ME02640B - Farmaceutske formulacije 514 - Google Patents
Farmaceutske formulacije 514Info
- Publication number
- ME02640B ME02640B MEP-2016-204A MEP20416A ME02640B ME 02640 B ME02640 B ME 02640B ME P20416 A MEP20416 A ME P20416A ME 02640 B ME02640 B ME 02640B
- Authority
- ME
- Montenegro
- Prior art keywords
- formulation
- active agent
- matrix polymer
- weight
- copovidone
- Prior art date
Links
Classifications
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- 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
- 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/502—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
-
- 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
- A61K47/02—Inorganic compounds
-
- 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
- A61K47/12—Carboxylic acids; Salts or anhydrides thereof
-
- 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
- A61K47/20—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing sulfur, e.g. dimethyl sulfoxide [DMSO], docusate, sodium lauryl sulfate or aminosulfonic acids
-
- 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
- A61K9/2095—Tabletting processes
-
- 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)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Inorganic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Claims (27)
1. Farmaceutska formulacija koja obuhvata aktivni agens u cvrštoj disperziji sa matriksnim polimerom, naznačena time što aktivni agens je 4-[3-( 4-ciklopropankarbonii-piperazin-1-karbonii)-4-fluoro-benzii]-2H-ftaiazin-1-on ili so ili solvat od toga, te matriksni polimer pokazuje nisku higroskopnost i visoku temperaturu omeksavanja.
2. Formuiacija kako se zahteva u patentnom zahtevu 1, naznačena time što je aktivni agens u stabiinom amorfnom obliku.
3. Formulacija kako se zahteva u patentnom zahtevu 2, naznačena time što je harem 90% aktivnog agensa u amorfnom obliku.
4. Formuiacija kako se zahteva u patentnom zahtevu 2, naznačena time što je barem 95% aktivnog agensa u amorfnom obliku.
5. Formuiacija kako se zahteva u patentnom zahtevu 2, naznačena time što je 100% aktivnog agensa u amorfnom obliku.
6. Formuiacija kako se zahteva u biio kojem od patentnih zahteva 1 do 5, naznačena time što je matriksni polimer odabran izmedu: kopovidona, hidroksipropil metilceluloza ftalata (HPMCP), hidroksipropil metilceluloza acetat sukcinata (HPMCAS), 2-hidroksipropil -P-ciklodekstrina (HPBCD), hidroksipropil metilceluloze (hipromeloza, HPMC), polimetakrilata, hidroksipropil celuloze (HPC) i celuloza acetat ftalata (CAP).
7. Formulacija kako se zahteva u bilo kojem od patentnih zahteva 1 do 5, naznačena time što matriksni polimer je kopovidon.
8.Formulacija kako se zahteva u patentnom zahtevu 7, naznačena time što je kopovidon ko-polimer sa 1-vinil-2-pirolidonom i vinil acetatom u srazmeri od 6:4 maseno.
9. Formulacija kako se zahteva u bilo kojem od patentnih zahteva 1 do 8, naznačena time što je srazmera aktivni agens:matriksni polimer težinski od 1:0,25 do 1:10.
10. Formulacija kako se zahteva u patentnom zahtevu 9, naznačena time što je srazmera aktivni agens:matriksni polimer težinski 1 :2:2 do 1: 10.
11. Formulacija kako se zahteva u patentnom zahtevu 9, naznačena time što je srazmera aktivni agens:matriksni polimer težinski 1 :2 do 1 :4.
12. Formulacija kako se zahteva u bilo kojem od prethodnih patentnih zahteva naznačena time što je količina aktivnog agensa po jedinicnoj dozi harem 20% težinski.
13. Formulacija kako se zahteva u patentnom zahtevu 12 naznačena time što je količina aktivnog agensa po jedinicnoj dozi od 20% do 30% težinski.
14. Formulacija kako se zahteva u bilo kojem od prethodnih patentnih zahteva, naznačena time što čvrsta disperzija ukljucuje popvršinski aktivni agens ilili plastiftkator.
15. Formulacija kako se zahteva u patentnom zahtevu 14, naznačena time što je površinski aktivan agens odabran izmedu: natrijum dodecil sulfata (natrijum lauril sulfat); dokusat natrijuma; cetrimida; benzetonijum hlorida; cetilpiridinijum hlorida; laurinske kiseline; polioksietilen alkil etara; polioksietilen sorbitan masna kiselina estara, npr. polisorbata 20, 40, 60 i 80; polioksietilen ulje ricinusa derivata, npr. Cremophor RH40™; polioksietilen stearatea i poloksamera.
16. Formulacija kako se zahteva u bilo kojem od prethodnih patentnih zahteva naznačena time što je ukupna količina aktivnog agensa u formulaciji od 25 mg do 400 mg.
17. Formulacija kako se zahteva u patentnom zahtevu 1, naznačena time što je matriksni polimer kopovidon i formulacija nadalje obuhvata glidant, rastvorljivi punioc I lubrikant.
18. Formulacija kako se zahteva u patentnom zahtevu 17, naznačena time što je glidant silicijum dioksid, rastvorljivi punioc je manito! i lubrikant je natrijum stearil fumarat.
19. Formulacija kako se zahteva u patentnom zahtevu 1, naznačena time što je matriksni polimer kopovidon, srazmera aktivni agens:matriksni polimer težinski je 1:2.3 I ukupna količina aktivnog agensaje 25% težinski.
20. Formulacija kako se zahteva u patentnom zahtevu 19, naznačena time što formulacija takode obuhvata 1,8% težinski koloidnog silicijum dioksida, 14.7%% težinski manitola i 1% težinski natrijum stearil fumarata.
21. Formulacija kako se zahteva u bilo kojem od prethodnih patentnih zahteva, naznačena time što se čvrsta disperzija radi isparavanjem rastvaraca ili ekstruzijom raštopa.
