drugset / Trial / NCT07184502

Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of ZT003 Injection Following Single and Multiple Subcutaneous Administration in Healthy Volunteers/Overweight or Obese Volunteers

NCT07184502 ↗

Phase 1 Recruiting 76 enrolled Beijing QL Biopharmaceutical Co.,Ltd
RandomizedSequentialQuadruple-blindTreatment

Summary

This is a Phase 1, randomized, double-blind, placebo-controlled, single-center study designed to evaluate the safety, tolerability, and pharmacokinetics of ZT003 following subcutaneous administration in healthy adult participants. The study includes both single ascending dose (SAD) and multiple ascending dose (MAD) parts.

Timeline

Start
2025-10-16
Primary completion
2026-06-06
Completion
2026-10-10

Drugs

EvaluationDrugModalityDoseRoute
Subject ZT003 Unknown — Subcutaneous

Indications

No indication recorded.