JP2013537525A - 新規な持続型グルカゴン結合体およびこれを含む肥満の予防および治療用薬学的組成物 - Google Patents
新規な持続型グルカゴン結合体およびこれを含む肥満の予防および治療用薬学的組成物 Download PDFInfo
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- JP2013537525A JP2013537525A JP2013520654A JP2013520654A JP2013537525A JP 2013537525 A JP2013537525 A JP 2013537525A JP 2013520654 A JP2013520654 A JP 2013520654A JP 2013520654 A JP2013520654 A JP 2013520654A JP 2013537525 A JP2013537525 A JP 2013537525A
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- glucagon
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- exendin
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- 238000002360 preparation method Methods 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
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- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
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- 235000010356 sorbitol Nutrition 0.000 description 1
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- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
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Abstract
【選択図】図1
Description
薬の製造のための使用を提供することである。
本発明による製造方法は:
1)化学式4のグルカゴン誘導体を、両末端にアルデヒドを有するPEGとpH9.0で反応させるステップと、
流速:2.0mL/分
勾配:溶出液A0%→溶出液B50%(A:20mMクエン酸、pH3.0、B:A+1M KCl)で50分間溶出
流速:7.0mL/分
勾配:溶出液A100%→0%(A:20mMトリス、pH7.5+2M NaCl)
で60分間溶出
流速:2.0mL/分
勾配:溶出液A0%→溶出液B20%(A:20mMトリス、pH9.0、B:A+1M NaCl)で70分間溶出
流速:2.0mL/分
勾配:溶出液A 0%→溶出液B20%(A:20mMトリス、pH9.0、B:A+
1M NaCl)で70分間溶出
流速:2.0mL/分
勾配:溶出液A0%→溶出液B50%(A:20mMクエン酸、pH3.0、B:A+
1M KCl)で50分間溶出
流速:2.0mL/分
勾配:溶出液A0%→溶出液B20%(A:20mMトリス、pH9.0、B:A+1M NaCl)で70分間溶出
流速:7.0mL/分
勾配:溶出液A100%→0%60分(A:20mMトリス、pH7.5+1.5M硫酸アンモニウム)で60分間溶出
Claims (45)
- グルカゴンまたはその誘導体が、非ペプチドリンカーによって重合体キャリアに共有的に連結された、持続型グルカゴン結合体。
- 前記グルカゴン誘導体が、天然型グルカゴンのN末端の1番目のアミノ酸であるヒスチジン残基のアルファ炭素またはそれに結合されたアルファアミン基が置換、修飾または除去されたものである、請求項1に記載の持続型グルカゴン結合体。
- 前記グルカゴン誘導体が、天然型グルカゴンの一番目のN末端ヒスチジン残基のアミン基が除去された誘導体、その一番目のN末端ヒスチジン残基のアミン基がヒドロキシル基(hydroxyl group)に置換された誘導体、その一番目のN末端ヒスチジン残基のアミン基が2個のメチル基で修飾された誘導体およびその一番目のN末端ヒスチジン残基のアルファ炭素およびアルファ炭素に結合されたアミン基が除去された誘導体からなる群より選択されるものである、請求項2に記載の持続型グルカゴン結合体。
- 前記グルカゴン誘導体が、下記化学式1〜4で表示される誘導体からなる群より選択されるものである、請求項3記載の持続型グルカゴン誘導体:
- 前記非ペプチドリンカーの一方の末端がグルカゴンまたはその誘導体に、他方の末端は重合体キャリアに共有的に連結されるものである、請求項1に記載の持続型グルカゴン結合体。
- 前記非ペプチドリンカーが、ポリエチレングリコール(PEG)、ポリプロピレングリコール、エチレングリコールとプロピレングリコールとの共重合体、ポリオキシエチル化ポリオール、ポリビニルアルコール、ポリサッカライド、デキストラン、ポリビニルエチルエーテル、生分解性高分子、脂質重合体、キチン、ヒアルロン酸およびこれらの組み合わせからなる群より選択されるものである、請求項1に記載の持続型グルカゴン結合体。
