JP2018535948A5 - - Google Patents
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- JP2018535948A5 JP2018535948A5 JP2018518592A JP2018518592A JP2018535948A5 JP 2018535948 A5 JP2018535948 A5 JP 2018535948A5 JP 2018518592 A JP2018518592 A JP 2018518592A JP 2018518592 A JP2018518592 A JP 2018518592A JP 2018535948 A5 JP2018535948 A5 JP 2018535948A5
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- Prior art keywords
- seq
- lepr
- antigen
- binding fragment
- antibody
- Prior art date
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- 102000005861 leptin receptors Human genes 0.000 claims description 41
- 108010019813 leptin receptors Proteins 0.000 claims description 41
- 239000000427 antigen Substances 0.000 claims description 40
- 102000036639 antigens Human genes 0.000 claims description 40
- 108091007433 antigens Proteins 0.000 claims description 40
- 239000012634 fragment Substances 0.000 claims description 38
- 150000001413 amino acids Chemical group 0.000 claims description 29
- 102000016267 Leptin Human genes 0.000 claims description 20
- 108010092277 Leptin Proteins 0.000 claims description 20
- NRYBAZVQPHGZNS-ZSOCWYAHSA-N leptin Chemical compound O=C([C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](N)CC(C)C)CCSC)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](CS)C(O)=O NRYBAZVQPHGZNS-ZSOCWYAHSA-N 0.000 claims description 20
- 229940039781 leptin Drugs 0.000 claims description 20
- 108010047041 Complementarity Determining Regions Proteins 0.000 claims description 19
- 101001129927 Homo sapiens Leptin receptor Proteins 0.000 claims description 19
- 102000007318 human leptin receptor Human genes 0.000 claims description 19
- 230000011664 signaling Effects 0.000 claims description 17
- 239000008194 pharmaceutical composition Substances 0.000 claims description 16
- 230000035772 mutation Effects 0.000 claims description 14
- 206010049287 Lipodystrophy acquired Diseases 0.000 claims description 13
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 13
- 208000006132 lipodystrophy Diseases 0.000 claims description 13
- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 claims description 10
- 201000010099 disease Diseases 0.000 claims description 9
- 210000004027 cell Anatomy 0.000 claims description 8
- 230000007812 deficiency Effects 0.000 claims description 8
- 239000003112 inhibitor Substances 0.000 claims description 8
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 claims description 8
- 238000002198 surface plasmon resonance spectroscopy Methods 0.000 claims description 8
- 230000019491 signal transduction Effects 0.000 claims description 7
- 101001063991 Homo sapiens Leptin Proteins 0.000 claims description 6
- 238000003556 assay Methods 0.000 claims description 6
- 102000049953 human LEP Human genes 0.000 claims description 6
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims description 6
- 102000006501 Angiopoietin-like Proteins Human genes 0.000 claims description 4
- 108010019425 Angiopoietin-like Proteins Proteins 0.000 claims description 4
- 102000051325 Glucagon Human genes 0.000 claims description 4
- 108060003199 Glucagon Proteins 0.000 claims description 4
- 108010063919 Glucagon Receptors Proteins 0.000 claims description 4
- 102100040890 Glucagon receptor Human genes 0.000 claims description 4
- 102000004877 Insulin Human genes 0.000 claims description 4
- 108090001061 Insulin Proteins 0.000 claims description 4
- 206010022489 Insulin Resistance Diseases 0.000 claims description 4
- 208000008589 Obesity Diseases 0.000 claims description 4
- 102100020888 Sodium/glucose cotransporter 2 Human genes 0.000 claims description 4
- 101710103228 Sodium/glucose cotransporter 2 Proteins 0.000 claims description 4
