JP2016525139A - 安定化された抗体組成物 - Google Patents
安定化された抗体組成物 Download PDFInfo
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- JP2016525139A JP2016525139A JP2016528526A JP2016528526A JP2016525139A JP 2016525139 A JP2016525139 A JP 2016525139A JP 2016528526 A JP2016528526 A JP 2016528526A JP 2016528526 A JP2016528526 A JP 2016528526A JP 2016525139 A JP2016525139 A JP 2016525139A
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Abstract
Description
抗ECSCR(内皮細胞特異的走化性制御因子(endothelial cell−specific chemotaxis regulator)モノクローナル抗体(クローンid 13G11 1A31 A7、内皮マーカーECSCRに結合するハイブリドーマ細胞から発現されたネズミIgG/k抗体)のF6H8中で25℃および40℃における安定性を、6ヶ月にわたって研究した。
Nunc MaxiSorp(商標)平底Elisaプレートを、ECSCR抗原および無関係な陰性抗原でコーティングすることによって調製した。抗原をコーティングバッファーで1μg/mLの濃度に希釈し、プレートと共に4℃において一晩インキュベートした。このプレートをその後200μLの3%のブロッキング溶液でブロックし、RTにおいてシェーカー上で1−2時間インキュベートし、次いでPBS−Tween20溶液で3回洗浄し、吸い取り乾燥させた(blotted dry)。抗体試料をPBSで1μg/mLに希釈した。100ngまたは10ngの各希釈試料を、ECSCR抗原でコーティングされたウェルおよび陰性対照抗原でコーティングされたウェルに加えた。プレートをシェーカー上でRTにおいて1時間インキュベートし、その後PBS−Tween20で洗浄して、吸い取り乾燥した。抗体のアリコートを、PBS中1:5000希釈のヤギ抗マウスIgG−HRP二次抗体コンジュゲート(Biorad,Catalogue Nr.170−6516)でプローブした。プレートをシェーカー上でRTにおいて1時間インキュベートし、次いでPBS−Tween20溶液で3回洗浄し、吸い取り乾燥した。プレートを37℃において10分間、100μLのTMB(3,3’,5,5’−テトラメチルベンジジン)と一緒にインキュベートし、次いで50μL/ウェルの1M HClを加えた。吸光度を、450nmにおいて分光光度計により測定した。
ベバシズマブ、Fsn1006およびFsn0503の安定性を、25℃、50℃および70℃において4週の期間にわたって研究した。
表2 Fsn1006活性(平均OD±2SD、450nmにおいて)
表3 Fsn0503活性(平均OD±2SD、450nmにおいて)
SFAおよびPBSバッファー中で50℃から80℃の間の温度において保存されたベバシズマブ、Fsn1006およびFsn0503の結合活性を検査した。
インフリキシマブ(ヒト定常領域とネズミ可変領域とのキメラモノクローナル抗体、分子量149kDa)、融合タンパク質のエタネルセプト(IgG1のFc部分と融合された、75kDaのTNFR(腫瘍壊死因子受容体)のリガンド結合部分を含む、分子量150kDaの組換えヒトタンパク質)およびセルトリズマブ(およそ40kDaのポリエチレングリコールとコンジュゲートされた組換えFab’を含む、分子量91kDaの抗体断片)またはこれらの後発生物製剤から選択される抗原結合ポリペプチドまたはタンパク質と、式RFRH(式中、RFは4から12の炭素原子を有する線形過フッ素化炭水化物セグメントであり、RHは4から8の炭素を有する線形アルキル基である)(例えばF4H5およびF6H8)の半フッ素化アルカンを含む液体ビヒクルとを含む組成物の安定性を研究し、異なる媒体中の製剤と比較する。
・ICH条件下の保存安定性(25および40℃)。
・ICH条件以外の温度安定性、すなわち熱変性
これらを実施例1−3に記載の方法と同様に実施する。これらの抗原結合ポリペプチドの安定性をアッセイするために適切な分析方法を実施する。抗体の活性および有効性をモニターするためのアッセイおよび上記の安定性実験の過程の間の凝集レベルをモニターするためのアッセイとしては、上記の実施例1−3のプロトコルと同様のELISAなどの技術が挙げられる。
Claims (15)
- 抗原結合ポリペプチドまたはタンパク質と、液体ビヒクルとを含み、前記液体ビヒクルが式
RFRH
(式中、RFは4から12の炭素原子を有する線形過フッ素化炭水化物セグメントであり、RHは4から8の炭素原子を有する線形アルキル基である)の半フッ素化アルカンを含み、前記抗原結合ポリペプチドまたはタンパク質が、分散液または懸濁液を形成するように組み込まれる、組成物。 - 前記抗原結合ポリペプチドまたはタンパク質が、モノクローナル抗体、ポリクローナル抗体、抗体断片、抗体断片を含む融合タンパク質、抗体薬物複合体またはこれらの任意の組み合わせから選択される、請求項1に記載の組成物。
- 前記抗体断片が、抗原結合断片(Fab)、単鎖可変断片(scFv)、単一ドメイン抗体、ミニボディまたはダイアボディである、請求項2に記載の組成物。