- 前記非ペプチドリンカーが、1〜100kDaの範囲の分子量を有するものである、請求項1に記載の持続型グルカゴン結合体。
- 前記非ペプチドリンカーが、両末端にそれぞれグルカゴンまたはその誘導体および重合体キャリアと共有的に連結できる官能基を有するものである、請求項1に記載の持続型グルカゴン結合体。
- 前記作用基がアルデヒド基、プロピオンアルデヒド基、ブチルアルデヒド基、マレイミド基、スクシンイミジルプロピオン酸、ヒドロキシスクシンイミジルカルボキシメチルおよびスクシンイミジルカーボネートからなる群より選択される官能基を有するものである、請求項8に記載の持続型グルカゴン結合体。
- 前記非ペプチドリンカーが、両末端にアルデヒド基を有するものである、請求項9に記載の持続型グルカゴン結合体。
- 前記非ペプチドリンカーが、両末端にアルデヒド基を有するポリエチレングリコール(PEG)である、請求項10に記載の持続型グルカゴン結合体。
- 前記重合体キャリアが、ポリエチレングリコール(PEG)、ポリアミノ酸、アルブミン、ゼラチン、兔疫グロブリン断片、デキストラン、脂肪酸、ポリサッカライドおよび高分子重合体からなる群より選択されるものである、請求項1に記載の持続型グルカゴン結合体。
- 前記重合体キャリアが、兔疫グロブリンFc断片である、請求項12に記載の持続型グルカゴン結合体。
- 前記兔疫グロブリンFc断片が、非糖鎖化されたものである、請求項13に記載の持続型グルカゴン結合体。
- 前記兔疫グロブリンFc断片が、CH1、CH2、CH3およびCH4ドメインからなる群より選択される1個〜4個のドメインからなるものである、請求項13に記載の持続型グルカゴン結合体。
- 前記兔疫グロブリンFc断片が、ヒンジ領域をさらに含むものである、請求項13に記載の持続型グルカゴン結合体。
- 前記兔疫グロブリンFc断片が、IgG、IgA、IgD、IgEおよびIgMからなる群より選択された兔疫グロブリンに由来するものである、請求項13に記載の持続型グルカゴン結合体。
- 前記兔疫グロブリンFc断片が、IgG4Fc断片である、請求項13に記載の持続型グルカゴン結合体。
- 前記兔疫グロブリンFc断片が、非糖鎖化したヒトIgG4Fc断片である、請求項18に記載の持続型グルカゴン結合体。
- 下記化学式5で表示される構造を有する、請求項1記載の持続型グルカゴン結合体:
R2は、−NH2、−OHおよびリシン(Lys)からなる群より選択され、
Xは、SQGTFTSDYSKYLDSRRAQDFVQWLMNTであり、
Yは、ポリエチレングリコール(PEG)であり、
Zは、兔疫グロブリンFc断片である。 - 下記のステップを含む請求項1による持続型グルカゴン結合体の製造方法:
1)グルカゴンまたはその誘導体を、両末端に官能基を有する非ペプチドリンカーと反応させるステップと、
2)ステップ1)の反応混合物から、非ペプチドリンカーの一方の末端にグルカゴンまたはその誘導体が共有的に連結された複合体を分離するステップと、
3)ステップ2)で分離された複合体を重合体キャリアと反応させるステップと、
4)ステップ3)の反応混合物から、非ペプチドリンカーの一方の末端にはグルカゴンまたはその誘導体が、他方の末端には重合体キャリアが共有的に連結された持続型グルカゴン結合体を分離するステップ。 - ステップ1)において、グルカゴンまたはその誘導体と非ペプチドリンカーとの反応が、1:5〜1:50の反応モル比で、pH7.5〜10.0の条件で行われるものである、請求項21に記載の製造方法。
- ステップ1)において、グルカゴンまたはその誘導体と非ペプチドリンカーとの反応が、還元剤の存在下で行われるものである、請求項21に記載の製造方法。
- 前記還元剤が、ナトリウムシアノボロハイドライド(NaCNBH3)、水素化ホウ素ナトリウム、ジメチルアミンホウ酸塩およびピリジンホウ酸塩からなる群より選択されるものである、請求項23に記載の製造方法。
- ステップ2)で分離された複合体が、ペプチドリンカーがグルカゴンまたはその誘導体のN末端以外のアミノ酸残基に非ペプチドリンカーの一方の末端が共有的に連結された、グルカゴン−非ペプチドリンカーの構造を有するものである、請求項21に記載の製造方法。
- 前記アミノ酸残基が、グルカゴンまたはその誘導体の12番目のリシン残基である、請求項25に記載の製造方法。
- ステップ3)において、複合体と重合体キャリアの反応が、1:2〜1:10の反応モル比で、pH5.0〜8.0で行われるものである、請求項21に記載の製造方法。
- ステップ3)において、複合体と重合体キャリアの反応が、還元剤の存在の下に行われるものである、請求項21に記載の製造方法。
- 還元剤が、ナトリウムシアノボロハイドライド(NaCNBH3)、水素化ホウ素ナトリウム、ジメチルアミンホウ酸塩およびピリジンホウ酸塩からなる群より選択されるものである、請求項28に記載の製造方法。
- ステップ4)で分離された持続型グルカゴン結合体が、グルカゴン−非ペプチドリンカー−重合体キャリアの構造を有するものである、請求項21に記載の製造方法。
- 下記のステップを含むものである、請求項21に記載の製造方法:
1)化学式4のグルカゴン誘導体を両末端にアルデヒドを有するPEGとpH9.0で反応させるステップ:
2)ステップ1)の反応混合物から、グルカゴン誘導体の12番目のリシン残基にPEGの一方の末端が共有的に連結されたグルカゴン−PEG複合体を分離するステップ;
3)ステップ2)で分離されたグルカゴン誘導体−PEG複合体を兔疫グロブリンFc断片と反応させるステップ;および