22. Formulacija kako se zahteva u patentnom zahtevu 21, naznačena time što se čvrsta disperzija radi ekstruzijom raštopa.
23. Formulacija prema bilo kojem od prethodnih patentnih zahteva, naznačena time što je formulacija tableta za oralnu primenu.
24. Dnevna farmaceutska doza 4-[3-( 4-ciklopropankarbonil-piperazin-1-karbonil)-4 fluoro-benzil]-2H-ftalazin-1-ona za lecenje kancera kod pacijenta, naznačena time što doza obuhvata 10 do 1000 mg 4-[3-( 4-ciklopropankarbonil-piperazin-1-karbonil)-4-fluoro-benzil]-2H-ftalazin-1-ona u cvrštoj disperziji sa matriksnim polimerom koji pokazuje nisku higroskopnost i visoku temperaturu omeksavanja.
25. Dnevna farmaceutska doza kako se zahteva u patentnom zahtevu 24, naznačena time što je matriksni polimer kopovidon i srazmera 4-[3-(4-ciklopropankarbonil-piperazin-1-karbonil)-4-fluoro-benzil]-2H-ftalazin-1-ona naprema matriksnom polimeru težinski je 1:2 do 1:4.
26. Dnevna farmaceutska doza kako se zahteva u patentnim zahtevima 24 ili 25, naznačena time što se dnevna farmaceutska doza dostavi u manje od 4 jedinice po danu.
27. Postupak proizvodnje čvrste amorfne disperzije 4-[3-(4-ciklopropankarbonilpiperazin-1-karbonil)-4-fluoro-benzil]-2H-ftalazin-1-ona naznacen time što obuhvata: (i) mesanje podesne koliCine 4-[3-(4-ciklopropankarbonil-piperazin-1-karbonil)-4-fluoro-benzil]-2H-ftalazin-1-ona ili farmaceutski prihvatlj ive soli ili solvata od toga sa zeljenom kolicinom harem jednog matriksnog polimera, u cemu matriksni polimer pokazuje nisku higroskopnost i visoku temperaturu omeksavanja; (ii) povecanje temperature smese da se dobije raštop; i (ili) ekstrudiranje raštopa da se dobije cvrsti proizvod.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10334708P | 2008-10-07 | 2008-10-07 | |
| EP09740728.2A EP2346495B2 (en) | 2008-10-07 | 2009-10-05 | Pharmaceutical formulation 514 |
| PCT/GB2009/051309 WO2010041051A1 (en) | 2008-10-07 | 2009-10-05 | Pharmaceutical formulation 514 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ME02640B true ME02640B (me) | 2017-06-20 |
Family
ID=41396997
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MEP-2016-204A ME02640B (me) | 2008-10-07 | 2009-10-05 | Farmaceutske formulacije 514 |
Country Status (42)
Families Citing this family (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR122021018683B1 (pt) * | 2008-10-07 | 2022-11-16 | Kudos Pharmaceuticals Limited | Formulação farmacêutica de 4-[3-(4-ciclopropanocarbonil- piperazina-1-carbonil)-4-flúor- benzil]-2h-ftalazin-1-ona, uso de um polímero de matriz, forma de dosagem e método para produzir uma dispersão amorfa sólida |
| AR077975A1 (es) | 2009-08-28 | 2011-10-05 | Irm Llc | Derivados de pirazol pirimidina y composiciones como inhibidores de cinasa de proteina |
| KR20130109092A (ko) | 2010-06-09 | 2013-10-07 | 아보트 러보러터리즈 | 키나제 억제제를 함유하는 고체 분산물 |
| WO2012008159A1 (en) * | 2010-07-14 | 2012-01-19 | Senju Pharmaceutical Co., Ltd. | Solid dispersion of alfa-ketoamide derivatives |
| UA113500C2 (xx) | 2010-10-29 | 2017-02-10 | Одержані екструзією розплаву тверді дисперсії, що містять індукуючий апоптоз засіб | |
| SG10201801794WA (en) * | 2010-10-29 | 2018-04-27 | Abbvie Inc | Solid dispersions containing an apoptosis-inducing agent |
| MY165884A (en) | 2010-11-23 | 2018-05-18 | Abbvie Ireland Unlimited Co | Methods of treatment using selective bcl-2 inhibitors |
| KR101923364B1 (ko) | 2010-11-23 | 2018-11-30 | 애브비 인코포레이티드 | 아폽토시스유도제의 염 및 결정형 |
| GB201103837D0 (en) * | 2011-03-07 | 2011-04-20 | Oxagen Ltd | Amorphous (5-Fluoro-2-Methyl-3-Quinolin-2-Ylmethyl-Indol-1-Yl)-acetic acid |
| US11007194B2 (en) | 2011-11-11 | 2021-05-18 | Array Biopharma Inc. | Method of treating a proliferative disease |
| WO2013078264A1 (en) | 2011-11-23 | 2013-05-30 | Novartis Ag | Pharmaceutical formulations |
| NL2009367C2 (en) * | 2012-08-27 | 2014-03-03 | Stichting Vu Vumc | Microscopic imaging apparatus and method to detect a microscopic image. |
| DK2938598T3 (en) | 2012-12-31 | 2017-02-13 | Cadila Healthcare Ltd | Substituted phthalazine-1 (2H) -one derivatives as selective inhibitors of poly (adp-ribose) polymerase-1 |
| US20140275082A1 (en) | 2013-03-14 | 2014-09-18 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| TW201618783A (zh) | 2014-08-07 | 2016-06-01 | 艾森塔製藥公司 | 以布魯頓(Bruton)氏酪胺酸激酶(BTK)佔據和BTK再合成速率為基礎之治療癌症、免疫和自體免疫疾病及發炎性疾病之方法 |
