JP2015521622A5 - - Google Patents
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- JP2015521622A5 JP2015521622A5 JP2015518505A JP2015518505A JP2015521622A5 JP 2015521622 A5 JP2015521622 A5 JP 2015521622A5 JP 2015518505 A JP2015518505 A JP 2015518505A JP 2015518505 A JP2015518505 A JP 2015518505A JP 2015521622 A5 JP2015521622 A5 JP 2015521622A5
- Authority
- JP
- Japan
- Prior art keywords
- amino acid
- peptide
- ala
- glucagon analog
- seq
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 150000001413 amino acids Chemical class 0.000 claims description 131
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 119
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 15
- 230000004048 modification Effects 0.000 claims description 14
- 238000012986 modification Methods 0.000 claims description 14
- 125000002252 acyl group Chemical group 0.000 claims description 10
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Chemical compound CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 claims description 9
- 108010067722 Dipeptidyl Peptidase 4 Proteins 0.000 claims description 8
- 102100025012 Dipeptidyl peptidase 4 Human genes 0.000 claims description 8
- 239000008194 pharmaceutical composition Substances 0.000 claims description 8
- 125000001433 C-terminal amino-acid group Chemical group 0.000 claims description 7
- 101001015516 Homo sapiens Glucagon-like peptide 1 receptor Proteins 0.000 claims description 7
- UCUNFLYVYCGDHP-BYPYZUCNSA-N L-methionine sulfone Chemical compound CS(=O)(=O)CC[C@H](N)C(O)=O UCUNFLYVYCGDHP-BYPYZUCNSA-N 0.000 claims description 7
- 125000000393 L-methionino group Chemical group [H]OC(=O)[C@@]([H])(N([H])[*])C([H])([H])C(SC([H])([H])[H])([H])[H] 0.000 claims description 7
- 239000000539 dimer Substances 0.000 claims description 7
- UKAUYVFTDYCKQA-UHFFFAOYSA-N -2-Amino-4-hydroxybutanoic acid Natural products OC(=O)C(N)CCO UKAUYVFTDYCKQA-UHFFFAOYSA-N 0.000 claims description 6
- UKAUYVFTDYCKQA-VKHMYHEASA-N L-homoserine Chemical compound OC(=O)[C@@H](N)CCO UKAUYVFTDYCKQA-VKHMYHEASA-N 0.000 claims description 6
- QEFRNWWLZKMPFJ-ZXPFJRLXSA-N L-methionine (R)-S-oxide Chemical compound C[S@@](=O)CC[C@H]([NH3+])C([O-])=O QEFRNWWLZKMPFJ-ZXPFJRLXSA-N 0.000 claims description 6
- QEFRNWWLZKMPFJ-UHFFFAOYSA-N L-methionine sulphoxide Natural products CS(=O)CCC(N)C(O)=O QEFRNWWLZKMPFJ-UHFFFAOYSA-N 0.000 claims description 6
- SNDPXSYFESPGGJ-UHFFFAOYSA-N L-norVal-OH Natural products CCCC(N)C(O)=O SNDPXSYFESPGGJ-UHFFFAOYSA-N 0.000 claims description 6
- 102000005962 receptors Human genes 0.000 claims description 6
- 108020003175 receptors Proteins 0.000 claims description 6
- 101000886868 Homo sapiens Gastric inhibitory polypeptide Proteins 0.000 claims description 5
- SNDPXSYFESPGGJ-BYPYZUCNSA-N L-2-aminopentanoic acid Chemical compound CCC[C@H](N)C(O)=O SNDPXSYFESPGGJ-BYPYZUCNSA-N 0.000 claims description 5
- 239000000556 agonist Substances 0.000 claims description 5
- 230000000694 effects Effects 0.000 claims description 5
