A Phase 2, Multiple Ascending Dose, Open-label, Proof-of-concept Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of HM15136 Treatment for 8 Weeks in Subjects Aged ≥2 Years With Congenital Hyperinsulinism (CHI)

This study is designed to evaluate the safety, tolerability, pharmacokinetics (PK), and efficacy of HM15136 when used as add-on therapy in subjects with CHI with persistent hypoglycemia while on standard of care treatment (SoC). HM15136 will be administered once weekly in multiple doses to subjects in multiple age including pediatric to find appropriate exposure-response data.

开始日期2021-10-28

申办/合作机构

Hanmi Pharmaceutical Co., Ltd.

NCT04167553 / Completed临床1期

A Phase 1, Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Doses of HM15136 in Obese or Overweight Subjects With Comorbidities

The planned period of each cohort is 22 weeks including subject screening, treatments for 12 weeks, and follow up period.

开始日期2019-08-30

申办/合作机构

Hanmi Pharmaceutical Co., Ltd.

NCT04032782 / Completed临床1期

A First-in-Human, Double-blind, Randomized, Placebo-controlled, Single Ascending Dose Study to Assess Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of HM15136 in Healthy Subjects

This is a double-blind, randomized, placebo controlled, single ascending dose (SAD) study to investigate the safety, tolerability, PK and PD of the SC administration of HM15136 in healthy subjects.
The study will be conducted in approximately 5 sequential dosing cohorts, enrolling 8 subjects per cohort. Subjects will be randomized to HM15136 or placebo in a ratio of 6:2 (6 active, 2 placebo).

开始日期2018-10-02

申办/合作机构

Hanmi Pharmaceutical Co., Ltd.

100 项与 Efpegerglucagon 相关的临床结果

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100 项与 Efpegerglucagon 相关的转化医学

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100 项与 Efpegerglucagon 相关的专利（医药）

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项与 Efpegerglucagon 相关的文献（医药）

2023-09-01·Diabetes, obesity & metabolism

Safety, tolerability, pharmacokinetics and pharmacodynamics of multiple ascending doses of the novel long-acting glucagon analogue HM15136 in overweight and obese patients with co-morbidities.

Article

作者: Baek, Seungjae ; Byeon, JinHee ; Choi, Jaehyuk ; Shin, Wonjung ; Kang, Seohyun ; Hompesch, Marcus

AIM:

To evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of multiple ascending doses of the novel long-acting glucagon analogue HM15136 in overweight/obese patients with co-morbidities, with and without type 2 diabetes (T2D).

MATERIALS AND METHODS:

This was a phase 1, double-blind, randomized, placebo-controlled, two-part trial with a 12-week treatment period of once-weekly subcutaneous HM15136 (0.02/0.04/0.06 mg/kg). Part 1 included patients with dyslipidaemia and/or hypertension and no T2D. Part 2 included patients with dyslipidaemia and/or hypertension plus T2D.

RESULTS:

In part 1, 23/27 (85.2%) patients receiving HM15136 and all patients receiving placebo (9/9 [100%]) experienced a treatment-emergent adverse event (TEAE). Five of 27 (18.5%) patients receiving HM15136 developed anti-HM15136 antibodies. Dose-dependent increases in mean HM15136 serum concentration and fasting plasma glucose (FPG) were observed, as were dose-dependent weight reductions of 0.5%/2.3%/2.6% at doses of 0.02/0.04/0.06 mg/kg, respectively. In part 2, 8/12 (66.7%) patients receiving HM15136 and all patients receiving placebo (4/4 [100.0%]) reported a TEAE. Two (16.7%) patients developed anti-HM15136 antibodies. Dose-dependent increases in mean HM15136 serum concentration were observed. FPG of more than 200 mg/dL was reported in 4/9 (44.4%) and 2/3 (66.7%) patients receiving 0.02 and 0.06 mg/kg, respectively. The 0.06 mg/kg dose was not tolerated in part 2 because of hyperglycaemia. Patients receiving 0.02 mg/kg showed a 0.9% weight reduction. No serious TEAEs leading to discontinuation were reported in either study part.

CONCLUSIONS:

This study of HM15136 provides a preliminary safety and tolerability profile with initial insights into its efficacy profile.

Scientific reports

A novel glucagon analog with an extended half-life, HM15136, normalizes glucose levels in rodent models of congenital hyperinsulinism

Article

作者: Shin, Seung-Hyun ; Kim, Ha Hyung ; Choi, In Young ; Lee, Sang-Hyun ; Kim, Jung Kuk ; Heo, Yong Ho ; Lee, Jong Suk

Abstract:

Congenital hyperinsulinism (CHI) is a rare genetic condition characterized by uncontrolled insulin secretion, resulting in hypoglycemia. Although glucagon has lately been regarded as a therapeutic option for CHI, its use is severely hampered by its poor solubility and stability at physiological pH, as well as its short duration of action. To address these constraints, we developed HM15136, a novel long-acting glucagon analog composed of a glucagon analog conjugated to the Fc fragment of human immunoglobulin G4 via a polyethylene glycol linker. In this study, we established that HM15136 was more soluble than natural glucagon (≥ 150 mg/mL vs 0.03 mg/mL). Next, we confirmed that HM15136 activated glucagon receptor in vitro and induced glycogenolysis and gluconeogenesis in rat primary hepatocytes. Pharmacokinetics (PK)/Pharmacodynamics (PD) analysis of HM15136 shows that HM15136 has a markedly longer half-life (36 h vs. < 5 min) and increased bioavailability (90%) compared to native glucagon in mice. Further, HM15136 could effectively reverse acute hypoglycemia induced by insulin challenge, and multiple doses of HM15136 could sustain increased blood glucose levels in CHI rats. In conclusion, our findings indicate that HM15136 promotes sustained elevation of blood glucose, demonstrating the potential for development as a once-weekly therapy for CHI.

