JP2022504805A - 薬物送達デバイスのプラットフォーム式組み立てプロセス - Google Patents
薬物送達デバイスのプラットフォーム式組み立てプロセス Download PDFInfo
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Abstract
Description
2018年10月15日に出願され、その全体が参照により本明細書に組み込まれる米国仮特許出願第62/745,739号明細書に対する優先権が主張される。
(i)米国特許出願公開第2006/0040358号明細書(2006年2月23日公開)、米国特許出願公開第2005/0008642号明細書(2005年1月13日公開)、米国特許出願公開第2004/0228859号明細書(2004年11月18日公開)に記載されている例えば抗体1A(DSMZ受託番号DSM ACC 2586)、抗体8(DSMZ受託番号DSM ACC 2589)、抗体23(DSMZ受託番号DSM ACC 2588)及び抗体18を含むが、これらに限定されない、
(ii)PCT国際公開第06/138729号パンフレット(2006年12月28日公開)及びPCT国際公開第05/016970号パンフレット(2005年2月24日公開)及びLu et al.(2004),J.Biol.Chem.279:2856-2865に記載されている抗体2F8、A12及びIMC-A12を含むが、これらに限定されない、
(iii)PCT国際公開第07/012614号パンフレット(2007年2月1日公開)、PCT国際公開第07/000328号パンフレット(2007年1月4日公開)、PCT国際公開第06/013472号パンフレット(2006年2月9日公開)、PCT国際公開第05/058967号パンフレット(2005年6月30日公開)及びPCT国際公開第03/059951号パンフレット(2003年7月24日公開)、
(iv)米国特許出願公開第2005/0084906号明細書(2005年4月21日公開)に記載される抗体7C10、キメラ抗体C7C10、抗体h7C10、抗体7H2M、キメラ抗体*7C10、抗体GM607、ヒト化抗体7C10バージョン1、ヒト化抗体7C10バージョン2、ヒト化抗体7C10バージョン3及び抗体7H2HMを含むが、これらに限定されない、
(v)米国特許出願公開第2005/0249728号明細書(2005年11月10日公開)、米国特許出願公開第2005/0186203号明細書(2005年8月25日公開)、米国特許出願公開第2004/0265307号明細書(2004年12月30日公開)及び米国特許出願公開第2003/0235582号明細書(2003年12月25日公開)並びにMaloney et al.(2003)Cancer Res.63:5073-5083に記載されている抗体EM164、再表面形成(resurfaced)EM164、ヒト化EM164、huEM164 v1.0、huEM164 v1.1、huEM164 v1.2及びhuEM164 v1.3を含むが、これらに限定されない、
(vi)米国特許第7,037,498号明細書(2006年5月2日発行)、米国特許出願公開第2005/0244408号明細書(2005年11月30日公開)及び米国特許出願公開第2004/0086503号明細書(2004年5月6日公開)並びにCohen,et al.(2005),Clinical Cancer Res.11:2063-2073に記載されている、ATCC受託番号PTA-2792、PTA-2788、PTA-2790、PTA-2791、PTA-2789、PTA-2793及び抗体2.12.1、2.13.2、2.14.3、3.1.1、4.9.2及び4.17.3を有するハイブリドーマによって産生された抗体の各々を含むが、これらに限定されない、例えば抗体CP-751,871、
(vii)米国特許出願公開第2005/0136063号明細書(2005年6月23日公開)及び米国特許出願公開第2004/0018191号明細書(2004年1月29日公開)に記載されている抗体19D12と、ATCCに受託番号PTA-5214で受託されているプラスミド15H12/19D12 HCA(γ4)のポリヌクレオチドによってコードされる重鎖及びATCCに受託番号PTA-5220で受託されているプラスミド15H12/19D12 LCF(κ)のポリヌクレオチドによってコードされる軽鎖を含む抗体とを含むが、これらに限定されない、並びに
