US20050267125A1 - High drug load tablet - Google Patents
High drug load tablet Download PDFInfo
- Publication number
- US20050267125A1 US20050267125A1 US10/512,171 US51217105A US2005267125A1 US 20050267125 A1 US20050267125 A1 US 20050267125A1 US 51217105 A US51217105 A US 51217105A US 2005267125 A1 US2005267125 A1 US 2005267125A1
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- Prior art keywords
- tablet
- compound
- tablet according
- pharmaceutically acceptable
- weight
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- KTUFNOKKBVMGRW-UHFFFAOYSA-N [H]N(C(=O)C1=CC=C(CN2CCN(C)CC2)C=C1)C1=CC=C(C)C(N([H])C2=NC(C3=CN=CC=C3)=CC=N2)=C1 Chemical compound [H]N(C(=O)C1=CC=C(CN2CCN(C)CC2)C=C1)C1=CC=C(C)C(N([H])C2=NC(C3=CN=CC=C3)=CC=N2)=C1 KTUFNOKKBVMGRW-UHFFFAOYSA-N 0.000 description 3
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- 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
- A61K47/32—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers, poly(meth)acrylates, or polyvinyl pyrrolidone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2009—Inorganic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/2027—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2072—Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2095—Tabletting processes; Dosage units made by direct compression of powders or specially processed granules, by eliminating solvents, by melt-extrusion, by injection molding, by 3D printing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C43/00—Compression moulding, i.e. applying external pressure to flow the moulding material; Apparatus therefor
- B29C43/003—Compression moulding, i.e. applying external pressure to flow the moulding material; Apparatus therefor characterised by the choice of material
Definitions
- the present invention relates to pharmaceutical tablets Comprising 4-(4-methylpiperazin-1-ylmethyl)-N-[4-methyl-3-(4-pyridin-3-yl)pyrimidin-2-ylamio)phenyl]-benzamide or pharmaceutically acceptable salts thereof and is hereinafter referred as Compound I.
- Compound I has the formula (1)
- the present invention provides a tablet with high drug loading comprising a pharmacologically effective amount of Compound I or a pharmaceutically acceptable salt thereof present in an amount of from about 30% to 80%, e.g. at least about 35, 40, 45, 50 or 55% to about e.g. 60, 65, 70, 75 or 80%, preferably more than 55%.
- the amount of Compound I may vary from 45 to 80%, e.g. 50 to 70% in weight based on the total weight of the tablet.
- Compound I may be in the free base form or pharmaceutically acceptable salts thereof, e.g. monomesylate form.
- the active moiety corresponds to Compound I in the free base form.
- 119.5 mg of Compound I mesylate salt correspond to 100 mg of Compound I free base active moiety.
- the present invention also provides a tablet comprising
- the present invention provides a tablet wherein the Compound I is in crystalline form.
- the monomesylate salt of Compound I is used.
- the monomesylate salt of Compound I is in crystalline form, e.g. alpha or beta crystal form, most preferably, the monomesylate salt of Compound I is in the beta crystal form.
- One or more pharmaceutically acceptable excipients may be present in the tablets, e.g. those conventionally used, e.g. (1.1) at least one binder, e.g. microcrystalline cellulose, hydroxypropylmethyl cellulose, (1.2) at least one disintegrant, e.g. cross-linked polyvinylpyrrolidinone, e.g. Crospovidone®, (13) at least one glidant, e.g. colloidal silicon dioxide, (1.4) at least one lubricant, e.g. magnesium stearate and/or (1.5) basic coating.
- binder e.g. microcrystalline cellulose, hydroxypropylmethyl cellulose
- disintegrant e.g. cross-linked polyvinylpyrrolidinone, e.g. Crospovidone®
- glidant e.g. colloidal silicon dioxide
- lubricant e.g. magnesium stearate and/or (1.5) basic coating.
