Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
• • 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
  • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
  • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
  • A61K31/404—Indoles, e.g. pindolol
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
  • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
  • A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
• • 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
  • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
• • 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
  • A61K9/19—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles lyophilised, i.e. freeze-dried, solutions or dispersions
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
  • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
  • A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
  • A61K47/16—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
  • A61K47/18—Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
  • A61K47/183—Amino acids, e.g. glycine, EDTA or aspartame
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
  • A61K47/24—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing atoms other than carbon, hydrogen, oxygen, halogen, nitrogen or sulfur, e.g. cyclomethicone or phospholipids
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
  • A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
  • A61K47/38—Cellulose; Derivatives thereof
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
  • C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
  • C07K16/28—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
  • C07K16/2803—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
  • C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
  • C07K16/28—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
  • C07K16/2803—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
  • C07K16/2818—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against CD28 or CD152
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
  • C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
  • C07K16/28—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
  • C07K16/2803—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
  • C07K16/2827—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against B7 molecules, e.g. CD80, CD86

Definitions

• DON 6-Diazo-5-oxo-L-norleucine
• the disclosure provides a lyophilate comprising Compound 1 for subcutaneous administration to a subject in need thereof.
• the disclosure provides a lyophilate comprising Compound 1 and a bulking agent, e.g., mannitol.
• the disclosure provides a lyophilate comprising Compound 1 and a cellulose-based suspension modulator, e.g., sodium carboxymethyl cellulose.
• a cellulose-based suspension modulator e.g., sodium carboxymethyl cellulose.
• the disclosure provides a lyophilate comprising Compound 1 and a poloxamer-based suspension modulator, e.g., Poloxamer 188.
• a poloxamer-based suspension modulator e.g., Poloxamer 188.
• the disclosure provides a lyophilate comprising Compound 1 and a lecithin-based suspension modulator, e.g., soy lecithin.
• a lecithin-based suspension modulator e.g., soy lecithin.
• the disclosure provides a lyophilate comprising Compound 1 and a buffering agent, e.g., L-histidine.
• a pharmaceutical composition comprising a lyophilate comprising Compound 1 that has been suspended in a pharmaceutically acceptable excipient, e.g., a solvent, e.g., water.
• the disclosure provides a method for treating a cancer in a subject in need thereof comprising subcutaneously administering a therapeutically effective amount of a pharmaceutical composition comprising a lyophilate comprising Compound 1.
• the disclosure provides a method of making the lyophilate comprising Compound 1.
• the disclosure provides a method of making the pharmaceutical composition comprising a lyophilate comprising Compound 1.
• the disclosure provides a kit comprising the lyophilate comprising Compound 1 packaged as single unit dose in a vial.
• Fig. 1 is an image showing the lyophilized cake appearance of five lyophilates comprising Compound 1.
• Fig. 2 is an image showing the appearance of a pharmaceutical composition comprising Compound 1 suspended in 2.5 mL of water for injection.
• the disclosure provides a lyophilate comprising Compound 1 for subcutaneous administration to a subject in need thereof.
• the disclosure provides a lyophilate comprising Compound 1 and a bulking agent.
• the Compound 1/bulking agent weight ratio is about 5 to about 0.05.
• the Compound 1/bulking agent weight ratio is about 3 to about 0.1.
• the Compound 1/bulking agent weight ratio is about 1 to about 0.2.
• the Compound 1/bulking agent weight ratio is about 3, about 2, about 1, about 0.9, about 0.8, about 0.7, about 0.6, about 0.5, about 0.4, about 0.3, about 0.2, or about 0.1.
• the bulking agent is mannitol.
• the disclosure provides a lyophilate comprising Compound 1 and a cellulose-based suspension modulator.
• the Compound 1/cellulose-based suspension modulator weight ratio is about 25 to about 0.3. In another embodiment, the Compound 1/cellulose-based suspension modulator weight ratio is about 15 to about 0.5. In another embodiment, the Compound 1/cellulose-based suspension modulator weight ratio is about 10 to about 1. In another embodiment, the Compound 1/cellulose-based suspension modulator weight ratio is about 5 to about 2. In another embodiment, the Compound 1/cellulose-based suspension modulator weight ratio is about 10, about 9, about 8, about 7.5, about 7, about 6, about 5, about 4, about 3, about 2.7, about 2, or about 1. In another embodiment, the cellulose-based suspension modulator is sodium carboxymethyl cellulose.
• the disclosure provides a lyophilate comprising Compound 1 and a poloxamer-based suspension modulator.
• the Compound 1/poloxamer-based suspension modulator weight ratio is about 80 to about 1.
• the Compound 1/poloxamer-based suspension modulator weight ratio is about 40 to about 2.
• the Compound 1/poloxamer-based suspension modulator weight ratio is about 20, about 19, about 18, about 17, about 16, about 15, about 14, about 13, about 12, about 11, about 10, about 9, about 8.8, about 7, about 6, about 5, about 4, about 3, or about 2.
• the poloxamer-based suspension modulator is Pol oxamer 188 (a copolymer of polyoxyethylene and polyoxypropylene).
• the disclosure provides a lyophilate comprising Compound 1 and lecithin-based suspension modulator.
• the Compound 1/lecithin-based suspension modulator weight ratio is about 15 to about 0.15.
• the Compound 1/lecithin-based suspension modulator weight ratio is about 8 to about 0.3.
• the Compound 1/lecithin-based suspension modulator weight ratio is about 5 to about 0.6.
• the Compound 1/lecithin-based suspension modulator weight ratio is about 3 to about 1.
• the Compound 1/lecithin-based suspension modulator weight ratio is about 5, about 4, about 3, about 2, about 1.5, about 1, about 0.6.
• the lecithin-based suspension modulator is soy lecithin.
• the disclosure provides a lyophilate comprising Compound 1 and a buffering agent.
• the Compound 1/buffering agent weight ratio is about 50 to about 1.
• the Compound l/buffering agent weight ratio is about 25 to about 10.
• the Compound l/buffering agent weight ratio is about 20 to about 15.
• the Compound l/buffering agent weight ratio is about 25, about 24, about 23, about 22, about 21, about 20, about 21, about 20, about 19, about 18, about 17.4, about 17, about 16, about 15, about 14, about 13, about 12, about 11, or about 10.
• the buffering agent is L-histidine.
• the disclosure provides a lyophilate comprising Compound 1, a bulking agent, at least one of a cellulose-based suspension modulator, a poloxamer-based suspension modulator, or a lecithin-based suspension modulator, and, optionally, a buffering agent.
• the disclosure provides a lyophilate comprising Compound 1, a bulking agent, and at least two of a cellulose-based suspension modulator, a poloxamer-based suspension modulator, or a lecithin-based suspension modulator, and, optionally, a buffering agent.
• the disclosure provides a lyophilate comprising Compound 1, a bulking agent, a cellulose-based suspension modulator, a poloxamer-based suspension modulator, and a lecithin-based suspension modulator, and, optionally, a buffering agent.
• the disclosure provides a lyophilate comprising about 20 % wt/wt to about 45 % wt/wt of Compound 1 and about 35 % wt/wt to about 55 % wt/wt of a bulking agent.
• the disclosure provides a lyophilate comprising Compound 1, mannitol, sodium carboxymethyl cellulose, pol oxamer 188, and soy lecithin, and, optionally, L-histidine.
• the disclosure provides a lyophilate comprising about 10 mg to about 120 mg of Compound 1. In another embodiment, the disclosure provides a lyophilate comprising about 20 mg to about 110 mg of Compound 1. In another embodiment, the disclosure provides a lyophilate comprising about 30 mg to about 100 mg of Compound 1. In another embodiment, the disclosure provides a lyophilate comprising about 40 mg to about 90 mg of Compound 1. In another embodiment, the disclosure provides a lyophilate comprising about 50 mg to about 80 mg of Compound 1. In another embodiment, the disclosure provides a lyophilate comprising about 60 mg to about 70 mg of Compound 1.
• the disclosure provides a lyophilate comprising about 10 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 42 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 62.5 mg, about 65 mg, about 67.5 mg, about 70 mg, about 75 mg, about 80 mg, about 85 mg, about 90 mg, about 95 mg, about 100 mg, about 105 mg, about 110 mg, or about 120 mg of Compound 1.
• the disclosure provides a lyophilate comprising about 50 mg to about 250 mg of a bulking agent. In another embodiment, the disclosure provides a lyophilate comprising about 60 mg to about 210 mg of a bulking agent. In another embodiment, the disclosure provides a lyophilate comprising about 70 mg to about 200 mg of a bulking agent. In another embodiment, the disclosure provides a lyophilate comprising about 80 mg to about 190 mg of a bulking agent. In another embodiment, the disclosure provides a lyophilate comprising about 90 mg to about 180 mg of a bulking agent. In another embodiment, the disclosure provides a lyophilate comprising about 100 mg to about 170 mg of a bulking agent.
• the disclosure provides a lyophilate comprising about 110 mg to about 160 mg of a bulking agent. In another embodiment, the disclosure provides a lyophilate comprising about 120 mg to about 150 mg of a bulking agent. In another embodiment, the disclosure provides a lyophilate comprising about 125 mg to about 140 mg of a bulking agent.
• the disclosure provides a lyophilate comprising about 50 mg, about 55 mg, about 60 mg, about 65 mg, about 70 mg, about 75 mg, about 80 mg, about 85 mg, about 90 mg, about 95 mg, about 100 mg, about 105, about 110 mg, about 115 mg, about 120 mg, about 125 mg, about 130 mg, about 135 mg, about 140 mg, about 145 mg, about 150 mg, about 155 mg, about 160 mg, about 165 mg, about 170 mg, about 175 mg, about 180, about 185 mg, about 190 mg, about 195 mg, about 200 mg, about 205 mg, about 210 mg, about 215 mg, or about 220 mg of a bulking agent.
• the bulking agent is mannitol.
• the disclosure provides a lyophilate comprising about 1 mg to about 100 mg of a cellulose-based suspension modulator. In another embodiment, the disclosure provides a lyophilate comprising about 5 mg to about 75 mg of a cellulose-based suspension modulator. In another embodiment, the disclosure provides a lyophilate comprising about 5 mg to about 50 mg of a cellulose- based suspension modulator. In another embodiment, the disclosure provides a lyophilate comprising about 5 mg to about 10 mg of a cellulose-based suspension modulator. In another embodiment, the disclosure provides a lyophilate comprising about 20 mg to about 30 mg of a cellulose-based suspension modulator.
• the disclosure provides a lyophilate comprising about 5 mg, about 6 mg, about 7 mg, about 8 mg, about 9 mg, about 10 mg, about 11 mg, about 12 mg, about 13 mg, about 14 mg, about 15 mg, about 16 mg, about 17 mg, about 18 mg, about 19 mg, about 20 mg, about 21 mg, about 22 mg, about 23 mg, about 24 mg, about 25 mg, about 25.2 mg, about 26 mg, about 27 mg, about 28 mg, about 29 mg, about 30 mg, about 31 mg, about 32 mg, about 33 mg, about 34 mg, about 35 mg, about 36 mg, about 37 mg, about 38 mg, about 39 mg, about 40 mg, about 41 mg, about 42 mg, about 43 mg, about 44 mg, about 45 mg, about 46 mg, about 47 mg, about 48 mg, about 49 mg, or about 50 mg of a cellulose-based suspension modulator.
• the cellulose-based suspension modulator is sodium carboxymethyl cellulose.
• the disclosure provides a lyophilate comprising about 0.5 mg to about 70 mg of a poloxamer-based suspension modulator. In another embodiment, the disclosure provides a lyophilate comprising about 1 mg to about 40 mg of a poloxamer-based suspension modulator. In another embodiment, the disclosure provides a lyophilate comprising about 2 mg to about 30 mg of a poloxamer-based suspension modulator. In another embodiment, the disclosure provides a lyophilate comprising about 3 mg to about 20 mg of a poloxamer-based suspension modulator. In another embodiment, the disclosure provides a lyophilate comprising about 4 mg to about 10 mg of a poloxamer-based suspension modulator.
• the disclosure provides a lyophilate comprising about 3 mg, about 4 mg, about 5 mg, about 6 mg, about 7 mg, about 7.65 mg, about 8, about 9, about 10 mg, about 11 mg, about 12 mg, about 13 mg, about 1 mg, about 15 mg, about 16 mg, about 17 mg, about 18 mg, about 19 mg, or about 20 mg of a poloxamer-based suspension modulator.
• the poloxamer-based suspension modulator is Poloxamer 188.
• the disclosure provides a lyophilate comprising about 1 mg to about 100 mg of a lecithin-based suspension modulator. In another embodiment, the disclosure provides a lyophilate comprising about 10 mg to about 80 mg of a lecithin-based suspension modulator. In another embodiment, the disclosure provides a lyophilate comprising about 20 mg to about 70 mg of a lecithin-based suspension modulator. In another embodiment, the disclosure provides a lyophilate comprising about 30 mg to about 60 mg of a lecithin-based suspension modulator. In another embodiment, the disclosure provides a lyophilate comprising about 40 mg to about 50 mg of a lecithin-based suspension modulator.
• the disclosure provides a lyophilate comprising about 30 mg, about 31 mg, about 32 mg, about 33 mg, about 34 mg, about 35 mg, about 36 mg, about 37 mg, about 38 mg, about 39 mg, about 40 mg, about 41 mg, about 42 mg, about 43 mg, about 44 mg, about 45 mg, about 46 mg, about 47 mg, about 48 mg, about 49 mg, about 50 mg, about 51 mg, about 52 mg, about 53 mg, about 54 mg, about 55 mg, about 56 mg, about 57 mg, about 58 mg, about 59, or about 60 mg of a lecithin-based suspension modulator.
