CA2640997C - Doxorubicin formulations for anti-cancer use - Google Patents
Doxorubicin formulations for anti-cancer use Download PDFInfo
- Publication number
- CA2640997C CA2640997C CA2640997A CA2640997A CA2640997C CA 2640997 C CA2640997 C CA 2640997C CA 2640997 A CA2640997 A CA 2640997A CA 2640997 A CA2640997 A CA 2640997A CA 2640997 C CA2640997 C CA 2640997C
- Authority
- CA
- Canada
- Prior art keywords
- composition
- weight
- doxorubicin
- copolymer
- parts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 281
- AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 title claims abstract description 232
- 229960004679 doxorubicin Drugs 0.000 title claims abstract description 116
- 238000009472 formulation Methods 0.000 title abstract description 62
- 230000001093 anti-cancer Effects 0.000 title description 2
- 229920001400 block copolymer Polymers 0.000 claims abstract description 47
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 claims abstract description 44
- 239000008101 lactose Substances 0.000 claims abstract description 44
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 claims abstract description 34
- 238000000034 method Methods 0.000 claims abstract description 20
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 17
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 claims abstract description 17
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 claims abstract description 17
- 229960002216 methylparaben Drugs 0.000 claims abstract description 17
- 239000007972 injectable composition Substances 0.000 claims abstract description 14
- 201000011510 cancer Diseases 0.000 claims abstract description 9
- 229920001577 copolymer Polymers 0.000 claims description 67
- 150000003839 salts Chemical class 0.000 claims description 60
- 239000012736 aqueous medium Substances 0.000 claims description 27
- 230000002209 hydrophobic effect Effects 0.000 claims description 27
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 26
- 239000007787 solid Substances 0.000 claims description 20
- 239000002552 dosage form Substances 0.000 claims description 19
- 229920001480 hydrophilic copolymer Polymers 0.000 claims description 19
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 claims description 14
- 239000007788 liquid Substances 0.000 claims description 13
- 238000002347 injection Methods 0.000 claims description 12
- 239000007924 injection Substances 0.000 claims description 12
- 238000004090 dissolution Methods 0.000 claims description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- 238000004108 freeze drying Methods 0.000 claims description 5
- 229920001600 hydrophobic polymer Polymers 0.000 claims description 4
- 239000003708 ampul Substances 0.000 claims 1
- 230000000087 stabilizing effect Effects 0.000 abstract description 2
- 230000003381 solubilizing effect Effects 0.000 abstract 1
- 230000004044 response Effects 0.000 description 26
- 239000000243 solution Substances 0.000 description 19
- 238000011282 treatment Methods 0.000 description 19
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 229920001992 poloxamer 407 Polymers 0.000 description 14
- -1 polyoxyethylene Polymers 0.000 description 14
- 238000012552 review Methods 0.000 description 14
- 239000011780 sodium chloride Substances 0.000 description 14
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 13
- 230000003902 lesion Effects 0.000 description 13
- 206010061289 metastatic neoplasm Diseases 0.000 description 8
- 238000001035 drying Methods 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- 230000004083 survival effect Effects 0.000 description 7
- 208000019505 Deglutition disease Diseases 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 6
- 239000002246 antineoplastic agent Substances 0.000 description 6
- 239000008280 blood Substances 0.000 description 6
- 210000004369 blood Anatomy 0.000 description 6
- 238000002591 computed tomography Methods 0.000 description 6
- 229940124301 concurrent medication Drugs 0.000 description 6
- 208000028653 esophageal adenocarcinoma Diseases 0.000 description 6
- 230000001394 metastastic effect Effects 0.000 description 6
- 206010030137 Oesophageal adenocarcinoma Diseases 0.000 description 5
- 108091006629 SLC13A2 Proteins 0.000 description 5
- 230000037396 body weight Effects 0.000 description 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 5
- 208000036764 Adenocarcinoma of the esophagus Diseases 0.000 description 4
- 229930006000 Sucrose Natural products 0.000 description 4
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 4
- 230000002411 adverse Effects 0.000 description 4
- 238000002512 chemotherapy Methods 0.000 description 4
- 229940127089 cytotoxic agent Drugs 0.000 description 4
- 201000010099 disease Diseases 0.000 description 4
- 208000037821 progressive disease Diseases 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- 239000005720 sucrose Substances 0.000 description 4
- 238000002562 urinalysis Methods 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 206010061818 Disease progression Diseases 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 238000011976 chest X-ray Methods 0.000 description 3
- 230000005750 disease progression Effects 0.000 description 3
- 238000002565 electrocardiography Methods 0.000 description 3