| CN104434809B (zh) * | 2014-12-10 | 2018-10-16 | 北京科莱博医药开发有限责任公司 | 一种奥拉帕尼固体分散体制剂及其制备方法 |
| CN105777651A (zh) * | 2015-01-13 | 2016-07-20 | 江苏豪森药业集团有限公司 | 聚腺苷酸二磷酸核糖转移酶抑制剂的晶型及其制备方法和医药用途 |
| WO2016155655A1 (zh) | 2015-04-03 | 2016-10-06 | 上海瑛派药业有限公司 | Parp抑制剂固体药物剂型及其应用 |
| CN106265580B (zh) * | 2015-05-18 | 2020-09-08 | 中国科学院上海药物研究所 | Somcl-9112固体分散体、其制备方法及包含其的somcl-9112固体制剂 |
| CN112010809A (zh) * | 2015-06-12 | 2020-12-01 | 苏州科睿思制药有限公司 | 奥拉帕尼的晶型i及其制备方法 |
| US20170105937A1 (en) * | 2015-10-16 | 2017-04-20 | Cadila Healthcare Limited | Olaparib co-precipitate and preparation method thereof |
| CN105254572A (zh) * | 2015-11-09 | 2016-01-20 | 北京科莱博医药开发有限责任公司 | 一种奥拉帕尼的晶型及其制备方法和应用 |
| ITUB20159206A1 (it) * | 2015-12-22 | 2017-06-22 | Olon Spa | Forme cristalline e amorfe di olaparib |
| US20170204067A1 (en) | 2016-01-14 | 2017-07-20 | Scinopharm Taiwan, Ltd. | Crystalline forms of olaparib and manufacturing processes therefor |
| CZ2016391A3 (cs) | 2016-06-29 | 2018-01-10 | Zentiva, K.S. | Farmaceutická formulace olaparibu |
| CN108201536A (zh) * | 2016-12-16 | 2018-06-26 | 中国科学院上海药物研究所 | 一种奥拉帕尼口服缓控释药物组合物及其用途 |
| JP7211980B2 (ja) * | 2017-06-12 | 2023-01-24 | プロテイン ダイナミック ソリューションズ インコーポレイテッド | 結晶及び結晶化を分析する方法及びシステム |
| US10519136B2 (en) | 2017-12-29 | 2019-12-31 | Accutar Biotechnology | Dual inhibitors of PARP1 and CDK |
| CA3031777A1 (en) | 2018-01-31 | 2019-07-31 | Apotex Inc. | Crystalline form of olaparib |
| CN109293576A (zh) * | 2018-11-08 | 2019-02-01 | 威海贯标信息科技有限公司 | 一种小粒度奥拉帕尼的制备方法 |
| US12318385B2 (en) * | 2018-11-16 | 2025-06-03 | Jiangsu Hengrui Medicine Co., Ltd. | Pharmaceutical composition comprising PARP inhibitors |
| CN113924300A (zh) * | 2019-04-11 | 2022-01-11 | 百时美施贵宝公司 | 用于达到治疗血浆浓度的增加效能的非晶形固体及经溶解调配物 |
| CN110013466B (zh) * | 2019-05-28 | 2021-11-30 | 天津中医药大学 | 一种小檗红碱固体分散体粉末及制备方法及应用 |
| US10703728B1 (en) * | 2019-06-18 | 2020-07-07 | Scinopharm Taiwan, Ltd. | Crystalline form of olaparib and a process for preparing the same |
| EP4079295A4 (en) * | 2019-12-20 | 2023-12-06 | Samyang Holdings Corporation | COMPOSITION HAVING IMPROVED SOLUBILITY AND BIOAVAILABILITY OF OLAPARIB |
| WO2021133886A1 (en) | 2019-12-23 | 2021-07-01 | Accutar Biotechnology | Combinations of estrogen receptor degraders and cyclin-dependent kinase inhibitors for treating cancer |
| JP2023509191A (ja) | 2020-01-09 | 2023-03-07 | アストラゼネカ・アクチエボラーグ | 癌を治療するための組み合わせ療法 |
| CN113288859B (zh) * | 2020-02-21 | 2024-11-22 | 上海宣泰医药科技股份有限公司 | 奥拉帕尼药物组合物及其制剂、制备方法和用途 |
| CN113350349B (zh) * | 2020-03-04 | 2022-11-11 | 中国科学院上海药物研究所 | 奥拉帕尼溶出增强组合物 |
| CN116710424A (zh) | 2020-09-16 | 2023-09-05 | 努福米克斯技术有限公司 | 奥拉帕利草酸共晶体及其药学用途 |
| KR102707060B1 (ko) * | 2020-12-01 | 2024-09-13 | 주식회사 삼양홀딩스 | 안정성 및 생체이용율이 개선된 올라파립 고체 분산체 조성물 |
| CN112843007A (zh) * | 2021-02-04 | 2021-05-28 | 石药集团中奇制药技术(石家庄)有限公司 | 一种奥拉帕利片 |
| AU2022248850A1 (en) | 2021-03-27 | 2023-11-09 | TRx Biosciences Limited | Compositions having improved bioavailability of therapeutics |
| US20240269073A1 (en) * | 2021-06-07 | 2024-08-15 | Zerion Pharma ApS | Co-amorphous forms for use in cancer therapy |
| EP4384501A4 (en) * | 2021-08-09 | 2025-01-22 | Glenmark Life Sciences Limited | Process for the preparation of olaparib, and crystalline form thereof |
| US12049452B2 (en) | 2021-11-10 | 2024-07-30 | Nuformix Technologies Limited | Olaparib hydroxybenzoic acid cocrystals and their pharmaceutical use |
| AU2023233811A1 (en) * | 2022-03-14 | 2024-09-19 | TRx Biosciences Limited | Compositions having improved bioavailability of therapeutics and uses thereof |
| TW202408509A (zh) * | 2022-07-14 | 2024-03-01 | 大陸商西藏海思科製藥有限公司 | 雜芳基衍生物的藥物組合物及其在醫藥上的應用 |
| CN115998699B (zh) * | 2023-02-13 | 2025-06-24 | 中国药科大学 | 一种3d打印奥拉帕利片及其制备方法 |
| CN117205169A (zh) * | 2023-10-26 | 2023-12-12 | 宁夏医科大学 | 一种奥拉帕利片及其制备方法 |
| WO2026013152A1 (en) | 2024-07-09 | 2026-01-15 | Stada Arzneimittel Ag | Pharmaceutical composition comprising olaparib |
| US12383633B1 (en) | 2024-10-01 | 2025-08-12 | Zymeron Corporation | Injectable formulations of PARP inhibitors and uses thereof |
Family Cites Families (142)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2143745A1 (de) | 1971-09-01 | 1973-03-08 | Hoechst Ag | 3,4-dihydro-2h-isochinolin-1-thione und verfahren zu ihrer herstellung |
| US3813384A (en) * | 1972-01-17 | 1974-05-28 | Asta Werke Ag Chem Fab | Basically substituted benzyl phthalazone derivatives,acid salts thereof and process for the production thereof |