- microcrystalline cellulose is used as
- Binders (1.1) include but are not restricted to starches, e.g. potato, wheat or corn starch; microcrystalline cellulose, e.g. products such as Avicel®, Filtrak®, Heweten® or Pharmacel®; hydroxypropyl cellulose; hydroxyethyl cellulose; hydroxypropylmethyl cellulose, e.g. hydroxypropylmethyl cellulose-Type 2910 USP, hypromellose, and polyvinylpyrrolidone, e.g. Povidone® K30 from BASF.
- hydroxypropylmethyl cellulose-Type 2910 USP is used.
- Suitable disintegrants (1.2) include but are not restricted to maize starch; CMC-Ca; CMC-Na; microcrystalline cellulose; cross-linked PVP, e.g. as known and commercially available under the trade names Crospovidone®, Polyplasdone®, available commercially from the ISP company, or Kollidon® XL; alginic acid; sodium alginate; and guar gum.
- cross-linked PVP e.g. Crospovidone® is used.
- glidants one or more of the following may be used: silica; colloidal silica, e.g. colloidal silica anhydrous, e.g. Aerosil® 200, magnesium trisilicat, powdered cellulose, starch and talc.
- colloidal silica anhydrous or/and colloidal silicon dioxide are used.
- lubricants (1.4) one or more of the following may be used Mg-, Al- or Ca-stearate, PEG 4000-8000 and/or talc.
- Mg-, Al- or Ca-stearate Preferably magnesium stearate is used.
- One or more of these excipients can be selected and used having regard to the particular desired properties of the tablet by routine experimentation.
- the amount of binder (1.1) may vary within a range of from about 1 to 40%, preferably 1 to 30%, in particular 1 to 25% in weight based on the total weight of the tablet.
- the amount of disintegrant (1.2) may vary within a range of from to 5 to 40%, e.g. 10 to 35% in weight based on the total weight of the tablet.
- the amount of glidant (1.3) may vary within ranges of from 0.1 to 10%, in particular 0.1 to 5%, e.g. 0.5 to 3% in weight based on the total weight of the tablet or 2 to 4% in weight based on the total weight of the tablet.
- the amount of lubricant (1.4) may vary within a range of from 0.1 to 5%, e.g. 0.5 to 2% in weight based on the total weight of the tablet.
- the amount of basic coating (1.5) may vary from 1 to 10%, preferably from 1.5 to 5% in weight based on the total weight of the tablet.
- any given excipient may serve more than one function e.g. as disintegrant, binder, glidant, and/or lubricant.
- the tablet comprises the following excipients, one or more binders in a total amount of about 1% to 25% in weight based on the total weight of the tablet, one or more disintegrants in a total amount of about 10% to 35% in weight based on the total weight of the tablet, one or more glidants in a total amount of about 0.5% to 3% in weight based on the total weight of the tablet, and/or one or more lubricants in a total amount of about 0.5% to 2% in weight based on the total weight of the tablet.
- each excipient and the amounts relative to other excipients is similarly dependent on the desired properties of the tablet and may also be chosen by routine experimentation.
- the tablet may be chosen to exhibit accelerated and/or delayed release of Compound I with or without quantitative control of the release of active agent.
- the tablet is chosen to exhibit immediate release of the Compound I, e.g. the Compound I monomesylate salt beta crystal form.
- compositions comprising Compound I are obtainable.
- pharmaceutically acceptable oral solid dosage forms in the form of tablets may be obtained by preparation of tablets by compression methods. More specifically, the tablets of the invention may be prepared by granulation, preferably wet-granulation, followed by compression methods.
- Compound I especially the mesylate salt, exhibits high particle size, e.g. 60% of the Compound I starting material having a particle size greater or equal to 100 ⁇ m, e.g. 90% of the particles are smaller or equal to 420 ⁇ m
- Wet-granulation process is usually performed with a starting material of particle size lower than 100 ⁇ m.
- the tablet according to the invention contains a high content of Compound I given the relatively small amount of excipients. This enables the production of physically small tablets.