• the lecithin-based suspension modulator is soy lecithin
• the disclosure provides a lyophilate comprising about 0.1 mg to about 20 mg of a buffering agent. In another embodiment, the disclosure provides a lyophilate comprising about 0.5 mg to about 15 mg of a buffering agent. In another embodiment, the disclosure provides a lyophilate comprising about 1 mg to about 10 mg of a buffering agent. In another embodiment, the disclosure provides a lyophilate comprising about 2 mg to about 8 mg of a buffering agent. In another embodiment, the disclosure provides a lyophilate comprising about 3 mg to about 5 mg of a buffering agent.
• the disclosure provides a lyophilate comprising about 0.1 mg, about 0.5 mg, about 1 mg, about 1.5 mg, about 2 mg, about 2.5 mg, about 3 mg, about 3.5 mg, about 3.9 mg, about 4 mg, about 4.5 mg, about
• the buffering agent is L-histidine.
• Embodiment I A lyophilate comprising about 60 mg to about 70 mg of Compound 1 for subcutaneous administration to a subject.
• Embodiment II The lyophilate of Embodiment I comprising about 125 mg to about 140 mg of bulking agent, e.g., mannitol.
• bulking agent e.g., mannitol.
• Embodiment III The lyophilate of Embodiments I or II comprising about 8 mg to about 30 mg of a cellulose-based suspension modulator, e.g., sodium carboxymethyl cellulose.
• a cellulose-based suspension modulator e.g., sodium carboxymethyl cellulose.
• Embodiment IV The lyophilate of any one of Embodiments I-III comprising about 5 mg to about 10 mg of a poloxamer-based suspension modulator, e.g., Poloxamer 188.
• a poloxamer-based suspension modulator e.g., Poloxamer 188.
• Embodiment V The lyophilate of any one of Embodiments I-IV comprising about 40 mg to about 50 mg of a lecithin-based suspension modulator, e.g., soy lecithin.
• a lecithin-based suspension modulator e.g., soy lecithin.
• Embodiment VI The lyophilate of any one of Embodiments I-V comprising about 2 mg to about 5 mg of a buffering agent, e.g., L-histidine.
• a buffering agent e.g., L-histidine.
• Embodiment LA A lyophilate comprising about 110 mg to about 130 mg of Compound 1 for subcutaneous administration to a subject.
• Embodiment ILA The lyophilate of Embodiment LA comprising about 110 mg to about 250 mg of bulking agent, e.g., mannitol.
• Embodiment IILA The lyophilate of Embodiments LA or ILA comprising about 5 mg to about 30 mg of a cellulose-based suspension modulator, e.g., sodium carboxymethyl cellulose.
• a cellulose-based suspension modulator e.g., sodium carboxymethyl cellulose.
• Embodiment IV-A The lyophilate of any one of Embodiments LA to IILA comprising about 5 mg to about 15 mg of a poloxamer-based suspension modulator, e.g., Poloxamer 188.
• Embodiment V-A The lyophilate of any one of Embodiments LA to IV-A comprising about 40 mg to about 90 mg of a lecithin-based suspension modulator, e.g., soy lecithin.
• Embodiment VI-A The lyophilate of any one of Embodiments LA to V-A comprising about 2 mg to about 10 mg of a buffering agent, e.g., L-histidine.
• a buffering agent e.g., L-histidine.
• Representative lyophilates (designated L1-L5) of the present disclosure comprise Compound 1, mannitol, NaCMC, Pol oxamer 188, NF, histidine, and soy lecithin in the following amounts:
• the moisture content of the lyophilate is about 4% or less as determined by the Karl Fischer method, In another embodiment, the moisture content of the lyophilate is about 3% or less, In another embodiment, the moisture content of the lyophilate is about 2% or less, In another embodiment, the moisture content of the lyophilate is about 1% or less. In another embodiment, the moisture content of the lyophilate is about 0.9%. In another embodiment, the moisture content of the lyophilate is about 0.8%. In another embodiment, the moisture content of the lyophilate is about 0.7%. another embodiment, the moisture content of the lyophilate is about 0.6%. In another embodiment, the moisture content of the lyophilate is about 0.5%.
• the moisture content of the lyophilate is about 0.4%. In another embodiment, the moisture content of the lyophilate is about 0.3%. In another embodiment, the moisture content of the lyophilate is about 0.2%. In another embodiment, the moisture content of the lyophilate is about 0.1%.
• the chemical purity of Compound 1 in the lyophilate is about 96% to about 99.9% as measured by HPLC. In another embodiment, the chemical purity of Compound 1 in the lyophilate is about 96%. In another embodiment, the chemical purity of Compound 1 in the lyophilate is about 96.5%. In another embodiment, the chemical purity of Compound 1 in the lyophilate is about 97%. In another embodiment, the chemical purity of Compound 1 in the lyophilate is about 97.5%. In another embodiment, the chemical purity of Compound 1 in the lyophilate is about 98 %. In another embodiment, the chemical purity of Compound 1 in the lyophilate is about 98.5%. In another embodiment, the chemical purity of Compound 1 in the lyophilate is about 99.0%. In another embodiment, the chemical purity of Compound 1 in the lyophilate is about 99.5%.
• the disclosure provides a lyophilate comprising about
• Compound 1 67.5 mg of Compound 1, about 135 mg of mannitol, about 25.2 mg of sodium carboxymethyl cellulose, about 7.65 mg of pol oxamer 188, about 3.88 mg of L-histidine, and about 45 mg of soy lecithin.
• the disclosure provides a lyophilate consisting essentially of about 67.5 mg of Compound 1, about 135 mg of mannitol, about 25.2 mg of sodium carboxymethyl cellulose, about 7.65 mg of poloxamer 188, about 3.88 mg of L-histidine, and about 45 mg of soy lecithin.
• the disclosure provides a lyophilate consisting of about
• Compound 1 67.5 mg of Compound 1, about 135 mg of mannitol, about 25.2 mg of sodium carboxymethyl cellulose, about 7.65 mg of poloxamer 188, about 3.88 mg of L-histidine, and about 45 mg of soy lecithin.
• the disclosure provides a lyophilate comprising about
• Compound 1 67.5 mg of Compound 1, about 135 mg of mannitol, about 9.0 mg of sodium carboxymethyl cellulose, about 7.65 mg of poloxamer 188, about 3.88 mg of L-histidine, and about 45 mg of soy lecithin.
• the disclosure provides a lyophilate consisting essentially of about 67.5 mg of Compound 1, about 135 mg of mannitol, about 9.0 mg of sodium carboxymethyl cellulose, about 7.65 mg of poloxamer 188, about 3.88 mg of L-histidine, and about 45 mg of soy lecithin.
• the disclosure provides a lyophilate consisting of about
• Compound 1 67.5 mg of Compound 1, about 135 mg of mannitol, about 9.0 mg of sodium carboxymethyl cellulose, about 7.65 mg of poloxamer 188, about 3.88 mg of L-histidine, and about 45 mg of soy lecithin.
• the disclosure provides a lyophilate comprising about
• Compound 1 62.5 mg of Compound 1, about 125 mg of mannitol, about 8.33 mg of sodium carboxymethyl cellulose, about 7.08 mg of poloxamer 188, about 4.31 mg of L-histidine, and about 41.7 mg of soy lecithin.
• the disclosure provides a lyophilate consisting essentially of about 62.5 mg of Compound 1, about 125 mg of mannitol, about 8.33 mg of sodium carboxymethyl cellulose, about 7.08 mg of poloxamer 188, about 4.31 mg of L-histidine, and about 41.7 mg of soy lecithin.
• the disclosure provides a lyophilate consisting of about
• Compound 1 62.5 mg of Compound 1, about 125 mg of mannitol, about 8.33 mg of sodium carboxymethyl cellulose, about 7.08 mg of poloxamer 188, about 4.31 mg of L-histidine, and about 41.7 mg of soy lecithin.
• the disclosure provides a lyophilate comprising about
• Compound 1 120.2 mg of Compound 1, about 240.4 mg of mannitol, about 16 mg of sodium carboxymethyl cellulose, about 13.6 mg of poloxamer 188, about 8.3 mg of L-histidine, about 80.2 mg of soy lecithin.
• the disclosure provides a lyophilate consisting essentially of about 120.2 mg of Compound 1, about 240.4 mg of mannitol, about 16 mg of sodium carboxymethyl cellulose, about 13.6 mg of poloxamer 188, about 8.3 mg of L-histidine, about 80.2 mg of soy lecithin.
• the disclosure provides a lyophilate consisting of about
• Compound 1 120.2 mg of Compound 1, about 240.4 mg of mannitol, about 16 mg of sodium carboxymethyl cellulose, about 13.6 mg of poloxamer 188, about 8.3 mg of L-histidine, about 80.2 mg of soy lecithin.
• the disclosure provides a lyophilate comprising about
• Compound 1 120.2 mg of Compound 1, about 120.2 mg of mannitol, about 8 mg of sodium carboxymethyl cellulose, about 6.8 mg of pol oxamer 188, about 4.1 mg of L-histidine, about 40.1 mg of soy lecithin.
• the disclosure provides a lyophilate consisting essentially of about 120.2 mg of Compound 1, about 120.2 mg of mannitol, about 8 mg of sodium carboxymethyl cellulose, about 6.8 mg of pol oxamer 188, about 4.1 mg of L-histidine, about 40.1 mg of soy lecithin.
• the disclosure provides a lyophilate consisting of about 120.2 mg of Compound 1, about 120.2 mg of mannitol, about 8 mg of sodium carboxymethyl cellulose, about 6.8 mg of pol oxamer 188, about 4.1 mg of L-histidine, about 40.1 mg of soy lecithin.
• the disclosure provides a pharmaceutical composition comprising a Lyophilate of the Disclosure suspended in a solvent.
• the solvent comprises water.
• the solvent is water, e.g., sterile water for injection, USP.
• the disclosure provides a pharmaceutical composition
• a pharmaceutical composition comprising a Lyophilate of the Disclosure suspended in a solvent, wherein the concentration of Compound 1 is about 20 mg/mL to about 60 mg/mL, e.g., about
• Compound 1 is about 25 mg/mL to about 30 mg/mL. In another embodiment, the concentration of Compound 1 is about 20 mg/mL. In another embodiment, the concentration of Compound 1 is about 21 mg/mL. In another embodiment, the concentration of Compound 1 is about 22 mg/mL. In another embodiment, the concentration of Compound 1 is about 23 mg/mL. In another embodiment, the concentration of Compound 1 is about 24 mg/mL. In another embodiment, the concentration of Compound 1 is about 25 mg/mL. In another embodiment, the concentration of Compound 1 is about 26 mg/mL. In another embodiment, the concentration of Compound 1 is about 27 mg/mL. In another embodiment, the concentration of Compound 1 is about 28 mg/mL.
• the concentration of Compound 1 is about 29 mg/mL. In another embodiment, the concentration of Compound 1 is about 30 mg/mL. In another embodiment, the concentration of Compound 1 is about 31 mg/mL. In another embodiment, the concentration of Compound 1 is about 32 mg/mL. In another embodiment, the concentration of Compound 1 is about 33 mg/mL. In another embodiment, the concentration of Compound 1 is about 34 mg/mL. In another embodiment, the concentration of Compound 1 is about 35 mg/mL. In another embodiment, the concentration of Compound 1 is about 40 mg/mL. In another embodiment, the concentration of Compound 1 is about 45 mg/mL. In another embodiment, the concentration of Compound 1 is about 50 mg/mL. In another embodiment, the concentration of Compound 1 is about 55 mg/mL. In another embodiment, the concentration of Compound 1 is about 60 mg/mL.
• the disclosure provides a pharmaceutical composition
• a pharmaceutical composition comprising a Lyophilate of the Disclosure suspended in a solvent, wherein the average particle size distribution of Compound 1 in the suspension is about 0.1 pm to about
• the average particle size distribution of Compound 1 in the suspension is about 1 pm to about 40 pm after 3 days at 2-8 °C. In another embodiment, the average particle size distribution of Compound 1 in the suspension is about 10 pm to about 30 pm after 3 days at 2-8 °C. In another embodiment, the average particle size distribution of Compound 1 in the suspension is about 10 pm to about 30 pm. In another embodiment, the average particle size distribution of Compound 1 in the suspension is about 10 pm after 3 days at 2-8 °C. In another embodiment, the average particle size distribution of Compound 1 in the suspension is about 15 pm after 3 days at 2-8 °C. In another embodiment, the average particle size distribution of Compound 1 in the suspension is about 20 pm after 3 days at 2-8 °C. In another embodiment, the average particle size distribution of Compound 1 in the suspension is about 25 pm after 3 days at 2-8 °C.
• the disclosure provides a pharmaceutical composition
• a pharmaceutical composition comprising about 67.5 mg of Compound 1, about 135 mg of mannitol, about 25.2 mg of sodium carboxymethyl cellulose, about 7.65 mg of poloxamer 188, about 3.88 mg of L-histidine, about 45 mg of soy lecithin, and about 2.5 mL of sterile water for injection, USP (WFI USP).
• the disclosure provides a pharmaceutical composition consisting essentially of about 67.5 mg of Compound 1, about 135 mg of mannitol, about 25.2 mg of sodium carboxymethyl cellulose, about 7.65 mg of pol oxamer 188, about 3.88 mg of L-histidine, about 45 mg of soy lecithin, and about 2.5 mL of sterile water for injection, USP.
• the disclosure provides a pharmaceutical composition consisting of about 67.5 mg of Compound 1, about 135 mg of mannitol, about 25.2 mg of sodium carboxymethyl cellulose, about 7.65 mg of poloxamer 188, about 3.88 mg of L-histidine, about 45 mg of soy lecithin, and about 2.5 mL of sterile water for injection, USP.