项与 Efpegerglucagon 相关的新闻（医药）

2022-12-20

·PRNewswire

DelveInsight Estimates a Promising Picture of Obesity Pipeline Space Landscape as Key 100+ Pharma Companies Working in the Space

The prevalence of obesity has been rising since the past few years, which prompts the growing demand for treatment options. The increasing prevalence of Obesity and the growing research and development activities to develop novel therapies to treat obesity drive the market. The Companies developing the potential therapies in the last stage of development include Novo Nordisk, Eli Lilly and Company, Saniona, and several others. LAS VEGAS, Dec. 20, 2022 /PRNewswire/ -- DelveInsight's ' Obesity Pipeline Insight – 2022 ' report provides comprehensive global coverage of available, marketed, and pipeline obesity therapies in various stages of clinical development, major pharmaceutical companies are working to advance the pipeline space and future growth potential of the obesity pipeline domain. Key Takeaways from the Obesity Pipeline Report DelveInsight's obesity pipeline report depicts a robust space with 100+ active players working to develop 130+ pipeline therapies for obesity treatment. Key obesity companies such as 180 Life Sciences, 9 meters, Aardvark Therapeutics, Adocia, Agentix, AgeX Therapeutics, Altimmune, Amgen, Antag Therapeutics, Aphaia Pharma, Aptorum Group, AstraZeneca, Bukwang Pharmaceutical, Caliway Biopharmaceutics Co Ltd, Can Fite Biopharma, Carmot Therapeutics, Inc., Cellivery Therapeutics Inc, CinFina Pharma, Clayton Biotech, Click Therapeutics, Corbus Pharma, DiscoveryBiomed Inc, Dong-A ST, Dongkook Pharmaceuticals, Eccogene, Elevian, Eli Lilly and Company, Empros Pharma, Enterin Inc., EraCal Therapeutics AG, ERX Pharmaceuticals, ERX Pharmaceuticals, Eternygen GmbH, Eurofarma, Gannex Pharma, Glaceum, Gmax Biopharm, GPER G-1 Development Group, LLC, Gubra Therapeutics, Hanmi Pharmaceutical, Hanmi Pharmaceuticals, Innovent Biologics, Jenrin Discovery, Jiangsu Hansoh Pharmaceutical, Kallyope, Kintai Therapeutics, Kriya Therapeutics, LG Life Sciences, Lipidio Pharmaceuticals, MakScientific, Nano Precision Medical, NeonMind Biosciences, Novartis, Novo Nordisk, NuSirt Biopharma, Otsuka Pharmaceutical Factory Inc, Pfizer, Raziel Therapeutics, Reata Pharmaceuticals, Regeneron Pharmaceuticals, Reviva Pharmaceuticals, Rivus Pharmaceuticals, Shionogi, SHIONOGI & Co., Ltd., Sigrid Therapeutics, SJT Molecular Research SL, Structure Therapeutics, Sun Pharmaceutical Industries, Techfields Pharma, Terns Pharmaceuticals, Tonix Pharmaceuticals, UGISense AG, Versanis Bio, Viking Therapeutics, YSOPIA Bioscience, Yuhan, Zealand Pharma, and others are evaluating new drugs for obesity to improve the treatment landscape. Promising obesity pipeline therapies in various stages of development include Semaglutide oral, Tirzepatide, Sibutramine/Topiramate, NNC0174-0833, Tesomet, SHR-20004, RZL-012, CT-868, PF-06882961, EMP-16, S-237648, LY3502970, ARD-101, NNC0165-1875, XW003, IBI362, TG103, Cotadutide, MBL949, PF-07081532, APHD-012, LY 3437943, HSG4112, Leucine/sildenafil, BI 456906, Pemvidutide, LY3841136, HM15136, GMA106, DD01, ZP8396, K833, NNC0480-0389, LB54640, CT-181, CB4211, CT-388, CIN-109, ERX-1000, DWP306001, SCO-094, S-309309, NO-13065, GDD3898, XW004, SCO-267, ASC41, AMG 133, LY3541105, AMG-786, HU6, BMS-963272, BI 1820237, Xla 1, Dapiglutide, PB-119, PB-718, AGTX-2004, ECC5004, Thermostem, XW017, HM 14320, TNX-2900, CF-102, XW 010, LR19020, LR19056, YH34160, NM-136, CIN 110, CIN 209, CIN 210, RSVI-301, PramExe, BC GlueExe, BC Pram GlueExe, AGEX BAT1, CLS-1, CRB-913, Tespria, AM 6545, LP-003, KT A522, JD5037, SJT4a, GL0034, TF0103, TERN-601, NEO-001, KTX 0200, ENT-03, Bimagrumab, VK2735, HUM-234, NPM 139, YHC2129, YHC2134, YHC1140, GSBR-2nd Gen, GSBR-3rd Gen, and others. In December 2022, Amgen announced new Phase I data from AMG 133. This first-in-human study was designed to evaluate the safety, tolerability, pharmacokinetic and pharmacodynamic effects of AMG 133 in people with obesity and without diabetes (NCT04478708). The MAD cohorts showed mean percent changes in body weight (BW), ranging from -7.2% at the lowest dose (140mg Q4W), to -14.5% at the highest dose (420mg Q4W) by day 85. A substantial degree of weight loss was maintained beyond the treatment period, which will be shared as part of the oral presentation. Most treatment-emergent adverse events (TEAEs) were mild and transient. The majority of the TEAEs were GI-related, with the most common being nausea and vomiting, most events resolved within 48 hours. In December 2022, Poolbeg Pharma, a clinical-stage infectious disease company, acquired the exclusive license from InsuCaps to use its proprietary microencapsulation and nanoencapsulation oral delivery technologies in metabolic syndrome-related diseases, including obesity, pre-diabetes, and diabetes. In November 2022, Rhythm Pharmaceuticals, Inc. announced that Great Britain's Medicines & Healthcare products Regulatory Agency (MHRA) has expanded the marketing authorization for IMCIVREE® (setmelanotide) to include the treatment of obesity and control of hunger associated with genetically confirmed Bardet-Biedl syndrome (BBS) in adult and pediatric patients 6 years of age and older. In November 2022, Reviva Pharmaceuticals Holdings, Inc. announced the issuance of a patent covering the composition of matter for RP1208 in Canada, adding to its existing protection in key markets around the world. The Canadian patent covers the compositions of novel phenylcycloalkylmethylamine derivatives and the use of the compositions for the treatment of obesity, related co-morbid conditions, and depression and related co-morbid conditions. In October 2022, Eli Lilly and Company announced that the U.S. Food and Drug Administration (FDA) had granted Fast Track designation for the investigation of tirzepatide for the treatment of adults with obesity or overweight with weight-related comorbidities. In September 2022, Rivus Pharmaceuticals Inc. announced the completion of a USD 132 million Series B financing led by RA Capital Management with participation from Bain Capital Life Sciences, BB Biotech AG, and existing investors Longitude Capital, Medicxi, and RxCapital. This financing will further support the clinical advancement of lead candidate HU6, a first-in-class Controlled Metabolic Accelerator (CMA) designed to treat cardio-metabolic disease by addressing obesity, a primary driver of disease. In June 2022, LG Chem's new drug for treating genetic obesity received additional ODD (Orphan Drug Designation) from the US FDA. LG Chem announced on the 16th that the FDA recently granted ODD to ' LB54640' for the treatment of 'POMC (Proopiomelanocortin) deficiency.' In April 2022, Saniona announced that it paused the Phase IIb clinical trials testing Tesomet for people with Prader–Willi syndrome (PWS) and hypothalamic obesity (HO). The decision "is not related to the safety or efficacy of Tesomet and is entirely due to funding limitations. The company also announced a reprioritization and restructuring effort to immediately reduce operating expenses while maximizing cash resources. Request a sample and discover the recent advances in obesity drug treatment @ Obesity Pipeline Report The obesity pipeline report provides detailed profiles of pipeline assets, a comparative analysis of clinical and non-clinical stage obesity drugs, inactive and dormant assets, a comprehensive assessment of driving and restraining factors, and an assessment of opportunities and risks in the obesity clinical trial landscape. Obesity Overview Obesity is a chronic disease that causes abnormal or excessive fat accumulation or adipose tissue in the body, posing a health risk. It is caused by an imbalance between calories consumed and calories burned. The factors responsible for the causes of obesity include heredity, a sedentary lifestyle, excessive fat, sugar consumption (energy-dense meals), certain medications, and endocrine issues. Changes in the environment or society, as well as in behavior and culture, all directly impact. Obesity