- the total amount of excipients in a given unit dosage may be about 70% or less by weight based on the total weight of the tablet, more particularly about 50% or less.
- the excipient content is in the range of about 30 to 55%, more particularly 35 to 50% in weight based on the total weight of the tablet
- Tablets according to the invention surprisingly provide for the administration of Compound I in a smaller size than was hitherto possible for a given unit dose of Compound I.
- the tablets of the invention are, despite the high drug loading, small, and, therefore, convenient to administer. This leads to a better patient compliance.
- this invention provides a tablet comprising from 50 mg to 600 mg Compound I, e.g. of from 100 mg to about 400 mg. Most preferably, tablets according to the invention are tablets containing 100 mg and/or tablets containing 400 mg of Compound I.
- the present invention provides for tablets containing an amount of Compound I mesylate, e.g. Compound I mesylate alpha crystal form and/or Compound I mesylate beta crystal form, equal to 100 mg and/or 400 mg of Compound I free base.
- the Compound I mesylate form used for the tablet according to the invention is the beta crystal form.
- the process for the preparation of the tablets consists in forming an inner phase, mixing it together with an outer phase, compressing the obtained mixture and optionally coating the tablet.
- the inner phase comprises Compound I.
- the inner phase comprises Compound I and one or more excipients, more preferably one or more binders and most preferably the amount of one or more binders in the inner phase is ranging from about 1 to 30%, preferably 1 to 20% and more preferably 1 to 15%.
- the binders of the inner phase according to the invention are preferably microcrystalline cellulose and hydroxypropylmethyl cellulose.
- the amount of microcrystalline cellulose in the inner phase may vary from about 10 to 29%, in particular 12 to 14% in weight based on the total weight of the tablet
- the amount of hydroxypropylmethyl cellulose in the inner phase may vary from 1 to 5%, preferably 1 to 2% in weight based on the total weight of the tablet.
- the Compound I and the pharmaceutically acceptable excipients of the inner phase are mixed together with water and the mixture is processed for granulation, e.g. using a wet high-shear granulator to form the wet-granulates.
- the wet-granulates may be then, dried, e.g. using a fluid bed dryer.
- the present invention pertains to a process for the preparation of tablets comprising an outer phase.
- the outer phase consists in a mixture of the inner phase with one or more excipients.
- the inner phase and one or more excipients of the outer phase are mixed together using, e.g. a diffusion mixer.
- one or more binders are added.
- Most preferably cellulose microcrystalline is added.
- microcrystalline cellulose is added in the range of 1 to 10% in weight based on the total weight of the tablet.
- the amount of microcrystalline cellulose is around 5% in weight based on the total weight of the tablet.
- the outer phase according to the invention may also contain one or more disintegrants, most preferably Crospovidone®.
- the amount of disintegrant in the outer phase is ranging from about 10 to 30%, preferably 12 to 25%, most preferably about 15%.
- one or more glidants are incorporated into the outer phase.
- one or more lubricants are incorporated into the outer phase.
- tablets are performed by compression of the mixture of the inner and the outer phases using, e.g. a tablet press.
- the tablets may be coated, preferably as described herein after.
- the present invention provides a process comprising:
- core is meant the granulate phase (steps (i) and (ii)) including the active drug Compound I and the outer phase consisting of the excipients.
- total weight of the tablet is meant the weight of a tablet being the inner and the outer phases and the coating (if any).
- the coating process may be performed at low temperature, e.g. between 30 and 40° C., preferably between 32 and 39° C., most preferably at a temperature ranging from around 35 to around 38° C.
- the coating process may be performed with a spray rate preferably in the range of 30 to 105 g of coating dispersion per kg of cores per hour, preferably of 35 to 105 g. It has surprisingly been found that swelling of the disintegrants, e.g. Crospovidone®, nor sticking of the cores occurred during spraying of the coating mixture, as it would be expected by the person skilled in the art by processing at low temperatures.