- 前記モノクローナル抗体がキメラ、ヒト化またはヒト抗体である、請求項2に記載の組成物。
- 前記抗原結合ポリペプチドまたはタンパク質が、少なくとも90kDaの分子量を有する、請求項1から4のいずれかに記載の組成物。
- 前記半フッ素化アルカンが、F4H5、F4H6、F4H8、F6H4、F6H6、F6H8およびF6H10から選択される、請求項1から5のいずれかに記載の組成物。
- 有効に水を含まない、請求項1から6のいずれかに記載の組成物。
- 前記組成物が、この初期の抗原結合活性の少なくとも85%を、RTから40℃の間の温度において6ヶ月の保存の間保持する、請求項1から7のいずれかに記載の組成物。
- 前記抗原結合ポリペプチドまたはタンパク質が少なくとも0.5mg/mLの濃度である、請求項1から8のいずれかに記載の組成物。
- 医薬品としての使用のための、請求項1から9のいずれかに記載の組成物。
- 皮下、経皮、筋肉内または局所領域注射による非経口投与用の医薬品としての使用のための、請求項10に記載の組成物。
- 抗原結合ポリペプチドまたはタンパク質と、式
RFRH
(式中、RFは4から12の炭素原子を有する線形過フッ素化炭水化物セグメントであり、RHは4から8の炭素原子を有する線形アルキル基である)の半フッ素化アルカンを含む液体ビヒクルとを、懸濁液または分散液を形成するように混合するステップを含む、抗原結合ポリペプチドまたはタンパク質を安定化させる方法。 - 前記抗原結合ポリペプチドまたはタンパク質が、初期の抗原結合活性の少なくとも85%を、RTから40℃の間の温度において6ヶ月の保存の間保持する、請求項12に記載の方法。
- がんまたは自己免疫疾患の治療用の医薬品としての使用のための、請求項10に記載の組成物。
- 前記抗原結合ポリペプチドまたはタンパク質が、血管新生阻害剤、抗増殖剤またはTNF阻害剤である、請求項1に記載の組成物。
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EP13177699.9 | 2013-07-23 | ||
EP13177699 | 2013-07-23 | ||
PCT/EP2014/065840 WO2015011199A1 (en) | 2013-07-23 | 2014-07-23 | Stabilized antibody compositions |
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US (3) | US10273298B2 (ja) |
EP (1) | EP3024484B1 (ja) |
JP (1) | JP6503349B2 (ja) |
KR (1) | KR102272568B1 (ja) |
CN (2) | CN114028560A (ja) |
AU (1) | AU2014295052B2 (ja) |
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CN111182893A (zh) | 2017-10-04 | 2020-05-19 | 诺瓦利克有限责任公司 | 包含f6h8的眼用组合物 |
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JP7137696B2 (ja) | 2019-05-14 | 2022-09-14 | プロヴェンション・バイオ・インコーポレイテッド | 1型糖尿病を予防するための方法および組成物 |
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CA2918419A1 (en) | 2015-01-29 |
PT3024484T (pt) | 2018-10-24 |
MX2016001018A (es) | 2016-09-06 |
US20160159902A1 (en) | 2016-06-09 |
JP6503349B2 (ja) | 2019-04-17 |
US20210340248A1 (en) | 2021-11-04 |
AU2014295052A1 (en) | 2016-02-11 |
KR102272568B1 (ko) | 2021-07-05 |
CA2918419C (en) | 2022-05-03 |
PL3024484T3 (pl) | 2018-11-30 |
CN105555311B (zh) | 2021-10-08 |
ES2687094T3 (es) | 2018-10-23 |
MX370207B (es) | 2019-12-05 |
EP3024484A1 (en) | 2016-06-01 |
BR112016001522B1 (pt) | 2019-10-01 |
US10273298B2 (en) | 2019-04-30 |
AU2014295052B2 (en) | 2018-08-30 |
WO2015011199A1 (en) | 2015-01-29 |
HK1224218A1 (zh) | 2017-08-18 |
CN105555311A (zh) | 2016-05-04 |
DK3024484T3 (en) | 2018-10-08 |
KR20160034307A (ko) | 2016-03-29 |
EP3024484B1 (en) | 2018-06-20 |
US20190256591A1 (en) | 2019-08-22 |
CN114028560A (zh) | 2022-02-11 |
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