drugset / Trial / NCT06732154

A Phase I Clinical Study of a Single Subcutaneous Injection of HRS-5632 in Healthy Subjects

NCT06732154 ↗

Phase 1 Completed 50 enrolled Fujian Shengdi Pharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The study is being conducted to evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of HRS-5632 Following a Single Subcutaneous Injection in Healthy Subjects

Timeline

Start
2024-12-02
Primary completion
2026-03-02
Completion
2026-03-02

Drugs

EvaluationDrugModalityDoseRoute
Subject HRS-5632 Unknown — Subcutaneous

Indications