- the tablets exhibit improved abrasion resistance.
- the physical and chemical stability may be tested in conventional manner, e.g. the tablets may be tested as such by measurement of dissolution, friability, disintegration time, assay for Compound I degradation products, appearance and/or microscopy, e.g. after storage at room temperature, i.e. 25° C., and/or storage at 40° C.
- the tablet cores may vary in shape and be, for example, round, oval, oblong, cylindrical or any other suitable shape.
- a characteristic of tablets according to the invention is their small size having regard to the amount of Compound I or Compound I salt contained therein.
- tablets obtained by the compression method described above are round or oval.
- the edges of the tablets may be beveled or rounded.
- the tablets are ovaloid and/or round.
- the tablets according to the invention may be scored.
- the ovaloid tablet may be small in dimension e.g. 10 to 20 mm in length, preferably 15 to 20 mm, most preferably 17 to 19 mm; 5 to 10 nun in width, preferably 6.5 to 8 mm.
- the thickness of the tablet is from 4 to 8 mm, preferably 6 to 8 mm.
- Compression forces of between 10 to 20 kN are used to prepare the compressed tablet, preferably, 12 to 18 kN.
- the ovaloid tablet contains 400 mg of Compound I.
- the round tablet may be of the following dimensions, e.g. 5 to 15 mm in diameter, preferably 7 to 10 mm, most preferably about 9 mm.
- the thickness of the tablet may be from 2 to 5 mm, preferably 2.5 to 4 mm Compression forces of between 6 to 18 kN are used to prepare the compressed tablet, preferably, 8 to 14 kN.
- the round tablet contains 100 mg of Compound I.
- the 100 mg tablet is a scored tablet, most preferably the tablet has a break score on one side.
- the tablets of the invention comprising about 100 mg of Compound I may furthermore have a hardness of from about 30 to 140 N, e.g. 40 to 140 N, 30 to 100 N, 40 to 100 N, preferably 50 to 80 N.
- the tablets of the invention comprising about 400 mg of Compound I may have a hardness of 100 to 270 N, e.g. 100 to 250 N, 160 to 270 N, 160 to 250 N, preferably 195 to 235 N.
- the disintegration time of the tablet may be of about 20 min or less.
- the disintegration time is ranging from about 2 to 10 min, preferably 4 to 10 min, e.g. 4 to 8 min.
- the disintegration time is, preferably ranging from about 7 to 15 min, preferably 8 to 15 min, e.g. 8 to 14 min.
- the friability of the tablets is measured according to the US Pharmacopeia.
- the friability of the tablets according to the invention monitored following the recommendation of the US Phramacopeia is 0%.
- the tablets of the invention may furthermore be colored and/or the tablets or coating marked so as to impart an individual appearance and to make them instantly recognizable.
- the use of dyes can serve to enhance the appearance as well as to identify the tablets.
- Dyes suitable for use in pharmacy typically include carotinoids, iron oxides or chlorophyll.
- the tablets of the invention may be marked using an imprint code.
- Procedures which may be used may be conventional or known in the art or based on such procedures e.g those described in L. Lachman et al. The Theory and Practice of Industrial Pharmacy, 3rd Ed, 1986, H. Sucker et al, Pharmazeutician Technologie, Thieme, 1991, Hagers Handbuch der pharmazuetician für für für Pharmazeutician Technologie, Thieme, 1991, Hagers Handbuch der pharmazuetician für für Praxis, 4th Ed. (Springer Verlag, 1971) and Remington's Pharmaceutical Sciences, 13th Ed., (Mack Publ., Co., 1970) or later editions.
- the tablets of the invention are useful for human indication of Compound I, e.g. anti-tumor treatment, as indicated by standard tests.
- the activity and characteristics of the tablets of the invention may be indicated in standard clinical trials and/or animal trials.
- the tablets of the invention are particular useful for, e.g. treatment of non-malignant and malignant proliferative disorders, e.g. leukemias, gliomas, sarcomas, prostate-, breast-, gastro-intestinal-, lung-, ovary tumors.
