JP2023538455A - オラパリブシュウ酸共結晶及びその医薬的使用 - Google Patents
オラパリブシュウ酸共結晶及びその医薬的使用 Download PDFInfo
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- JP2023538455A JP2023538455A JP2023518150A JP2023518150A JP2023538455A JP 2023538455 A JP2023538455 A JP 2023538455A JP 2023518150 A JP2023518150 A JP 2023518150A JP 2023518150 A JP2023518150 A JP 2023518150A JP 2023538455 A JP2023538455 A JP 2023538455A
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- olaparib
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- A61P35/00—Antineoplastic agents
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C55/00—Saturated compounds having more than one carboxyl group bound to acyclic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
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- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
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- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
本出願は、2020年9月16日に出願された米国仮出願第63/079,018号の優先権を主張し、その開示は参照により組み込まれる。
本開示は、オラパリブ(olaparib)シュウ酸共結晶、該共結晶の治療的使用、及びそれらを含む医薬組成物に関する。
本発明は、新規のオラパリブシュウ酸共結晶に関する。オラパリブシュウ酸共結晶は、1:1から2:3までのオラパリブ:シュウ酸の比率で変化する。特に、本発明は、2:3オラパリブシュウ酸共結晶、1:1オラパリブシュウ酸共結晶、及び2:1オラパリブシュウ酸共結晶に関する。これらの本発明のオラパリブシュウ酸共結晶、その調製及びその特性は、以下の実施例に記載され、図に示される。本発明は、治療上有効量の本発明のオラパリブシュウ酸共結晶と、薬学的に許容される担体とを含む医薬組成物に関する。本発明はまた、本明細書に記載の疾患、障害及び状態の治療方法、並びにその治療のための、治療有効量の本発明のオラパリブシュウ酸共結晶、又はそれを含む医薬組成物の使用に関する。本発明はさらに、本明細書に記載の疾患、障害及び状態の治療に使用するための医薬の製造における本発明のオラパリブシュウ酸共結晶の使用も提供する。
Bruker 2nd Gen D2‐Phaser回折計で取得した1:1オラパリブシュウ酸共結晶の実験的XRPDパターンを、図5に示す。表2は、図5の実験的XRPDパターンにおいて特定されたピークの角度、°2θ±0.2°2θ、及びd値を列挙する。ピークのリスト全体又は対応するd値、又はそのサブセットは、図5に実質的に類似するXRPDパターンによるのと同様に、共結晶を特徴付けるのに十分である場合がある。例えば、共結晶は、12.7、13.7、14.8、16.2、18.1、22.6、及び24.3°2θ±0.2°2θのピークから選択される、少なくとも2つ、少なくとも3つ、少なくとも4つ、少なくとも5つ、少なくとも6つ、又はすべてのピークにより特徴付けられることがある。
Bruker 2nd Gen D2‐Phaser回折計で取得した2:1オラパリブシュウ酸共結晶の実験的XRPDパターンを図8に示す。表3は、図8の実験的XRPDパターンで特定されたピークの角度、°2θ±0.2°2θ、及びd値を列挙する。ピークのリスト全体又は対応するd値、又はそのサブセットは、図8に実質的に類似するXRPDパターンによるのと同様に、共結晶を特徴付けるのに十分である場合がある。例えば、共結晶は、6.5、7.9、12.0、13.1、14.3、15.9、18.7、及び19.7°2θ±0.2°2θにおけるピークから選択される少なくとも2つ、少なくとも3つ、少なくとも4つ、少なくとも5つ、少なくとも6つ、少なくとも7つのピーク、又はすべてのピークにより特徴付けられることがある。