| FR2262513A1 (en) | 1974-03-01 | 1975-09-26 | Delalande Sa | 3,4,5-Triphenyl-delta-1,2,4-oxadiazolines - with bronchodilator, anti-cholinergic, hypertensive, analgesic and sedative activity |
| JPS54156526A (en) | 1978-05-31 | 1979-12-10 | Asahi Chemical Ind | Dry picture forming material |
| US4283539A (en) | 1979-12-18 | 1981-08-11 | Pfizer Inc. | Isoquinoline acetic acids |
| JPS58164577A (ja) | 1982-03-24 | 1983-09-29 | Taiho Yakuhin Kogyo Kk | 4―ベンジル―1―(2h)イソキノロン誘導体 |
| US4665181A (en) * | 1984-05-17 | 1987-05-12 | Pennwalt Corporation | Anti-inflammatory phthalazinones |
| US5041653A (en) * | 1985-05-03 | 1991-08-20 | Sri International | Substituted benzamide radiosensitizers |
| US5032617A (en) * | 1985-05-03 | 1991-07-16 | Sri International | Substituted benzamide radiosensitizers |
| US5215738A (en) * | 1985-05-03 | 1993-06-01 | Sri International | Benzamide and nicotinamide radiosensitizers |
| ES2031813T3 (es) * | 1985-11-11 | 1993-01-01 | Asta Pharma Ag | Procedimiento para la preparacion de derivados de 4-bencil-1-(2h)-ftalazinona. |
| DE3612211A1 (de) * | 1986-04-11 | 1987-10-15 | Basf Ag | Kontinuierliches verfahren zum tablettieren |
| DE3612212A1 (de) * | 1986-04-11 | 1987-10-15 | Basf Ag | Verfahren zur herstellung von festen pharmazeutischen formen |
| GB8610018D0 (en) | 1986-04-24 | 1986-05-29 | Fujisawa Pharmaceutical Co | Phthalazine derivatives |
| DE3640641A1 (de) * | 1986-11-28 | 1988-07-14 | Thomae Gmbh Dr K | Neue heteroaromatische aminderivate, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung |
| ZA882639B (en) | 1987-05-02 | 1988-09-30 | Asta-Pharma Aktiengesellschaft | New 2-aminoalkyl-4-benzyl-1(2h)-phthalazinone derivatives |
| DE3812567A1 (de) * | 1988-04-15 | 1989-10-26 | Basf Ag | Verfahren zur herstellung pharmazeutischer mischungen |
| DE68920798T2 (de) | 1988-08-19 | 1995-05-18 | Warner Lambert Co | Substituierte Dihydroisochinolinone und verwandte Verbindungen als Verstärker der letalen Effekte von Bestrahlung und bestimmten Chemotherapeutika; ausgewählte Verbindungen, Analoga und Verfahren. |
| EP0389995B1 (en) | 1989-03-28 | 1995-05-31 | Nisshin Flour Milling Co., Ltd. | Isoquinoline derivatives for the treatment of glaucoma or ocular hypertension |
| DD287032A5 (de) | 1989-07-28 | 1991-02-14 | Karl-Marx-Universitaet Leipzig,De | Verfahren zur herstellung von 3-carbamoyl-4-aryl-1,2-di-hydro-isochinolin-1h-onen |
| GB9011833D0 (en) | 1990-05-25 | 1990-07-18 | Collins Mary K L | Inhibition of viral infection |
| US6004979A (en) * | 1991-02-07 | 1999-12-21 | Hoechst Marion Roussel | Nitrogenous bicycles |
| MX9200299A (es) * | 1991-02-07 | 1992-12-01 | Roussel Uclaf | Nuevos derivados biciclicos nitrogenados, su procedimiento de preparacion los nuevos compuestos intermedios obtenidos su aplicacion como medicamentos y las composiciones farmaceuticas que los contienen. |
| EP0502575A1 (en) | 1991-03-06 | 1992-09-09 | Merck & Co. Inc. | Substituted 1-(2H)-isoquinolinones |
| IL104406A0 (en) | 1992-01-17 | 1993-05-13 | Syntex Inc | Substituted 1-isoquinolone derivatives,their preparation and pharmaceutical compositions containing them |
| CZ199593A3 (en) * | 1992-10-02 | 1994-04-13 | Asta Medica Ag | Phthalazinone derivatives exhibiting anti-arrhythmic and analgesic activity and eliminating resistance to a plurality of medicaments (mdr) |
| JPH08502973A (ja) | 1992-11-02 | 1996-04-02 | メルク エンド カンパニー インコーポレーテッド | ニューロテンシンアンタゴニストとしての置換フタラジノン |
| EP0634404A1 (en) | 1993-07-13 | 1995-01-18 | Rhone Poulenc Agriculture Ltd. | Phtalazin derivatives and their use as pesticides |
| US5587384A (en) * | 1994-02-04 | 1996-12-24 | The Johns Hopkins University | Inhibitors of poly(ADP-ribose) synthetase and use thereof to treat NMDA neurotoxicity |
| US5648355A (en) * | 1994-02-09 | 1997-07-15 | Kos Pharmaceutical, Inc. | Method of treatment of endogenous, painful gastrointestinal conditions of non-inflammatory, non-ulcerative origin |
| GB9404485D0 (en) | 1994-03-09 | 1994-04-20 | Cancer Res Campaign Tech | Benzamide analogues |
| PT699754E (pt) | 1994-08-12 | 2001-04-30 | Us Health | Metodo para diagnosticar uma predisposicao para cancro da mama e do ovario |
| WO1996005306A2 (en) | 1994-08-12 | 1996-02-22 | Myriad Genetics, Inc. | IN VIVO MUTATIONS AND POLYMORPHISMS IN THE 17q-LINKED BREAST AND OVARIAN CANCER SUSCEPTIBILITY GENE |