• the disclosure provides a pharmaceutical composition
• a pharmaceutical composition comprising about 67.5 mg of Compound 1, about 135 mg of mannitol, about 9.0 mg of sodium carboxymethyl cellulose, about 7.65 mg of poloxamer 188, about 3.88 mg of L-histidine, about 45 mg of soy lecithin, and about 2.25 mL of sterile water for injection, USP.
• the disclosure provides a pharmaceutical composition consisting essentially of about 67.5 mg of Compound 1, about 135 mg of mannitol, about 9.0 mg of sodium carboxymethyl cellulose, about 7.65 mg of poloxamer 188, about 3.88 mg of L-histidine, about 45 mg of soy lecithin, and about 2.25 mL of sterile water for injection, USP.
• the disclosure provides a pharmaceutical composition consisting of about 67.5 mg of Compound 1, about 135 mg of mannitol, about 9.0 mg of sodium carboxymethyl cellulose, about 7.65 mg of poloxamer 188, about 3.88 mg of L-histidine, about 45 mg of soy lecithin, and about 2.25 mL of sterile water for injection, USP.
• the disclosure provides a pharmaceutical composition
• a pharmaceutical composition comprising about 62.5 mg of Compound 1, about 125 mg of mannitol, about 8.33 mg of sodium carboxymethyl cellulose, about 7.08 mg of poloxamer 188, about 4.31 mg of L-histidine, about 41.7 mg of soy lecithin, and about 2.5 mL of sterile water for injection, USP.
• the disclosure provides a pharmaceutical composition consisting essentially of about 62.5 mg of Compound 1, about 125 mg of mannitol, about 8.33 mg of sodium carboxymethyl cellulose, about 7.08 mg of poloxamer 188, about 4.31 mg of L-histidine, about 41.7 mg of soy lecithin, and about 2.5 mL of sterile water for injection, USP.
• the disclosure provides a pharmaceutical composition consisting of about 62.5 mg of Compound 1, about 125 mg of mannitol, about 8.33 mg of sodium carboxymethyl cellulose, about 7.08 mg of poloxamer 188, about 4.31 mg of L-histidine, about 41.7 mg of soy lecithin, and about 2.5 mL of sterile water for injection, USP.
• the disclosure provides a pharmaceutical composition
• a pharmaceutical composition comprising about 120.2 mg of Compound 1, about 240.4 mg of mannitol, about 16 mg of sodium carboxymethyl cellulose, about 13.6 mg of poloxamer 188, about 8.3 mg of L-histidine, about 80.2 mg of soy lecithin, and about 2.5 mL of sterile water for injection, USP.
• the disclosure provides a pharmaceutical composition consisting essentially of about 120.2 mg of Compound 1, about 240.4 mg of mannitol, about 16 mg of sodium carboxymethyl cellulose, about 13.6 mg of poloxamer 188, about 8.3 mg of L-histidine, about 80.2 mg of soy lecithin, and about 2.5 mL of sterile water for injection, USP.
• the disclosure provides a pharmaceutical composition consisting of about 120.2 mg of Compound 1, about 240.4 mg of mannitol, about 16 mg of sodium carboxymethyl cellulose, about 13.6 mg of poloxamer 188, about 8.3 mg of L-histidine, about 80.2 mg of soy lecithin, and about 2.5 mL of sterile water for injection, USP.
• the disclosure provides a pharmaceutical composition
• a pharmaceutical composition comprising about 120.2 mg of Compound 1, about 120.2 mg of mannitol, about 8.0 mg of sodium carboxymethyl cellulose, about 6.8 mg of poloxamer 188, about 4.1 mg of L-histidine, about 40.1 mg of soy lecithin, and about 2.5 mL of sterile water for injection, USP.
• the disclosure provides a pharmaceutical composition consisting essentially of about 120.2 mg of Compound 1, about 120.2 mg of mannitol, about 8.0 mg of sodium carboxymethyl cellulose, about 6.8 mg of poloxamer 188, about 4.1 mg of L-histidine, about 40.1 mg of soy lecithin, and about 2.5 mL of sterile water for injection, USP.
• the disclosure provides a pharmaceutical composition consisting of about 120.2 mg of Compound 1, about 120.2 mg of mannitol, about 8.0 mg of sodium carboxymethyl cellulose, about 6.8 mg of poloxamer 188, about 4.1 mg of L-histidine, about 40.1 mg of soy lecithin, and about 2.5 mL of sterile water for injection, USP.
• the disclosure provides a pharmaceutical composition comprising lyophilate LI, L2, L3, L4, or L5, see table above, and 1 mL WFI USP, 1.5 mL WFI USP, 2.0 mL WFI USP, 2.5 mL WFI USP, 3.0 mL WFI USP, 3.5 mL WFI USP, 4.0 mL WFI USP, 4.5 mL WFI USP, or 5 mL WFI USP.
• compositions described in this section are collectively referred to as a "Pharmaceutical Composition of the Disclosure.”
• the disclosure provides a method for treating cancer in a subject in need thereof comprising subcutaneously administering a therapeutically effective amount of a Pharmaceutical Composition of the Disclosure to the subject.
• the disclosure provides a method for treating cancer in a subject in need thereof comprising subcutaneously administering a therapeutically effective amount of a Pharmaceutical Composition of the Disclosure to the subject in combination with one or more optional therapeutic agents.
• the disclosure provides a Pharmaceutical Composition of the Disclosure for use in treating cancer in a subject.
• the disclosure provides a Pharmaceutical Composition of the Disclosure for use in treating cancer in a subject, wherein the Pharmaceutical Composition of the Disclosure is to be subcutaneously administered in combination with one or more optional therapeutic agents.
• the Pharmaceutical Composition of the Disclosure is subcutaneously administered to the subject according to an intermittent dosing schedule.
• the Pharmaceutical Composition of the Disclosure may be administered to a subject three days a week on non-consecutive days, e.g., Monday- Wednesday-Friday, or two days a week on non-consecutive days, e.g., Monday and Thursday.
• the cancer is a solid tumor.
• the cancer is a hematological cancer.
• the hematological cancer is acute lymphocytic leukemia, chronic lymphocytic leukemia (including B-cell chronic lymphocytic leukemia), or acute myeloid leukemia.
• the cancer is any one or more of the cancers of Table 1.
• Table 1
• the cancer is any one or more of the cancers of Table 2.
• the cancer is selected from the group consisting of squamous cell carcinoma of the head and neck (SCCHN), adenocarcinoma squamous cell carcinoma of the esophagus, adenocarcinoma of the stomach, adenocarcinoma of the colon, hepatocellular carcinoma, cholangiocarcinoma of the biliary system, adenocarcinoma of gall bladder, adenocarcinoma of the pancreas, ductal carcinoma in situ of the breast, adenocarcinoma of the breast, adenocarcinoma of the lungs, squamous cell carcinoma of the lungs, transitional cell carcinoma of the bladder, squamous cell carcinoma of the bladder, squamous cell carcinoma of the cervix, adenocarcinoma of the cervix, endometrial carcinoma, penile squamous cell carcinoma, and squamous cell carcinoma of
• SCCHN head and neck
• a precancerous tumor is selected from the group consisting of leukoplakia of the head and neck, Barrett's esophagus, metaplasia of the stomach, adenoma of the colon, chronic hepatitis, bile duct hyperplasia, pancreatic intraepithelial neoplasia, atypical adenomatous hyperplasia of the lungs, dysplasia of the bladder, cervical initraepithelial neoplasia, penile intraepithelial neoplasia, and actinic keratosis of the skin.
• the cancer is selected from the group consisting of hepatocellular carcinoma, glioblastoma, lung cancer, breast cancer, head and neck cancer, prostate cancer, melanoma, and colorectal cancer.
• the cancer is selected from the group consisting of colorectal cancer, breast cancer, lymphoma, melanoma, kidney cancer, and lung cancer.
• the cancer has become resistant to conventional cancer treatments.
• conventional cancer treatments refers to any cancer drugs, biologies, or radiotherapy, or combination of cancer drugs and/or biologies and/or radiotherapy that have been tested and/or approved for therapeutic use in humans by the U.S. Food and Drug Administration, European Medicines Agency, or similar regulatory agency.
• a Pharmaceutical Composition of the Disclosure is administered to a subject having cancer as a single agent.
• a Pharmaceutical Composition of the Disclosure is administered to a subject having cancer in combination with one or more optional therapeutic agents.
• a Pharmaceutical Composition of the Disclosure is administered in combination with one optional therapeutic agent.
• a Pharmaceutical Composition of the Disclosure is administered in combination with two optional therapeutic agents.
• a Pharmaceutical Composition of the Disclosure is administered in combination with three optional therapeutic agents.
• Optional therapeutic agents useful in treating cancer patients include those known in the art as well as those developed in the future.
• Optional therapeutic agents are administered in an amount to provide their desired therapeutic effect.
• the effective dosage range for each optional therapeutic agent is known in the art, and the optional therapeutic agent is administered to an individual in need thereof within such established ranges.
• a Pharmaceutical Composition of the Disclosure and the optional therapeutic agent(s) can be administered separately as multi-unit doses in any order, e.g., wherein a Pharmaceutical Composition of the Disclosure is administered before the optional therapeutic agent(s), or vice versa.
• One or more doses of a Pharmaceutical Composition of the Disclosure and the optional therapeutic agent(s) can be administered to the subject.
• the optional therapeutic agent comprises one or more immune checkpoint inhibitors.
• immune checkpoint inhibitors include PD- 1 inhibitors, PD-L1 inhibitors, CTLA-4 inhibitors, LAG3 inhibitors, TIM3 inhibitors, cd47 inhibitors, TIGIT inhibitors, and B7-H1 inhibitors.
• the immune checkpoint inhibitor is selected from the group consisting of a PD-1 inhibitor, a PD-L1 inhibitor, a CTLA-4 inhibitor, a LAG3 inhibitor, a TIM3 inhibitor, and a cd47 inhibitor.
• the immune checkpoint inhibitor is a programmed cell death (PD-1) inhibitor.
• PD-1 is a T-cell coinhibitory receptor that plays a pivotal role in the ability of tumor cells to evade the host's immune system. Blockage of interactions between PD-1 and PD-L1, a ligand of PD-1, enhances immune function and mediates antitumor activity.
• PD-1 inhibitors include antibodies that specifically bind to PD-1. Particular anti-PD-1 antibodies include, but are not limited to nivolumab, pembrolizumab, STI-A1014, pidilzumab, and cemiplimab-rwlc.
• the immune checkpoint inhibitor is a PD-L1 (also known as B7-H1 or CD274) inhibitor.
• PD-L1 inhibitors include antibodies that specifically bind to PD-L1.
• Particular anti-PD-Ll antibodies include, but are not limited to, avelumab, atezolizumab, durvalumab, and BMS-936559.
• the immune checkpoint inhibitor is a CTLA-4 inhibitor.
• CTLA-4 also known as cytotoxic T-lymphocyte antigen 4
• CTLA-4 is a protein receptor that downregulates the immune system.
• CTLA-4 is characterized as a "brake” that binds costimulatory molecules on antigen-presenting cells, which prevents interaction with CD28 on T cells and also generates an overtly inhibitory signal that constrains T cell activation.
• CTLA-4 inhibitors include antibodies that specifically bind to CTLA-4.
• Particular anti-CTLA-4 antibodies include, but are not limited to, ipilimumab and tremelimumab.
• the immune checkpoint inhibitor is a LAG3 inhibitor.
• LAG3, Lymphocyte Activation Gene 3 is a negative co-stimulatory receptor that modulates T cell homeostasis, proliferation, and activation.
• LAG3 has been reported to participate in regulatory T cells (Tregs) suppressive function. A large proportion of LAG3 molecules are retained in the cell close to the microtubuleorganizing center, and only induced following antigen specific T cell activation.
• Regs regulatory T cells
• Examples of LAG3 inhibitors include antibodies that specifically bind to LAG3. Particular anti-LAG3 antibodies include, but are not limited to, GSK2831781.
• the immune checkpoint inhibitor is a TIM3 inhibitor.
• TIM3, T-cell immunoglobulin and mucin domain 3 is an immune checkpoint receptor that functions to limit the duration and magnitude of T H 1 and T C 1 T-cell responses.
• the TIM3 pathway is considered a target for anticancer immunotherapy due to its expression on dysfunctional CD8 + T cells and Tregs, which are two reported immune cell populations that constitute immunosuppression in tumor tissue.
• Examples of TIM 3 inhibitors include antibodies that specifically bind to TIM3.
• the immune checkpoint inhibitor is a cd47 inhibitor. See Unanue, E.R., PNAS 110: 10886-87 (2013).
• the immune checkpoint inhibitor is a TIGIT inhibitor. See Harjunpaa 1 and Guillerey, Clin Exp Immunol 200: 108-119 (2019).
• the one or more immune checkpoint inhibitors are administered to the subject in therapeutically effective amounts. These amounts are guided by standard clinical practice, e.g., according to the prescribing information associated with the immune checkpoint inhibitors.
• about 1 to about 2000 mg can be administered as an intravenous infusion every 2-4 weeks.
• immune checkpoint inhibitor is nivolumab
• 240 mg may be administered to the subject by intravenous infusion every two weeks, or 480 mg may be administered by intravenous infusion every for weeks.
• the immune checkpoint inhibitors is pembrolizumab
• 200 mg may be administered to the subject by intravenous infusion every three weeks
• 400 mg may be administered to the subject by intravenous infusion every six weeks.
• the immune checkpoint inhibitors is avelumab
• 800 mg may be administered to the subject by intravenous infusion every two weeks.
• immune checkpoint inhibitors is atezolizumab
• 840 mg may be administered by intravenous infusion every two weeks
• 1200 mg may be administered by intravenous infusion every three weeks
• 1680 mg may be administered by intravenous infusion every four weeks.