Claims (15)
- オラパリブシュウ酸共結晶。
- 2:3オラパリブシュウ酸共結晶、1:1オラパリブシュウ酸共結晶、及び2:1オラパリブシュウ酸共結晶の群から選択される、請求項1に記載のオラパリブシュウ酸共結晶。
- 以下の少なくとも1つを特徴とする2:3オラパリブシュウ酸共結晶である、請求項2に記載のオラパリブシュウ酸共結晶:
10.9、12.0、13.7、16.1、17.0、19.1、19.8及び20.7°2θ±0.2°2θのピークから選ばれる少なくとも2つ、少なくとも3つ、少なくとも4つ、少なくとも5つ、少なくとも6つ、少なくとも7つ、又はすべてのピークを有するパワーX線回折パターン;又は
図1とほぼ同様のパワーX線回折パターン。 - パワーX線回折パターンが、10.9、12.0、13.7、16.1、17.0、19.1、19.8、20.7°2θ±0.2°2θのピークから選ばれる少なくとも5つのピークを有する、請求項3に記載のオラパリブシュウ酸共結晶。
- 以下の少なくとも1つを特徴とする1:1オラパリブシュウ酸共結晶である、請求項2に記載のオラパリブシュウ酸共結晶:
12.7、13.7、14.8、16.2、18.1、22.6及び24.3°2θ±0.2°2θのピークから選ばれる少なくとも2つ、少なくとも3つ、少なくとも4つ、少なくとも5つ、少なくとも6つ、又はすべてのピークを有するパワーX線回折パターン;又は
図5とほぼ同様のパワーX線回折パターン。 - 動力X線回折パターンが、12.7、13.7、14.8、16.2、18.1、22.6、24.3°2θ±0.2°2θのピークから選ばれる少なくとも4つのピークを有する、請求項5に記載のオリパラブシュウ酸共結晶。
- 以下の少なくとも1つを特徴とする2:1オラパリブシュウ酸共結晶である、請求項2に記載のオラパリブシュウ酸共結晶:
6.5、7.9、12.0、13.1、14.3、15.9、18.7、及び19.7°2θ±0.2°2θのピークから選ばれる少なくとも2つ、少なくとも3つ、少なくとも4つ、少なくとも5つ、少なくとも6つ、少なくとも7つ、又は全てのピークを有するパワーX線回折パターン;又は
図8とほぼ同様のパワーX線回折パターン。 - パワーX線回折パターンが、6.5、7.9、12.0、13.1、14.3、15.9、18.7、及び19.7°2θ±0.2°2θのピークから選ばれる少なくとも5つのピークを有する、請求項7記載のオラパリブシュウ酸共結晶。
- 請求項1~8のいずれか1項に記載のオラパリブシュウ酸共結晶と、薬学的に許容される担体とを含む医薬組成物。
- ポリ(ADP‐リボース)ポリメラーゼ(PARP)の阻害によって疾患、障害、又は状態を治療する方法であって、治療有効量の請求項1~8のいずれか1項に記載のオラパリブシュウ酸共結晶、請求項2に記載のオラパリブシュウ酸共結晶、又は請求項9に記載の医薬組成物をそれを必要とする患者に投与するステップを含む、上記方法。
- 癌、線維症、炎症性疾患、神経疾患、心血管疾患、眼科変性疾患、血管疾患、又は敗血症性ショック、ALI、及び急性肝不全の群から選択される重症の疾患を治療する方法であって、請求項1~8のいずれか1項に記載のオラパリブシュウ酸共結晶、請求項2に記載のオラパリブシュウ酸共結晶、又は請求項9に記載の医薬組成物の治療有効量をそれを必要とする患者に投与するステップを含む、上記方法。
- ポリ(ADP‐リボース)ポリメラーゼ(PARP)の阻害によって疾患、障害、又は状態を治療するための、請求項1~8のいずれか1項に記載のオラパリブシュウ酸共結晶又は請求項9に記載の医薬組成物の使用。
- 癌、線維症、炎症性疾患、神経疾患、心血管疾患、眼科変性疾患、血管疾患、又は敗血症性ショック、ALI、及び急性肝不全の群から選択される重症疾患を治療するための、請求項1~8のいずれか一項に記載のオラパリブシュウ酸共結晶又は請求項9に記載の医薬組成物の使用。
- オラパリブとシュウ酸の混合物を溶媒中でスラリー化するステップを含む、オラパリブシュウ酸共結晶の調製方法。
- オラパリブとシュウ酸の混合物を粉砕するステップを含む、オラパリブシュウ酸共結晶の調製方法。
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WO2017191562A1 (en) * | 2016-05-04 | 2017-11-09 | Alembic Pharmaceuticals Limited | Process for the preparation of olaparib and polymorphs thereof |
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