[go: up one dir, main page]

RU2006105645A - Лиофилизированные композиции cci-779 - Google Patents

Лиофилизированные композиции cci-779 Download PDF

Info

Publication number
RU2006105645A
RU2006105645A RU2006105645/15A RU2006105645A RU2006105645A RU 2006105645 A RU2006105645 A RU 2006105645A RU 2006105645/15 A RU2006105645/15 A RU 2006105645/15A RU 2006105645 A RU2006105645 A RU 2006105645A RU 2006105645 A RU2006105645 A RU 2006105645A
Authority
RU
Russia
Prior art keywords
solution
cci
specified
solvent
butyl alcohol
Prior art date
Application number
RU2006105645/15A
Other languages
English (en)
Other versions
RU2345772C2 (ru
Inventor
Джозеф Т. РУБИНО (US)
Джозеф Т. Рубино
Original Assignee
Уайт (Us)
Уайт
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=34115376&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=RU2006105645(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Уайт (Us), Уайт filed Critical Уайт (Us)
Publication of RU2006105645A publication Critical patent/RU2006105645A/ru
Application granted granted Critical
Publication of RU2345772C2 publication Critical patent/RU2345772C2/ru

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/436Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/10Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/16Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
    • A61K47/18Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
    • A61K47/183Amino acids, e.g. glycine, EDTA or aspartame
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/26Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0019Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/19Particulate 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Rheumatology (AREA)
  • Dermatology (AREA)
  • Neurology (AREA)
  • Pain & Pain Management (AREA)
  • Hematology (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Neurosurgery (AREA)
  • Oncology (AREA)
  • Biomedical Technology (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Claims (22)

1. Раствор, пригодный для приготовления лиофилизированного CCI-779, указанный раствор содержит от 0,1 до 250 мг/мл CCI-779 и по меньшей мере 30% об./об. растворителя, выбранного из группы, состоящей из диметилсульфоксида, ацетонитрила, этанола, изопропанола, т-бутилового спирта и их смесей, которые необязательно дополнительно содержат воду.
2. Раствор по п.1, который содержит 40% об./об. воды и имеет pH от 4 до 6.
3. Раствор по п.1, который содержит от 40 до 70% об./об. растворителя.
4. Раствор по п.1, в котором растворитель содержит т-бутиловый спирт.
5. Раствор по п.1, в котором растворитель представляет собой этанол.
6. Раствор по п.4, в котором указанный растворитель, содержит т-бутиловый спирт в диапазоне от 40 до 60% об./об. т-бутилового спирта в воде.
7. Раствор по п.1, содержащий воду, где pH равен приблизительно 5,5.
8. Раствор по любому из пп.1-7, содержащий от 10 до 100 мг/мл CCI-779.
9. Раствор по любому из пп.1-7, в котором указанный раствор дополнительно содержит от 2 до 5% мас./об. наполнителя.
10. Раствор по п.9, в котором указанный наполнитель представляет собой маннит.
11. Раствор по любому из пп.1-7, в котором указанный раствор дополнительно содержит антиоксидант.
12. Способ приготовления лиофилизированной препаративной формы CCI-779, включающий стадию лиофилизации раствора по любому из пп.1-11.
13. Способ приготовления лиофилизированной препаративной формы CCI-779, включающий стадии
(a) приготовления раствора, имеющего pH от 4 до 6, и содержащего от 10 до 100 мг/мл CCI-779, 2-5% мас./об. маннита и т-бутиловый спирт в воде, и
(b) лиофилизации указанного раствора для получения лиофилизированного CCI-779.
14. Лиофилизированная препаративная форма CCI-779, полученная лиофилизацией раствора по любому из пп.1-7.
15. Способ приготовления CCI-779 для введения в жидкой форме, включающий стадию восстановления CCI-779 с помощью подходящего для парентерального введения растворителя, чтобы создать концентрированный раствор CCI-779, и смешивание указанного концентрированного раствора с разбавителем, содержащим воду, чтобы создать жидкую лекарственную форму CCI-779.
16. Способ по п.15, в котором указанный разбавитель дополнительно содержит 5-8% мас./об. полисорбата 80.
17. Способ по п.15 или 16, в котором указанный разбавитель дополнительно содержит абсолютный спирт.
18. Способ по п.15, в котором указанный концентрированный раствор разбавлен 1:9 0,9% раствором хлорида натрия.
19. Жидкая дозированная форма CCI-779, полученная способом по любому из п.15 или 16.
20. Способ повышения стабильности при хранении CCI-779, включающий стадию лиофилизации раствора, содержащего от 25 мг/мл до 100 CCI-779, т-бутиловый спирт и имеющего pH от 4 до 6.
21. Способ по п.20, в котором указанный раствор дополнительно содержит от 2 до 5% мас./об. маннита.
22. Набор, содержащий емкость для лиофилизированного CCI-779 по п.14 и растворитель для его восстановления.
RU2006105645/15A 2003-07-25 2004-07-15 Лиофилизированные композиции cci-779 RU2345772C2 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US49029303P 2003-07-25 2003-07-25
US60/490,293 2003-07-25

