drugset / Trial / NCT07238647

A Trial of HRS-5817 in Obese Participants

NCT07238647 ↗

Phase 0 Active not recruiting 40 enrolled Atridia Pty Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess safety, PK, Pharmacodynamic and immunogenicity profile of a single dose of HRS-5817 in obese participants

Timeline

Start
2026-01-05
Primary completion
2027-01-30
Completion
2027-01-30

Drugs

EvaluationDrugModalityDoseRoute
Subject HRS-5817 Unknown — Subcutaneous

Indications