(viii)特にIGF-1受容体を標的とする前述の抗体、ペプチボディ及び関連タンパク質等に関して参照により各々の全体が本明細書に組み込まれる米国特許出願公開第2004/0202655号明細書(2004年10月14日公開)に記載されている抗体PINT-6A1、PINT-7A2、PINT-7A4、PINT-7A5、PINT-7A6、PINT-8A1、PINT-9A2、PINT-11A1、PINT-11A2、PINT-11A3、PINT-11A4、PINT-11A5、PINT-11A7、PINT-11A12、PINT-12A1、PINT-12A2、PINT-12A3、PINT-12A4及びPINT-12A5を含むが、これらに限定されない。
Claims (27)
- プラットフォーム式薬物送達デバイスを組み立てる方法であって、
前記薬物送達デバイスのベース構成要素の組を提供することと、
前記薬物送達デバイスの少なくとも1つの所望の特性に基づき、後部サブアセンブリの群から前記薬物送達デバイスの後部サブアセンブリを特定することと、
前記特定された後部サブアセンブリを選択することと、
前記薬物送達デバイスの少なくとも1つの所望の特性に基づき、前部サブアセンブリの群から前記薬物送達デバイスの前部サブアセンブリを特定することと、
前記特定された前部サブアセンブリを選択することと、
前記ベース構成要素の組、前記後部サブアセンブリ及び前記前部サブアセンブリを使用して前記薬物送達デバイスを組み立てることと
を含む方法。 - 前記少なくとも1つの所望の特性は、薬物粘度又は薬物量の少なくとも1つを含む、請求項1に記載の方法。
- 前記後部サブアセンブリの群内の各後部サブアセンブリは、異なる駆動機構を含む、請求項1又は2に記載の方法。
- 各前部サブアセンブリは、異なるシリンジアセンブリを含む、請求項1~3のいずれか一項に記載の方法。
- 前記シリンジアセンブリは、ガラス又はポリマー材料の1つから作成される、請求項4に記載の方法。
- 前記ベース構成要素の組は、前記薬物送達デバイスの構成間で幾何学的に同一である、請求項1~5のいずれか一項に記載の方法。
- 前記薬物送達デバイスにスキンを適用することを更に含む、請求項1~6のいずれか一項に記載の方法。
- 前記スキンは、所期の使用者群からの少なくとも1つの属性に基づいて選択される、請求項7に記載の方法。
- プラットフォーム式薬物送達デバイスを組み立てる方法であって、
前記薬物送達デバイスのベース構成要素の組を提供すること、
前記薬物送達デバイスの少なくとも1つの所望の特性に基づき、選択可能なサブアセンブリの第1群から前記薬物送達デバイスの第1サブアセンブリを特定すること、
前記特定された第1サブアセンブリを選択すること、
前記少なくとも1つの所望の特性に基づき、選択可能なサブアセンブリの第2群から前記薬物送達デバイスの第2サブアセンブリを特定すること、
前記特定された第2サブアセンブリを選択すること、
前記少なくとも1つの所望の特性に基づき、選択可能なサブアセンブリの第3群から前記薬物送達デバイスの第3サブアセンブリを特定すること、
前記特定された第3サブアセンブリを選択すること、
前記ベース構成要素の組、前記第1サブアセンブリ、前記第2サブアセンブリ及び前記第3サブアセンブリを使用して前記薬物送達デバイスを組み立てること
を含む方法。 - 前記少なくとも1つの特性は、薬物粘度又は薬物量の少なくとも1つを含む、請求項9に記載の方法。
- 前記選択可能なサブアセンブリの第1群は、複数のプレフィルドシリンジアセンブリを含む、請求項9又は10に記載の方法。
- 前記選択可能なサブアセンブリの第2群は、複数の駆動アセンブリを含む、請求項9~11のいずれか一項に記載の方法。
- 前記複数の駆動アセンブリは、複数のトルクばねを含み、前記複数のトルクばねのそれぞれは、変化する特性を有する、請求項12に記載の方法。
- 前記選択可能なサブアセンブリの第3群は、複数のボリュームアダプタを含む、請求項9~13のいずれか一項に記載の方法。
- 前記薬物送達デバイスにスキンを適用することを更に含む、請求項9~14のいずれか一項に記載の方法。
- 前記スキンは、所期の使用者群からの少なくとも1つの属性に基づいて選択される、請求項15に記載の方法。
- 前記ベース構成要素の組は、前記薬物送達デバイスの構成間で幾何学的に同一である、請求項8~16のいずれか一項に記載の方法。