- 102000050325 human granulocyte inhibitory Human genes 0.000 claims description 5
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 5
- 239000002131 composite material Substances 0.000 claims description 4
- 230000004584 weight gain Effects 0.000 claims description 4
- 235000019786 weight gain Nutrition 0.000 claims description 4
- 230000004580 weight loss Effects 0.000 claims description 4
- 230000001939 inductive effect Effects 0.000 claims description 3
- MEMAWYPPJAGKPA-UHFFFAOYSA-N C(C)(=O)CC(C(C)N)N Chemical compound C(C)(=O)CC(C(C)N)N MEMAWYPPJAGKPA-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 206010012601 diabetes mellitus Diseases 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 2
- 230000007123 defense Effects 0.000 claims 1
- MASNOZXLGMXCHN-ZLPAWPGGSA-N glucagon Chemical compound C([C@@H](C(=O)N[C@H](C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O)C(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC=1NC=NC=1)[C@@H](C)O)[C@@H](C)O)C1=CC=CC=C1 MASNOZXLGMXCHN-ZLPAWPGGSA-N 0.000 description 91
- 125000003275 alpha amino acid group Chemical group 0.000 description 50
- 230000002378 acidificating effect Effects 0.000 description 12
- -1 aliphatic amino acid Chemical class 0.000 description 12
- 108010004460 Gastric Inhibitory Polypeptide Proteins 0.000 description 9
- 102100039994 Gastric inhibitory polypeptide Human genes 0.000 description 9
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 9
- 108010036598 gastric inhibitory polypeptide receptor Proteins 0.000 description 9
- 125000003892 C18 acyl group Chemical group 0.000 description 8
- 125000006850 spacer group Chemical group 0.000 description 8
- 102000051325 Glucagon Human genes 0.000 description 7
- 108060003199 Glucagon Proteins 0.000 description 7
- 229960004666 glucagon Drugs 0.000 description 7
- 230000001681 protective effect Effects 0.000 description 7
- 108010086246 Glucagon-Like Peptide-1 Receptor Proteins 0.000 description 6
- 102100032882 Glucagon-like peptide 1 receptor Human genes 0.000 description 6
- 125000002883 imidazolyl group Chemical group 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 101710198884 GATA-type zinc finger protein 1 Proteins 0.000 description 5
- DTHNMHAUYICORS-KTKZVXAJSA-N Glucagon-like peptide 1 Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC=1N=CNC=1)[C@@H](C)O)[C@@H](C)O)C(C)C)C1=CC=CC=C1 DTHNMHAUYICORS-KTKZVXAJSA-N 0.000 description 5
- LRQKBLKVPFOOQJ-YFKPBYRVSA-N L-norleucine Chemical compound CCCC[C@H]([NH3+])C([O-])=O LRQKBLKVPFOOQJ-YFKPBYRVSA-N 0.000 description 5
- 102100040918 Pro-glucagon Human genes 0.000 description 5
- SCOZOHWKTFBYNS-UHFFFAOYSA-N 2,2-diamino-3-methyl-4-oxopentanoic acid Chemical compound CC(=O)C(C)C(N)(N)C(O)=O SCOZOHWKTFBYNS-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 101001040075 Homo sapiens Glucagon receptor Proteins 0.000 description 3
- 125000000998 L-alanino group Chemical group [H]N([*])[C@](C([H])([H])[H])([H])C(=O)O[H] 0.000 description 3
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 description 3