symptoms go beyond an increase in body fat. It can cause skin issues, shortness of breath, sleeping difficulties, and other symptoms. Some obesity symptoms have even been linked to an increased risk of developing certain diseases and disorders. In some cases, these can be life-threatening or even fatal. Find out more about drugs for obesity @ FDA-approved Obesity Drugs A snapshot of the Obesity Pipeline Drugs mentioned in the report: Learn more about the emerging obesity pipeline therapies @ Obesity Clinical Trials Obesity Therapeutics Assessment The obesity pipeline report proffers an integral view of obesity emerging novel therapies segmented by stage, product type, molecule type, mechanism of action, and route of administration. Scope of the Obesity Pipeline Report Coverage: Global Therapeutic Assessment By Product Type: Mono, Combination, Mono/Combination Therapeutic Assessment By Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III Therapeutics Assessment By Route of Administration: Oral, Parenteral, Intravenous, Subcutaneous, Topical Therapeutics Assessment By Molecule Type: Monoclonal Antibody, Peptides, Polymer, Small molecule, Gene therapy Therapeutics Assessment By Mechanism of Action: Glucagon like peptide 1 receptor agonists, Gastric inhibitory polypeptide receptor agonists, Beta 1 adrenergic receptor antagonists, Biogenic monoamine uptake inhibitors, Lipolysis modulators, Alpha-glucosidase inhibitors, Amylase inhibitors, Lipase inhibitors, Glucagon like peptide 1 receptor agonists, Glucagon receptor agonists, Islet amyloid polypeptide replacements Key Obesity Companies: 180 Life Sciences, 9 meters, Aardvark Therapeutics, Adocia, Agentix, AgeX Therapeutics, Altimmune, Amgen, Antag Therapeutics, Aphaia Pharma, Aptorum Group, AstraZeneca, Bukwang Pharmaceutical, Caliway Biopharmaceutics Co Ltd, Can Fite Biopharma, Carmot Therapeutics, Inc., Cellivery Therapeutics Inc, CinFina Pharma, Clayton Biotech, Click Therapeutics, Corbus Pharma, DiscoveryBiomed Inc, Dong-A ST, Dongkook Pharmaceuticals, Eccogene, Elevian, Eli Lilly and Company, Empros Pharma, Enterin Inc., EraCal Therapeutics AG, ERX Pharmaceuticals, ERX Pharmaceuticals, Eternygen GmbH, Eurofarma, Gannex Pharma, Glaceum, Gmax Biopharm, GPER G-1 Development Group, LLC, Gubra Therapeutics, Hanmi Pharmaceutical, Hanmi Pharmaceuticals, Innovent Biologics, Jenrin Discovery, Jiangsu Hansoh Pharmaceutical, Kallyope, Kintai Therapeutics, Kriya Therapeutics, LG Life Sciences, Lipidio Pharmaceuticals, MakScientific, Nano Precision Medical, NeonMind Biosciences, Novartis, Novo Nordisk, NuSirt Biopharma, Otsuka Pharmaceutical Factory Inc, Pfizer, Raziel Therapeutics, Reata Pharmaceuticals, Regeneron Pharmaceuticals, Reviva Pharmaceuticals, Rivus Pharmaceuticals, Shionogi, SHIONOGI & Co., Ltd., Sigrid Therapeutics, SJT Molecular Research SL, Structure Therapeutics, Sun Pharmaceutical Industries, Techfields Pharma, Terns Pharmaceuticals, Tonix Pharmaceuticals, UGISense AG, Versanis Bio, Viking Therapeutics, YSOPIA Bioscience, Yuhan, Zealand Pharma, and others. Key Obesity Pipeline Therapies: Semaglutide oral, Tirzepatide, Sibutramine/Topiramate, NNC0174-0833, Tesomet, SHR-20004, RZL-012, CT-868, PF-06882961, EMP-16, S-237648, LY3502970, ARD-101, NNC0165-1875, XW003, IBI362, TG103, Cotadutide, MBL949, PF-07081532, APHD-012, LY 3437943, HSG4112, Leucine/sildenafil, BI 456906, Pemvidutide, LY3841136, HM15136, GMA106, DD01, ZP8396, K833, NNC0480-0389, LB54640, CT-181, CB4211, CT-388, CIN-109, ERX-1000, DWP306001, SCO-094, S-309309, NO-13065, GDD3898, XW004, SCO-267, ASC41, AMG 133, LY3541105, AMG-786, HU6, BMS-963272, BI 1820237, Xla 1, Dapiglutide, PB-119, PB-718, AGTX-2004, ECC5004, Thermostem, XW017, HM 14320, TNX-2900, CF-102, XW 010, LR19020, LR19056, YH34160, NM-136, CIN 110, CIN 209, CIN 210, RSVI-301, PramExe, BC GlueExe, BC Pram GlueExe, AGEX BAT1, CLS-1, CRB-913, Tespria, AM 6545, LP-003, KT A522, JD5037, SJT4a, GL0034, TF0103, TERN-601, NEO-001, KTX 0200, ENT-03, Bimagrumab, VK2735, HUM-234, NPM 139, YHC2129, YHC2134, YHC1140, GSBR-2nd Gen, GSBR-3rd Gen, and others. Dive deep into rich insights for new drug for obesity treatment; visit @ Obesity Medications Table of Contents For further information on the obesity pipeline therapeutics, reach out @ Obesity Drug Treatment Related Reports Obesity Epidemiology Forecast Obesity Epidemiology Forecast – 2032 report delivers an in-depth understanding of the disease, historical and forecasted epidemiology as well as the obesity epidemiology trends. Obesity Market Obesity Market Insights, Epidemiology, and Market Forecast – 2032 report delivers an in-depth understanding of the disease, historical and forecasted epidemiology, market share of the individual therapies, and key hypothalamic obesity companies, including Saniona, YSOPIA Bioscience, Innovent Biologics, Glaceum, Shionogi, Aardvark Therapeutics, among others. Hypothalamic Obesity Market Hypothalamic Obesity Market Insights, Epidemiology, and Market Forecast – 2032 report delivers an in-depth understanding of the disease, historical and forecasted epidemiology, market share of the individual therapies, and key hypothalamic obesity companies, including Altimmune, Saniona, YSOPIA Bioscience, Innovent Biologics, among others. Hypothalamic Obesity Pipeline Hypothalamic Obesity Pipeline Insight – 2022 report provides comprehensive insights about the pipeline landscape, including clinical and non-clinical stage products and the key hypothalamic obesity companies, including Altimmune, Saniona, YSOPIA Bioscience, Innovent Biologics, among others. HET Obesity/POMC Deficiency Obesity Pipeline HET Obesity/POMC Deficiency Obesity Pipeline Insight – 2022 report provides comprehensive insights about the pipeline landscape, including clinical and non-clinical stage products and the key HET obesity/POMC deficiency obesity companies, including Novo Nordisk, Eli Lilly, and Company, MedImmune, Boehringer Ingelheim, Raziel Therapeutics, among others. HET Obesity/POMC Deficiency Obesity Market HET Obesity/POMC Deficiency Obesity Market Insights, Epidemiology, and Market Forecast – 2032 report delivers an in-depth understanding of the disease, historical and forecasted epidemiology, market share of the individual therapies, and key HET obesity/POMC deficiency obesity companies, including Novo Nordisk, Eli Lilly, and Company, MedImmune, Boehringer Ingelheim, Raziel Therapeutics, among others. Other Trending Reports Goitre Market | Thymus Cancer Market | US Healthcare Outlook Report | Venous Stenosis Market | Negative Pressure Wound Therapy Systems Market | Metrorrhagia Market | Dysfunctional Uterine Bleeding Market | Hypereosinophilic Syndrome Market | Age-related Vision Dysfunction Market | Dental Lasers Market | CRISPR Therapies Pipeline Insight | Cell And Gene Therapy For Multiple Myeloma Market | Drug Hypersensitivity Market | Dysthymia Market | Persistent Depressive Disorder Market | Cancer Vaccines Market | Weight Loss/Weight Management (Obesity) Market | Food Allergy Market | Obsessive-Compulsive Disorder Market | Tumor Ablation Market | Physiotherapy Equipment Market | CAR-T Pipeline Insight | Anti-hypertension Market | Radiofrequency Ablation Devices Market | Global Messenger RNA (mRNA)-based Vaccines and Therapeutics Market | Gastro Intestinal Bleeding Market | Trastuzumab Biosimilars Insight | Varicose Veins Market | Germ Cell Tumor Market | Intracardiac Echocardiography Devices Market | India Healthcare Outlook Report | Crows Feet Market Insight | Seborrhoeic Dermatitis Market | Injectable Drug Delivery Devices Market | Structural Heart Devices Market | Substance (Drug) Abuse Market Related Healthcare Blogs Obesity: A Global Concern Weight Loss and Obesity Market Obesity Treatment Market Related Healthcare Services Healthcare Business Consulting Healthcare Competitive Intelligence Services Healthcare Asset Prioritization Services About DelveInsight DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. Connect with us at LinkedIn Contact Us Shruti Thakur [email protected] +1(919)321-6187 Logo: SOURCE DelveInsight Business Research, LLP

