drugset / Trial / NCT06547775
A Study to Evaluate Features of KN069 in Participants With Obesity or Overweight
RandomizedSequentialQuadruple-blindTreatment
Summary
This is a Phase 1, First-in-human, double-blinded, placebo-controlled study which aims to investigate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and the immunogenicity of KN069 in Chinese male participants with Obesity or Overweight.
Timeline
- Start
- 2024-08-02
- Primary completion
- 2027-04-30
- Completion
- 2027-06-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | KN069 | Unknown | 12 mg | Subcutaneous |
| Subject | KN069 | Unknown | 30 mg | Subcutaneous |
| Subject | KN069 | Unknown | 60 mg | Subcutaneous |
| Subject | KN069 | Unknown | 120 mg | Subcutaneous |
| Subject | KN069 | Unknown | 240 mg | Subcutaneous |