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 |
|---|---|---|---|---|
| US9150632B2 (en) | 2009-06-16 | 2015-10-06 | Indiana University Research And Technology Corporation | GIP receptor-active glucagon compounds |
| HRP20181591T1 (hr) | 2011-06-10 | 2018-11-30 | Hanmi Science Co., Ltd. | Novi derivati oksintomodulina i farmaceutski pripravci za liječenje pretilosti koji ih sadrže |
| AU2012270366C1 (en) | 2011-06-17 | 2017-07-13 | Hanmi Science Co., Ltd. | A conjugate comprising oxyntomodulin and an immunoglobulin fragment, and use thereof |
| EA031230B1 (ru) | 2011-06-22 | 2018-12-28 | Индиана Юниверсити Рисерч Энд Текнолоджи Корпорейшн | Агонисты глюкагонового рецептора/glp-1-рецептора |
| 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 |
| NZ739063A (en) | 2012-11-06 | 2019-11-29 | Hanmi Pharm Ind Co Ltd | Liquid formulation of protein conjugate comprising the oxyntomodulin and an immunoglobulin fragment |
| KR101993393B1 (ko) | 2012-11-06 | 2019-10-01 | 한미약품 주식회사 | 옥신토모듈린 유도체를 포함하는 당뇨병 또는 비만성 당뇨병 치료용 조성물 |
| SG10201705097PA (en) | 2012-12-21 | 2017-07-28 | Sanofi Sa | Functionalized exendin-4 derivatives |
| LT3004155T (lt) | 2013-05-28 | 2021-12-27 | Takeda Pharmaceutical Company Limited | Peptidų junginys |
| AR098614A1 (es) * | 2013-12-18 | 2016-06-01 | Lilly Co Eli | Compuesto para el tratamiento de hipoglicemia severa |
| AR100306A1 (es) | 2014-02-18 | 2016-09-28 | Novo Nordisk As | Análogos de glucagón estables y uso para el tratamiento de la hipoglucemia |
| 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 |
| ES2822994T3 (es) * | 2014-09-24 | 2021-05-05 | Univ Indiana Res & Tech Corp | Conjugados de incretina-insulina |
| 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 |
| TN2017000271A1 (en) | 2014-12-30 | 2018-10-19 | Hanmi Pharm Ind Co Ltd | Glucagon derivative having improved stability |
| KR102418477B1 (ko) | 2014-12-30 | 2022-07-08 | 한미약품 주식회사 | 글루카곤 유도체 |
| 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 |
| TN2017000555A1 (en) | 2015-06-30 | 2019-04-12 | Hanmi Pharm Ind Co Ltd | Glucagon derivative and a composition comprising a long acting conjugate of the same |
| TWI622596B (zh) | 2015-10-26 | 2018-05-01 | 美國禮來大藥廠 | 升糖素受體促效劑 |
| PH12018501409B1 (en) * | 2015-12-31 | 2023-03-10 | Hanmi Pharmaceutical Co Ltd | Triple glucagon/glp-1/gip receptor agonist |
| CN109477094B (zh) | 2016-05-24 | 2022-04-26 | 武田药品工业株式会社 | 肽化合物 |
| JP7208020B2 (ja) | 2016-06-29 | 2023-01-18 | 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、その結合体、及びそれを含む組成物、並びにその治療的用途 |
| AR110300A1 (es) | 2016-12-02 | 2019-03-13 | Sanofi Sa | Compuestos como agonistas peptídicos trigonales de los receptores de glp1 / glucagón / gip |
| AR110301A1 (es) | 2016-12-02 | 2019-03-13 | Sanofi Sa | Compuestos como agonistas peptídicos de receptores de glp1 / glucagón / gip |
| 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 |
| KR102793451B1 (ko) | 2018-04-10 | 2025-04-11 | 사노피-아벤티스 도이칠란트 게엠베하 | 고체상으로부터 고체상-결합된 펩타이드를 절단하는 방법 |