- プラットフォーム式薬物送達デバイスであって、
前記薬物送達デバイスのベース構成要素の組を提供する工程、
前記薬物送達デバイスの少なくとも1つの所望の特性に基づき、選択可能なサブアセンブリの第1群から前記薬物送達デバイスの第1サブアセンブリを特定する工程、
前記特定された第1サブアセンブリを選択する工程、
前記少なくとも1つの所望の特性に基づき、選択可能なサブアセンブリの第2群から前記薬物送達デバイスの第2サブアセンブリを特定する工程、
前記特定された第2サブアセンブリを選択する工程、
前記少なくとも1つの所望の特性に基づき、選択可能なサブアセンブリの第3群から前記薬物送達デバイスの第3サブアセンブリを特定する工程、
前記特定された第3サブアセンブリを選択する工程、
前記ベース構成要素の組、前記第1サブアセンブリ、前記第2サブアセンブリ及び前記第3サブアセンブリを使用して前記薬物送達デバイスを組み立てる工程
を含むプロセスによって用意されるプラットフォーム式薬物送達デバイス。 - 前記選択可能なサブアセンブリの第1群は、複数のプレフィルドシリンジアセンブリを含む、請求項18に記載のプラットフォーム式薬物送達デバイス。
- 前記選択可能なサブアセンブリの第2群は、複数の駆動アセンブリを含む、請求項18又は19に記載のプラットフォーム式薬物送達デバイス。
- 前記選択可能なサブアセンブリの第3群は、複数のボリュームアダプタを含む、請求項18~20のいずれか一項に記載のプラットフォーム式薬物送達デバイス。
- 薬物送達デバイスを組み立てるためのプラットフォームシステムであって、
前記薬物送達デバイスのベース構成要素の組と、
前記薬物送達デバイスの選択可能なサブアセンブリの第1群と、
前記薬物送達デバイスの選択可能なサブアセンブリの第2群と、
前記薬物送達デバイスの選択可能なサブアセンブリの第3群と
を含み、前記薬物送達デバイスは、前記薬物送達デバイスの少なくとも1つの所望の特性を使用して、前記選択可能なサブアセンブリの第1群から第1サブアセンブリを、前記選択可能なサブアセンブリの第2群から第2サブアセンブリを、且つ前記選択可能なサブアセンブリの第3群から第3サブアセンブリを特定及び選択し、且つ前記ベース構成要素の組を前記選択可能なサブアセンブリの第1群、前記選択可能なサブアセンブリの第2群及び前記選択可能なサブアセンブリの第3群に結合することによって組み立てられる、プラットフォームシステム。 - 前記少なくとも1つの特性は、薬物粘度又は薬物量の少なくとも1つを含む、請求項22に記載のプラットフォームシステム。
- 前記選択可能なサブアセンブリの第1群は、複数のプレフィルドシリンジアセンブリを含む、請求項22又は23に記載のプラットフォームシステム。
- 前記選択可能なサブアセンブリの第2群は、複数の駆動アセンブリを含む、請求項22~24のいずれか一項に記載のプラットフォームシステム。
- 前記複数の駆動アセンブリは、複数のトルクばねを含み、前記複数のトルクばねのそれぞれは、変化する特性を有する、請求項25に記載のプラットフォームシステム。
- 前記選択可能なサブアセンブリの第3群は、複数のボリュームアダプタを含む、請求項22~26のいずれか一項に記載のプラットフォームシステム。
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EA202191038A1 (ru) | 2021-07-06 |
MA53913A (fr) | 2022-01-19 |
AR116703A1 (es) | 2021-06-02 |
US20210346596A1 (en) | 2021-11-11 |
CN112689523A (zh) | 2021-04-20 |
SG11202101824VA (en) | 2021-03-30 |
CA3109988A1 (en) | 2020-04-23 |
AU2019359801A1 (en) | 2021-03-18 |
TW202031306A (zh) | 2020-09-01 |
EP3866889A1 (en) | 2021-08-25 |
IL281895A (en) | 2021-05-31 |
WO2020081480A1 (en) | 2020-04-23 |
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