• the immune checkpoint inhibitors is ipilumumab
• 3 mg/kg may be administered to the subject by intravenous infusion every three weeks.
• the immune checkpoint inhibitors is tremelimumab
• 3 to 20 mg/kg may be administered to the subject by intravenous infusion every four weeks.
• immune checkpoint inhibitors is GSK2831781
• 1.5 to 5 mg/kg may be administered to the subject by intravenous infusion every 2-4 weeks.
• the immune checkpoint inhibitor(s) is an antibody, and 1 to 20 mg/kg is administered to the subject by intravenous infusion every 2-4 weeks. In another embodiment, 20-2000 mg of the antibody is administered to the subject by intravenous infusion every 2-4 weeks. In another embodiment, Compound 1 is administered prior to administration of the antibody. In another embodiment, Compound 1 is administered to the subject 1, 2, 3, 4, 5, 6, or 7 days prior to the day of administration of the antibody. In another embodiment, Compound 1 is administered to the subject the day the antibody is administered. In another embodiment, Compound 1 is administered to the subject 1, 2, 3, 4, 5, 6, or 7 days after the day of administration of the antibody.
• the subject receives pembrolizumab administered by intravenous infusion every three weeks and Compound 1 administered two times a week by subcutaneous infusion, wherein the first dose of Compound 1 is administered prior to the first dose of pembrolizumab, the first dose of Compound 1 is administered on the same day as the first dose of pembrolizumab, or the first dose of Compound 1 is administered after to the first dose of pembrolizumab, e.g., until disease progression or until there is no therapeutic benefit.
• the subject receives nivolumab administered by intravenous infusion every two weeks and Compound 1 administered two times a week by subcutaneous infusion, wherein the first dose of Compound 1 is administered prior to the first dose of nivolumab, the first dose of Compound 1 is administered on the same day as the first dose of nivolumab, or the first dose of Compound 1 is administered after to the first dose of nivolumab, e.g., until disease progression or until there is no therapeutic benefit.
• the treatment of the cancer patient with Compound 1 and one or more an immune checkpoint inhibitors induces anti-proliferative response faster than when the immune checkpoint inhibitor is administered alone.
• antibody is meant to include intact monoclonal antibodies, polyclonal antibodies, multispecific antibodies formed from at least two intact antibodies, and antibody fragments, so long as they exhibit the desired biological activity.
• antibody is meant to include soluble receptors that do not possess the Fc portion of the antibody.
• the antibodies are humanized monoclonal antibodies and fragments thereof made by means of recombinant genetic engineering.
• Another class of immune checkpoint inhibitors include polypeptides that bind to and block PD-1 receptors on T-cells without triggering inhibitor signal transduction.
• Such peptides include B7-DC polypeptides, B7-H1 polypeptides, B7-1 polypeptides and B7-2 polypeptides, and soluble fragments thereof, as disclosed in U.S. Pat. 8,114,845.
• Another class of immune checkpoint inhibitors include compounds with peptide moieties that inhibit PD-1 signaling. Examples of such compounds are disclosed in U.S. Pat. 8,907,053.
• Another class of immune checkpoint inhibitors include inhibitors of certain metabolic enzymes, such as indoleamine 2,3 dioxygenase (IDO), which is expressed by infiltrating myeloid cells and tumor cells, and isocitrate dehydrogenase (IDH), which is mutated in leukemia cells. Mutants of the IDH enzyme lead to increased levels of 2- hydroxyglutarate (2-HG), which prevent myeloid differentiation. Stein et al., Blood 130:122-3 (2017); Wouters, Blood 730:693-94 (2017).
• IDO indoleamine 2,3 dioxygenase
• IDH isocitrate dehydrogenase
• IDH blocking agents include, but are not limited to, ivosidenib and enasidenib mesylate. Dalle and DiNardo, Ther Adv Hematol 9 7):163-73 (2016); Nassereddine et al., Onco Targets Ther 72:303-08 (2016).
• the IDO enzyme inhibits immune responses by depleting amino acids that are necessary for anabolic functions in T cells or through the synthesis of particular natural ligands for cytosolic receptors that are able to alter lymphocyte functions. Pardoll, Nature Reviews. Cancer 72:252-64 (2012); Lob, Cancer Immunol Immunother 55:153-57 (2009).
• IDO blocking agents include, but are not limited to, levo-l-methyl typtophan (L-1MT) and 1-methyl- tryptophan (1MT).
• L-1MT levo-l-methyl typtophan
• 1MT 1-methyl- tryptophan
• the immune checkpoint inhibitor is nivolumab, pembrolizumab, pidilizumab, STI-A1110, avelumab, atezolizumab, durvalumab, STI-A1014, ipilimumab, tremelimumab, GSK2831781, BMS-936559 or MED14736.
• the optional therapeutic agent is an epigenetic drug.
• epigenetic drug refers to a therapeutic agent that targets an epigenetic regulator.
• epigenetic regulators include the histone lysine methyltransferases, histone arginine methyl transferases, histone demethylases, histone deacetylases, histone acetylases, and DNA methyltransferases.
• Histone deacetylase inhibitors include, but are not limited to, vorinostat and panobinostat lactate.
• Additional examples of conventional therapies and anticancer agents that can be used in combination with a Pharmaceutical Composition of the Disclosure include surgery, radiotherapy, e.g., gamma-radiation, neutron beam radiotherapy, electron beam radiotherapy, proton therapy, brachytherapy, and systemic radioactive isotopes, endocrine therapy, a biologic response modifier, e.g., an interferon, an interleukin, tumor necrosis factor (TNF), hyperthermia and cryotherapy, an agent to attenuate any adverse effect (e.g., an antiemetic), and any other approved biologic therapy or chemotherapy, e.g., a treatment regimen that uses drugs to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing.
• Chemotherapy may be given by mouth, injection, or infusion, or on the skin, depending on the type and stage of the cancer being treated.
• Nonlimiting exemplary antiproliferative compounds include an aromatase inhibitor; an anti-estrogen; an anti-androgen; a gonadorelin agonist; a topoisomerase I inhibitor; a topoisomerase II inhibitor; a microtubule active agent; an alkylating agent, e.g., temozolomide; a retinoid, a carontenoid, or a tocopherol; a cyclooxygenase inhibitor; an MMP inhibitor; an mTOR inhibitor; an antimetabolite; a platin compound; a methionine aminopeptidase inhibitor; a bisphosphonate; an antiproliferative antibody; a heparanase inhibitor; an inhibitor of Ras oncogenic isoforms; a telomerase inhibitor; a proteasome inhibitor; a compound used in the treatment of hematologic malignancies; a Fit- 3 inhibitor; an Hsp90 inhibitor; a kinesin
• Nonlimiting exemplary aromatase inhibitors include steroids, such as atamestane, exemestane, and formestane, and non-steroids, such as aminoglutethimide, roglethimide, pyridoglutethimide, trilostane, testolactone, ketokonazole, vorozole, fadrozole, anastrozole, and letrozole.
• steroids such as atamestane, exemestane, and formestane
• non-steroids such as aminoglutethimide, roglethimide, pyridoglutethimide, trilostane, testolactone, ketokonazole, vorozole, fadrozole, anastrozole, and letrozole.
• Nonlimiting anti-estrogens include tamoxifen, fulvestrant, raloxifene, and raloxifene hydrochloride.
• Anti-androgens include, but are not limited to, bicalutamide and apalutamide.
• Gonadorelin agonists include, but are not limited to, abarelix, goserelin, and goserelin acetate.
• Nonlimiting exemplary topoisomerase I inhibitors include topotecan, gimatecan, irinotecan, camptothecin and its analogues, 9-nitrocamptothecin, and the macromolecular camptothecin conjugate PNU-166148.
• Topoisomerase II inhibitors include, but are not limited to, anthracyclines, such as doxorubicin, daunorubicin, epirubicin, idarubicin, and nemorubicin; anthraquinones, such as mitoxantrone and losoxantrone; and podophillotoxines, such as etoposide and teniposide.
• Microtubule active agents include microtubule stabilizing, microtubule destabilizing compounds, and microtubulin polymerization inhibitors including, but not limited to, taxanes, such as paclitaxel and docetaxel; discodermolides; cochicine and epothilones and derivatives thereof.
• Nonlimiting exemplary alkylating agents include cyclophosphamide, ifosfamide, melphalan, trabectedin, and nitrosoureas, such as carmustine and lomustine.
• MMP inhibitors include collagen peptidomimetic and nonpeptidomimetic inhibitors, tetracycline derivatives, batimastat, marimastat, prinomastat, metastat, BMS-279251, BAY 12- 9566, TAA211, MMI270B, and AAJ996.
• Nonlimiting exemplary mTOR inhibitors include compounds that inhibit the mammalian target of rapamycin (mTOR) and possess antiproliferative activity such as sirolimus, everolimus, CCI-779, and ABT578.
• Nonlimiting exemplary antimetabolites include 5 -fluorouracil (5-FU), capecitabine, gemcitabine, DNA demethylating compounds, such as 5-azacytidine and decitabine, methotrexate and edatrexate, and folic acid antagonists, such as pemetrexed.
• 5-FU 5 -fluorouracil
• capecitabine gemcitabine
• gemcitabine DNA demethylating compounds, such as 5-azacytidine and decitabine
• methotrexate and edatrexate methotrexate and edatrexate
• folic acid antagonists such as pemetrexed.
• Nonlimiting exemplary platin compounds include carboplatin, cis-platin, cisplatinum, and oxaliplatin.
• Nonlimiting exemplary methionine aminopeptidase inhibitors include bengamide or a derivative thereof and PPI-2458.
• Nonlimiting exemplary bisphosphonates include etridonic acid, clodronic acid, tiludronic acid, pamidronic acid, alendronic acid, ibandronic acid, risedronic acid, and zoledronic acid.
• Nonlimiting exemplary heparanase inhibitors include compounds that target, decrease, or inhibit heparin sulfate degradation, such as PI-88 and OGT2115.
• Nonlimiting exemplary compounds which target, decrease, or inhibit the oncogenic activity of Ras include famesyl transferase inhibitors, such as L-744832, DK8G557, tipifarnib, and lonafarnib.
• Nonlimiting exemplary telomerase inhibitors include compounds that target, decrease, or inhibit the activity of telomerase, such as compounds that inhibit the telomerase receptor, such as telomestatin.
• Nonlimiting exemplary proteasome inhibitors include compounds that target, decrease, or inhibit the activity of the proteasome including, but not limited to, bortezomib.
• the proteasome inhibitor is carfilzomib or ixazomib.
• Nonlimiting exemplary FMS-like tyrosine kinase inhibitors which are compounds targeting, decreasing or inhibiting the activity of FMS-like tyrosine kinase receptors (Flt-3R), include gilteritinib, interferon, I-P-D-arabinofuransylcytosine (ara- c), and bisulfan; and ALK inhibitors, which are compounds that target, decrease, or inhibit anaplastic lymphoma kinase, include alectinib, brigatinib, and lorlatinib.
• Nonlimiting exemplary Flt-3 inhibitors include PKC412, midostaurin, a staurosporine derivative, SU11248, MLN518, and gilteritinib.
• Nonlimiting exemplary HSP90 inhibitors include compounds targeting, decreasing, or inhibiting the intrinsic ATPase activity of HSP90; or degrading, targeting, decreasing or inhibiting the HSP90 client proteins via the ubiquitin proteosome pathway.
• Compounds targeting, decreasing or inhibiting the intrinsic ATPase activity of HSP90 are especially compounds, proteins, or antibodies that inhibit the ATPase activity of HSP90, such as 17-allylamino,17-demethoxygeldanamycin (17AAG), a geldanamycin derivative; other geldanamycin related compounds; radicicol and HD AC inhibitors.
• Nonlimiting exemplary protein tyrosine kinase and/or serine and/or threonine kinase inhibitors or lipid kinase inhibitors include a) a compound targeting, decreasing, or inhibiting the activity of the platelet-derived growth factor-receptors (PDGFR), such as a compound that targets, decreases, or inhibits the activity of PDGFR, including olaratumab and N-phenyl-2-pyrimidine-amine derivatives, such as imatinib, SU1O1, SU6668, and GFB-111; b) a compound targeting, decreasing, or inhibiting the activity of the fibroblast growth factor-receptors (FGFR), such as erdafitinib and lenvatinib; c) a compound targeting, decreasing, or inhibiting the activity of the insulin-like growth factor receptor I (IGF-IR), such as brigatinib; d) a compound targeting, decreasing, or inhibiting the activity
• Bcr-Abl kinase and mutants, such as an N-phenyl-2-pyrimidine-amine derivative, such as imatinib or nilotinib; PD180970; AG957; NSC 680410; PD173955; or dasatinib; k) a compound targeting, decreasing, or inhibiting the activity of members of the protein kinase C (PKC) and Raf family of serine/threonine kinases, members of the MEK, SRC, JAK, FAK, PDK1, PKB/Akt, and Ras/MAPK family members, and/or members of the cyclin-dependent kinase family (CDK), such as a staurosporine derivative disclosed in U.S.
• PKC protein kinase C
• Raf family of serine/threonine kinases members of the MEK, SRC, JAK, FAK, PDK1, PKB/Akt, and Ras/MAPK family members,
• Patent No. 5,093,330 such as midostaurin
• examples of further compounds include UCN-01, safingol, BAY 43-9006, bryostatin 1, perifosine; ilmofosine; RO 318220 and RO 320432; GO 6976; Isis 3521; LY333531/LY379196; a isochinoline compound; a farnesyl transferase inhibitor; PD 184352 or QAN697, or AT7519; abemaciclib; binimetinib; cobimetinib; encorafenib; neratinib; palbociclib; ribociclib; 1) a compound targeting, decreasing or inhibiting the activity of a protein-tyrosine kinase, such as acalabrutinib, imatinib mesylate or a tyrphostin, such as Tyrphostin A23/RG- 50810; AG 99; Tyrp
• Nonlimiting exemplary compounds that target, decrease, or inhibit the activity of a protein or lipid phosphatase include inhibitors of phosphatase 1, phosphatase 2 A, or CDC25, such as okadaic acid or a derivative thereof.
