS58604B2 (sr) 2009-08-13 2010-02-18 Formulacija n-[2,4-bis(1,1-dimetiletil)-5-hidroksifenil]-1,4-dihidro-4-oksohinolin-3-karboksamida u obliku tablete za upotrebu u tretmanu cistične fibroze
SI201031871T SI2464337T2 (sl) 2009-08-13 2010-02-18 Formulacija tablete N-(2,4-bis(1,1-dimetiletil)-5-hidroksifenil)-1,4-dihidro-4-oksokinolin -3-karboksamida za uporabo v zdravljenju cistične fibroze
RU2012109390/15A RU2012109390A (ru) 2009-08-13 2010-02-18 Фармацевтическая композиция и способы ее введения
KR1020127006386A KR20120061875A (ko) 2009-08-13 2010-02-18 제약 조성물 및 그의 투여
SM20190210T SMT201900210T1 (it) 2009-08-13 2010-02-18 Formulazione in compressa di n-[2,4-bis(1,1-dimetiletil)-5-idrossifenil]-1,4-diidro-4-ossochinolin-3-carbossammide per uso nel trattamento di fibrosi cistica
MEP-2019-101A ME03356B (me) 2009-08-13 2010-02-18 Formulacija n-[2,4-bis(1,1-dimetiletil)-5-hidroksifenil]-1,4-dihidr0-4-oksohinolin-3-karboksamida u obliku tablete za upotrebu u tretmanu cistićne fibroze
ZA2012/00722A ZA201200722B (en) 2009-08-13 2012-01-30 Pharmaceutical composition and administrations thereof
IL218057A IL218057A0 (en) 2009-08-13 2012-02-12 Compositions comprising carboxamide compounds and uses thereof
CY20191100385T CY1121572T1 (el) 2009-08-13 2019-04-08 Σκευασμα δισκιου του ν-[2,4-δις(1,1-διμεθυλαιθυλ)-5-υδροξυφαινυλ]-1,4-διυδρο-4-οξοκινολινο-3-καρβοξαμιδιου για χρηση στη θεραπεια κυστικης ινωσης

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SI2464337T1 (sl) 2019-05-31
RU2012109390A (ru) 2013-09-20
EP2464337B2 (en) 2024-06-26
HUE042437T2 (hu) 2019-07-29
DK2464337T3 (en) 2019-04-23
ES2718273T3 (es) 2019-06-28
ME03356B (me) 2019-10-20
PT2464337T (pt) 2019-05-03
HRP20190660T4 (hr) 2024-10-11
CN102497859A (zh) 2012-06-13
EP2464337A1 (en) 2012-06-20
FI2464337T4 (fi) 2024-07-18
ES2718273T5 (en) 2025-02-06
US11564916B2 (en) 2023-01-31
KR20120061875A (ko) 2012-06-13
SI2464337T2 (sl) 2024-08-30
RS58604B1 (sr) 2019-05-31
CL2012000348A1 (es) 2012-09-14
CY1121572T1 (el) 2020-05-29
US20100074949A1 (en) 2010-03-25
BR112012008082A2 (pt) 2016-03-01
PL2464337T5 (pl) 2024-10-14

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