| BR112020020647A2 (pt) | 2018-04-10 | 2021-02-23 | Sanofi-Aventis Deutschland Gmbh | síntese de lixisenatida com capeamento |
| TWI707865B (zh) * | 2018-05-04 | 2020-10-21 | 丹麥商諾佛 儂迪克股份有限公司 | Gip衍生物及其用途 |
| 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 |
| EP3856768A2 (en) * | 2018-09-24 | 2021-08-04 | Takeda Pharmaceutical Company Limited | Gip receptor agonist peptide compounds and uses thereof |
| KR102779458B1 (ko) * | 2018-11-12 | 2025-03-12 | 톈진 인스티튜트 오브 파마슈티컬 리서치 씨오., 엘티디. | 글루카곤 유도 펩티드 및 이의 용도 |
| US12297250B2 (en) * | 2018-12-03 | 2025-05-13 | 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 |
| EP4311578A3 (en) * | 2019-06-28 | 2024-04-10 | Hanmi Pharm. Co., Ltd. | Triple agonist having activity with respect to all of glucagon, glp-1, and gip receptors for treating liver disease |
| WO2021169512A1 (zh) * | 2020-02-24 | 2021-09-02 | 中山大学 | 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 |
| AU2021278157A1 (en) * | 2020-05-29 | 2022-11-24 | Jiangsu Hengrui Pharmaceuticals Co., Ltd. | Dual-agonist compound for both GLP-1 and GIP receptors and application thereof |
| JP2023534949A (ja) * | 2020-07-15 | 2023-08-15 | ハンミ ファーマシューティカル カンパニー リミテッド | グルカゴン誘導体又はその結合体の肝臓疾患に対する治療的用途 |
| JP2023535382A (ja) * | 2020-07-17 | 2023-08-17 | ハンミ ファーマシューティカル カンパニー リミテッド | 三重作用性持続型結合体又は三重作用剤を含む組合せ物の治療学的用途 |
| JP2023537895A (ja) * | 2020-08-14 | 2023-09-06 | ハンミ ファーマシューティカル カンパニー リミテッド | 三重活性体持続型結合体を有効成分として含む薬学組成物 |
| 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 |
| EP4204440A1 (en) * | 2020-10-17 | 2023-07-05 | Sun Pharmaceutical Industries Limited | Glp-1/gip dual agonists |
| JP2023550594A (ja) * | 2020-10-30 | 2023-12-04 | ノヴォ ノルディスク アー／エス | Ｇｌｐ－１、ｇｉｐ、およびグルカゴン受容体三重作動薬 |
| EP4249505A4 (en) * | 2020-12-23 | 2024-08-21 | Zhejiang Doer Biologics Co., Ltd. | GLUCAGONE DERIVATIVE WITH LONG-TERM EFFECTS |
| US20240174728A1 (en) * | 2021-01-22 | 2024-05-30 | Shenzhen Turier Biotech Co., Ltd. | A use of a polypeptide compound in the preparation of drugs for preventing or treating inflammatory bowel diseases and related intestinal fibrosis |
| 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 CA CA2877358A patent/CA2877358A1/en not_active Abandoned
- 2013-06-18 WO PCT/US2013/046228 patent/WO2013192129A1/en not_active Ceased
- 2013-06-18 TW TW102121606A patent/TWI599575B/zh not_active IP Right Cessation
- 2013-06-18 CN CN201380040322.2A patent/CN104583232B/zh not_active Expired - Fee Related
- 2013-06-18 EP EP13731619.6A patent/EP2864351B1/en not_active Not-in-force
- 2013-06-18 HK HK15110472.9A patent/HK1209764A1/xx unknown
- 2013-06-18 ES ES13731619.6T patent/ES2602486T3/es active Active
- 2013-06-18 MX MX2014015558A patent/MX2014015558A/es unknown
- 2013-06-18 US US13/920,188 patent/US9340600B2/en active Active
- 2013-06-18 AR ARP130102142 patent/AR091477A1/es unknown
- 2013-06-18 JP JP2015518505A patent/JP6311708B2/ja active Active
- 2013-06-18 KR KR20157000956A patent/KR20150023013A/ko not_active Withdrawn
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