4)ステップ3)の反応混合物から、PEGの一方の末端にはグルカゴン誘導体が、他方の末端には兔疫グロブリンFc断片が共有的に連結された持続型グルカゴン結合体を分離するステップ。 - 有効成分として請求項1記載の持続型グルカゴン結合体および薬学的に許容可能な担体を含む、肥満の予防または治療用薬学的組成物。
- 抗肥満薬物をさらに含むものである、請求項32に記載の薬学的組成物。
- 前記抗肥満薬物が、GLP−1作動剤、レプチン(Leptin)作動剤、DPP−IV阻害剤、Y5受容体拮抗剤(antagonist)、メラニン濃縮ホルモン(melanin−concentrating hormone、MCH)拮抗剤、Y2/3作動剤、MC3/4作動剤、胃/膵臓リパーゼ(gastric/pancreatic lipase)阻害剤、5HT2c作動剤、β3A作動剤、アミリン(amylin)作動剤、グレリン(ghrelin)拮抗剤およびこれらの組み合わせからなる群より選択されるものである、請求項33に記載の薬学的組成物。
- 前記GLP−1作動剤が、エキセンディン−4、エキセンディン−4誘導体およびこれらの持続型結合体である、請求項34に記載の薬学的組成物。
- 前記エキセンディン−4誘導体が、天然型エキセンディン−4の一番目のN末端ヒスチジン残基のアミン基が除去された誘導体、その一番目のN末端ヒスチジン残基のアミン基がヒドロキシル基に置換された誘導体、その一番目のN末端ヒスチジン残基のアミン基が2個のメチル基で修飾された誘導体およびその一番目のN末端ヒスチジン残基のアルファ炭素およびアルファ炭素に結合されたアミン基が除去された誘導体からなる群より選択されるものである、請求項35に記載の薬学的組成物。
- 前記持続型エキセンディン−4結合体が、非ペプチドリンカーを介してエキセンディン−4またはその誘導体と兔疫グロブリンFc断片が共有的に連結された構造を有するものである、請求項35に記載の薬学的組成物。
- 前記持続型エキセンディン−4結合体が、非ペプチドリンカーの一方の末端にはエキセンディン−4誘導体が、他方の末端には兔疫グロブリンFc断片が共有的に連結された構造を有するものである、請求項37に記載の薬学的組成物。
- 治療学的に有効な量の請求項1記載の持続型グルカゴン結合体を、これを必要とする対象に投与するステップを含む、肥満を予防または治療する方法。
- 前記持続型グルカゴン結合体とともに抗肥満薬物を併用投与するものである、請求項39に記載の方法。
- 前記抗肥満薬物が、GLP−1作動剤、レプチン(Leptin)作動剤、DPP−IV阻害剤、Y5受容体拮抗剤(antagonist)、メラニン濃縮ホルモン(melanin−concentrating hormone、MCH)拮抗剤、Y2/3作動剤、MC3/4作動剤、胃/膵臓リパーゼ(gastric/pancreatic lipase)阻害剤、5HT2c作動剤、βA作動剤、アミリン(amylin)作動剤、グレリン(ghrelin)拮抗剤およびこれらの組み合わせからなる群より選択されるものである、請求項40に記載の方法。
- 前記GLP−1作動剤が、エキセンディン−4、エキセンディン−4誘導体およびこれらの持続型結合体である、請求項41に記載の方法。
- 前記エキセンディン−4誘導体が、天然型エキセンディン−4一番目のN末端ヒスチジン残基のアミン基が除去された誘導体、その一番目のN末端ヒスチジン残基のアミン基がヒドロキシル基に置換された誘導体、その一番目のN末端ヒスチジン残基アミン基が2個のメチル基で修飾された誘導体およびその一番目のN末端ヒスチジン残基のアルファ炭素およびアルファ炭素に結合されたアミン基が除去された誘導体からなる群より選択されるものである、請求項42に記載の方法。
- 前記持続型エキセンディン−4結合体が、非ペプチドリンカーを介してエキセンディン−4またはその誘導体と兔疫グロブリンFc断片が共有的に連結された構造を有するものである、請求項42に記載の方法。
- 前記持続型エキセンディン−4結合体が、非ペプチドリンカーの一方の末端にはエキセンディン−4誘導体が、他方の末端には兔疫グロブリンFc断片が共有的に連結された構造を有し、前記エキセンディン−4誘導体がその一番目のN末端ヒスチジン残基のアルファ炭素およびアルファ炭素に結合されたアミン基が除去されたものである、請求項44に記載の方法。
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Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2014518209A (ja) * | 2011-06-17 | 2014-07-28 | ハンミ サイエンス カンパニー リミテッド | オキシントモジュリンと免疫グロブリン断片とを含む結合体及びその用途 |
US9522946B2 (en) | 2011-06-10 | 2016-12-20 | Hanmi Science Co., Ltd. | Oxyntomodulin derivatives and pharmaceutical composition for treating obesity comprising the same |
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Families Citing this family (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9458444B2 (en) | 2006-02-03 | 2016-10-04 | Opko Biologics Ltd. | Long-acting coagulation factors and methods of producing same |