• Further anti-angiogenic compounds include compounds having another mechanism for their activity unrelated to protein or lipid kinase inhibition, e.g., thalidomide and TNP-470.
• Additional, nonlimiting, exemplary chemotherapeutic compounds include: avastin, daunorubicin, adriamycin, Ara-C, VP-16, teniposide, mitoxantrone, idarubicin, carboplatinum, PKC412, 6-mercaptopurine (6-MP), fludarabine phosphate, octreotide, SOM230, FTY720, 6-thioguanine, cladribine, 6- mercaptopurine, pentostatin, hydroxyurea, 2-hydroxy-lH-isoindole-l, 3-dione derivatives, l-(4-chloroanilino)-4-(4-pyridylmethyl)phthalazine or a pharmaceutically acceptable salt thereof, l-(4-chloroanilino)-4-(4-pyridylmethyl)phthalazine
• a number of suitable optional therapeutic, e.g., anticancer, agents are contemplated for use in the therapeutic methods provided herein. Indeed, the methods provided herein can include, but are not limited to, administration of numerous optional therapeutic agents such as: agents that induce apoptosis; polynucleotides (e.g., antisense, ribozymes, siRNA); polypeptides (e.g., enzymes and antibodies); biological mimetics (e.g., gossypol or BH3 mimetics); agents that bind (e.g., oligomerize or complex) with a Bcl-2 family protein such as Bax; alkaloids; alkylating agents; antitumor antibiotics; antimetabolites; hormones; platinum compounds; monoclonal or polyclonal antibodies (e.g., antibodies conjugated with anticancer drugs, toxins, defensins), toxins; radionuclides; biological response modifiers (e.g., interferons (e
• optional therapeutic agents comprise agents that induce or stimulate apoptosis.
• Agents that induce or stimulate apoptosis include, for example, agents that interact with or modify DNA, such as by intercalating, cross-linking, alkylating, or otherwise damaging or chemically modifying DNA.
• Agents that induce apoptosis include, but are not limited to, radiation (e.g., X-rays, gamma rays, UV); tumor necrosis factor (TNF)-related factors (e.g., TNF family receptor proteins, TNF family ligands, TRAIL, antibodies to TRAIL-R1 or TRAIL-R2); kinase inhibitors (e.g., epidermal growth factor receptor (EGFR) kinase inhibitor).
• radiation e.g., X-rays, gamma rays, UV
• TNF tumor necrosis factor
• TRAIL TNF family receptor proteins
• TRAIL TRAIL
• TRAIL antibodies to TRAIL-R1 or TRAIL-R2
• kinase inhibitors e.g., epidermal growth factor receptor (EGFR) kinase inhibitor
• vascular growth factor receptor (VGFR) kinase inhibitor vascular growth factor receptor (VGFR) kinase inhibitor, fibroblast growth factor receptor (FGFR) kinase inhibitor, platelet-derived growth factor receptor (PDGFR) kinase inhibitor, and Bcr-Abl kinase inhibitors (such as GLEEVEC)); antisense molecules; antibodies (e.g., HERCEPTIN, RITUXAN, ZEVALIN, and AVASTIN); anti-estrogens (e.g., raloxifene and tamoxifen); anti-androgens (e.g., flutamide, apalutamide, bicalutamide, finasteride, aminoglutethamide, ketoconazole, and corticosteroids); BCL-2 inhibitors (e.g., venetoclax); cyclooxygenase 2 (COX-2) inhibitors (e.g., celecoxib, meloxicam, NS-398,
• the therapeutic methods provided herein include administering to a subject having cancer (a cancer patient) therapeutically effective amounts of a Pharmaceutical Composition of the Disclosure, an immune checkpoint inhibitor, and at least one additional optional therapeutic agent, e.g., an anti- hyperproliferative or antineoplastic agent selected from alkylating agents, antimetabolites, and natural products (e.g., herbs and other plant and/or animal derived compounds).
• a pharmaceutical Composition of the Disclosure e.g., an immune checkpoint inhibitor selected from alkylating agents, antimetabolites, and natural products (e.g., herbs and other plant and/or animal derived compounds).
• Alkylating agents suitable for use in the present methods include, but are not limited to: 1) nitrogen mustards (e.g., mechlorethamine, cyclophosphamide, ifosfamide, melphalan (L-sarcolysin); and chlorambucil); 2) ethylenimines and methylmelamines (e.g., hexamethylmelamine and thiotepa); 3) alkyl sulfonates (e.g., busulfan); 4) nitrosoureas (e.g., carmustine (BCNU); lomustine (CCNU); semustine (methyl- CCNU); and streptozocin (streptozotocin)); and 5) triazenes (e.g., dacarbazine (DTIC; dimethyltri azenoimid-azolecarboxami de).
• nitrogen mustards e.g., mechlorethamine, cyclophosphamide,
• antimetabolites suitable for use in the present methods include, but are not limited to: 1) folic acid analogs (e.g., methotrexate (amethopterin)); 2) pyrimidine analogs (e.g., fluorouracil (5-fluorouracil; 5-FU), floxuridine (fluorode- oxyuridine; FudR), and cytarabine (cytosine arabinoside)); and 3) purine analogs (e.g., mercaptopurine (6-mercaptopurine; 6-MP), thioguanine (6-thioguanine; TG), and pentostatin (2'-deoxycoformycin)).
• folic acid analogs e.g., methotrexate (amethopterin)
• pyrimidine analogs e.g., fluorouracil (5-fluorouracil; 5-FU), floxuridine (fluorode- oxyuridine; FudR), and cytarabine (
• chemotherapeutic agents suitable for use in the methods of the present disclosure include, but are not limited to: 1) vinca alkaloids (e.g., vinblastine (VLB), vincristine); 2) epipodophyllotoxins (e.g., etoposide and teniposide); 3) antibiotics (e.g., dactinomycin (actinomycin D), daunorubicin (daunomycin; rubidomycin), doxorubicin, bleomycin, plicamycin (mithramycin), and mitomycin (mitomycin C)); 4) enzymes (e.g., L-asparaginase); 5) biological response modifiers (e.g., interferon-alfa); 6) platinum coordinating complexes (e.g., cisplatin (cis-DDP) and carboplatin); 7) anthracenediones (e.g., mitoxantrone); 8)
• vinca alkaloids e
• any oncolytic agent that is routinely used in a cancer therapy context finds use in the therapeutic methods of the present disclosure.
• the U.S. Food and Drug Administration (FDA) maintains a formulary of oncolytic agents approved for use in the United States. International counterpart agencies to the FDA maintain similar formularies.
• FDA Food and Drug Administration
• product labels required on all U.S. approved chemotherapeutics describe approved indications, dosing information, toxicity data, and the like, for the exemplary agents.
• Anticancer agents further include compounds which have been identified to have anticancer activity. Examples include, but are not limited to, 3-AP, 12-0- tetradecanoylphorbol- 13 -acetate, 17AAG, 852A, ABI-007, ABR-217620, ABT-751, ADI-PEG 20, AE-941, AG-013736, AGRO 100, alanosine, AMG 706, antibody G250, antineoplastons, AP23573, apaziquone, APC8015, atiprimod, ATN-161, atrasenten, azacitidine, BB-10901, BCX-1777, bevacizumab, BG00001, bicalutamide, BMS 247550, bortezomib, bryostatin-1, buserelin, calaspargase pegol-mknl, calcitriol, CCI- 779, CDB-2914, cefixime, cetuximab, CG0070
• the optional therapeutic agent comprises one of the anti-cancer drugs or anti-cancer drug combinations listed in Table 5.
• the methods of treating cancer provided herein comprise administering a Pharmaceutical Composition of the Disclosure to a subject in combination with radiation therapy and, optionally, an immune checkpoint inhibitor.
• the methods provided herein are not limited by the types, amounts, or delivery and administration systems used to deliver the therapeutic dose of radiation to a patient.
• the patient may receive photon radiotherapy, particle beam radiation therapy, other types of radiotherapies, and combinations thereof.
• the radiation is delivered to the patient using a linear accelerator. In still other embodiments, the radiation is delivered using a gamma knife.
• the source of radiation can be external or internal to the patient.
• External radiation therapy is most common and involves directing a beam of high-energy radiation to a tumor site through the skin using, for instance, a linear accelerator. While the beam of radiation is localized to the tumor site, it is nearly impossible to avoid exposure of normal, healthy tissue. However, external radiation is usually well tolerated by patients.
• Internal radiation therapy involves implanting a radiation-emitting source, such as beads, wires, pellets, capsules, particles, and the like, inside the body at or near the tumor site including the use of delivery systems that specifically target cancer cells (e.g., using particles attached to cancer cell binding ligands). Such implants can be removed following treatment, or left in the body inactive.
• Types of internal radiation therapy include, but are not limited to, brachytherapy, interstitial irradiation, intracavity irradiation, radioimmunotherapy, and the like.
• the patient may optionally receive radiosensitizers (e.g., metronidazole, misonidazole, intra-arterial Budr, intravenous iododeoxyuridine (ludR), nitroimidazole, 5-substituted-4-nitroimidazoles, 2H-isoindolediones, [[(2-bromoethyl)-amino]methyl]- nitro-lH-imidazole-l-ethanol, nitroaniline derivatives, DNA-affinic hypoxia selective cytotoxins, halogenated DNA ligand, 1,2,4 benzotriazine oxides, 2-nitroimidazole derivatives, fluorine-containing nitroazole derivatives, benzamide, nicotinamide, acridine-intercalator, 5-thiotretrazole derivative, 3-nitro-l,2,4-triazole, 4,5- dinitroimidazole derivative, hydroxylated texaphrin
• any type of radiation can be administered to a patient, so long as the dose of radiation is tolerated by the patient without unacceptable negative side-effects.
• Suitable types of radiotherapy include, for example, ionizing (electromagnetic) radiotherapy (e.g., X-rays or gamma rays) or particle beam radiation therapy (e.g., high linear energy radiation).
• Ionizing radiation is defined as radiation comprising particles or photons that have sufficient energy to produce ionization, i.e., gain or loss of electrons (as described in, for example, U.S. 5,770,581 incorporated herein by reference in its entirety).
• the effects of radiation can be at least partially controlled by the clinician.
• the dose of radiation is fractionated for maximal target cell exposure and reduced toxicity.
• the total dose of radiation administered to a patient is about .01 Gray (Gy) to about 100 Gy.
• about 10 Gy to about 65 Gy e.g., about 15 Gy, 20 Gy, 25 Gy, 30 Gy, 35 Gy, 40 Gy, 45 Gy, 50 Gy, 55 Gy, or 60 Gy
• a complete dose of radiation can be administered over the course of one day
• the total dose is ideally fractionated and administered over several days.
• radiotherapy is administered over the course of at least about 3 days, e.g., at least 5, 7, 10, 14, 17, 21, 25, 28, 32, 35, 38, 42, 46, 52, or 56 days (about 1-8 weeks).
• a daily dose of radiation will comprise approximately 1-5 Gy (e.g., about 1 Gy, 1.5 Gy, 1.8 Gy, 2 Gy, 2.5 Gy, 2.8 Gy, 3 Gy, 3.2 Gy, 3.5 Gy, 3.8 Gy, 4 Gy, 4.2 Gy, or 4.5 Gy), or 1-2 Gy (e.g., 1.5-2 Gy).
• the daily dose of radiation should be sufficient to induce destruction of the targeted cells.
• radiation is not administered every day, thereby allowing the animal to rest and the effects of the therapy to be realized.
• radiation desirably is administered on 5 consecutive days, and not administered on 2 days, for each week of treatment, thereby allowing 2 days of rest per week.
• radiation can be administered 1 day/week, 2 days/week, 3 days/week, 4 days/week, 5 days/week, 6 days/week, or all 7 days/week, depending on the animal's responsiveness and any potential side effects.
• Radiation therapy can be initiated at any time in the therapeutic period. In one embodiment, radiation is initiated in week 1 or week 2, and is administered for the remaining duration of the therapeutic period. For example, radiation is administered in weeks 1-6 or in weeks 2-6 of a therapeutic period comprising 6 weeks for treating, for instance, a solid tumor. Alternatively, radiation is administered in weeks 1-5 or weeks 2-5 of a therapeutic period comprising 5 weeks.
• These exemplary radiotherapy administration schedules are not intended, however, to limit the methods provided herein.
• the disclosure provides a method of making a Lyophilate of the Disclosure, the method comprising:
• the bulking agent is mannitol.
• the pre-lyophilization solution further comprises ethanol. In another embodiment, the pre-lyophilization solution further comprises t-butanol.
• the disclosure provides a method of making a Lyophilate of the Disclosure, the method comprising:
• Compound 1 is dissolved in a mixture of t-butanol, ethanol, and water at a temperature of about 25 °C to about 35°C. In another embodiment, the temperature is about 25 °C to about 30°C. In another embodiment, the temperature is about 25 °C. In another embodiment, the temperature is about 30 °C.
• the pre-lyophilization solution further comprises sodium carboxymethyl cellulose. In another embodiment, the pre-lyophilization solution further comprises poloxamer 188. In another embodiment, the pre-lyophilization solution further comprises soy lecithin. In another embodiment, the pre-lyophilization solution further comprises L-histidine. In another embodiment, the pre-lyophilization solution further comprises ethanol, t-butanol, sodium carboxymethyl cellulose, poloxamer 188, soy lecithin, and L-histidine.
