drugset / Trial / NCT06714955

Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of BGM0504 Injection in Non-diabetic Overweight or Obese Adult Subjects

NCT06714955

Phase 1 Completed 30 enrolled BrightGene Bio-Medical Technology Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a Phase 1, double-blind, parallel-arm ,placebo-controlled study. The study will evaluate the pharmacokinetics (PK), pharmacodynamic (PD), safety and tolerability of BGM0504 following multiple subcutaneous (SC) administrations in non-diabetic overweight or obese adult subjects.

Timeline

Start
2024-10-21
Primary completion
2025-01-21
Completion
2025-03-03

Drugs

EvaluationDrugModalityDoseRoute
Subject BGM0504 Unknown 10 mg Subcutaneous
Subject BGM0504 Unknown 15 mg Subcutaneous

Indications

No indication recorded.