US20150038413A1 (en) | 2006-02-03 | 2015-02-05 | Opko Biologics Ltd. | Long-acting polypeptides and methods of producing and administering same |
US8048849B2 (en) | 2006-02-03 | 2011-11-01 | Modigene, Inc. | Long-acting polypeptides and methods of producing same |
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US20140113860A1 (en) | 2006-02-03 | 2014-04-24 | Prolor Biotech Ltd. | Long-acting polypeptides and methods of producing and administering same |
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US9663778B2 (en) | 2009-07-09 | 2017-05-30 | OPKO Biologies Ltd. | Long-acting coagulation factors and methods of producing same |
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US20150158926A1 (en) | 2013-10-21 | 2015-06-11 | Opko Biologics, Ltd. | Long-acting polypeptides and methods of producing and administering same |
US10039809B2 (en) | 2013-12-18 | 2018-08-07 | The California Institute For Biomedical Research | Modified therapeutic agents, stapled peptide lipid conjugates, and compositions thereof |
MA43289B1 (fr) | 2014-01-20 | 2019-12-31 | Hanmi Pharm Ind Co Ltd | Insuline à action prolongée et utilisation associée |
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ES2893616T3 (es) | 2015-06-19 | 2022-02-09 | Opko Biologics Ltd | Factores de coagulación de acción prolongada y métodos para la producción de los mismos |
UY36870A (es) | 2015-08-28 | 2017-03-31 | Hanmi Pharm Ind Co Ltd | Análogos de insulina novedosos |
TWI622596B (zh) | 2015-10-26 | 2018-05-01 | 美國禮來大藥廠 | 升糖素受體促效劑 |
EP3463415A4 (en) * | 2016-06-02 | 2020-03-25 | Indiana University Research & Technology Corporation | WATER-SOLUBLE AND CHEMICALLY STABLE GLUCAGON PEPTIDES |
EP3479841A4 (en) * | 2016-06-29 | 2020-03-04 | Hanmi Pharm. Co., Ltd. | GLUCAGON DERIVATIVE, CONJUGATE THEREOF, COMPOSITION COMPRISING SAME, AND THERAPEUTIC USE THEREOF |
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WO2018056764A1 (ko) | 2016-09-23 | 2018-03-29 | 한미약품 주식회사 | 인슐린 수용체와의 결합력이 감소된, 인슐린 아날로그 및 이의 용도 |
TWI798209B (zh) | 2017-03-23 | 2023-04-11 | 南韓商韓美藥品股份有限公司 | 對胰島素受體有降低親和性之胰島素類似物之接合物及其用途 |
WO2019136158A1 (en) * | 2018-01-03 | 2019-07-11 | Spitfire Pharma, Inc. | Improved peptide pharmaceuticals for treatment of nash and other disorders |
KR20200038878A (ko) * | 2018-10-04 | 2020-04-14 | 한미약품 주식회사 | 글루카곤 및 이를 포함하는 조합물의 치료학적 용도 |