- non-malignant and malignant proliferative disorders e.g. leukemias, gliomas, sarcomas, prostate-, breast-, gastro-intestinal-, lung-, ovary tumors.
- the tablets of the invention comprising a pharmacologically effective amount of Compound I or Compound I salt may be administered as the sole active drug or with another active drug may be envisaged, e.g. together with simultaneous or separate administration of other drugs.
- the tablets of the invention obtained are stable both to the production process and during storage, e.g. for 2 years or even 3 years in conventional packaging, e.g. sealed aluminium blister packs. Less than about 5%, e.g. 2 or 3% or less of Compound I or Compound I salt may degrade during this time as determined in conventional tests.
- the tablets of the invention e.g. the 100 and 400 mg tablets, are bioequivalent with the marketed hard gelatine capsules (100 mg) of Compound I.
- the administration of 400 mg of Compound I in hard gelatine capsules (4 ⁇ 100 mg) in the form of a single film coated tablet is well tolerated.
- effective doses for example daily dosing of tablets of the invention comprising, e.g. 100-1000 mg, e.g. 100 to 800 mg, preferably 100 to 600 mg, especially 400 mg of Compound 1, are administered to patients of about 70 kg bodyweight
- the invention relates also to a method for administering to a human subject in need of such a treatment, Compound I or a pharmaceutically acceptable salt thereof in the form of a tablet, once daily for a period exceeding 3 months.
- the invention relates especially to such method wherein a daily dose of 100 to 1000 mg, preferably 100 to 800 mg, especially 200 to 600 mg, preferably 400 mg, of Compound I is administered to an adult.
- a daily dose of 100 to 1000 mg, preferably 100 to 800 mg, especially 200 to 600 mg, preferably 400 mg, of Compound I is administered to an adult.
- the specific dose level for any particular patient will depend upon a variety of factors including the age, the body weight, general health, drug combination with one or more active drugs, type and severity of the disease.
- the present invention provides a method of treating a subject which comprises administering a tablet according to the invention comprising a pharmacologically effective amount of Compound I salt to a subject in need of such a treatment, optionally with the simultaneous, sequential or separate administration of another drug e.g. a cyclosporin, a rapamycin, an ascomycin, corticosteroids, cyclophosphamide, azathioprine, methotrexate, brequinar, leflunomide, mizoribine, mycophenolic acid and/or mycophenolate mofetil.
- another drug e.g. a cyclosporin, a rapamycin, an ascomycin, corticosteroids, cyclophosphamide, azathioprine, methotrexate, brequinar, leflunomide, mizoribine, mycophenolic acid and/or mycophenolate mofetil.
- the dosages of the Compound I mesylate may be reduced e.g. to one-half to one-third their dosages when used alone.
- the medicament package comprises tablets according to the invention and printed instructions directing that one or more tablets of Compound I be administered orally.
- Tablets of 100 mg of Compound I free base according to the invention and of the above tablet were prepared by wet granulation of a mixture of Compound I salt with (1.1), mixing with 3 (1.1), (1.2), (1.3) and (1.4), compressing and coating the resultant tablets with an aqueous dispersion of the coating mixture (1.5).
- the coating process may be performed at low temperature, e.g. ranging from around 35 to around 38° C.
- the coating process may be performed with a spray rate preferably in the range of 30 to 105 g of coating dispersion per kg of cores (“core” corresponds to the compressed inner and outer phase) per hour, e.g. 35 to 105 g per kg of cores per h.
- Tablets of 400 mg of Compound I according to the invention and of the following tablet were prepared by wet granulation of a mixture of Compound I salt with (1.1), mixing with 3 (1.1), (1.2), (1.3) and (1.4), compressing and coating the resultant tablets with an aqueous dispersion of the coating mixture (1.5).
- the coating process may be performed at low temperature, e.g. ranging from around 35 to around 38° C.