Publications (2)

Publication Number Publication Date
RU2006105645A true RU2006105645A (ru) 2006-06-27
RU2345772C2 RU2345772C2 (ru) 2009-02-10

Family

ID=34115376

Family Applications (1)

Application Number Title Priority Date Filing Date
RU2006105645/15A RU2345772C2 (ru) 2003-07-25 2004-07-15 Лиофилизированные композиции cci-779

Country Status (20)

Country Link
US (1) US20050020615A1 (ru)
EP (1) EP1648454A1 (ru)
JP (1) JP2007500191A (ru)
KR (1) KR20060052880A (ru)
CN (1) CN1829514A (ru)
AR (1) AR045094A1 (ru)
AU (1) AU2004261163A1 (ru)
BR (1) BRPI0412916A (ru)
CA (1) CA2532251A1 (ru)
CO (1) CO5680425A2 (ru)
CR (1) CR8153A (ru)
EC (1) ECSP066394A (ru)
IL (1) IL172573A0 (ru)
MX (1) MXPA05013865A (ru)
NO (1) NO20056178L (ru)
RU (1) RU2345772C2 (ru)
SG (1) SG144165A1 (ru)
TW (1) TW200505501A (ru)
WO (1) WO2005011688A1 (ru)
ZA (1) ZA200600684B (ru)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2493878C (en) 2002-07-30 2013-07-23 Wyeth Parenteral formulations containing a rapamycin hydroxyester
KR20060130162A (ko) * 2004-01-08 2006-12-18 와이어쓰 Cci-779 의 경구 투여용, 직접 압축식 약학적 조성물
US7393952B2 (en) 2004-08-27 2008-07-01 Cordis Corporation Solvent free amorphous rapamycin
US7464012B2 (en) * 2004-12-10 2008-12-09 L'air Liquide, Societe Anonyme A Directoire Et Conseil De Surveillance Pour L'etude Et L'exploitation Des Procedes Georges Claude Simplified process simulator
US7582312B2 (en) * 2004-11-15 2009-09-01 Discovery Laboratories, Inc. Methods to produce lung surfactant formulations via lyophilization and formulations and uses thereof
US8436190B2 (en) * 2005-01-14 2013-05-07 Cephalon, Inc. Bendamustine pharmaceutical compositions
US8158152B2 (en) 2005-11-18 2012-04-17 Scidose Llc Lyophilization process and products obtained thereby
AR072777A1 (es) 2008-03-26 2010-09-22 Cephalon Inc Formas solidas de clorhidrato de bendamustina
CA2735899A1 (en) 2008-09-25 2010-04-01 Cephalon, Inc. Liquid formulations of bendamustine
BRPI1004922A2 (pt) * 2009-01-15 2019-09-24 Cephalon Inc composição farmacêutica, forma cristalina da base livre de bendamustina e método de tratamento de leucemia linfocítica crônica, doença de hodgkin, linfoma não-hodgkin, mieloma múltiplo ou câncer da mama
AU2011260016B2 (en) * 2010-06-02 2013-08-22 Fresenius Kabi Oncology Ltd. Stable pharmaceutical compositions of Rapamycin esters
EP2811984B1 (en) 2012-02-06 2015-08-26 Fresenius Kabi Oncology Limited Process for preparing stable pharmaceutical compositions of compounds susceptible to hydrolysis
CN102940630A (zh) * 2012-11-16 2013-02-27 浙江海正药业股份有限公司 含有西罗莫司酯化物的药物组合物及其制备方法
WO2014118696A2 (en) * 2013-01-29 2014-08-07 Gland Pharma Limited Pharmacuetical compositions of rapamycin esters and its derivatives
US10682415B2 (en) 2013-07-22 2020-06-16 Wisconsin Alumni Research Foundation Thermogel formulation for combination drug delivery
CN104510708B (zh) * 2013-09-29 2018-04-24 正大天晴药业集团股份有限公司 一种米铂冻干制剂及其制备方法
US10342769B2 (en) 2014-11-14 2019-07-09 Navinta Iii Inc Carmustine pharmaceutical composition
WO2017129772A1 (en) 2016-01-29 2017-08-03 Xellia Phamaceuticals Aps Stable pharmaceutical compositions of temsirolimus
CN105687132B (zh) * 2016-03-17 2020-06-12 鲁南贝特制药有限公司 一种坦西莫司注射用浓溶液及其制备方法
CN107773539A (zh) * 2016-08-27 2018-03-09 鲁南制药集团股份有限公司 一种注射用坦西莫司及其制备方法
CN111165656A (zh) * 2020-01-09 2020-05-19 南京大学(溧水)生态环境研究院 一种黑水虻冻干粉高效制备方法