| US5589483A (en) * | 1994-12-21 | 1996-12-31 | Geron Corporation | Isoquinoline poly (ADP-ribose) polymerase inhibitors to treat skin diseases associated with cellular senescence |
| US5834466A (en) | 1994-12-22 | 1998-11-10 | The Regents Of The University Of California | Method for protecting of heart by limiting metabolic and ionic abnormalities developed during ischemia, following ischemia or resulting from ischemia |
| EP0721286A3 (en) | 1995-01-09 | 2000-07-26 | Matsushita Electric Industrial Co., Ltd. | Video signal decoding apparatus with artifact reduction |
| CA2217351C (en) | 1995-04-07 | 2003-03-18 | Schering Corporation | Carbonyl-piperazinyl and piperidinyl compounds which inhibit farnesyl protein transferase |
| IL120264A0 (en) | 1996-02-29 | 1997-06-10 | Pfizer | Method of reducing tissue damage associated with non-cardiac ischemia |
| US5939557A (en) * | 1996-04-03 | 1999-08-17 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| JP2000504023A (ja) | 1996-04-03 | 2000-04-04 | メルク エンド カンパニー インコーポレーテッド | 癌治療方法 |
| US5874452A (en) * | 1996-04-03 | 1999-02-23 | Merck & Co., Inc. | Biheteroaryl inhibitors of farnesyl-protein transferase |
| US5859035A (en) * | 1996-04-03 | 1999-01-12 | Merck & Co., Inc. | Arylheteroaryl inhibitors of farnesyl-protein transferase |
| US6080870A (en) * | 1996-04-03 | 2000-06-27 | Merck & Co., Inc. | Biaryl substituted imidazole compounds useful as farnesyl-protein transferase inhibitors |
| US5872136A (en) * | 1996-04-03 | 1999-02-16 | Merck & Co., Inc. | Arylheteroaryl inhibitors of farnesyl-protein transferase |
| US5854265A (en) * | 1996-04-03 | 1998-12-29 | Merck & Co., Inc. | Biheteroaryl inhibitors of farnesyl-protein transferase |
| US6063930A (en) * | 1996-04-03 | 2000-05-16 | Merck & Co., Inc. | Substituted imidazole compounds useful as farnesyl-protein transferase inhibitors |
| US5880140A (en) * | 1996-04-03 | 1999-03-09 | Merck & Co., Inc. | Biheteroaryl inhibitors of farnesyl-protein transferase |
| US5883105A (en) * | 1996-04-03 | 1999-03-16 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| WO1997038664A2 (en) | 1996-04-18 | 1997-10-23 | Merck & Co., Inc. | A method of treating cancer |
| US5880128A (en) * | 1996-05-08 | 1999-03-09 | Schering Corporation | Carbonyl piperazinyl and piperidinyl compounds |
| CA2205757C (en) * | 1996-05-30 | 2006-01-24 | F. Hoffmann-La Roche Ag | Pyridazinone derivatives and their use as inhibitors of prostaglandin g/h synthase i and ii(cox i and ii) |
| EP0934270A1 (en) | 1996-05-30 | 1999-08-11 | Merck & Co., Inc. | A method of treating cancer |
| EP1014941B2 (en) * | 1996-06-26 | 2017-05-17 | The Board Of Regents, The University Of Texas System | Hot-melt extrudable pharmaceutical formulation |
| DE19629753A1 (de) * | 1996-07-23 | 1998-01-29 | Basf Ag | Verfahren zur Herstellung von festen Arzneiformen |
| US5854264A (en) * | 1996-07-24 | 1998-12-29 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| US5888529A (en) | 1997-03-28 | 1999-03-30 | The Regents Of The University Of California | Ileus treatment method |
| AU7484798A (en) | 1997-05-13 | 1998-12-08 | Octamer, Inc. | Methods for treating inflammation, inflammatory diseases, arthritis and strok e using padprt inhibitors |
| US6060038A (en) * | 1997-05-15 | 2000-05-09 | Merck & Co., Inc. | Radiolabeled farnesyl-protein transferase inhibitors |
| AU8784698A (en) | 1997-08-15 | 1999-03-08 | Johns Hopkins University, The | Method of using selective parp inhibitors to prevent or treat neurotoxicity |
| US6426415B1 (en) * | 1997-09-03 | 2002-07-30 | Guilford Pharmaceuticals Inc. | Alkoxy-substituted compounds, methods and compositions for inhibiting parp activity |
| US6291425B1 (en) | 1999-09-01 | 2001-09-18 | Guilford Pharmaceuticals Inc. | Compounds, methods and pharmaceutical compositions for treating cellular damage, such as neural or cardiovascular tissue damage |
| US6514983B1 (en) | 1997-09-03 | 2003-02-04 | Guilford Pharmaceuticals Inc. | Compounds, methods and pharmaceutical compositions for treating neural or cardiovascular tissue damage |
| US20020022636A1 (en) | 1997-09-03 | 2002-02-21 | Jia-He Li | Oxo-substituted compounds, process of making, and compositions and methods for inhibiting parp activity |