• the concentration of Compound 1 in the pre-lyophilization solution is about 1 mg/mL to about 15 mg/mL. In another embodiment, the concentration of Compound 1 in the pre-lyophilization solution is about 10 mg/mL.
• the disclosure provides a method of making a Pharmaceutical Composition of the Disclosure, the method comprising suspending a Lyophilate of the Disclosure in a solvent.
• the solvent comprises water.
• the disclosure provides a kit comprising a Lyophilate of the Disclosure packaged as single unit dose in a vial.
• the vial has a stopper and a cap.
• the vial is glass.
• the disclosure provides a kit comprising a Lyophilate of the Disclosure packaged as single unit dose in a vial for the treatment of cancer in a subject.
• the kit further comprises instructions for suspending the lyophilate in a solvent to give a Pharmaceutical Composition of the Disclosure.
• the kit further comprises instructions for administering the Pharmaceutical Composition of the Disclosure to a subject.
• the kit further comprises an optional therapeutic agent.
• the kit further comprises a device suitable for administering the Pharmaceutical Composition of the Disclosure to a subject subcutaneously.
• lyophilate refers to a powder obtained by lyophilization.
• lyophilization refers to a freeze-drying process by which Compound 1 is frozen and, while still in the frozen state, water and other solvents, if present, are removed by sublimation under vacuum.
• Compound 1 may be lyophilized in the presence of other agents, e.g., bulking agents, cellulose-based suspension modulators, poloxamer-based suspension modulators, lecithin-based suspension modulators, buffering agents, in order to enhance the properties of the lyophilate thus obtained and/or the properties of any pharmaceutical composition comprising the lyophilate.
• solvent refers to a liquid e.g., water, or mixture of liquids, e.g., water and ethanol, that is suitable for administration to a subject as part of a pharmaceutical composition or formulation.
• the solvent comprises a combination of water and one, two, three, or four additional pharmaceutically acceptable water miscible solvents, e.g., dioxolanes, dimethylacetamide, butylene glycol, polyethylene glycol, glycerin, ethanol, and the like, or a combination thereof.
• the solvent is water.
• the solvent is a combination of water and one additional pharmaceutically acceptable water miscible solvent.
• the solvent is a combination of water and ethanol.
• the solvent comprises a combination of water and one, two, three, or four additional pharmaceutically acceptable water immiscible solvents, e.g., peanut oil, ethyl oleate, and the like.
• the solvent comprises about 10% to about 30% of water and about 70% to about 90% of a water miscible solvent, e.g., ethanol.
• the solvent comprises about 15% to about 25% of water and about 75% to about 85% of a water miscible solvent.
• the solvent consists essentially of about 20% of water and about 80% of a water miscible solvent.
• bulking agent refers to a pharmaceutically acceptable excipient that provides structure to the lyophilized cake to prevent shrinkage and collapse.
• exemplary non-limiting bulking agents include mannitol, lactose, sucrose, polyethylene glycol, and glycine.
• cellulose-based suspension modulator refers to a polysaccharide consisting of a linear chain of (1— >4) linked D-glucose units.
• exemplary non-limiting cellulose-based suspension modulators include hydroxypropylcellulose, hydroxymethylcellulose, and sodium carboxymethyl cellulose.
• polyxamer-based suspension modulator refers to nonionic triblock copolymer comprising a central hydrophobic chain of polyoxypropylene flanked by two hydrophilic chains of polyoxyethylene.
• exemplary non-limiting poloxamer-based suspension modulators include pol oxamer 188, NF (Pluronic® F-68) and poloxamer 407 (Pluronic® F-127).
• lecithin-based suspension modulator refers to a mixture comprising glycerophospholipids, e.g., phosphatidyl choline, phosphatidyl ethanolamine, phosphatidyl inositol, phosphatidyl serine, and phosphatidic acid.
• glycerophospholipids e.g., phosphatidyl choline, phosphatidyl ethanolamine, phosphatidyl inositol, phosphatidyl serine, and phosphatidic acid.
• An exemplary non-limiting lecithin-based suspension modulator is soy lecithin.
• buffering agent refers to a pharmaceutically acceptable excipient that helps maintain the pH during lyophilization and after reconstitution of the resulting lyophilate.
• buffering agents include glycine, L- histidine, phosphate, acetic acid, lactic acid, citric acid, and Tris.
• diluent refers to a liquid used to dilute a pharmaceutical composition before parenteral administration to a subject.
• the diluent is normal saline, 5% dextrose, lactated Ringer’s solution, or any other sterile fluid designed to be compatible with administration, e.g., by intravenous infusion, to humans.
• the diluent is normal saline.
• weight ratio refers to mass of Compound 1 divided by the mass of another agent, e.g., a bulking agent or a buffering agent, in the lyophilate.
• another agent e.g., a bulking agent or a buffering agent
• the Compound 1/bulking agent weight ratio in a lyophilate comprising 67.5 mg of Compound 1 and 135 mg of mannitol is 0.5.
• the Compound 1/buffering agent weight ratio in a lyophilate comprising 67.5 mg of Compound 1, 135 mg of mannitol, and 3.88 mg of L-histidine is 17.4.
• % wt/wt refers to the mass of one lyophilate ingredient divided by the combined mass of all lyophilate ingredients, times 100.
• average particle size distribution or "Dso" as used herein is the diameter where 50 mass-% of the particles have a larger equivalent diameter, and the other 50 mass-% have a smaller equivalent diameter as determined by laser diffraction.
• intermittent dose administration refers to non-continuous administration of a Pharmaceutical Composition of the Disclosure to a subject.
• Intermittent dose administration regimens useful in the present disclosure encompass any discontinuous administration regimen that provides a therapeutically effective amount of a Pharmaceutical Composition of the Disclosure to a subject in need thereof.
• Intermittent dosing regimens can use equivalent, lower, or higher doses of a Pharmaceutical Composition of the Disclosure than would be used in continuous dosing regimens.
• Advantages of intermittent dose administration include, but are not limited to, improved safety, decreased toxicity, e.g., decreased weight loss, increased exposure, increased efficacy, and/or increased subject compliance. These advantages may be realized when a Pharmaceutical Composition of the Disclosure is administered as a single agent or when administered in combination with one or more additional therapeutic agents, e.g., an immune checkpoint inhibitor.
• a Pharmaceutical Composition of the Disclosure is administered to the subject according to an intermittent dosing schedule to treat cancer.
• the intermittent dosing schedule increases the therapeutic index of the Pharmaceutical Composition of the Disclosure.
• the therapeutic index is a comparison of the amount of the Pharmaceutical Composition of the Disclosure that causes the therapeutic effect, e.g., decrease in tumor mass, increase in time to tumor progression, and/or increase in subject survival time, to the amount that causes toxicity, e.g. body weight loss.
• the Pharmaceutical Composition of the Disclosure is administered to the subject every other day.
• the Pharmaceutical Composition of the Disclosure is administered to the subject once a week.
• the Pharmaceutical Composition of the Disclosure is administered to the subject twice a week on consecutive days, e.g., on Monday and Tuesday.
• the Pharmaceutical Composition of the Disclosure is administered to the subject twice a week on non-consecutive days, e.g., on Monday and Wednesday, on Monday and Thursday, or on Tuesday and Friday.
• the Pharmaceutical Composition of the Disclosure is administered to the subject twice a week on Monday and Thursday.
• the Pharmaceutical Composition of the Disclosure is administered to the subject twice a week on Tuesday and Friday.
• the Pharmaceutical Composition of the Disclosure is administered to the subject three times a week on consecutive days, e.g., on Monday, Tuesday, and Wednesday.
• the Pharmaceutical Composition of the Disclosure is administered to the subject three times a week on non-consecutive days, e.g., on Monday, Wednesday, and Friday.
• the Pharmaceutical Composition of the Disclosure is administered to the subject four times a week on consecutive days, e.g., on Monday, Tuesday, Wednesday and Thursday.
• the Pharmaceutical Composition of the Disclosure is administered to the subject four times a week on nonconsecutive days, e.g., on Monday, Tuesday, Thursday, and Friday.
• the Pharmaceutical Composition of the Disclosure is administered to the subject five times a week on consecutive days, e.g., on Monday, Tuesday, Wednesday, Thursday and Friday.
• Concurrent administration means that two or more agents are administered concurrently to the subject being treated.
• concurrently it is meant that each agent is administered either simultaneously or sequentially in any order at different points in time. However, if not administered simultaneously, it is meant that they are administered to an individual in a sequence and sufficiently close in time so as to provide the desired therapeutic effect and can act in concert.
• a Pharmaceutical Composition of the Disclosure can be administered to a subject at the same time or sequentially in any order at different points in time as the optional therapeutic agent.
• a Pharmaceutical Composition of the Disclosure and an optional therapeutic agent can be administered separately, in any appropriate form and by any suitable route.
• a Pharmaceutical Composition of the Disclosure and an optional therapeutic agent are not administered concurrently, it is understood that they can be administered in any order to a subject in need thereof.
• a Pharmaceutical Composition of the Disclosure can be administered prior to (e.g., 5 minutes, 15 minutes, 30 minutes, 45 minutes, 1 hour, 2 hours, 4 hours, 6 hours, 12 hours, 24 hours, 48 hours, 72 hours, 96 hours, 1 week, or more before), concomitantly with, or subsequent to (e.g., 5 minutes, 15 minutes, 30 minutes, 45 minutes, 1 hour, 2 hours, 4 hours, 6 hours, 12 hours, 24 hours, 48 hours, 72 hours, 96 hours, 1 week, or more after) an optional therapeutic agent.
• the terms “treat,” “treating,” “treatment,” “therapeutic methods,” and the like refer to eliminating, reducing, or ameliorating a disease or condition, and/or symptoms associated therewith. Although not precluded, treating a disease or condition does not require that the disease, condition, or symptoms associated therewith be completely eliminated. However, in one embodiment, administration of Compound 1 and, optionally, one or more optional therapeutic agents leads to remission of the cancer.
• a therapeutically effective amount refers to that amount of the therapeutic agent sufficient to result in amelioration of one or more symptoms of a disorder, or prevent advancement of a disorder, or cause regression of the disorder.
• a therapeutically effective amount will refer to the amount of a therapeutic agent that causes a therapeutic response, e.g., normalization of blood counts, decrease in the rate of tumor growth, decrease in tumor mass, decrease in the number of metastases, increase in time to tumor progression, and/or increase subject survival time by at least about 2%, at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, or
• pharmaceutically acceptable carrier or “pharmaceutically acceptable vehicle” encompasses any of the standard pharmaceutical carriers, solvents, surfactants, or vehicles. Suitable pharmaceutically acceptable vehicles include aqueous vehicles and nonaqueous vehicles. Standard pharmaceutical carriers and their formulations are described in Remington's Pharmaceutical Sciences, Mack Publishing Co., Easton, PA, 19th ed. 1995.
• container means any receptacle and closure therefore suitable for storing, shipping, dispensing, and/or handling a pharmaceutical product. In one embodiment, the container is a vial.
• the term "insert” means information accompanying a pharmaceutical product that provides a description of how to administer the product, along with the safety and efficacy data required to allow the physician, pharmacist, and patient to make an informed decision regarding use of the product.
• the package insert generally is regarded as the "label" for a pharmaceutical product.
• two or more agents when administered in combination, two or more agents can have a synergistic effect.
• the terms “synergy,” “synergistic,” “synergistically” and derivations thereof, such as in a “synergistic effect” or a “synergistic combination” or a “synergistic composition” as used herein refer to circumstances under which the biological activity of a combination of an agent and at least one additional therapeutic agent is greater than the sum of the biological activities of the respective agents when administered individually.
• the term “synergistically effective” as used herein refers to the interaction between Compound 1 and one or more immune checkpoint inhibitors that causes the total effect of the drugs to be greater than the sum of the individual effects of each drug. See, e.g, Berenbaum, Pharmacological Reviews 47:93-141 (1989).
• the disclosure provides the following particular embodiments.
• Embodiment 1 A lyophilate comprising Compound 1 and a bulking agent.
• Embodiment 2 The lyophilate of Embodiment 1 comprising about 67.5 mg of Compound 1.
• Embodiment s The lyophilate of Embodiments 1 or 2, wherein the Compound 1/bulking agent weight ratio is about 5 to about 0.05.
• Embodiment 4 The lyophilate of Embodiment 3, wherein the
• Compound 1/bulking agent weight ratio is about 1 to about 0.2.
• Embodiment 5 The lyophilate of Embodiment 5, wherein the
• Compound 1/bulking agent weight ratio is about 0.5 [0231] Embodiment 6.
• Embodiment 7 The lyophilate of Embodiment 6 comprising about
• Embodiment 8 The lyophilate of any one of Embodiments 1-7 further comprising a cellulose-based suspension modulator.
• Embodiment 9 The lyophilate of Embodiment 8, wherein the
• Compound 1/cellulose-based suspension modulator ratio is about 25 to about 0.3.
• Embodiment 10 The lyophilate of Embodiment 9, wherein the
• Compound 1/cellulose-based suspension modulator weight ratio is about 5 to about 2.
• Embodiment 11 The lyophilate of Embodiment 10, wherein the
• Compound 1/cellulose-based suspension modulator weight ratio is about 2.7 or about 7.5.
• Embodiment 12 The method of any one of Embodiments 8-11, wherein the cellulose-based suspension modulator is sodium carboxymethyl cellulose.
• Embodiment 13 The lyophilate of Embodiment 12 comprising about
• Embodiment 14 The lyophilate of any one of Embodiments 1-13 further comprising a poloxamer-based suspension modulator.
• Embodiment 15 The lyophilate of Embodiment 14, wherein the
• Compound 1/poloxamer-based suspension modulator ratio is about 80 to about 1.
• Embodiment 16 The lyophilate of Embodiment 15, wherein the
• Compound 1/poloxamer-based suspension modulator weight ratio is about 10 to about 6.