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1204775B (it) * 1986-01-31 1989-03-10 Rosella Silvestrini Kit per la determinazione dell'attivita' proliferativa nei tumori umani
US5352783A (en) * 1993-06-09 1994-10-04 Merck & Co., Inc. Microbial transformation product having immunosuppressive activity
US5362735A (en) * 1994-02-23 1994-11-08 Smithkline Beecham Corporation Rapamycin derivatives
US5362718A (en) * 1994-04-18 1994-11-08 American Home Products Corporation Rapamycin hydroxyesters
CN1124276C (zh) * 1995-06-09 2003-10-15 诺瓦蒂斯有限公司 雷帕霉素衍生物
GB9514594D0 (en) * 1995-07-17 1995-09-13 Johnson & Johnson Clin Diag Chemiluminescent analytical method
US5780462A (en) * 1995-12-27 1998-07-14 American Home Products Corporation Water soluble rapamycin esters
DE19936281C2 (de) * 1999-08-02 2002-04-04 Bayer Ag Verfahren zur Gefriertrocknung
US6277983B1 (en) * 2000-09-27 2001-08-21 American Home Products Corporation Regioselective synthesis of rapamycin derivatives
GB0008785D0 (en) * 2000-04-10 2000-05-31 Novartis Ag Organic compounds
PT1318837E (pt) * 2000-08-11 2004-12-31 Wyeth Corp Metodo de tratamenton de carcinoma positivo a receptor de estrogenio
US6399625B1 (en) * 2000-09-27 2002-06-04 Wyeth 1-oxorapamycins
TWI286074B (en) * 2000-11-15 2007-09-01 Wyeth Corp Pharmaceutical composition containing CCI-779 as an antineoplastic agent
CA2493878C (en) * 2002-07-30 2013-07-23 Wyeth Parenteral formulations containing a rapamycin hydroxyester
BR0314397A (pt) * 2002-09-17 2005-08-09 Wyeth Corp Formulações orais
UA83484C2 (ru) * 2003-03-05 2008-07-25 Уайт Способ лечения рака молочной железы комбинацией производного рапамицина и ингибитора ароматазы - летрозола, фармацевтическая композиция