| US6635642B1 (en) | 1997-09-03 | 2003-10-21 | Guilford Pharmaceuticals Inc. | PARP inhibitors, pharmaceutical compositions comprising same, and methods of using same |
| US6197785B1 (en) * | 1997-09-03 | 2001-03-06 | Guilford Pharmaceuticals Inc. | Alkoxy-substituted compounds, methods, and compositions for inhibiting PARP activity |
| CA2310250A1 (en) * | 1997-11-14 | 1999-05-27 | August Masaru Watanabe | Treatment for alzheimer's disease |
| WO1999044612A1 (en) | 1998-03-02 | 1999-09-10 | Cocensys, Inc. | Substituted quinazolines and analogs and the use thereof |
| FR2776291B1 (fr) | 1998-03-18 | 2000-06-16 | Pf Medicament | Nouveaux derives bis-benzamides, leur procede de fabrication, les compositions pharmaceutiques les contenant et leur utilisation comme medicament |
| US6310059B1 (en) * | 1998-06-30 | 2001-10-30 | Neuromed Technologies, Inc. | Fused ring calcium channel blockers |
| US6492375B2 (en) * | 1998-06-30 | 2002-12-10 | Neuromed Technologies, Inc. | Partially saturated calcium channel blockers |
| US20040266784A1 (en) * | 1998-06-30 | 2004-12-30 | Snutch Terrance P. | Calcium channel inhibitors comprising benzhydril spaced from piperazine |
| US6951862B2 (en) * | 1998-06-30 | 2005-10-04 | Neuromed Technologies, Inc. | Calcium channel blockers comprising two benzhydril moieties |
| US6387897B1 (en) * | 1998-06-30 | 2002-05-14 | Neuromed Technologies, Inc. | Preferentially substituted calcium channel blockers |
| US7186726B2 (en) * | 1998-06-30 | 2007-03-06 | Neuromed Pharmaceuticals Ltd. | Preferentially substituted calcium channel blockers |
| US6011035A (en) * | 1998-06-30 | 2000-01-04 | Neuromed Technologies Inc. | Calcium channel blockers |
| US6943168B2 (en) * | 1998-06-30 | 2005-09-13 | Neuromed Technologies Inc. | Calcium channel inhibitors comprising benzhydril spaced from piperazine |
| US20060084660A1 (en) * | 1998-06-30 | 2006-04-20 | Neuromed Technologies Inc. | Calcium channel blockers comprising two benzhydril moieties |
| US20040259866A1 (en) * | 1998-06-30 | 2004-12-23 | Snutch Terrance P. | Calcium channel blockers comprising two benzhydril moieties |
| ITMI981671A1 (it) * | 1998-07-21 | 2000-01-21 | Zambon Spa | Derivati ftalazinici inibitori della fosfodisterasi 4 |
| EE05006B1 (et) | 1999-01-11 | 2008-04-15 | Agouron Pharmaceuticals, Inc. | Polü(ADP-riboos)polümeraaside tritsüklilised inhibiitorid ja neid sisaldavad farmatseutilised kompositsioonid |
| KR20010101675A (ko) * | 1999-01-26 | 2001-11-14 | 우에노 도시오 | 2h-프탈라진-1-온 유도체 및 그 유도체를 유효 성분으로하는 약제 |
| DE19921567A1 (de) * | 1999-05-11 | 2000-11-16 | Basf Ag | Verwendung von Phthalazine-Derivaten |
| US6465467B1 (en) * | 1999-05-21 | 2002-10-15 | Biovitrum Ab | Certain aryl-aliphatic and heteroaryl-aliphatic piperazinyl pyrazines and their use in the treatment of serotonin-related diseases |
| DE60010476T2 (de) | 1999-08-11 | 2005-04-14 | Bristol-Myers Squibb Co. | Verfahren zur Herstellung eines C-4-Methylcarbonat-Analogons von Paclitaxel |
| US6465448B1 (en) | 1999-08-13 | 2002-10-15 | Case Western Reserve University | Methoxyamine potentiation of temozolomide anti-cancer activity |
| ECSP003637A (es) | 1999-08-31 | 2002-03-25 | Agouron Pharma | Inhibidores triciclicos de poli (adp-ribosa) polimerasas |
| WO2001021615A1 (fr) | 1999-09-17 | 2001-03-29 | Yamanouchi Pharmaceutical Co., Ltd. | Dérivés de benzimidazole |
| BR0007174A (pt) | 1999-09-28 | 2001-09-04 | Basf Ag | Composto, preparação farmacêutica e uso de compostos |
| US6552016B1 (en) * | 1999-10-14 | 2003-04-22 | Curis, Inc. | Mediators of hedgehog signaling pathways, compositions and uses related thereto |
| US6476048B1 (en) * | 1999-12-07 | 2002-11-05 | Inotek Pharamaceuticals Corporation | Substituted phenanthridinones and methods of use thereof |
| DE19963607B4 (de) * | 1999-12-23 | 2005-12-15 | Schering Ag | Verfahren zur Herstellung von 4-(Heteroaryl-methyl) halogen-1(2H)-phthalazinonen |
| US7041675B2 (en) * | 2000-02-01 | 2006-05-09 | Abbott Gmbh & Co. Kg | Heterocyclic compounds and their use as PARP inhibitors |
| WO2001079184A1 (en) | 2000-04-18 | 2001-10-25 | Sumitomo Pharmaceuticals Company, Limited | Substituted piperazine compounds |
| US7122679B2 (en) | 2000-05-09 | 2006-10-17 | Cephalon, Inc. | Multicyclic compounds and the use thereof |
| DE10022925A1 (de) * | 2000-05-11 | 2001-11-15 | Basf Ag | Substituierte Indole als PARP-Inhibitoren |