- SNPPWIUOZRMYNY-UHFFFAOYSA-N bupropion Chemical compound CC(C)(C)NC(C)C(=O)C1=CC=CC(Cl)=C1 SNPPWIUOZRMYNY-UHFFFAOYSA-N 0.000 claims description 4
- 229960001058 bupropion Drugs 0.000 claims description 4
- 208000035475 disorder Diseases 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 4
- 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 claims description 4
- 229960004666 glucagon Drugs 0.000 claims description 4
- 229940125396 insulin Drugs 0.000 claims description 4
- 235000020824 obesity Nutrition 0.000 claims description 4
- DHHVAGZRUROJKS-UHFFFAOYSA-N phentermine Chemical compound CC(C)(N)CC1=CC=CC=C1 DHHVAGZRUROJKS-UHFFFAOYSA-N 0.000 claims description 4
- 229940124597 therapeutic agent Drugs 0.000 claims description 4
- 230000002950 deficient Effects 0.000 claims description 3
- 230000006735 deficit Effects 0.000 claims description 3
- 230000009885 systemic effect Effects 0.000 claims description 3
- 208000024827 Alzheimer disease Diseases 0.000 claims description 2
- 201000000736 Amenorrhea Diseases 0.000 claims description 2
- 206010001928 Amenorrhoea Diseases 0.000 claims description 2
- 206010003694 Atrophy Diseases 0.000 claims description 2
- PWDLDBWXTVILPC-WGAVTJJLSA-N CC(C)(N)CC1=CC=CC=C1.C1O[C@@]2(COS(N)(=O)=O)OC(C)(C)O[C@H]2[C@@H]2OC(C)(C)O[C@@H]21 Chemical compound CC(C)(N)CC1=CC=CC=C1.C1O[C@@]2(COS(N)(=O)=O)OC(C)(C)O[C@H]2[C@@H]2OC(C)(C)O[C@@H]21 PWDLDBWXTVILPC-WGAVTJJLSA-N 0.000 claims description 2
- 206010010356 Congenital anomaly Diseases 0.000 claims description 2
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical group [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims description 2
- 201000005948 Donohue syndrome Diseases 0.000 claims description 2
- 208000003929 Familial Partial Lipodystrophy Diseases 0.000 claims description 2
- 206010056465 Food craving Diseases 0.000 claims description 2
- 229940121710 HMGCoA reductase inhibitor Drugs 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 108010001127 Insulin Receptor Proteins 0.000 claims description 2
- 102100036721 Insulin receptor Human genes 0.000 claims description 2
- 229940122199 Insulin secretagogue Drugs 0.000 claims description 2
- 208000013262 Localized lipodystrophy Diseases 0.000 claims description 2
- 208000001145 Metabolic Syndrome Diseases 0.000 claims description 2
- 229940100389 Sulfonylurea Drugs 0.000 claims description 2
- KJADKKWYZYXHBB-XBWDGYHZSA-N Topiramic acid Chemical compound C1O[C@@]2(COS(N)(=O)=O)OC(C)(C)O[C@H]2[C@@H]2OC(C)(C)O[C@@H]21 KJADKKWYZYXHBB-XBWDGYHZSA-N 0.000 claims description 2
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims description 2
- 230000003187 abdominal effect Effects 0.000 claims description 2
- 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 claims description 2
- 208000015228 acquired partial lipodystrophy Diseases 0.000 claims description 2
- 230000003213 activating effect Effects 0.000 claims description 2
- 210000000577 adipose tissue Anatomy 0.000 claims description 2
- 231100000540 amenorrhea Toxicity 0.000 claims description 2
- 230000037444 atrophy Effects 0.000 claims description 2
- 229940012191 bupropion / naltrexone Drugs 0.000 claims description 2
- 102220429788 c.1226C>A Human genes 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 229910052805 deuterium Inorganic materials 0.000 claims description 2
- 230000037213 diet Effects 0.000 claims description 2
- 235000005911 diet Nutrition 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- OLNTVTPDXPETLC-XPWALMASSA-N ezetimibe Chemical compound N1([C@@H]([C@H](C1=O)CC[C@H](O)C=1C=CC(F)=CC=1)C=1C=CC(O)=CC=1)C1=CC=C(F)C=C1 OLNTVTPDXPETLC-XPWALMASSA-N 0.000 claims description 2
- 229960000815 ezetimibe Drugs 0.000 claims description 2