Also Published As

Publication number Publication date
NO20056178L (no) 2006-02-17
SG144165A1 (en) 2008-07-29
TW200505501A (en) 2005-02-16
KR20060052880A (ko) 2006-05-19
AR045094A1 (es) 2005-10-12
CR8153A (es) 2006-05-26
CA2532251A1 (en) 2005-02-10
US20050020615A1 (en) 2005-01-27
ECSP066394A (es) 2006-08-30
AU2004261163A1 (en) 2005-02-10
EP1648454A1 (en) 2006-04-26
WO2005011688A1 (en) 2005-02-10
RU2345772C2 (ru) 2009-02-10
CN1829514A (zh) 2006-09-06
CO5680425A2 (es) 2006-09-29
MXPA05013865A (es) 2006-02-28
ZA200600684B (en) 2008-07-30
JP2007500191A (ja) 2007-01-11
BRPI0412916A (pt) 2006-09-26
IL172573A0 (en) 2006-04-10

Similar Documents

Publication Publication Date Title
RU2006105645A (ru) Лиофилизированные композиции cci-779
RU2399628C2 (ru) Производные циклоспорина, замещенные 3-эфиром и 3-тиоэфиром, для лечения и профилактики инфекционного гепатита с
KR880002366B1 (ko) 비-수성 아이버멕틴 제제
AU2009212762A1 (en) Topical anthelmintic veterinary formulations
AR033859A1 (es) Inhibidores de la metaloproteinasa de la matriz
KR920003331B1 (ko) 활성성분으로 스페르구알린(Spergualin)을 함유하는 주사제 조성물과 그 제조방법.
KR100376192B1 (ko) 정맥내주사용라파마이신제형및이의제조방법
MXPA04010925A (es) Formulaciones que contienen amiodarona y eter sulfoalquilico de ciclodextrina.
KR20000068991A (ko) 사이클로스포린과 음이온성 계면활성제를 포함하는 고형제제
PT503988E (pt) Composicoes para o tratamento de onicomicoses
NZ285122A (en) Stable, concentrated medicament containing docetaxel (or derivatives), at least 1 unsaturated phospholipid and small amount of at least 1 negative phospholipid
WO2007117581A3 (en) Stabilized transdermal bupropion preparations
CA2215327A1 (en) Formulations for lipophilic compounds
PE20030201A1 (es) Formulacion farmaceutica de sabor enmascarado y procedimiento para su preparacion
DK2922530T3 (en) Caspofunginacetatformuleringer
JP5723031B2 (ja) エキノカンジン系抗真菌剤であるミカファンギンを含む液体薬用組成物
DK2620153T3 (en) 5 ALPHA-ANDROSTAN (ALKYL) -3 BETA, 5,6 BETA-TRIOL INJECTION AND PROCEDURE FOR PREPARING THEREOF
ES2846820T3 (es) Composición de lactonas macrocíclicas, levamisol, un aminoazúcar y un agente antiparasitario adicional
TW200621310A (en) A process for preparing formulations of lypophilic active substances by spray freeze drying
CN1046516C (zh) 化合物dx-52-1的稳定方法和其冻干组合物
US9393230B2 (en) Pharmaceutical composition on the basis of phyto-nutrients with increased bioavailability, having anti-tumor activity, and method for producing said composition (alternatives)
EP0949923A1 (fr) Compositions pharmaceutiques stabilisees, a base de quinupristine et de dalfopristine et leur preparation
KR19980702109A (ko) 인돌-카르복실산을 함유하는 비경구 투여용 제약 조성물
Barthomeuf et al. Stabilization of Octastatin®, a somatostatin analogue: comparative accelerated stability studies of two formulations for freeze-dried products
BR0302470A (pt) Composições antiácidas lìquidas

Legal Events

Date Code Title Description
MM4A The patent is invalid due to non-payment of fees

Effective date: 20090716