• Embodiment 17 The lyophilate of Embodiment 16, wherein the
• Compound 1/poloxamer-based suspension modulator weight ratio is about 8.8.
• Embodiment 18 The lyophilate of any one of Embodiments 14-17, wherein the poloxamer-based suspension modulator is Poloxamer 188.
• Embodiment 19 The lyophilate of Embodiment 18 comprising about
• Embodiment 20 The lyophilate of any one of Embodiments 1-19 further comprising a lecithin-based suspension modulator.
• Embodiment 21 The lyophilate of Embodiment 20, wherein the
• Compound 1/lecithin-based suspension modulator ratio is about 20 to about 0.1.
• Embodiment 22 The lyophilate of Embodiment 21, wherein the
• Compound 1/lecithin-based suspension modulator weight ratio is about 10 to about 0.5.
• Embodiment 23 The lyophilate of Embodiment 22, wherein the
• Compound 1/lecithin-based suspension modulator weight ratio is about 1.5.
• Embodiment 24 The lyophilate of any one of Embodiments 20-23, wherein the lecithin-based suspension modulator is soy lecithin.
• Embodiment 25 The lyophilate of Embodiment 24 comprising about
• Embodiment 26 The lyophilate of any one of Embodiments 1-25 further comprising a buffering agent.
• Embodiment 27 The lyophilate of Embodiment 26, wherein the
• Compound 1/buffering agent weight ratio is about 50 to about 1.
• Embodiment 28 The lyophilate of Embodiment 27, wherein the
• Compound l/buffering agent weight ratio is about 20 to about 10.
• Embodiment 29 The lyophilate of Embodiment 28, wherein the
• Compound l/buffering agent weight ratio is about 17.4.
• Embodiment 30 The lyophilate of any one of Embodiments 26-29, wherein buffering agent is L-histidine.
• Embodiment 31 The lyophilate of Embodiment 30 comprising about 3.88 mg of L-histidine.
• Embodiment 32 A pharmaceutical composition comprising the lyophilate of any one of Embodiments 1-31, wherein the lyophilate is suspended in a solvent.
• Embodiment 33 The pharmaceutical composition of Embodiment 32, wherein the solvent comprises water.
• Embodiment 34 The pharmaceutical composition of Embodiments 32 or
• Embodiment 35 The pharmaceutical composition of any one of
• Embodiments 32-34 wherein the average particle size distribution of Compound 1 in the suspension is about 1 pm to about 30 pm after 3 days at 2-8 °C.
• Embodiment 36 A method for treating cancer in a subject in need thereof, the method comprising administering a therapeutically effective amount of the pharmaceutical composition of any one of Embodiments 32-35 to the subject.
• Embodiment 37 The method of Embodiment 36, wherein the pharmaceutical composition is administered subcutaneous to the subject.
• Embodiment 38 The method of Embodiments 36 or 37 further comprising administering an optional therapeutic agent to the subject.
• Embodiment 39 A method of making the lyophilate of Embodiment 1, the method comprising:
• Embodiment 40 The method of Embodiment 39, wherein the bulking agent is mannitol.
• Embodiment 41 The method of Embodiments 39 or 40, wherein the pre- lyophilization solution further comprises ethanol.
• Embodiment 42 The method of any one of Embodiments 39-41, wherein the pre-lyophilization solution further comprises t-butanol.
• Embodiment 43 The method of any one of Embodiments 39-42, wherein the pre-lyophilization solution further comprises sodium carboxymethyl cellulose.
• Embodiment 44 The method of any one of Embodiments 39-43, wherein the pre-lyophilization solution further comprises poloxamer 188.
• Embodiment 45 The method of any one of Embodiments 39-44, wherein the pre-lyophilization solution further comprises soy lecithin.
• Embodiment 46 The method of any one of Embodiments 39-45, wherein the pre-lyophilization solution further comprises L-histidine.
• Embodiment 47 A method of making the pharmaceutical composition of
• Embodiment 32 the method comprising suspending the lyophilate in a solvent.
• Embodiment 48 The method of Embodiment 47, wherein the solvent comprises water.
• Embodiment 49 A kit comprising the lyophilate of any one of
• Embodiment 50 The kit of Embodiment 49 for the treatment of cancer in a subject in need thereof.
• Embodiment 51 The kit of Embodiments 49 or 50 further comprising instructions for suspending the lyophilate in a solvent to give a pharmaceutical composition.
• Embodiment 52 The kit of Embodiments 49-51 further comprising instructions for administering the pharmaceutical composition to the subject.
• the disclosure provides the following particular embodiments.
• Embodiment Al A lyophilate comprising about 20 % wt/wt to about 45 % wt/wt of Compound 1 and about 35 % wt/wt to about 55 % wt/wt of a bulking agent.
• Embodiment A2 The lyophilate of Embodiment Al further comprising about 1 % wt/wt to about 10 % wt/wt of a cellulose-based suspension modulator.
• Embodiment A3 The lyophilate of Embodiments Al or A2 further comprising about 1 % wt/wt to about 5 % wt/wt of a poloxamer-based suspension modulator.
• Embodiment A4 The lyophilate of any one of Embodiments Al -A3 further comprising about 10 % wt/wt to about 20 % wt/wt of a lecithin-based suspension modulator.
• Embodiment A5 The lyophilate of any one of Embodiments A1-A5 further comprising about 0.5 % wt/wt to about 2.5 % wt/wt of a buffer.
• Embodiment A6 The lyophilate of any one of Embodiments A1-A5 comprising:
• Embodiment A7 The lyophilate of any one of Embodiments A1-A6 comprising about 25.1 % wt/wt of Compound 1.
• Embodiment A8 The lyophilate of any one of Embodiments A1-A7 comprising about 50.2 % wt/wt of the bulking agent.
• Embodiment A9 The lyophilate of any one of Embodiments A1-A8 comprising about 3.3 % wt/wt of a cellulose-based suspension modulator.
• Embodiment A10 The lyophilate of any one of Embodiments A1-A9 comprising about 2.8 % wt/wt poloxamer-based suspension modulator.
• Embodiment Al 1. The lyophilate of any one of Embodiments A1-A10 comprising about 16.8 % wt/wt of a lecithin-based suspension modulator.
• Embodiment A12 The lyophilate of any one of Embodiments Al-Al l comprising about 1.7 % wt/wt of a buffer.
• Embodiment Al 3. The lyophilate of any one of Embodiments A1-A12, wherein the bulking agent is mannitol.
• Embodiment A14 The lyophilate of any one of Embodiments A1-A13, wherein the cellulose-based suspension modulator is sodium carboxymethyl cellulose.
• Embodiment Al 5. The lyophilate of any one of Embodiments A1-A14, wherein the poloxamer-based suspension modulator is Pol oxamer 188 (copolymer of ethylene oxide and propylene oxide).
• Embodiment Al The lyophilate of any one of Embodiments A1-A15, wherein the lecithin-based suspension modulator is soy lecithin.
• Embodiment Al 7 The lyophilate of any one of Embodiments A1-A16, wherein the buffer is histidine.
• Embodiment Al 8. The lyophilate of Embodiment Al comprising:
• Embodiment Al 9. A pharmaceutical composition comprising the lyophilate of any one of Embodiments A1-A18, wherein the lyophilate is suspended in a pharmaceutically acceptable carrier.
• Embodiment A20 The pharmaceutical composition of Embodiment A19, wherein the pharmaceutically acceptable carrier comprises water.
• Embodiment A21 The pharmaceutical composition of Embodiments A19 or
• A20 wherein the Compound 1 concentration is about 20 mg/mL to about 60 mg/mL.
• Embodiment A22 The pharmaceutical composition of Embodiment A21, wherein the Compound 1 concentration is about 25 mg/mL.
• Embodiment A23 The pharmaceutical composition of any one of
• Embodiments Al 9-22 wherein the average particle size distribution of Compound 1 in the suspension is about 1 pm to about 30 pm.
• Embodiment A24 A method for treating cancer in a subject in need thereof, the method comprising administering a therapeutically effective amount of the pharmaceutical composition of any one of Embodiments A19-A23 to the subject.
• Embodiment A25 The method of Embodiment A24, wherein the cancer is a solid tumor.
• Embodiment A26 The method of Embodiment A24, wherein the cancer is a hematological cancer.
• Embodiment A27 The method of Embodiment A24, wherein the cancer is one or more of cancers listed in Table 1.
• Embodiment A28 The method of Embodiment A24, wherein the cancer is of hepatocellular carcinoma, glioblastoma, lung cancer, breast cancer, head and neck cancer, prostate cancer, melanoma, or colorectal cancer.
• Embodiment A29 The method of Embodiment A24, wherein the cancer is colorectal cancer, breast cancer, lymphoma, melanoma, kidney cancer, or lung cancer.
• Embodiment A30 The method of Embodiment A24, wherein the cancer is an advanced solid tumor, non-small cell lung cancer, or squamous cell carcinoma of head and neck.
• Embodiment A31 The method of any one of Embodiments A24-30, wherein the pharmaceutical composition is administered subcutaneously to the subject.
• Embodiment A32 The method of Embodiment A31, wherein the pharmaceutical composition is administered to the subject according to an intermittent dosing schedule.
• Embodiment A33 The method of Embodiment A32, wherein the wherein the pharmaceutical composition is administered to the subject twice a week on non- consecutive days.
• Embodiment A34 The method of any one of Embodiments A24-3A3 further comprising administering one or more optional therapeutic agents to the subject.
• Embodiment A35 The method of Embodiment A34, wherein the one or more optional therapeutic agents comprise one or more immune checkpoint inhibitors.
• Embodiment A36 The method of Embodiment A35, wherein the one or more immune checkpoint inhibitors comprise a PD-1 inhibitor, a PD-L1 inhibitor, a CTLA-4 inhibitor, a LAG3 inhibitor, a TIM3 inhibitor, or a TIGIT inhibitor, or a combination thereof.
• Embodiment A37 The method of Embodiment A36, wherein the one or more immune checkpoint inhibitors comprise an anti -PD-1 antibody.
• Embodiment A38 The method of Embodiment A37, wherein the anti-PD-1 antibody is nivolumab, pembrolizumab, pidilizumab, STI-Al l 10, (spartalizumab), JTX-4014, sintilimab, MEDI 0680, AGEN2034, BGB-A317, AB122, dostarlimab, PF- 06801591, cemiplimab, tislelizumab, toripalimab, camrelizumab, SYM021, JNJ 63723283, HLX10, LZM009, or MGA012.
• Embodiment A39 The method of any one of Embodiments A35-A38, wherein the one or more immune checkpoint inhibitors comprise an anti-PD-Ll antibody.
• Embodiment A40 The method of Embodiment A39, wherein the anti-PD-
• Ll antibody is avelumab, atezolizumab, durvalumab, KN035, or STI-A1014.
• Embodiment A41 The method of any one of Embodiments A35-A40, wherein the one or more immune checkpoint inhibitors comprise an anti-CTLA-4 antibody.
• Embodiment A42 The method of Embodiment A41, wherein the anti- CTLA-4 antibody is ipilimumab or tremelimumab.
• Embodiment A43 The method of any one of Embodiments A35-A42, wherein the one or more immune checkpoint inhibitors comprise an anti-LAG3 antibody.
• Embodiment A44 The method of Embodiment A43, wherein the anti-LAG3 antibody is GSK283178 E
• Embodiment A45 The method of any one of Embodiments A35-A44, wherein the one or more immune checkpoint inhibitors comprise an anti-TIM3 antibody.
• Embodiment A46 The method of any one of Embodiments A35-A45, wherein the one or more immune checkpoint inhibitors comprise an anti-TIGIT antibody.
• Embodiment A47 The method of Embodiment A46, wherein the anti-TIGIT antibody is vibostolimab (MK-7684), tiragolumab (RG6058), EOS-448, BMS-986207, BGB-A1217, MTIG7192A, AB154, ASP8374, or MK-7684.
• MK-7684 vibostolimab
• RG6058 tiragolumab
• EOS-448 EOS-448
• BMS-986207 BGB-A1217
• MTIG7192A MTIG7192A
• AB154 AB154
• ASP8374 ASP8374
• Embodiment A48 The method of any one of Embodiments A35-A47, wherein the cancer is or has become resistant to treatment with at least one immune checkpoint inhibitor.
• Embodiment A49 A kit comprising the lyophilate of any one of
• Embodiment A50 The kit of Embodiment A49 further comprising instructions for suspending the lyophilate in a solvent to give a pharmaceutical composition.
• Embodiment A51 The kit of Embodiments A49 or A50 further comprising a label with instructions on how to use the kit according to the methods of any one of Embodiments A24-48.
• Embodiment A52 The kit of Embodiment A51 wherein the label is approved by the United States Food and Drug Administration (FDA), the European Medicines Agency (EMA), the China Food and Drug Administration (CFDA) or the Japanese Ministry of Health Labor and Welfare (MHLW)
• FDA United States Food and Drug Administration
• EMA European Medicines Agency
• CFDA China Food and Drug Administration
• MHLW Japanese Ministry of Health Labor and Welfare
• Embodiment A53 A method of making the lyophilate of Embodiment Al, the method comprising: [0347] (i) preparing a pre-lyophilization solution comprising Compound 1, a bulking agent, and water;
• Embodiment A54 The method of Embodiment A54, wherein the bulking agent is mannitol.
• Embodiment A55 The method of Embodiments A53 or A54, wherein the pre-lyophilization solution further comprises ethanol.
• Embodiment A56 The method of any one of Embodiments A53-A55, wherein the pre-lyophilization solution further comprises t-butanol.
• Embodiment A57 The method of any one of Embodiments A53-A56, wherein the pre-lyophilization solution further comprises sodium carboxymethyl cellulose.