- the coating process may be performed with a spray rate preferably in the range of 30 to 105 g of coating dispersion per kg of cores (“core” corresponds to the compressed inner and outer phase) per hour, e.g. 35 to 105 g per kg of cores per h.
- Compound I free base/tablet Shape and Dimensions 100 mg Round, 9.1-9.3 mm diameter, curved, bevelled edges, thickness: 2.8-3.4 mm break score on one side 400 mg Ovaloid, 18.1-18.3 ⁇ 7.2-7.4 mm, curved, bevelled edges, thickness: 6.6-7.2 mm 100 mg Round, 9.1-9.4 mm diameter, curved, bevelled edges, thickness: 2.8-3.4 mm break score on one side 400 mg Ovaloid, 18.1-18.4 ⁇ 7.2-7.5 mm, curved, bevelled edges, thickness: 6.6-7.2 mm
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Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
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US14/679,076 Abandoned US20150209291A1 (en) | 2002-04-23 | 2015-04-06 | High drug load tablet |
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US14/679,076 Abandoned US20150209291A1 (en) | 2002-04-23 | 2015-04-06 | High drug load tablet |
US14/974,658 Abandoned US20160101105A1 (en) | 2002-04-23 | 2015-12-18 | High drug load tablet |
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US (6) | US20050267125A1 (ru) |
EP (1) | EP1501485B1 (ru) |
JP (4) | JP2005529126A (ru) |
KR (1) | KR100728846B1 (ru) |
CN (2) | CN101653424A (ru) |
AR (3) | AR039335A1 (ru) |
AT (1) | ATE374016T1 (ru) |
AU (1) | AU2003229705C1 (ru) |
BR (1) | BR0309528A (ru) |
CA (1) | CA2483199C (ru) |
CY (1) | CY1106996T1 (ru) |
DE (1) | DE60316552T2 (ru) |
DK (1) | DK1501485T3 (ru) |
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GB (1) | GB0209265D0 (ru) |
GE (1) | GEP20094627B (ru) |
HK (1) | HK1073253A1 (ru) |
HR (1) | HRP20040996B1 (ru) |
IL (1) | IL164678A (ru) |
MX (1) | MXPA04010496A (ru) |
MY (1) | MY136406A (ru) |
NO (1) | NO341027B1 (ru) |
NZ (1) | NZ536046A (ru) |
PE (1) | PE20031045A1 (ru) |
PL (1) | PL199779B1 (ru) |
PT (1) | PT1501485E (ru) |
RU (2) | RU2363450C2 (ru) |
SI (1) | SI1501485T1 (ru) |
TN (1) | TNSN04213A1 (ru) |
TW (1) | TWI350184B (ru) |
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- 2002-04-23 GB GB0209265A patent/GB0209265D0/en not_active Ceased
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2003
- 2003-04-21 TW TW092109221A patent/TWI350184B/zh not_active IP Right Cessation
- 2003-04-22 MX MXPA04010496A patent/MXPA04010496A/es active IP Right Grant
- 2003-04-22 KR KR20047016991A patent/KR100728846B1/ko active IP Right Review Request
- 2003-04-22 CN CN200910142577A patent/CN101653424A/zh active Pending
- 2003-04-22 PL PL371495A patent/PL199779B1/pl unknown
- 2003-04-22 GE GEAP200310694A patent/GEP20094627B/en unknown
- 2003-04-22 RU RU2004134323A patent/RU2363450C2/ru active
- 2003-04-22 AT AT03722519T patent/ATE374016T1/de active
- 2003-04-22 DK DK03722519T patent/DK1501485T3/da active
- 2003-04-22 DE DE2003616552 patent/DE60316552T2/de not_active Expired - Lifetime
- 2003-04-22 BR BR0309528A patent/BR0309528A/pt not_active Application Discontinuation
- 2003-04-22 WO PCT/EP2003/004151 patent/WO2003090720A1/en active IP Right Grant
- 2003-04-22 ES ES03722519T patent/ES2290457T3/es not_active Expired - Lifetime
- 2003-04-22 AU AU2003229705A patent/AU2003229705C1/en not_active Expired
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- 2003-04-22 MY MYPI20031513 patent/MY136406A/en unknown
- 2003-04-22 AR ARP030101383 patent/AR039335A1/es not_active Application Discontinuation