US20230000950A1 (en) * | 2019-10-04 | 2023-01-05 | Hanmi Pharm. Co., Ltd. | Composition comprising glucagon and glp-1 and gip receptor dual agonist and therapeutic use of same |
KR20220140443A (ko) * | 2021-04-09 | 2022-10-18 | 한미약품 주식회사 | 글루카곤 유도체를 포함하는 만성 신장 질환 예방 또는 치료용 약학 조성물 |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007528346A (ja) * | 2003-03-13 | 2007-10-11 | ハンミ ファーム. シーオー., エルティーディー. | 長い生体内半減期を有する生理活性ポリペプチド結合体 |
JP2007536211A (ja) * | 2003-11-13 | 2007-12-13 | ハンミ ファーム.インダストリー カンパニー リミテッド | 免疫グロブリン断片を用いた蛋白質結合体およびその製造方法 |
JP2008169195A (ja) * | 2007-01-05 | 2008-07-24 | Hanmi Pharmaceutical Co Ltd | キャリア物質を用いたインスリン分泌ペプチド薬物結合体 |
JP2008534676A (ja) * | 2005-04-08 | 2008-08-28 | ハンミ ファーマシューティカル カンパニー リミテッド | 非ペプチド性重合体で改質された免疫グロブリンFc断片およびこれを含む薬学的組成物 |
WO2009011544A2 (en) * | 2007-07-16 | 2009-01-22 | Hanmi Pharmaceutical Co., Ltd. | Insulinotropic peptide derivative wherein its n-terminal amino acid is modified |
WO2009069983A2 (en) * | 2007-11-29 | 2009-06-04 | Hanmi Pharmaceutical Co., Ltd. | A pharmaceutical composition for treating obesity-related disease comprising insulinotropic peptide conjugate |
WO2009155257A1 (en) * | 2008-06-17 | 2009-12-23 | Indiana University Research And Technology Corporation | Glucagon analogs exhibiting enhanced solubility and stability physiological ph buffers |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5480867A (en) * | 1993-12-29 | 1996-01-02 | The Rockefeller University | Glucagon analogs with serine replacements |
US6096871A (en) | 1995-04-14 | 2000-08-01 | Genentech, Inc. | Polypeptides altered to contain an epitope from the Fc region of an IgG molecule for increased half-life |
DE69731289D1 (de) | 1996-03-18 | 2004-11-25 | Univ Texas | Immunglobulinähnliche domäne mit erhöhten halbwertszeiten |
US6277375B1 (en) * | 1997-03-03 | 2001-08-21 | Board Of Regents, The University Of Texas System | Immunoglobulin-like domains with increased half-lives |
US7157555B1 (en) * | 1997-08-08 | 2007-01-02 | Amylin Pharmaceuticals, Inc. | Exendin agonist compounds |
US6756480B2 (en) | 2000-04-27 | 2004-06-29 | Amgen Inc. | Modulators of receptors for parathyroid hormone and parathyroid hormone-related protein |
SI1355942T1 (sl) | 2000-12-07 | 2009-02-28 | Lilly Co Eli | Glp-1 fuzijski proteini |
US8658174B2 (en) * | 2005-07-27 | 2014-02-25 | Qinghua Wang | GLP/1/exendin 4 IgG Fc fusion constructs for treatment of diabetes |
DK2158214T3 (da) | 2007-06-15 | 2011-12-05 | Zealand Pharma As | Glukagonanaloger |