临床1期孤儿药快速通道临床2期引进/卖出

2022-08-13

·药时代

【收藏】深度梳理国内外抗肥胖药物管线

‍‍正文共： 6000字 8图预计阅读时间： 8分钟来源：药渡撰文：杨哲编辑：丸子前段时间，饶毅与BGI于烨的“伪科学”之战再一次引发大众热议。也将“益生菌”产品推上了风口浪尖。与健康、减肥相挂钩的益生菌产品在近两年格外的火爆，反映了我国国内减肥药市场的庞大。根据《中国居民营养与慢性病状况报告（2020）年》与弗若斯特沙利文统计数据：中国成年居民的超重或肥胖人群占比已达50.7%，中国肥胖人口总数量预计在 2030 年达到 3.3 亿人。随着居民健康意识的提高，人们对于体重管理的需求也在不断增加。而我国抗肥胖药物（anti-obesity medications, AOMs）产业却处在十分尴尬的境地。目前我国CFDA批准上市的抗肥胖药物仅有奥利司它一款产品。国内生产奥利司他的厂商众多（图1），同质化竞争严重。同时奥利司他作为一种强效胰脂肪酶抑制剂，不良反应较多，减肥效果并不显著。随着国家对AOMs相关政策的放开，市场急需新型AOMs药物的入场。本文将对目前国内外主流抗肥胖药物产品管线及入局公司进行简要梳理。图1：国内奥利司他药物上市产品（来源：CFDA官网）1国外抗肥胖药物主要管线国外抗肥胖药物的发展较早，政策较为宽松。截至2021年，除奥利司他外，FDA还批准了其余6款具有抗肥胖功能的药物。但出于安全性及成熟性考虑，目前这些药物均未在中国获批用于抗肥胖治疗，6款AOMs药物列表整理如下：表1：目前FDA批准上市的减肥药物及其存在风险目前已上市的减肥药物均以抑制中枢神经食欲为主要方式。然而部分药物作用具体机理未知，药物安全性成问题，这也是目前国家迟迟不批准新的AOMs药物入局的根本原因。但随着部分药物使用的长期安全性得到验证以及全国肥胖人口的增多，目前我国的相关政策正在逐步放宽。其中，诺和诺德旗下的GLP-1受体激动剂系列药物最有希望突出重围。根据2021年柳叶刀杂志对目前已上市减肥药物临床试验数据的分析可知，芬特明-托吡酯（phentermine–topiramate）是目前上市药物中最有效的减肥药（体重减轻≥5%的优势比[OR] 8.02, 95% CI 5.24-12.27；体重减轻百分比的平均差[MD] -7.97, 95% CI -9.28~-6.66），其次是GLP-1受体激动剂（[OR] 6.33, 95% CI 5.0-8.0; [MD] -5.76, 95% CI -6.3~-5.21），但GLP-1受体激动剂相对芬特明-托吡酯诱发严重不良反应的几率更低，这证实了GLP-1受体激动剂在抗肥胖药物应用领域的强发展潜力。除上述成熟的抗肥胖药物产品外，目前国外药企也在迅速布局涵盖GLP-1受体激动剂在内的多种新型抗肥胖及减重产品，其主要入局公司如下：1Novo Nordisk目前诺和诺德主要还是围绕GLP-1受体激动剂进行抗肥胖药物开发，意在攻克GLP-1受体激动剂药物的长效性壁垒。其官网数据显示，目前诺和诺德共有四条AOMs管线处于临床开发阶段，如下图所示（图2）：图2：诺和诺德AOMs管线分布（来源：诺和诺德官网）Cagrisema及LA-GDF15均为长效GLP-1类似物。Cagrisema为长效amylin（胰淀素）类似物cagrilintide和长效GLP-1受体激动剂司美格鲁肽的双重复合制剂。其中，司美格鲁肽是目前诺和诺德公司的降糖王牌产品之一，仅2022年第一季度营业额便达到18.29亿美元。将其与cagrilintide这一能促进饱腹感的长效胰淀素类似物共同应用，意在加强司美格鲁肽的减重效果。目前该药物处于临床I期开发阶段，效果值得期待。CDE数据显示，诺和诺德于今年6月10日递交了Cagrisema国内临床试验申请，国内市场野心巨大。Oral Sema Obesity为口服型司美格鲁肽，也属于GLP-1受体激动剂，主要是改善司美格鲁肽注射剂患者依从性不好的缺陷。事实上，司美格鲁肽对于肥胖患者减重的实验结果十分惊艳。18年发表在柳叶刀杂志上的II期大规模实验结果显示，在受试的957名患者中， 0.1-0.4mg/天的司美格鲁肽注射量治疗组与安慰剂治疗组相比，受试者体重均产生了显著下降，减重效果强于0.3mg/天注射的利拉鲁肽治疗组。在第52周，司美格鲁肽0.4mg/天治疗组患者平均体重下降了16.3%（图3），且所有受试者均未产生任何不良反应。司美格鲁肽口服剂型的开发更利于其在抗肥胖药物市场的应用，真正做到“无痛减肥”，市场前景巨大。据悉，诺和诺德将在今年内于国内提交Oral Sema Obesity的上市申请。目前辉瑞制药也有口服小分子GLP-1受体激动剂药物正处于临床II期阶段。图3：司美格鲁肽的减重效果（来源：诺和诺德官网）除了GLP-1受体激动剂系列产品外，诺和诺德也布局了肽酪氨酸酪氨酸（PYY）类似物的药物管线开发，即PYY1875。肽酪氨酸酪氨酸（PYY）是神经肽Y（NPY）家族的成员，可抑制中枢神经，减少食欲，从而达到减轻体重的效果。PYY1875的安全性良好，目前已进入II期临床阶段。2Eli Lily GLP-1图4：礼来官网中对Trizepatide的报道在礼来官网最显著的位置，标注着Trizepatide三期临床的惊人效果。受试的的2539名志愿者在经过72周的治疗后，服用Trizepatide 5mg，10mg，15mg及安慰剂的患者体重分别下降了原始体重的16%，21.4%，22.5%及3.1%。在15mg Trizepatide治疗组中，有人在经历72周Trizepatide的治疗后体重竟减少了24千克，且无任何强烈的不良反应。Trizepatide的优异成效使其成为了目前抗肥胖药物市场的明日之星。Trizepatide是一种同时具有GIP（葡萄糖依赖性促胰岛素多肽）受体和GLP-1（胰高血糖素样肽-1）受体激动效果的新型药物。礼来利用将两种肠促胰岛素的作用整合到一个新的分子中的策略，补充了GLP-1受体激动剂作用效果，达到了1+1>2的惊艳疗效。