drugset / Trial / NCT06760455

A Safety and Tolerability Study of BPR-30221616 Injection in Healthy Subjects

NCT06760455 ↗

Phase 1 Recruiting 48 enrolled Chengdu Brilliant Pharmaceutical Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to determine the safety, tolerability, pharmacokinetics、 pharmacodynamics and immunogenicity of BPR-30221616 in healthy subjects.

Timeline

Start
2025-01-10
Primary completion
2026-01-24
Completion
2026-12-05

Drugs

EvaluationDrugModalityDoseRoute
Subject BPR-30221616 Unknown — Subcutaneous

Indications

No indication recorded.