- 210000003236 esophagogastric junction Anatomy 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 201000007492 gastroesophageal junction adenocarcinoma Diseases 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 229940102223 injectable solution Drugs 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920001983 poloxamer Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 230000002861 ventricular Effects 0.000 description 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 229920011250 Polypropylene Block Copolymer Polymers 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000000973 chemotherapeutic effect Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000008121 dextrose Substances 0.000 description 2
- 201000007550 esophagus adenocarcinoma Diseases 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 229920001477 hydrophilic polymer Polymers 0.000 description 2
- 238000001802 infusion Methods 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 125000006353 oxyethylene group Chemical group 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000011343 solid material Substances 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- 150000008163 sugars Chemical class 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 230000003442 weekly effect Effects 0.000 description 2
- 208000000461 Esophageal Neoplasms Diseases 0.000 description 1
- 206010062878 Gastrooesophageal cancer Diseases 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical class Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 208000007433 Lymphatic Metastasis Diseases 0.000 description 1
- 206010027476 Metastases Diseases 0.000 description 1
- 206010027457 Metastases to liver Diseases 0.000 description 1
- 206010027459 Metastases to lymph nodes Diseases 0.000 description 1
- 101100113998 Mus musculus Cnbd2 gene Proteins 0.000 description 1
- 206010030155 Oesophageal carcinoma Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000000259 anti-tumor effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 210000001185 bone marrow Anatomy 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000009096 combination chemotherapy Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 239000012738 dissolution medium Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 201000004101 esophageal cancer Diseases 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 238000011354 first-line chemotherapy Methods 0.000 description 1
- 201000006974 gastroesophageal cancer Diseases 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 230000002440 hepatic effect Effects 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000010253 intravenous injection Methods 0.000 description 1
- 238000002642 intravenous therapy Methods 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000009401 metastasis Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 238000009597 pregnancy test Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 238000001959 radiotherapy Methods 0.000 description 1
- 238000011519 second-line treatment Methods 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000011255 standard chemotherapy Methods 0.000 description 1
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
- A61K9/0012—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
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7028—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages
- A61K31/7034—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin
- A61K31/704—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
-
- 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
- A61K47/14—Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
-
- 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
- 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
- A61K47/34—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Dermatology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Biochemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/359,352 US8148338B2 (en) | 2006-02-22 | 2006-02-22 | Doxorubicin formulations for anti-cancer use |
| US11/359,352 | 2006-02-22 | ||
| PCT/CA2007/000182 WO2007095722A1 (en) | 2006-02-22 | 2007-02-08 | Doxorubicin formulations for anti-cancer use |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2640997A1 CA2640997A1 (en) | 2007-08-30 |
| CA2640997C true CA2640997C (en) | 2013-11-19 |
Family
ID=38428501
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2640997A Active CA2640997C (en) | 2006-02-22 | 2007-02-08 | Doxorubicin formulations for anti-cancer use |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8148338B2 (enExample) |
| EP (1) | EP1991239B1 (enExample) |
| JP (1) | JP5449784B2 (enExample) |
| KR (1) | KR101074430B1 (enExample) |
| CN (1) | CN101389343B (enExample) |
| CA (1) | CA2640997C (enExample) |
| WO (1) | WO2007095722A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8314151B2 (en) | 2008-04-29 | 2012-11-20 | Enzo Therapeutics, Inc. | Sphingosine kinase type 1 inhibitors, and processes for using same |
| US8372888B2 (en) * | 2008-04-29 | 2013-02-12 | Enzo Therapeutics, Inc. | Sphingosine kinase type 1 inhibitors, compositions and processes for using same |
| US8912215B2 (en) * | 2011-12-13 | 2014-12-16 | Everon Biosciences, Inc. | Rapamycin composition |
| US20130150311A1 (en) * | 2011-12-13 | 2013-06-13 | Grzegorz Pietrzynski | Mixed poloxamer excipients |