- 230000000087 stabilizing effect Effects 0.000 description 3
- 108010016626 Dipeptides Proteins 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 150000001408 amides Chemical group 0.000 description 2
- 125000000539 amino acid group Chemical group 0.000 description 2
- 210000004899 c-terminal region Anatomy 0.000 description 2
- 125000001924 fatty-acyl group Chemical group 0.000 description 2
- 125000001475 halogen functional group Chemical group 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 150000003573 thiols Chemical group 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- 0 C*(C)(C)C(C(O)=O)N Chemical compound C*(C)(C)C(C(O)=O)N 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- UEQUQVLFIPOEMF-UHFFFAOYSA-N Mianserin Chemical compound C1C2=CC=CC=C2N2CCN(C)CC2C2=CC=CC=C21 UEQUQVLFIPOEMF-UHFFFAOYSA-N 0.000 description 1
- JRLGPAXAGHMNOL-LURJTMIESA-N N(2)-acetyl-L-ornithine Chemical compound CC(=O)N[C@H](C([O-])=O)CCC[NH3+] JRLGPAXAGHMNOL-LURJTMIESA-N 0.000 description 1
- 208000008589 Obesity Diseases 0.000 description 1
- 230000009435 amidation Effects 0.000 description 1
- 238000007112 amidation reaction Methods 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261662868P | 2012-06-21 | 2012-06-21 | |
| US61/662,868 | 2012-06-21 | ||
| US201261716878P | 2012-10-22 | 2012-10-22 | |
| US61/716,878 | 2012-10-22 | ||
| PCT/US2013/046228 WO2013192129A1 (en) | 2012-06-21 | 2013-06-18 | Glucagon analogs exhibiting gip receptor activity |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015521622A JP2015521622A (ja) | 2015-07-30 |
| JP2015521622A5 true JP2015521622A5 (enExample) | 2016-08-04 |
| JP6311708B2 JP6311708B2 (ja) | 2018-04-18 |
Family
ID=48699335
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015518505A Active JP6311708B2 (ja) | 2012-06-21 | 2013-06-18 | Ｇｉｐ受容体活性を示すグルカゴンアナローグ |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US9340600B2 (enExample) |
| EP (1) | EP2864351B1 (enExample) |
| JP (1) | JP6311708B2 (enExample) |
| KR (1) | KR20150023013A (enExample) |
| CN (1) | CN104583232B (enExample) |
| AR (1) | AR091477A1 (enExample) |
| CA (1) | CA2877358A1 (enExample) |
| ES (1) | ES2602486T3 (enExample) |
| HK (1) | HK1209764A1 (enExample) |
| MX (1) | MX2014015558A (enExample) |
| RU (1) | RU2015101697A (enExample) |
| TW (1) | TWI599575B (enExample) |
| WO (1) | WO2013192129A1 (enExample) |
Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102459325B (zh) | 2009-06-16 | 2015-03-25 | 印第安纳大学科技研究有限公司 | 胃抑胜肽受体活化的胰高血糖素化合物 |
| WO2012169798A2 (en) | 2011-06-10 | 2012-12-13 | Hanmi Science Co., Ltd. | Novel oxyntomodulin derivatives and pharmaceutical composition for treating obesity comprising the same |
| EP3502129B1 (en) | 2011-06-17 | 2021-04-07 | Hanmi Science Co., Ltd. | A conjugate comprising oxyntomodulin and an immunoglobulin fragment, and use thereof |
| JP6179864B2 (ja) | 2011-06-22 | 2017-08-16 | インディアナ ユニヴァーシティ リサーチ アンド テクノロジー コーポレイション | グルカゴン／ｇｌｐ−１レセプタコ−アゴニスト |
| KR101968344B1 (ko) | 2012-07-25 | 2019-04-12 | 한미약품 주식회사 | 옥신토모듈린 유도체를 포함하는 고지혈증 치료용 조성물 |