| WO2001087845A2 (en) | 2000-05-15 | 2001-11-22 | Fujisawa Pharmaceutical Co., Ltd. | N-containing heterocyclic compounds and their use as 5-ht antagonists |
| WO2001090077A1 (en) | 2000-05-19 | 2001-11-29 | Guilford Pharmaceuticals, Inc. | Sulfonamide and carbamide derivatives of 6(5h)phenanthridinones and their uses |
| AU7549501A (en) * | 2000-06-16 | 2002-01-02 | Biogen Inc | Angiogenesis-modulating compositions and uses |
| US7498304B2 (en) * | 2000-06-16 | 2009-03-03 | Curis, Inc. | Angiogenesis-modulating compositions and uses |
| WO2002035991A2 (en) * | 2000-10-30 | 2002-05-10 | The Board Of Regents, The University Of Texas System | Spherical particles produced by a hot-melt extrusion/spheronization process |
| AU9578901A (en) | 2000-10-30 | 2002-05-15 | Kudos Pharm Ltd | Phthalazinone derivatives |
| US7151102B2 (en) * | 2000-10-30 | 2006-12-19 | Kudos Pharmaceuticals Limited | Phthalazinone derivatives |
| WO2002044157A2 (en) | 2000-12-01 | 2002-06-06 | Iconix Pharmaceuticals, Inc. | Parb inhibitors |
| EP1217000A1 (en) * | 2000-12-23 | 2002-06-26 | Aventis Pharma Deutschland GmbH | Inhibitors of factor Xa and factor VIIa |
| GB0104752D0 (en) * | 2001-02-27 | 2001-04-18 | Astrazeneca Ab | Pharmaceutical compositions |
| JPWO2002068407A1 (ja) | 2001-02-28 | 2004-06-24 | 山之内製薬株式会社 | ベンゾイミダゾール化合物 |
| DE60218458T2 (de) | 2001-05-08 | 2007-11-15 | Kudos Pharmaceuticals Ltd. | Isochinolinon derivate als parp inhibitoren |
| EP1396488A1 (en) * | 2001-05-23 | 2004-03-10 | Mitsubishi Pharma Corporation | Fused heterocyclic compound and medicinal use thereof |
| WO2003007959A1 (en) | 2001-07-16 | 2003-01-30 | Fujisawa Pharmaceutical Co., Ltd. | Quinoxaline derivatives which have parp inhibitory action |
| US20030073692A1 (en) * | 2001-08-07 | 2003-04-17 | Pharmacia & Upjohn S.P.A. | Amino-phthalazinone derivatives active as kinase inhibitors, process for their preparation and pharmaceutical compositions containing them |
| WO2003051879A1 (en) | 2001-12-14 | 2003-06-26 | Altana Pharma Ag | Known and novel 4,5-dihydro-imidazo[4,5,1-ij]quinolin-6-ones useful as poly(adp-ribose)polymerase inhibitors |
| AUPR975601A0 (en) | 2001-12-24 | 2002-01-31 | Fujisawa Pharmaceutical Co., Ltd. | Quinazolinone derivatives |
| US7396542B2 (en) * | 2001-12-28 | 2008-07-08 | Teva Pharmaceutical Industries Ltd. | Stable pharmaceutical formulation of paroxetine hydrochloride anhydrous and a process for preparation thereof |
| AU2002360733A1 (en) | 2001-12-31 | 2003-07-24 | Guilford Pharmaceuticals Inc. | SUBSTITUTED 4,9-DIHYDROCYCLOPENTA(imn)PHENANTHRIDINE-5-ONES DERIVATIVES THEREOF AND THEIR USES |
| AUPS019702A0 (en) | 2002-01-29 | 2002-02-21 | Fujisawa Pharmaceutical Co., Ltd. | Condensed heterocyclic compounds |
| US7402580B2 (en) | 2002-02-19 | 2008-07-22 | Ono Pharmaceutical Co., Ltd. | Fused pyridazine derivative compounds and drugs containing these compounds as the active ingredient |
| ATE451365T1 (de) | 2002-02-25 | 2009-12-15 | Kudos Pharm Ltd | Als atm-inhibitoren geeignete pyranone |
| US20030195192A1 (en) * | 2002-04-05 | 2003-10-16 | Fortuna Haviv | Nicotinamides having antiangiogenic activity |
| AUPS137402A0 (en) | 2002-03-26 | 2002-05-09 | Fujisawa Pharmaceutical Co., Ltd. | Novel tricyclic compounds |
| US20040014744A1 (en) * | 2002-04-05 | 2004-01-22 | Fortuna Haviv | Substituted pyridines having antiangiogenic activity |
| US7196085B2 (en) * | 2002-04-30 | 2007-03-27 | Kudos Pharmaceuticals Limited | Phthalazinone derivatives |
| US7449464B2 (en) * | 2003-03-12 | 2008-11-11 | Kudos Pharmaceuticals Limited | Phthalazinone derivatives |
| AU2004220321B2 (en) * | 2003-03-12 | 2010-02-25 | Kudos Pharmaceuticals Ltd | Phthalazinone derivatives |
| US20060251724A1 (en) * | 2003-05-06 | 2006-11-09 | Farrell Thomas P | Method for preparing thermoformed compositions containing acrylic polymer binders, pharmaceutical dosage forms and methods of preparing the same |
| US20050048112A1 (en) * | 2003-08-28 | 2005-03-03 | Jorg Breitenbach | Solid pharmaceutical dosage form |
| US8025899B2 (en) † | 2003-08-28 | 2011-09-27 | Abbott Laboratories | Solid pharmaceutical dosage form |
| TWI338000B (en) * | 2003-12-01 | 2011-03-01 | Kudos Pharm Ltd | Dna damage repair inhibitors for treatment of cancer |
| EP1744751A4 (en) * | 2004-03-18 | 2010-03-10 | Brigham & Womens Hospital | METHOD FOR THE TREATMENT OF SYNUCLEINOPATHIES |