- 2003-04-22 JP JP2003587357A patent/JP2005529126A/ja not_active Withdrawn
- 2003-04-22 EP EP03722519A patent/EP1501485B1/en not_active Revoked
- 2003-04-22 US US10/512,171 patent/US20050267125A1/en not_active Abandoned
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- 2003-04-22 PE PE2003000398A patent/PE20031045A1/es not_active Application Discontinuation
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- 2004-10-18 IL IL16467804A patent/IL164678A/en active IP Right Grant
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2005
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2007
- 2007-11-08 CY CY071101448T patent/CY1106996T1/el unknown
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2009
- 2009-04-08 RU RU2009112955A patent/RU2405540C1/ru active
- 2009-06-09 AR ARP090102074 patent/AR072755A2/es not_active Application Discontinuation
- 2009-09-25 JP JP2009220815A patent/JP2010031019A/ja not_active Withdrawn
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2010
- 2010-04-21 US US12/764,696 patent/US20100203133A1/en not_active Abandoned
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2012
- 2012-03-19 US US13/423,990 patent/US20120177737A1/en not_active Abandoned
- 2012-12-26 JP JP2012283244A patent/JP5752107B2/ja not_active Expired - Lifetime
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2014
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2015
- 2015-03-23 JP JP2015060091A patent/JP5798269B2/ja not_active Expired - Lifetime
- 2015-04-06 US US14/679,076 patent/US20150209291A1/en not_active Abandoned
- 2015-12-18 US US14/974,658 patent/US20160101105A1/en not_active Abandoned
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Cited By (12)
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US20090324718A1 (en) * | 2006-09-01 | 2009-12-31 | Ilan Zalit | Imatinib compositions |
EP2251042A2 (en) | 2006-09-22 | 2010-11-17 | Novartis AG | Method of optimizing the treatment of philadelphia-positive leukemia with abl tyrosine kinase inhibitors |
US20090092669A1 (en) * | 2007-09-25 | 2009-04-09 | Bella Gerber | Stable imatinib compositions |
US8414918B2 (en) | 2007-09-25 | 2013-04-09 | Teva Pharmaceutical Industries Ltd. | Stable imatinib compositions |
US8933082B2 (en) | 2008-06-27 | 2015-01-13 | Indiana University Research And Technology Corp. | Materials and methods for suppressing and/or treating neurofibroma and related tumors |
US9345704B2 (en) | 2008-06-27 | 2016-05-24 | Indiana University Research And Technology Corporation | Materials and methods for suppressing and/or treating neurofibroma and related tumors |
WO2010065433A1 (en) | 2008-12-01 | 2010-06-10 | Novartis Ag | Method of optimizing the treatment of philadelphia-positive leukemia with imatinib mesylate |
US20120329810A1 (en) * | 2011-06-22 | 2012-12-27 | Natco Pharma Limited | Imatinib mesylate oral pharmaceutical composition and process for preparation thereof |
US9750700B2 (en) * | 2011-06-22 | 2017-09-05 | Natco Pharma Limited | Imatinib mesylate oral pharmaceutical composition and process for preparation thereof |
WO2013063000A1 (en) | 2011-10-28 | 2013-05-02 | Novartis Ag | Method of treating gastrointestinal stromal tumors |
WO2013063003A1 (en) | 2011-10-28 | 2013-05-02 | Novartis Ag | Method of treating gastrointestinal stromal tumors |
WO2014011284A1 (en) | 2012-07-11 | 2014-01-16 | Novartis Ag | Method of treating gastrointestinal stromal tumors |
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