- 239000003877 glucagon like peptide 1 receptor agonist Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 230000002267 hypothalamic effect Effects 0.000 claims description 2
- 230000003993 interaction Effects 0.000 claims description 2
- 238000002955 isolation Methods 0.000 claims description 2
- 229960005060 lorcaserin Drugs 0.000 claims description 2
- XTTZERNUQAFMOF-QMMMGPOBSA-N lorcaserin Chemical compound C[C@H]1CNCCC2=CC=C(Cl)C=C12 XTTZERNUQAFMOF-QMMMGPOBSA-N 0.000 claims description 2
- XZWYZXLIPXDOLR-UHFFFAOYSA-N metformin Chemical compound CN(C)C(=N)NC(N)=N XZWYZXLIPXDOLR-UHFFFAOYSA-N 0.000 claims description 2
- 229960003105 metformin Drugs 0.000 claims description 2
- 108700008455 metreleptin Proteins 0.000 claims description 2
- 229960000668 metreleptin Drugs 0.000 claims description 2
- 229960003562 phentermine Drugs 0.000 claims description 2
- 229960003611 pramlintide Drugs 0.000 claims description 2
- 108010029667 pramlintide Proteins 0.000 claims description 2
- NRKVKVQDUCJPIZ-MKAGXXMWSA-N pramlintide acetate Chemical compound C([C@@H](C(=O)NCC(=O)N1CCC[C@H]1C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(=O)N1[C@@H](CCC1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@H](CC=1NC=NC=1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@H](CS)NC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CS)NC(=O)[C@@H](N)CCCCN)[C@@H](C)O)[C@@H](C)O)[C@@H](C)O)C(C)C)C1=CC=CC=C1 NRKVKVQDUCJPIZ-MKAGXXMWSA-N 0.000 claims description 2
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 claims description 2
- 208000011580 syndromic disease Diseases 0.000 claims description 2
- 229960004394 topiramate Drugs 0.000 claims description 2
- 229960002911 zonisamide Drugs 0.000 claims description 2
- UBQNRHZMVUUOMG-UHFFFAOYSA-N zonisamide Chemical compound C1=CC=C2C(CS(=O)(=O)N)=NOC2=C1 UBQNRHZMVUUOMG-UHFFFAOYSA-N 0.000 claims description 2
- 240000006409 Acacia auriculiformis Species 0.000 claims 1
- 229940127355 PCSK9 Inhibitors Drugs 0.000 claims 1
- 238000004587 chromatography analysis Methods 0.000 claims 1
- 230000007547 defect Effects 0.000 claims 1
- 239000002471 hydroxymethylglutaryl coenzyme A reductase inhibitor Substances 0.000 claims 1
- 238000000034 method Methods 0.000 description 8
- 230000004936 stimulating effect Effects 0.000 description 2
- 238000002560 therapeutic procedure Methods 0.000 description 2
- 229940122392 PCSK9 inhibitor Drugs 0.000 description 1
- 230000001668 ameliorated effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000000249 far-infrared magnetic resonance spectroscopy Methods 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- AHLBNYSZXLDEJQ-FWEHEUNISA-N orlistat Chemical compound CCCCCCCCCCC[C@H](OC(=O)[C@H](CC(C)C)NC=O)C[C@@H]1OC(=O)[C@H]1CCCCCC AHLBNYSZXLDEJQ-FWEHEUNISA-N 0.000 description 1
- 229960001243 orlistat Drugs 0.000 description 1
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562240021P | 2015-10-12 | 2015-10-12 | |
| US62/240,021 | 2015-10-12 | ||
| US201662359757P | 2016-07-08 | 2016-07-08 | |
| US62/359,757 | 2016-07-08 | ||
| US201662375495P | 2016-08-16 | 2016-08-16 | |
| US62/375,495 | 2016-08-16 | ||
| US201662393143P | 2016-09-12 | 2016-09-12 | |
| US62/393,143 | 2016-09-12 | ||
| PCT/US2016/056465 WO2017066204A1 (en) | 2015-10-12 | 2016-10-11 | Antigen-binding proteins that activate the leptin receptor |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021039405A Division JP7165225B2 (ja) | 2015-10-12 | 2021-03-11 | レプチン受容体を活性化させる抗原結合タンパク質 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018535948A JP2018535948A (ja) | 2018-12-06 |
| JP2018535948A5 true JP2018535948A5 (enExample) | 2019-11-21 |
| JP7034068B2 JP7034068B2 (ja) | 2022-03-11 |
Family
ID=57184864
Family Applications (5)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018518592A Active JP7034068B2 (ja) | 2015-10-12 | 2016-10-11 | レプチン受容体を活性化させる抗原結合タンパク質 |