EP2217701B9 (en) | 2007-10-30 | 2015-02-18 | Indiana University Research and Technology Corporation | Glucagon antagonists |
DK2718318T3 (en) * | 2011-06-10 | 2018-11-05 | Hanmi Science Co Ltd | New oxyntomodulin derivatives and pharmaceutical compositions for the treatment of obesity comprising these |
-
2011
- 2011-07-15 KR KR20110070535A patent/KR101382593B1/ko active IP Right Grant
- 2011-07-21 EP EP17178273.3A patent/EP3248611B1/en active Active
- 2011-07-21 TW TW100125894A patent/TWI593422B/zh active
- 2011-07-21 EP EP11809879.7A patent/EP2595648A4/en not_active Withdrawn
- 2011-07-21 WO PCT/KR2011/005375 patent/WO2012011752A2/en active Application Filing
- 2011-07-21 US US13/810,999 patent/US9072794B2/en active Active
- 2011-07-21 JP JP2013520654A patent/JP6076902B2/ja active Active
- 2011-07-21 AR ARP110102650 patent/AR082320A1/es unknown
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007528346A (ja) * | 2003-03-13 | 2007-10-11 | ハンミ ファーム. シーオー., エルティーディー. | 長い生体内半減期を有する生理活性ポリペプチド結合体 |
JP2007536211A (ja) * | 2003-11-13 | 2007-12-13 | ハンミ ファーム.インダストリー カンパニー リミテッド | 免疫グロブリン断片を用いた蛋白質結合体およびその製造方法 |
JP2007537992A (ja) * | 2003-11-13 | 2007-12-27 | ハンミ ファーム.インダストリー カンパニー リミテッド | 免疫グロブリンFc領域をキャリアとして含む薬剤学的組成物 |
JP2008534676A (ja) * | 2005-04-08 | 2008-08-28 | ハンミ ファーマシューティカル カンパニー リミテッド | 非ペプチド性重合体で改質された免疫グロブリンFc断片およびこれを含む薬学的組成物 |
JP2008169195A (ja) * | 2007-01-05 | 2008-07-24 | Hanmi Pharmaceutical Co Ltd | キャリア物質を用いたインスリン分泌ペプチド薬物結合体 |
JP2010515677A (ja) * | 2007-01-05 | 2010-05-13 | ハンミ ファーマシューティカル カンパニー リミテッド | 免疫グロブリン断片を用いたインスリン分泌結合体 |
WO2009011544A2 (en) * | 2007-07-16 | 2009-01-22 | Hanmi Pharmaceutical Co., Ltd. | Insulinotropic peptide derivative wherein its n-terminal amino acid is modified |
JP2009019027A (ja) * | 2007-07-16 | 2009-01-29 | Hanmi Pharmaceutical Co Ltd | アミノ末端のアミノ酸が変異したインスリン分泌ペプチド誘導体 |
WO2009069983A2 (en) * | 2007-11-29 | 2009-06-04 | Hanmi Pharmaceutical Co., Ltd. | A pharmaceutical composition for treating obesity-related disease comprising insulinotropic peptide conjugate |
WO2009155257A1 (en) * | 2008-06-17 | 2009-12-23 | Indiana University Research And Technology Corporation | Glucagon analogs exhibiting enhanced solubility and stability physiological ph buffers |
Cited By (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9522946B2 (en) | 2011-06-10 | 2016-12-20 | Hanmi Science Co., Ltd. | Oxyntomodulin derivatives and pharmaceutical composition for treating obesity comprising the same |