| PT2716291T (pt) * | 2012-10-08 | 2020-03-04 | Univ Ulm | Associação de opióides e fármacos anticancerígenos para o tratamento de cancro |
| EP3068364B1 (en) * | 2013-11-14 | 2021-11-03 | Metro Biotech NSW Pty Ltd | Nad+ precursor selected from nmn, naad, namn, or a pharmaceutically acceptable salt thereof, for use in treating a side effect of chemotherapy and/or radiotherapy in a subject |
| US10613007B2 (en) | 2015-03-13 | 2020-04-07 | Corning Incorporated | Edge strength testing methods and apparatuses |
| CA2984379C (en) | 2015-04-28 | 2024-06-11 | Newsouth Innovations Pty Limited | Targeting nad+ to treat chemotherapy and radiotherapy induced cognitive impairment, neuropathies, and inactivity |
| US10660879B2 (en) | 2017-06-23 | 2020-05-26 | Enzo Biochem, Inc. | Sphingosine pathway modulating compounds for the treatment of cancers |
| US10675255B2 (en) | 2017-06-23 | 2020-06-09 | Enzo Bochem, Inc. | Sphingosine pathway modulating compounds for the treatment of cancers |
| WO2023220641A2 (en) | 2022-05-11 | 2023-11-16 | Juno Therapeutics, Inc. | Methods and uses related to t cell therapy and production of same |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8426672D0 (en) * | 1984-10-22 | 1984-11-28 | Erba Farmitalia | Pharmaceutical compositions |
| US4927571A (en) * | 1987-05-18 | 1990-05-22 | Liposome Technology, Inc. | Preparation of injectable doxorubicin/liposome suspension |
| US6277410B1 (en) | 1992-10-08 | 2001-08-21 | Supratek Pharma Inc. | Copolymer compositions for oral delivery |
| US5817321A (en) * | 1992-10-08 | 1998-10-06 | Supratek Pharma, Inc. | Biological agent compositions |
| US6060518A (en) * | 1996-08-16 | 2000-05-09 | Supratek Pharma Inc. | Polymer compositions for chemotherapy and methods of treatment using the same |
| WO2003065006A2 (en) * | 2002-01-31 | 2003-08-07 | Millennium Pharmaceuticals, Inc. | Methods and compositions for treating cancer |
| JP2004010479A (ja) * | 2002-06-03 | 2004-01-15 | Japan Science & Technology Corp | ブロック共重合体とアンスラサイクリン系抗癌剤を含む新規固型製剤及びその製造法 |
| GB0312309D0 (en) * | 2003-05-29 | 2003-07-02 | Gaslini Children S Hospital G | Targeted liposome |
-
2006
- 2006-02-22 US US11/359,352 patent/US8148338B2/en not_active Expired - Fee Related
-
2007
- 2007-02-08 CA CA2640997A patent/CA2640997C/en active Active
- 2007-02-08 KR KR1020087023127A patent/KR101074430B1/ko not_active Expired - Fee Related
- 2007-02-08 WO PCT/CA2007/000182 patent/WO2007095722A1/en not_active Ceased
- 2007-02-08 JP JP2008555579A patent/JP5449784B2/ja not_active Expired - Fee Related
- 2007-02-08 CN CN2007800064317A patent/CN101389343B/zh not_active Expired - Fee Related
- 2007-02-08 EP EP07701771.3A patent/EP1991239B1/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| HK1130661A1 (en) | 2010-01-08 |
| US20070196493A1 (en) | 2007-08-23 |
| KR101074430B1 (ko) | 2011-10-17 |
| KR20080110755A (ko) | 2008-12-19 |
| WO2007095722A1 (en) | 2007-08-30 |
| EP1991239B1 (en) | 2014-09-17 |
| EP1991239A1 (en) | 2008-11-19 |
| CN101389343B (zh) | 2012-08-22 |
| US8148338B2 (en) | 2012-04-03 |
| JP2009527505A (ja) | 2009-07-30 |
| CN101389343A (zh) | 2009-03-18 |
| CA2640997A1 (en) | 2007-08-30 |
| EP1991239A4 (en) | 2012-09-19 |
| JP5449784B2 (ja) | 2014-03-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2640997C (en) | Doxorubicin formulations for anti-cancer use | |
| TW201909904A (zh) | 高濃度調配物 | |
| NL2023661B1 (en) | Pharmaceutical Eutectic Salt Formulation | |
| CA2867295A1 (en) | Formulations of bendamustine | |
| CN111249229A (zh) | 一种稳定的法匹拉韦注射液及其制备方法 | |
| Gaur et al. | Formulation and characterization of fast disintegrating tablet of aceclofenac by using sublimation method | |
| RU2557919C1 (ru) | Сыпучий прессуемый порошок рапамицина и фармацевтическая композиция на его основе | |
| US20200138840A1 (en) | Pharmaceutical composition and tumor immunoactivity promoter | |
| ES2900171T3 (es) | Composición inyectable | |
| Olajide et al. | Physicochemical properties of some paediatric and adult products of dihydroartemisinin-piperaquine antimalarial marketed in Nigeria | |
| Seelam et al. | Preparation and evaluation of alginate microspheres of piroxicam for controlled release | |
| HK1130661B (en) | Doxorubicin formulations for anti-cancer use | |
| Lukkad Harish et al. | Formulation and Evaluation of Modified Disintegrating Sustained Release Tablets of Diclofenac Sodium | |
| Kumar et al. | Non Aqueous Formulations and Evaluation of Fosaprepitant Liquid Injectable Dosage Form | |
| Bhat et al. | Design and characterization of chronopharmaceutical drug delivery of theophylline | |
| Yadav et al. | FORMULATION AND EVALUATION OF SUSTAINED RELEASE MATRIX TABLETS OF ATENOLOL | |
| TWI489985B (zh) | 吉西他濱之不含有機溶劑的水性溶液組合物 | |
| Nasser et al. | Preparation and Evaluation of Oral Disintegrating Tablets of Ketoprofen by Dirct Compression | |
| CN119546305A (zh) | 泛raf激酶抑制剂的口服液体悬浮液 | |
| AU2024223940A1 (en) | Compositions and methods of using eflornithine | |
| CN119136818A (zh) | 用于早产婴儿的联合疗法 | |
| Rao et al. | Formulation and Evaluation of Modified Pulsincap Technique for Oral Controlled Release of Glipizide | |
| Madhusudhana | Formulation and in vitro evaluation of microparticulate carrier for antiviral drug |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request |