Drug intelligence / Profile preview

olatorepatide

Development stage
Phase 3
Lead developer
Hansoh Pharmaceutical Group
Modality
Peptides
Administration
Subcutaneous
01

Overview

**Olatorepatide (HS-20094)** is a synthetic peptide dual agonist of the glucagon-like peptide 1 receptor (**GLP-1R**) and gastric inhibitory polypeptide receptor (**GIPR**), developed by **Jiangsu Hansoh Pharmaceutical Co., Ltd.** (Hansoh Pharma). Administered as a once-weekly subcutaneous injection, it promotes insulin secretion, slows gastric emptying, suppresses appetite, and reduces food intake, leading to glycemic control, weight loss, and metabolic improvements. Phase 2 trials in type 2 diabetes mellitus (**T2DM**) patients showed dose-dependent reductions in HbA1c, fasting glucose, and body weight (up to 4.8% at 15 mg), with good tolerability and primarily mild gastrointestinal adverse events; it outperformed placebo and showed advantages over semaglutide 1 mg in some measures. **Regeneron** in-licensed ex-China rights in 2025 for $80M upfront plus up to $1.93B milestones and low double-digit royalties.[1][2][3][6]

Other names
olatorepatide
02

Targets

GIPR (Gastric inhibitory polypeptide receptor)GLP1R (GLP-1R)

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