US9527898B2 (en) | 2011-06-10 | 2016-12-27 | Hanmi Science Co., Ltd. | Oxyntomodulin derivatives and pharmaceutical composition for treating obesity comprising the same |
US9765131B2 (en) | 2011-06-10 | 2017-09-19 | Hanmi Science Co., Ltd. | Oxyntomodulin derivatives and pharmaceutical composition for treating obesity comprising the same |
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US10550168B2 (en) | 2012-11-06 | 2020-02-04 | Hanmi Pharm. Co., Ltd. | Composition for treating diabetes or diabesity comprising oxyntomodulin analog |
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US10513550B2 (en) | 2014-12-30 | 2019-12-24 | Hanmi Pharm Co., Ltd | Glucagon derivatives |
JP2021102618A (ja) * | 2015-06-30 | 2021-07-15 | ハンミ ファーマシューティカル カンパニー リミテッド | グルカゴン誘導体及びその持続型結合体を含む組成物 |
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JP2018526333A (ja) * | 2015-06-30 | 2018-09-13 | ハンミ ファーマシューティカル カンパニー リミテッド | グルカゴン誘導体及びその持続型結合体を含む組成物 |
JP2018528234A (ja) * | 2015-09-24 | 2018-09-27 | ハンミ ファーマシューティカル カンパニー リミテッド | 免疫グロブリン断片の特定位置を連結部位として用いたタンパク質結合体 |
JP2022025098A (ja) * | 2015-12-02 | 2022-02-09 | ハンミ ファーマシューティカル カンパニー リミテッド | 脂肪酸誘導体を用いたタンパク質結合体及びその製造方法 |
US10894076B2 (en) | 2015-12-29 | 2021-01-19 | Pegbio Co., Ltd. | Composition comprising GLP-1 receptor agonist and glucagon receptor agonist and application thereof |
JP2019500399A (ja) * | 2015-12-29 | 2019-01-10 | 派格生物医薬(蘇州)有限公司Pegbio Co.,Ltd. | Glp−1受容体作動薬とグルカゴン受容体作動薬とを含む組成物、及びその用途 |
US11332508B2 (en) | 2015-12-31 | 2022-05-17 | Hanmi Pharm. Co., Ltd. | Triple glucagon/GLP-1/GIP receptor agonist |
JP2022532445A (ja) * | 2019-07-18 | 2022-07-14 | ハンミ ファーマシューティカル カンパニー リミテッド | 新規な中間体製造による持続型薬物結合体の製造方法 |
US11717577B2 (en) | 2019-07-18 | 2023-08-08 | Hanmi Pharm. Co., Ltd. | Method for preparing long-acting drug conjugate through preparation of intermediate |
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US9072794B2 (en) | 2015-07-07 |
WO2012011752A3 (en) | 2012-05-31 |
EP3248611A1 (en) | 2017-11-29 |
AR082320A1 (es) | 2012-11-28 |
EP2595648A2 (en) | 2013-05-29 |
EP3248611B1 (en) | 2021-07-21 |
KR20120010146A (ko) | 2012-02-02 |
KR101382593B1 (ko) | 2014-04-10 |
TW201309323A (zh) | 2013-03-01 |
JP6076902B2 (ja) | 2017-02-08 |
US20130122023A1 (en) | 2013-05-16 |
TWI593422B (zh) | 2017-08-01 |
WO2012011752A2 (en) | 2012-01-26 |
EP2595648A4 (en) | 2014-07-02 |
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