| JP2021039405A Active JP7165225B2 (ja) | 2015-10-12 | 2021-03-11 | レプチン受容体を活性化させる抗原結合タンパク質 |
| JP2022169008A Active JP7436603B2 (ja) | 2015-10-12 | 2022-10-21 | レプチン受容体を活性化させる抗原結合タンパク質 |
| JP2023202680A Active JP7699191B2 (ja) | 2015-10-12 | 2023-11-30 | レプチン受容体を活性化させる抗原結合タンパク質 |
| JP2024018406A Active JP7759417B2 (ja) | 2015-10-12 | 2024-02-09 | レプチン受容体を活性化させる抗原結合タンパク質 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021039405A Active JP7165225B2 (ja) | 2015-10-12 | 2021-03-11 | レプチン受容体を活性化させる抗原結合タンパク質 |
| JP2022169008A Active JP7436603B2 (ja) | 2015-10-12 | 2022-10-21 | レプチン受容体を活性化させる抗原結合タンパク質 |
| JP2023202680A Active JP7699191B2 (ja) | 2015-10-12 | 2023-11-30 | レプチン受容体を活性化させる抗原結合タンパク質 |
| JP2024018406A Active JP7759417B2 (ja) | 2015-10-12 | 2024-02-09 | レプチン受容体を活性化させる抗原結合タンパク質 |
Country Status (32)
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6799001B2 (ja) | 2015-03-10 | 2020-12-09 | リジェネロン・ファーマシューティカルズ・インコーポレイテッドＲｅｇｅｎｅｒｏｎ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ， Ｉｎｃ． | 注入装置 |
| TWI824372B (zh) | 2015-10-12 | 2023-12-01 | 美商再生元醫藥公司 | 活化瘦素受體的抗原結合蛋白 |
| SI3538554T1 (sl) | 2016-11-08 | 2025-10-30 | Regeneron Pharmaceuticals, Inc. | Proteini, ki vežejo antigen, ki antagonizirajo leptinski receptor |
| EP3618895B1 (en) | 2017-05-05 | 2022-04-13 | Regeneron Pharmaceuticals, Inc. | Auto-injector |
| MX2020006508A (es) | 2017-12-18 | 2020-09-17 | Regeneron Pharma | Moleculas de union a antigeno biespecificas que se unen al receptor de leptina y/o gp130, y metodos para el uso de estas. |
| US11608381B2 (en) | 2018-04-06 | 2023-03-21 | Regeneron Pharmaceuticals, Inc. | Methods of treatment using a leptin receptor agonist antibody |
| EP3868743B8 (en) * | 2018-10-11 | 2023-06-07 | Sumitomo Chemical Company Limited | Propylene oxide purification system and method for producing propylene oxide |
| JP7565287B2 (ja) * | 2019-01-31 | 2024-10-10 | シーメンス・ヘルスケア・ダイアグノスティックス・インコーポレイテッド | 抗ナロキソンおよび抗ナルトレキソンモノクローナル抗体ならびにその作製方法および使用方法 |
| US20220288169A1 (en) * | 2019-05-24 | 2022-09-15 | The Board of Supervisors of Louisiana State University and Agriculyural and Mechanical College | Compositions and methods for the treatment and prevention of hypoglycemic complications |
| US20220275097A1 (en) * | 2019-07-02 | 2022-09-01 | Shanghaitech University | Antibody to leptin receptor |
| US11392515B2 (en) | 2019-12-03 | 2022-07-19 | Micron Technology, Inc. | Cache architecture for a storage device |
| KR20210095781A (ko) | 2020-01-24 | 2021-08-03 | 주식회사 에이프릴바이오 | 항원결합 단편 및 생리활성 이펙터 모이어티로 구성된 융합 컨스트럭트를 포함하는 다중결합항체 및 이를 포함하는 약학조성물 |
| KR20230069969A (ko) * | 2020-09-15 | 2023-05-19 | 리제너론 파마슈티칼스 인코포레이티드 | 통증에 대한 lepr 아고니스트의 사용 |
| WO2022178382A1 (en) | 2021-02-22 | 2022-08-25 | Regeneron Pharmaceuticals, Inc. | Method for diagnosing and treating partial lipodystrophy |
| CN114456124B (zh) * | 2021-12-30 | 2023-04-21 | 华南农业大学 | 一种新利司他半抗原、人工抗原、抗体及其制备方法和应用 |
| AU2024304341A1 (en) | 2023-06-16 | 2026-01-22 | Regeneron Pharmaceuticals, Inc. | Medical device packaging and related methods |
| US20250108173A1 (en) | 2023-10-02 | 2025-04-03 | Regeneron Pharmaceuticals, Inc. | Drug delivery device safety system |
| JP2025148269A (ja) | 2024-03-15 | 2025-10-07 | イーライ リリー アンド カンパニー | 肥満を治療するための単独又は併用療法としてのレプチン受容体アゴニスト抗体 |
| WO2025227054A1 (en) * | 2024-04-25 | 2025-10-30 | The Board Of Regents Of The University Of Texas System | Monoclonal antibodies binding to leptin and uses thereof |
| US12303604B1 (en) | 2024-10-16 | 2025-05-20 | Currax Pharmaceuticals Llc | Pharmaceutical formulations comprising naltrexone and/or bupropion |
Family Cites Families (58)
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|---|---|---|---|---|
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