• Embodiment A58 The method of any one of Embodiments A53-A57, wherein the pre-lyophilization solution further comprises poloxamer 188.
• Embodiment A59 The method of any one of Embodiments A53-A58, wherein the pre-lyophilization solution further comprises soy lecithin.
• Embodiment A60 The method of any one of Embodiments A53-A59, wherein the pre-lyophilization solution further comprises L-histidine.
• Embodiment A61 A method of making the pharmaceutical composition of
• Embodiment Al 9 the method comprising suspending the lyophilate in a solvent.
• Embodiment A62 The method of Embodiment A61, wherein the solvent comprises water.
• Embodiment A63 A kit for carrying out the methods of any one of
• Embodiments A24-A48 the kit comprising a single unit dose of the lyophilate of any one of Embodiments Al-18 packaged in a container.
• Embodiment A64 The kit of Embodiment A63 further comprising instructions for suspending the lyophilate in a solvent to give a pharmaceutical composition.
• Embodiment A65 The kit of Embodiments A63 or A64 further comprising a label that is approved by the United States Food and Drug Administration (FDA), the European Medicines Agency (EMA), the China Food and Drug Administration (CFDA) or the Japanese Ministry of Health Labor and Welfare (MHLW).
• FDA United States Food and Drug Administration
• EMA European Medicines Agency
• CFDA China Food and Drug Administration
• MHLW Japanese Ministry of Health Labor and Welfare
• Embodiment A66 The pharmaceutical composition of any one of Embodiments A19-A23 for use in treating cancer in a subject in need thereof.
• Embodiment A67 The pharmaceutical composition for use of Embodiment
• A66 wherein the cancer is a solid tumor.
• Embodiment A68 The pharmaceutical composition for use of Embodiment
• A66 wherein the cancer is a hematological cancer.
• Embodiment A69 The pharmaceutical composition for use of Embodiment
• A66 wherein the cancer is one or more of cancers listed in Table 1.
• Embodiment A70 The pharmaceutical composition for use of Embodiment
• cancer wherein the cancer is of hepatocellular carcinoma, glioblastoma, lung cancer, breast cancer, head and neck cancer, prostate cancer, melanoma, or colorectal cancer.
• Embodiment A71 The pharmaceutical composition for use of Embodiment A66, wherein the cancer is colorectal cancer, breast cancer, lymphoma, melanoma, kidney cancer, or lung cancer.
• Embodiment A72 The pharmaceutical composition for use of Embodiment A66, wherein the cancer is an advanced solid tumor, non-small cell lung cancer, or squamous cell carcinoma of head and neck.
• Embodiment A73 The pharmaceutical composition for use of any one of Embodiments A66-A72, wherein the pharmaceutical composition is to be administered subcutaneously to the subject.
• Embodiment A74 The pharmaceutical composition for use of Embodiment A73, wherein the pharmaceutical composition is to be administered to the subject according to an intermittent dosing schedule.
• Embodiment A75 The pharmaceutical composition for use of Embodiment A74, wherein the wherein the pharmaceutical composition is to be administered to the subject twice a week on non-consecutive days.
• Embodiment A76 The pharmaceutical composition for use of any one of Embodiments A66-A75, wherein the pharmaceutical composition is to be administered with one or more optional therapeutic agents to the subject.
• Embodiment A77 The pharmaceutical composition for use of Embodiment A76, wherein the one or more optional therapeutic agents comprise one or more immune checkpoint inhibitors.
• Embodiment A78 The pharmaceutical composition for use of Embodiment A77, wherein the one or more immune checkpoint inhibitors comprise a PD-1 inhibitor, a PD-L1 inhibitor, a CTLA-4 inhibitor, a LAG3 inhibitor, a TIM3 inhibitor, or a TIGIT inhibitor, or a combination thereof.
• Embodiment A79 The pharmaceutical composition for use of Embodiment A78, wherein the one or more immune checkpoint inhibitors comprise an anti -PD-1 antibody.
• Embodiment A80 The pharmaceutical composition for use of Embodiment A79, wherein the anti-PD-1 antibody is nivolumab, pembrolizumab, pidilizumab, STI- Al l 10, (spartalizumab), JTX-4014, sintilimab, MEDI 0680, AGEN2034, BGB-A317, AB122, dostarlimab, PF-06801591, cemiplimab, tislelizumab, toripalimab, camrelizumab, SYM021, JNJ 63723283, HLX10, LZM009, or MGA012.
• the anti-PD-1 antibody is nivolumab, pembrolizumab, pidilizumab, STI- Al l 10, (spartalizumab), JTX-4014, sintilimab, MEDI 0680, AGEN2034, BGB-A317, AB122, do
• Embodiment A81 The pharmaceutical composition for use of any one of Embodiments A77-A80, wherein the one or more immune checkpoint inhibitors comprise an anti-PD-Ll antibody.
• Embodiment A82 The pharmaceutical composition for use of Embodiment A81, wherein the anti-PD-Ll antibody is avelumab, atezolizumab, durvalumab, KN035, or STI-A1014.
• Embodiment A83 The pharmaceutical composition for use of any one of Embodiments A77-A82, wherein the one or more immune checkpoint inhibitors comprise an anti-CTLA-4 antibody.
• Embodiment A84 The pharmaceutical composition for use of Embodiment
• anti-CTLA-4 antibody is ipilimumab or tremelimumab.
• Embodiment A85 The pharmaceutical composition for use of any one of
• Embodiments A77-A84, wherein the one or more immune checkpoint inhibitors comprise an anti-LAG3 antibody.
• Embodiment A86 The pharmaceutical composition for use of Embodiment A85, wherein the anti-LAG3 antibody is GSK2831781.
• Embodiment A87 The pharmaceutical composition for use of any one of Embodiments A77-A86, wherein the one or more immune checkpoint inhibitors comprise an anti-TIM3 antibody.
• Embodiment A88 The pharmaceutical composition for use of any one of Embodiments A77-A87, wherein the one or more immune checkpoint inhibitors comprise an anti-TIGIT antibody.
• Embodiment A89 The pharmaceutical composition for use of Embodiment A88, wherein the anti-TIGIT antibody is vibostolimab (MK-7684), tiragolumab (RG6058), EOS-448, BMS-986207, BGB-A1217, MTIG7192A, AB154, ASP8374, or MK-7684.
• the anti-TIGIT antibody is vibostolimab (MK-7684), tiragolumab (RG6058), EOS-448, BMS-986207, BGB-A1217, MTIG7192A, AB154, ASP8374, or MK-7684.
• Embodiment A90 The pharmaceutical composition for use of any one of
• Embodiments A77-A89 wherein the cancer is or has become resistant to treatment with at least one immune checkpoint inhibitor.
• Embodiment A91 Use of the pharmaceutical composition of any one of
• Embodiments A19-A23 in the manufacture of a medicament for treating cancer in a subject in need thereof.
• Embodiment A92 The use of Embodiment A91, wherein the cancer is a solid tumor.
• Embodiment A93 The use of Embodiment A91, wherein the cancer is a hematological cancer.
• Embodiment A94 The use of Embodiment A91, wherein the cancer is one or more of cancers listed in Table 1.
• Embodiment A95 The use of Embodiment A91, wherein the cancer is of hepatocellular carcinoma, glioblastoma, lung cancer, breast cancer, head and neck cancer, prostate cancer, melanoma, or colorectal cancer.
• Embodiment A96 The use of Embodiment A91, wherein the cancer is colorectal cancer, breast cancer, lymphoma, melanoma, kidney cancer, or lung cancer.
• Embodiment A97 The use of Embodiment A91, wherein the cancer is an advanced solid tumor, non-small cell lung cancer, or squamous cell carcinoma of head and neck.
• Embodiment A98 The use of any one of Embodiments A91-A97, wherein the pharmaceutical composition is to be administered subcutaneously to the subject.
• Embodiment A99 The use of Embodiment A98, wherein the pharmaceutical composition is to be administered to the subject according to an intermittent dosing schedule.
• Embodiment Al 00 The use of Embodiment A99, wherein the wherein the pharmaceutical composition is to be administered to the subject twice a week on non- consecutive days.
• Embodiment A101 The use of any one of Embodiments A91-A100, wherein the pharmaceutical composition is to be administered with one or more optional therapeutic agents to the subject.
• Embodiment A102 The use of Embodiment A101, wherein the one or more optional therapeutic agents comprise one or more immune checkpoint inhibitors.
• Embodiment A103 The use of Embodiment A102, wherein the one or more immune checkpoint inhibitors comprise a PD-1 inhibitor, a PD-L1 inhibitor, a CTLA-4 inhibitor, a LAG3 inhibitor, a TIM3 inhibitor, or a TIGIT inhibitor, or a combination thereof.
• Embodiment A104 The use of Embodiment A103, wherein the one or more immune checkpoint inhibitors comprise an anti -PD-1 antibody.
• Embodiment Al 05 The use of Embodiment A104, wherein the anti-PD-1 antibody is nivolumab, pembrolizumab, pidilizumab, STI-Al l 10, (spartalizumab), JTX-4014, sintilimab, MEDI 0680, AGEN2034, BGB-A317, AB122, dostarlimab, PF- 06801591, cemiplimab, tislelizumab, toripalimab, camrelizumab, SYM021, JNJ 63723283, HLX10, LZM009, or MGA012.
• Embodiment Al 06.
• Embodiment Al 07.
• the anti-PD-Ll antibody is avelumab, atezolizumab, durvalumab, KN035, or STLA1014.
• Embodiment A108 The use of any one of Embodiments A102-A107, wherein the one or more immune checkpoint inhibitors comprise an anti-CTLA-4 antibody.
• Embodiment A109 The use of Embodiment A108, wherein the anti-CTLA-4 antibody is ipilimumab or tremelimumab.
• Embodiment Al 10. The use of any one of Embodiments A102-A109, wherein the one or more immune checkpoint inhibitors comprise an anti-LAG3 antibody.
• Embodiment Al 11 The use of Embodiment Al 10, wherein the anti-LAG3 antibody is GSK2831781.
• Embodiment Al 12 The use of any one of Embodiments A102-A111, wherein the one or more immune checkpoint inhibitors comprise an anti-TIM3 antibody.
• Embodiment Al 13 The use of any one of Embodiments A102-A112, wherein the one or more immune checkpoint inhibitors comprise an anti-TIGIT antibody.
• Embodiment Al 14 The use of Embodiment Al 13, wherein the anti-TIGIT antibody is vibostolimab (MK-7684), tiragolumab (RG6058), EOS-448, BMS-986207, BGB-A1217, MTIG7192A, AB154, ASP8374, or MK-7684.
• the anti-TIGIT antibody is vibostolimab (MK-7684), tiragolumab (RG6058), EOS-448, BMS-986207, BGB-A1217, MTIG7192A, AB154, ASP8374, or MK-7684.
• Embodiment Al 15. The use of any one of Embodiments A102-A114, wherein the cancer is or has become resistant to treatment with at least one immune checkpoint inhibitor.
• Time includes time for suspension, plus 1 additional minute.
• composition comprising Compound 1 in unit dosage form for subcutaneous administration to a subject
• mannitol, sodium carboxymethyl cellulose, pol oxamer 188, and histidine are dissolved in water at 40 °C. After dissolution the solution may be cooled without precipitation to 25°C.
• Compound 1 is fully dissolved in the solution at 30°C (this may take several hours).
• the solution is, optionally, protected from light.
• the solution is brought to the correct mass (or volume) using the target QS value, adding room temperature WFI until the target is reached.
• the L2 pre-lyophilization solution contained precipitated solids that could be re-dissolved by mixing at 30 °C.
• step 1 The drug product solution of step 1 was sterile filtered using redundant 1) Millipore Polysep II prefilter and 2) redundant Millipore Durapore 0.22 micron capsule filters. The pressure should be maintained at 20 PSI or less.
• the initial shelf temperature is room temperature.
• the shelf temperature is decreased to -40 °C, and the pressure is dropped to 45 mTorr. This condition is held for 44.5 h.
• the shelf temperature is ramped up to 0 °C over 5 hours and held at that temperature for 12 hours.
• the shelf temperature is ramped up to 35 °C over 1 h and held at that temperature for 28 hours.
• the shelf temperature is ramped back to room temperature over 1 h prior to nitrogen equilibration and then insertion of stoppers.
• the freezing/drying is accomplished according to one of the following programs.
• PSD particle size distribution
• the LI and L2 pharmaceutical compositions described in EXAMPLE 2 were administered to dogs via subcutaneous (SC) injection at 0.83 mg/kg.
• Blood samples were collected from all animals via the saphenous vein or cephalic vein at pre-dose, 0.25, 0.5, 1, 2, 4, 6, 8, 12, 24, 36, 48, 60 and 72 hours post-dose in the SC group into test tubes containing potassium ethylenediaminotetraacetic acid (K2EDTA).
• Plasma was separated from the blood by centrifugation at 4°C and stored at -80°C until analysis.
• Compound 1 and DON concentration in plasma was quantified using a liquid chromatography with tandem mass spectrometry (LC-MS/MS) method.
• the mean terminal TI/2 was 8.71 ⁇ 3.90 hours.
• the AUCiast and AUCinf were calculated to be 1270 ⁇ 469 and 1430 ⁇ 468 hr*nM, respectively.
• the MRTiast and MRTINF was 9.31 ⁇ 2.30 hr and 13.0 ⁇ 4.98 hr, respectively.
• the mean terminal TI/2 was 12.1 ⁇ 12.3 hours.
• the AUCiast and AUCinf were calculated to be 759 ⁇ 230 and 1030 ⁇ 478 hr*nM, respectively.
• the MRTiast and MRTINF was 7.61 ⁇ 2.09 hr and 17.0 ⁇ 16.5 hr, respectively.

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