与此同时，礼来更是借着Trizepatide的东风开启了肥胖患者关爱计划，意图深耕抗肥胖药物市场。目前礼来除了Trizepatide还在同时开发的AOMs临床管线如下图所示（图5）：图5：礼来的AOMs研发管线（来源：礼来官网）目前礼来处于I期临床的产品是一种长效胰淀素类似物。处于II期临床的GGG Tri-Agonist则是在Trizepatide的基础上，开发出的一种能同时激动GIP,GLP,GLP-1受体的三重激动剂，希望达到1+1+1>3的效果，重现Trizepatide的成功。同样处于II期开发阶段的GLP-1 Receptor NPA产品则是礼来最新研发的的化学小分子GLP-1受体激动剂。它能跨过大分子药物的吸收和代谢壁垒，适用于后期开发的更多剂型，如缓释制剂等等，有望解决目前GLP-1受体激动剂大多半衰期短的瓶颈，其临床结果同样值得期待。3韩美制药韩美制药是韩国的第一大制药公司，目前其在减肥药物研发方面有一款药物正处于临床前研发阶段，名为HM15136。HM15136是一种长效胰高血糖素类似物，通过非肽基柔性连接物（LAPSCOVERY）与人免疫球蛋白恒定区化学结合增强其体内半衰期。其利用的是胰高血糖素受体兴奋的生理效应（抑制食物摄入、增加能量消耗和改善脂质代谢）。在临床前研究中，观察到该药物显著的减肥效果和改善血脂状况。其具体原理如图6所示：图6：HM15136治疗肥胖的简要机理（来源：韩美制药官网）4Versanis bioVersanis bio是一家诺华背景的公司，于2021年成立，主攻肥胖治疗方向，其主要管线产品为Bimagrumab。Bimagrumab是一种独特的单抗，能靶向激活素II型受体（ActRII），通过与相关受体的结合，阻断包括激活素A和肌生长抑制素在内的激素的作用，刺激骨骼肌生长。在临床前实验中发现，Bimagrumab可以促进褐色脂肪细胞的分化和活性，促进机体燃烧能量。其机理可简要概括成在增肌的同时，完成了脂肪细胞的转化，是理想中的减肥产品。目前该产品已进入了II期临床阶段，在对于569名非糖尿病患者的随机临床试验中，最高剂量治疗组在24周减掉了14.6%的纯脂肪重量，在48周减掉了20.5%的纯脂肪重量，且肌肉重量增加了3.6%，而安慰剂组各项指标基本不变。该临床实验结果是十分惊人的，真正做到了只减脂肪并增加肌肉的效果，期待后续临床结果的披露。2国内抗肥胖药物主要管线相比于国外抗肥胖药物研究的繁荣，目前国内制药企业在AOMs领域主要集中于GLP-1受体激动剂药物的开发，尤其是在利拉鲁肽核心专利到期（化合物专利2017年已到期，晶体专利2022年到期），2022年1月21日CDE发布了《利拉鲁肽用于体重管理的临床试验设计指导原则》后，以华东医药为首的各国内厂商快速挤入利拉鲁肽仿制药及多靶点GLP-1受体激动剂药物研究赛道。1华东医药从华东医药官网上披露的其内分泌及肥胖药物研发管线中不难看出其对于GLP-1受体激动剂药物的前瞻性布局（图7）。其直接对标诺和诺德Saxenda的仿制药物利拉鲁肽注射液一骑绝尘，2022年第二季度便进入了上市申请阶段，有望成为国内第一家GLP-1受体激动剂抗肥胖药物的吃螃蟹玩家。同时其GLP-1相关创新性药物也层出不穷，TTP273作为全球创新小分子GLP-1受体激动剂，走的是First-in-class药物快速审批通道，已于2022年1季度完成II期临床试验的末例受试者出组。DR10624作为GLP-1R/GCGR/FGF21R靶点的多重激动剂，可用于2型糖尿病、肥胖和代谢综合征等疾病的治疗，已于2022年4月获批在新西兰开展I期临床试验。与此同时，由于诺和诺德司美格鲁肽的核心专利将于2026年到期，华东医药迅速布局了司美格鲁肽仿制药的临床试验申请，目前其IND已于2022年4月获得受理。华东医药在抗肥胖药物的产业布局之深可见一斑，是我国当之无愧的抗肥胖药物研发“卷中之王”。图7：华东医药内分泌及减肥药物研发管线（来源：华东医药官网）2爱美客截止2022年08月11日收盘，爱美客（300896）收盘价579.00元，可谓是中国的医美第一股，可看出投资者们对于中国大健康及医美市场的极高信心。从光大证券对爱美客的企业分析报告中可以了解到，目前爱美客在抗肥胖药物领域主要有布局有两款产品，一款是诺和诺德利拉鲁肽的仿制药，目前已经进入了I期临床阶段，一款是溶脂针产品去氧胆酸。去氧胆酸可溶解局部的脂肪细胞膜，导致脂肪细胞分解，从而达到去除脂肪的目的。目前全球范围内，已上市的去氧胆酸溶脂药物只有艾尔建旗下的 Kybella ，且适应症被严格限定于去除颏下脂肪（双下巴）。该款产品在 2015 年被 FDA 批准。当前，国内在研的溶脂针产品的企业仅有爱美客，科笛生物及南京诺瑞特生物三家。爱美客的溶脂针产品预计于2023年进入临床试验阶段。3上海仁会仁会生物的官网近日发布了其创新药贝那鲁肽的真实世界临床研究数据，其减重效果尤为振奋人心。贝那鲁肽是中国糖尿病领域第一个创新药，也是国内首个拥有自主知识产权的 GLP-1 受体激动剂，于 2017 年上市。对中国两家医院（唐山市迁安燕山医院、秦皇岛市中医医院）的 314 例 T2DM 患者数据进行分析，贝那鲁肽治疗3个月后患者体重平均降低10.05kg（图8），HbA1c 平均降低 2.87%。作为完全我国自研的创新药，其具备和人体完全同源的氨基酸序列，更加适合国人体质。贝那鲁肽已被收录入《中国II型糖尿病防治指南（2017年版）》中。作为临床常用GLP-1受体激动剂制剂，有望超过利拉鲁肽，成为国产减肥药物的后来居上者。目前其治疗肥胖适应症的临床试验已经进行到临床III期，药渡将关注其是否会在后期对贝那鲁肽进行长效性和口服制剂的开发。图8：贝那鲁肽的减重效果（来源：上海仁会生物官网）4恒瑞医药/信达生物/东阳光GLP-1受体激动剂等抗肥胖药物的火爆及国家政策的放开使得国内制药巨头们也加入抗肥胖药物研发大军。目前恒瑞医药，信达生物，东阳光均有一款GLP-1受体激动剂自研创新药进入临床阶段。