| US20050227999A1 (en) * | 2004-04-09 | 2005-10-13 | Neuromed Technologies Inc. | Diarylamine derivatives as calcium channel blockers |
| JP5315611B2 (ja) | 2004-06-23 | 2013-10-16 | 小野薬品工業株式会社 | S1p受容体結合能を有する化合物およびその用途 |
| GB0419072D0 (en) * | 2004-08-26 | 2004-09-29 | Kudos Pharm Ltd | Phthalazinone derivatives |
| CA2598204C (en) * | 2004-11-09 | 2015-01-13 | Board Of Regents, The University Of Texas System | Stabilized hme composition with small drug particles |
| US7517870B2 (en) * | 2004-12-03 | 2009-04-14 | Fondazione Telethon | Use of compounds that interfere with the hedgehog signaling pathway for the manufacture of a medicament for preventing, inhibiting, and/or reversing ocular diseases related with ocular neovascularization |
| DE102005011822A1 (de) * | 2005-03-15 | 2006-09-21 | Merck Patent Gmbh | Phthalazinone |
| GB0521373D0 (en) * | 2005-10-20 | 2005-11-30 | Kudos Pharm Ltd | Pthalazinone derivatives |
| WO2008017867A2 (en) * | 2006-08-10 | 2008-02-14 | Cipla Limited | Antiretroviral solid oral composition with at least one water insoluble polymer |
| UY30639A1 (es) * | 2006-10-17 | 2008-05-31 | Kudos Pharm Ltd | Derivados sustituidos de 2h-ftalazin-1-ona, sus formas cristalinas, proceso de preparacion y aplicaciones |
| JPWO2008081829A1 (ja) * | 2006-12-27 | 2010-04-30 | アステラス製薬株式会社 | 難水溶性薬物の溶解性維持用アミノアルキルメタアクリレートコポリマーe |
| PT2698062E (pt) | 2006-12-28 | 2015-10-19 | Abbvie Inc | Inibidores da poli (adp-ribose) polimerase |
| EP1958615A1 (en) * | 2007-02-13 | 2008-08-20 | Bayer Schering Pharma Aktiengesellschaft | Solid pharmaceutical formulations of a homogeneous dispersion of active principles having pH-dependent solubility |
| TW200900396A (en) * | 2007-04-10 | 2009-01-01 | Kudos Pharm Ltd | Phthalazinone derivatives |
| BR122021018683B1 (pt) * | 2008-10-07 | 2022-11-16 | Kudos Pharmaceuticals Limited | Formulação farmacêutica de 4-[3-(4-ciclopropanocarbonil- piperazina-1-carbonil)-4-flúor- benzil]-2h-ftalazin-1-ona, uso de um polímero de matriz, forma de dosagem e método para produzir uma dispersão amorfa sólida |
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- 2011-04-07 CO CO11043258A patent/CO6361906A2/es not_active Application Discontinuation
- 2011-04-07 CL CL2011000774A patent/CL2011000774A1/es unknown
- 2011-05-06 ZA ZA2011/03333A patent/ZA201103333B/en unknown
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2013
- 2013-06-06 US US13/911,151 patent/US20140066447A1/en not_active Abandoned
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2015
- 2015-04-16 US US14/688,326 patent/US20160008473A1/en not_active Abandoned
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2016
- 2016-09-20 CY CY20161100928T patent/CY1118190T1/el unknown
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2017
- 2017-03-03 US US15/449,353 patent/US20170173010A1/en not_active Abandoned
- 2017-09-18 US US15/707,376 patent/US20180133216A1/en not_active Abandoned
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2018
- 2018-11-06 FI FIEP09740728.2T patent/FI2346495T4/fi active
- 2018-11-06 CY CY2018030C patent/CY2018030I1/el unknown
- 2018-11-07 NO NO2018038C patent/NO2018038I1/no unknown
- 2018-11-07 HU HUS1800043C patent/HUS1800043I1/hu unknown
- 2018-11-08 LT LTPA2018014C patent/LTPA2018014I1/lt unknown
- 2018-12-18 US US16/224,096 patent/US20190365751A1/en not_active Abandoned
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2019
- 2019-08-29 AR ARP190102461A patent/AR116035A2/es not_active Application Discontinuation
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2020
- 2020-04-30 US US16/863,074 patent/US20200323847A1/en not_active Abandoned
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2021
- 2021-09-23 US US17/483,070 patent/US20220249474A1/en not_active Abandoned
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2022
- 2022-08-24 US US17/821,833 patent/US11633396B2/en active Active
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2023
- 2023-05-04 US US18/312,333 patent/US11975001B2/en active Active
- 2023-05-04 US US18/312,375 patent/US12048695B2/en active Active
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2024
- 2024-07-26 US US18/785,063 patent/US12178816B2/en active Active
- 2024-07-26 US US18/785,092 patent/US12144810B1/en active Active
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