| UA116217C2 (uk) | 2012-10-09 | 2018-02-26 | Санофі | Пептидна сполука як подвійний агоніст рецепторів glp1-1 та глюкагону |
| KR101993393B1 (ko) | 2012-11-06 | 2019-10-01 | 한미약품 주식회사 | 옥신토모듈린 유도체를 포함하는 당뇨병 또는 비만성 당뇨병 치료용 조성물 |
| CA2890324C (en) | 2012-11-06 | 2021-02-23 | Hanmi Pharm. Co., Ltd. | Liquid formulation of protein conjugate comprising the oxyntomodulin and an immunoglobulin fragment |
| EP2934568B1 (en) | 2012-12-21 | 2017-10-18 | Sanofi | Dual glp1/gip or trigonal glp1/gip/glucagon agonists |
| UA118558C2 (uk) | 2013-05-28 | 2019-02-11 | Такеда Фармасьютікал Компані Лімітед | Пептидна сполука |
| AR098614A1 (es) * | 2013-12-18 | 2016-06-01 | Lilly Co Eli | Compuesto para el tratamiento de hipoglicemia severa |
| US9963496B2 (en) | 2014-02-18 | 2018-05-08 | Novo Nordisk A/S | Stable glucagon analogues and use for treatment of hypoglycaemia |
| TWI772252B (zh) | 2014-09-16 | 2022-08-01 | 南韓商韓美藥品股份有限公司 | 長效glp-1/高血糖素受體雙促效劑治療非酒精性脂肝疾病之用途 |
| CN106519015B (zh) * | 2014-09-23 | 2020-04-17 | 深圳市图微安创科技开发有限公司 | 胃泌酸调节素类似物 |
| WO2016049190A1 (en) * | 2014-09-24 | 2016-03-31 | Indiana University Research And Technology Corporation | Incretin-insulin conjugates |
| JP2018012644A (ja) * | 2014-11-26 | 2018-01-25 | 武田薬品工業株式会社 | ペプチド化合物 |
| KR102418477B1 (ko) | 2014-12-30 | 2022-07-08 | 한미약품 주식회사 | 글루카곤 유도체 |
| EP3575314B1 (en) | 2014-12-30 | 2024-02-14 | Hanmi Pharm. Co., Ltd. | Glucagon derivative |
| JOP20200119A1 (ar) * | 2015-01-09 | 2017-06-16 | Lilly Co Eli | مركبات مساعد مشترك من gip وglp-1 |
| AR105319A1 (es) | 2015-06-05 | 2017-09-27 | Sanofi Sa | Profármacos que comprenden un conjugado agonista dual de glp-1 / glucagón conector ácido hialurónico |
| MA49545B1 (fr) | 2015-06-30 | 2022-03-31 | Hanmi Pharm Ind Co Ltd | Dérivé de glucagon et composition comprenant un conjugué à action prolongée de celui-ci |
| TWI622596B (zh) | 2015-10-26 | 2018-05-01 | 美國禮來大藥廠 | 升糖素受體促效劑 |
| CN115920077B (zh) * | 2015-12-31 | 2025-07-04 | 韩美药品株式会社 | 胰高血糖素/glp-1/gip受体三重激动剂的长效缀合物 |
| CN109477094B (zh) | 2016-05-24 | 2022-04-26 | 武田药品工业株式会社 | 肽化合物 |
| CA3029518A1 (en) | 2016-06-29 | 2018-01-04 | Hanmi Pharm. Co., Ltd. | Glucagon derivative, conjugate thereof, composition comprising same, and therapeutic use thereof |
| AR110300A1 (es) | 2016-12-02 | 2019-03-13 | Sanofi Sa | Compuestos como agonistas peptídicos trigonales de los receptores de glp1 / glucagón / gip |
| TW201833131A (zh) | 2016-12-02 | 2018-09-16 | 法商賽諾菲公司 | 作為胜肽類ｇｌｐ１／升糖素／ｇｉｐ受體促效劑之新化合物 |
| GB201620611D0 (en) | 2016-12-05 | 2017-01-18 | Univ Of Lancaster | Treatment of neurological diseases |
| JOP20180028A1 (ar) | 2017-03-31 | 2019-01-30 | Takeda Pharmaceuticals Co | مركب ببتيد |
| CA3096493A1 (en) | 2018-04-10 | 2019-10-17 | Sanofi-Aventis Deutschland Gmbh | Method for cleavage of solid phase-bound peptides from the solid phase |
| JP7332620B2 (ja) | 2018-04-10 | 2023-08-23 | サノフィ－アベンティス・ドイチュラント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | キャップ付加を伴うリキシセナチドの合成 |