恒瑞医药的诺利糖肽（HS-20004）目前已经进入了II期临床阶段，是一款经棕榈酸修饰的GLP-1类似物。通过氨基酸序列的改造，诺利糖肽既保证了生物学活性，又增强了抵抗DPP-IV酶解的能力。诺利糖肽结构中的棕榈酸还会与血清蛋白结合，延长其体内半衰期，达到长效作用的效果。而信达生物则选择了和礼来Trizepatide 1+1策略的相似研发方案，其GLP-1R/胰高血糖素受体（GCGR）双重激动剂mazdutide (研发代号：IBI362)目前也进入了II期临床。东阳光则是在寻找减肥新靶点的道路上另辟蹊径，其创新药物HEC88473是国内首个获批临床的GLP-1/FGF21双重激动剂，FGF21在与其体内受体结合后，能促进体细胞的脂肪酸代谢以及胰岛素敏感性，目前位于I期临床阶段。5甘李药业对于中国糖尿病患者来说，甘李药业绝不陌生。甘李药业于1998 年成立，是国内首家掌握产业化生产重组胰岛素类似物技术的企业，深耕于国内糖尿病胰岛素领域。甘李药业是国内首家实现三代胰岛素生产的糖尿病头部企业，突破了三代胰岛素由外企垄断的国内尴尬局面，据CDE官网数据显示，目前三代胰岛素中的门冬胰岛素仅有甘李药业一家国产企业于2020年获批上市。GLP-1受体激动剂药物的发现发展与糖尿病治疗密不可分，其研发初始治疗方向便是II型糖尿病。因此，深耕于糖尿病治疗领域的甘李药业也早早布局了GLP-1受体激动剂药物。其自主研发的长效GLP-1受体激动剂GZR18目前也进入了I期临床阶段，并已完成了首例受试者给药，预计给药每周一次。作为糖尿病治疗领域研发头部企业，手握中国众多糖尿病患者一手数据，其能否在GLP-1受体激动剂药物与胰岛素联合用药治疗肥胖的方案上做出新的尝试，为肥胖治疗提出国产化联合用药方案，突出重围，药渡将持续关注。3结语中国的减肥药物产业在经过了长久的沉寂之后，众多制药企业纷纷入局，究竟谁能脱颖而出，吃下国产减肥药物的第一口螃蟹，值得期待。而减肥药物的市场在GLP-1受体激动剂药物火爆之后，能否在肠脑轴，基因治疗，肠道菌群等研究中发现新的治疗靶点，则是众多研发者和制药企业们值得深思的方向。参考文献：1.Shi Qingyang,Wang Yang,Hao Qiukui et al. Pharmacotherapy for adults with overweight and obesity: a systematic review and network meta-analysis of randomised controlled trials.[J] .Lancet, 2022, 399: 259-269.2.Müller Timo D,Blüher Matthias,Tschöp Matthias H et al. Anti-obesity drug discovery: advances and challenges.[J] .Nat Rev Drug Discov, 2022, 21: 201-223.3.O'Leary Karen,An anti-obesity drug from the diabetes toolbox.[J] .Nat Med, 2022, 4.Geng Leiluo,Lam Karen S L,Xu Aimin,The therapeutic potential of FGF21 in metabolic diseases: from bench to clinic.[J] .Nat Rev Endocrinol, 2020, 16: 654-667.5.O'Neil Patrick M,Birkenfeld Andreas L,McGowan Barbara et al. Efficacy and safety of semaglutide compared with liraglutide and placebo for weight loss in patients with obesity: a randomised, double-blind, placebo and active controlled, dose-ranging, phase 2 trial.[J] .Lancet, 2018, 392: 637-649.6.光大证券，2022，《爱美客（300896）投资价值分析报告：医美赛道长期主义的践行者》。【备注】原文题目：不只奥利司他！深度梳理国内外抗肥胖药物管线版权声明/免责声明本文为授权转载文章，版权归拥有者。仅供感兴趣的个人谨慎参考，非商用，非医用、非投资用。欢迎朋友们批评指正！衷心感谢！文中图片、视频为授权正版作品，或来自微信公共图片库，或取自公司官网/网络根据CC0协议使用，版权归拥有者。任何问题，请与我们联系（电话：13651980212。微信：27674131。邮箱：contact@drugtimes.cn）。衷心感谢！推荐阅读又一个首款！FDA加快批准Enhertu（DS-8201）治疗HER2突变非小细胞肺癌患者药企们的「过冬」策略，裁员不尽兴，他还要收租...Aβ假说“被锤”后，离开4年的默沙东又被勾回来，买了一个连靶点都不知道的产品...54亿美金，买！歇了不到3个月的辉瑞，又开始溢价收购了...104家中国新药企业扬帆出海！ADC赛道喜讯频传！科伦博泰势头赶超老大哥石药 | 药时代出海系列对话RNA靶向新兴企业施能康（SynerK）：从Alnylam公司APOLLO-B的成功看RNAi药物的研发提前4个月！FDA批准ADC药物Enhertu（DS-8201）用于治疗「HER2低表达」乳腺癌患者，市场有望扩大5倍！接连7款药物试验失败！新药研发既要有毅力，更要有「及时止损」的智慧万字长文：从理论到生产，一文读懂mRNA-LNP制剂技术药时代第111期直播笔记 | 欧美儿童药物开发相关的法规和指导原则2022上半年成绩单出炉！勃林格殷格翰保持稳健增长，夯实研发管线！点击这里，欢聚药时代！

仿制药创新药小分子药物信使RNA专利到期

2022-06-14

·BioSpace

VectivBio Announces Launch of Public Offering of Ordinary Shares - June 14, 2022

BASEL, Switzerland, June 14, 2022 (GLOBE NEWSWIRE) -- VectivBio Holding AG (“VectivBio”) (Nasdaq: VECT), a clinical-stage biopharmaceutical company pioneering novel transformational treatments for severe rare conditions, today announced the launch of a follow-on public offering of its ordinary shares. In addition, VectivBio expects to grant the underwriters a 30-day option to purchase up to an additional 15% of the ordinary shares to be sold in the offering on the same terms and conditions. The offering is subject to market and other conditions, and there can be no assurance as to whether or when the offering may be completed. All of the ordinary shares in the offering are to be sold by VectivBio. Also today, VectivBio entered into an agreement with Forbion Growth Opportunities Fund II Coöperatief U.A., represented by Forbion Growth II Management B.V. ("Forbion") pursuant to which VectivBio has agreed to sell 3,478,260 ordinary shares to Forbion at the price of $5.75 per ordinary share, for gross proceeds of approximately $20 million, in a private placement transaction that is expected to close concurrently with the public offering. The sale of these ordinary shares will not be registered under the Securities Act of 1933, as amended. The closing of the private placement transaction is not contingent on any public offering. VectivBio intends to use the net proceeds from the public offering and concurrent private placement, together with its existing cash and cash equivalents, available for sale and short-term deposits: to fund (i) clinical development and pre-commercialization activities for its lead product candidate and (ii) general corporate purposes, including general and administrative expenses and working capital. SVB Securities and Piper Sandler are acting as joint book-running managers for the public offering. LifeSci Capital is acting as a co-manager for the public offering. A registration statement relating to these securities has been filed with the U.S. Securities and Exchange Commission on Form F-3 (File No. 333-264653) and declared effective on May 12, 2022. The public offering will be made only by means of a prospectus supplement. Copies of the preliminary prospectus supplement and the accompanying prospectus related to the public offering may be obtained, when available, from: SVB Securities LLC, Attention: Syndicate Department, 53 State Street, 40th Floor, Boston, MA 02109, or by telephone at (800) 8-8-7525, ext. 6105, or by email at syndicate@svbsecurities.com; Piper Sandler & Co., Attention: Prospectus Department, 800 Nicollet Mall, J12S03, Minneapolis, Minnesota 55402, or by telephone at (800) 747-3924, or by email at prospectus@psc.com; or by accessing the U.S. Securities and Exchange Commission’s website at This press release shall not constitute an offer to sell or the solicitation of an offer to buy these securities, nor shall there be any sale of these securities, in any state or jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction. The ordinary shares offered in the concurrent private placement have not been registered under the Securities Act of 1933, as amended, and may not be offered or sold in the United States except pursuant to an effective registration statement or an applicable exemption from the registration requirements. About VectivBio AG VectivBio is a global clinical-stage biotechnology company focused on transforming and improving the lives of patients with severe rare conditions. Lead product candidate apraglutide is a next-generation, long-acting synthetic GLP-2 analog being developed for a range of rare gastrointestinal diseases where GLP-2 can play a central role in addressing disease pathophysiology, including short bowel syndrome with intestinal failure (SBS-IF) and Acute Graft-Versus-Host Disease (aGVHD). VectivBio is also advancing its modular, small molecule CoMET platform to address a broad range of previously undruggable Inherited Metabolic Diseases (IMDs). CoMET leverages innovative chemistry, based on a proprietary stabilized pantetheine backbone, to restore fundamental cellular metabolism in pediatric populations with IMDs characterized by a deficit of energy metabolism caused by the depletion of functional Coenzyme A (“CoA”). Candidates from the CoMET platform are initially being evaluated in methylmalonic acidemia (MMA), propionic acidemia (PA), and other organic acidimias. Forward Looking Statements Forward-looking statements are statements that are not historical facts. Words and phrases such as “anticipated,” “forward,” “will,” “would,” “may,” “remain,” “potential,” “prepare,” “expected,” “believe,” “plan,” “near future,” “belief,” “guidance,” and similar expressions are intended to identify forward-looking statements. These statements include, but are not limited to, whether VectivBio will offer the ordinary shares or consummate the offering and the concurrent private placement, the timing, size and use of proceeds of the public offering and concurrent private placement described herein, and its expectations with respect to granting the underwriters a 30-day option to purchase additional ordinary shares. All of such statements are subject to risks and uncertainties, and assumptions, including those that are described in the Risk Factor sections of the preliminary prospectus supplement for such offering to be filed with the U.S. Securities and Exchange Commission (the “SEC”), and the documents incorporated by reference therein, including without limitation those risks and uncertainties identified in the “Risk Factors” section of VectivBio’s Registration Statement on Form F-3 declared effective by the SEC on May 12, 2022, the accompanying prospectus, VectivBio’s Annual Report on Form 20-F filed with the SEC on April 7, 2022, and other filings that VectivBio makes with the SEC from time to time. All forward-looking statements contained in this press release speak only as of the date on which they were made. Except to the extent required by law, VectivBio undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made. VectivBio Contacts: Patrick Malloy VectivBio SVP, Investor Relations and Strategic Communications Patrick.malloy@vectivbio.com