| BR112020022027A2 (pt) * | 2018-05-04 | 2021-02-02 | Novo Nordisk A/S | derivados de gip e seus usos |
| TW202015735A (zh) | 2018-05-30 | 2020-05-01 | 法商賽諾菲公司 | 包含ｇｌｐ－１／升糖素／ｇｉｐ三重受體促效劑、連接子及透明質酸之接合物 |
| JP2022503793A (ja) * | 2018-09-24 | 2022-01-12 | 武田薬品工業株式会社 | Ｇｉｐ受容体アゴニストペプチド化合物及びその使用 |
| CN111171134B (zh) | 2018-11-12 | 2023-08-15 | 天津药物研究院有限公司 | 胰高血糖素衍生肽及其用途 |
| WO2020115048A1 (en) * | 2018-12-03 | 2020-06-11 | Antag Therapeutics Aps | Modified gip peptide analogues |
| CN110128526B (zh) * | 2019-05-30 | 2021-07-23 | 江苏诺泰澳赛诺生物制药股份有限公司 | 长效化艾塞那肽衍生物及其盐与制备方法和用途 |
| WO2020263063A1 (ko) * | 2019-06-28 | 2020-12-30 | 한미약품 주식회사 | 글루카곤, glp-1 및 gip 수용체 모두에 활성을 갖는 삼중 활성체 또는 이의 결합체의 간 질환에 대한 치료적 용도 |
| CN114945589B (zh) * | 2020-02-24 | 2024-05-24 | 深圳市图微安创科技开发有限公司 | 多肽化合物及其在预防或治疗糖尿病或糖尿病并发症中的应用 |
| KR20230018395A (ko) * | 2020-05-29 | 2023-02-07 | 베이징 투오 지에 바이오파마수티컬 컴퍼니 리미티드 | Glp-1 및 gip 수용체 둘 모두에 대한 이중 작용제 화합물 및 이의 적용 |
| KR20220009354A (ko) * | 2020-07-15 | 2022-01-24 | 한미약품 주식회사 | 글루카곤 유도체 또는 이의 결합체의 간질환에 대한 치료적 용도 |
| EP4183419A4 (en) * | 2020-07-17 | 2025-04-02 | Hanmi Pharm. Co., Ltd. | THERAPEUTIC USE OF A COMBINATION WITH A LONG-ACTING TRIPLE AGONIST CONJUGATE OR TRIPLE AGONIST |
| KR20220021890A (ko) * | 2020-08-14 | 2022-02-22 | 한미약품 주식회사 | 삼중 활성체 지속형 결합체를 유효성분으로 포함하는 약학 조성물 |
| EP4218791A4 (en) * | 2020-09-25 | 2024-11-06 | Hanmi Pharm. Co., Ltd. | THERAPEUTIC USE OF TRIPLE AGONISTS WITH ACTIVITY TOWARDS ALL GLUCAGON, GLP-1 AND GIP RECEPTORS FOR NEURODEGENERATIVE DISEASES OR CONJUGATES THEREOF |
| US20240020543A1 (en) * | 2020-10-17 | 2024-01-18 | Sun Pharmaceutical Industries Limited | Glp-1/gip dual agonists |
| EP4236991A1 (en) * | 2020-10-30 | 2023-09-06 | Novo Nordisk A/S | Glp-1, gip and glucagon receptor triple agonists |
| CN118184764A (zh) * | 2020-12-23 | 2024-06-14 | 浙江道尔生物科技有限公司 | 一种长效胰高血糖素衍生物 |
| CN117120462A (zh) * | 2021-01-22 | 2023-11-24 | 深圳市图微安创科技开发有限公司 | 多肽化合物在预防或治疗炎症性肠病及其相关的肠纤维化中的应用 |
| JP2024512895A (ja) * | 2021-04-09 | 2024-03-21 | ハンミ ファーマシューティカル カンパニー リミテッド | グルカゴン誘導体を含む慢性腎臓疾患予防又は治療用薬学組成物 |
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2013
- 2013-06-18 RU RU2015101697A patent/RU2015101697A/ru unknown
- 2013-06-18 MX MX2014015558A patent/MX2014015558A/es unknown
- 2013-06-18 AR ARP130102142 patent/AR091477A1/es unknown
- 2013-06-18 EP EP13731619.6A patent/EP2864351B1/en not_active Not-in-force
- 2013-06-18 ES ES13731619.6T patent/ES2602486T3/es active Active
- 2013-06-18 TW TW102121606A patent/TWI599575B/zh not_active IP Right Cessation
- 2013-06-18 CA CA2877358A patent/CA2877358A1/en not_active Abandoned
- 2013-06-18 JP JP2015518505A patent/JP6311708B2/ja active Active
- 2013-06-18 US US13/920,188 patent/US9340600B2/en active Active
- 2013-06-18 CN CN201380040322.2A patent/CN104583232B/zh not_active Expired - Fee Related
- 2013-06-18 WO PCT/US2013/046228 patent/WO2013192129A1/en not_active Ceased
- 2013-06-18 KR KR20157000956A patent/KR20150023013A/ko not_active Withdrawn
- 2013-06-18 HK HK15110472.9A patent/HK1209764A1/xx unknown
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