合作小分子药物

100 项与 Efpegerglucagon 相关的药物交易

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研发状态

10 条进展最快的记录,

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适应症	最高研发状态	国家/地区	公司	日期
先天性高胰岛素血症	临床2期	美国	Hanmi Pharmaceutical Co., Ltd.	2021-10-28
先天性高胰岛素血症	临床2期	德国	Hanmi Pharmaceutical Co., Ltd.	2021-10-28
先天性高胰岛素血症	临床2期	以色列	Hanmi Pharmaceutical Co., Ltd.	2021-10-28
先天性高胰岛素血症	临床2期	英国	Hanmi Pharmaceutical Co., Ltd.	2021-10-28
2型糖尿病	临床1期	美国	Hanmi Pharmaceutical Co., Ltd.	2019-08-30
肥胖	临床1期	美国	Hanmi Pharmaceutical Co., Ltd.	2019-08-30

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临床结果

适应症

分期

评价

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研究	分期	人群特征	评价人数	分组	结果	评价	发布日期


EASD2022	N/A	代谢性疾病	-	HM15136	製醖膚窪齋壓艱網範簾(廠積獵糧夢鹹築積簾製) = 遞夢夢膚鏇製廠夢鑰遞簾遞鬱製憲網製遞衊範 (鹹範壓網鬱獵憲願艱網 ) 更多	-	2022-09-21
EASD2021	N/A	代谢性疾病	-	Efpeglenatide	鏇艱顧築壓餘夢鬱顧糧(鑰窪壓鬱壓齋憲鏇願鹹) = 夢願鹹憲齋遞淵鏇鏇範膚積選願網襯網壓觸獵 (簾簾鑰憲壓積餘願餘餘 ) 更多	-	2021-09-29
EASD2021	N/A	代谢性疾病	-	HM15136	鏇艱顧築壓餘夢鬱顧糧(鑰窪壓鬱壓齋憲鏇願鹹) = 積醖簾鬱鹽衊鹽壓齋艱膚積選願網襯網壓觸獵 (簾簾鑰憲壓積餘願餘餘 ) 更多	-	2021-09-29
ADA2021	N/A	代谢性疾病	-	HM15136	遞鏇繭廠網鹽廠獵壓遞(鹽顧積鏇簾淵範網築繭) = 選醖網壓遞憲製鏇糧憲願顧餘餘糧廠顧願遞選 (鹹簾膚夢淵襯積簾衊憲 ) 更多	-	2021-06-01
EASD2020	N/A	肥胖	-	HM15136	夢觸築壓構獵淵鹽淵餘(衊觸構艱顧夢膚壓繭壓) = 構衊餘衊襯齋遞淵夢繭蓋膚鑰壓蓋願壓選鹹製 (積衊願醖獵鑰艱築夢蓋 )	-	2020-09-23
EASD2020	N/A	肥胖	-	GLP-1RAs (liraglutide, dulaglutide, semaglutide)	夢觸築壓構獵淵鹽淵餘(衊觸構艱顧夢膚壓繭壓) = 築糧艱鹹範製衊遞憲選蓋膚鑰壓蓋願壓選鹹製 (積衊願醖獵鑰艱築夢蓋 )	-	2020-09-23
EASD2020	N/A	肥胖 \| 代谢性疾病	-	HM15136	廠襯築襯選蓋糧鑰蓋糧(繭遞壓餘壓築壓積鏇築) = 選鑰淵廠網顧鬱鑰醖廠艱構網憲齋鹹鹹獵鑰鹹 (窪築築淵糧鏇鑰築蓋顧 ) 更多	-	2020-09-23
ADA2020	N/A	-	-	HM15136	製艱蓋鏇獵範壓餘淵網(糧膚蓋衊鏇艱憲齋齋鬱) = 廠窪壓鹹壓艱鑰齋網製獵觸膚糧願艱蓋獵繭簾 (製蓋築繭膚獵夢醖鬱艱 ) 更多	-	2020-06-01
ADA2020	N/A	-	-	Placebo	製艱蓋鏇獵範壓餘淵網(糧膚蓋衊鏇艱憲齋齋鬱) = 觸簾壓選糧鏇廠鹽積構獵觸膚糧願艱蓋獵繭簾 (製蓋築繭膚獵夢醖鬱艱 ) 更多	-	2020-06-01
EASD2019	N/A	肥胖	-	HM15136	選淵積簾餘鏇窪醖醖構(憲齋壓顧齋衊鏇憲鹽遞) = 觸積網衊構觸構鏇築壓鏇壓鬱蓋獵鑰觸繭製願 (範選鑰鑰鬱夢蓋蓋窪簾 ) 更多	-	2019-09-17
EASD2019	N/A	胰岛素抵抗 HbA1c \| HOMA-IR \| FGF21 ... 更多	-	HM15136	憲膚選糧觸鬱鏇齋餘憲(鏇製衊遞夢製繭願選淵) = an initial BG elevation was rapidly normalized and maintained normal thereafter with no HbA1c increase (3.4±0.08 and 3.7±0.09% for Veh and HM15136) 齋艱製繭製餘簾遞糧觸 (鏇窪願憲選衊鹽襯鏇鹽 )	积极	2019-09-17