Trials / Recruiting
RecruitingNCT07072195
A Study of AMC6156 in People With Sarcopenia
A Multicenter, Randomized, Double-Blind, Placebo-controlled, Phase 2 Clinical Trial to Evaluate the Efficacy and Safety of AMC6156 in Patients With Sarcopenia
- Status
- Recruiting
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 80 (estimated)
- Sponsor
- Animuscure Inc. · Industry
- Sex
- All
- Age
- 65 Years
- Healthy volunteers
- Not accepted
Summary
This clinical trial aims to find out whether AMC6156 can improve physical function and is safe in older adults with sarcopenia. Participants will take AMC6156 or a placebo daily for 12 weeks, and their movement, strength, and safety will be regularly monitored through tests and checkups.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | AMC6156 0.1mg | Oral administration of AMC6156 in tablet form at a dose of 0.1 mg once daily for 12 weeks. |
| DRUG | AMC6156 0.3mg | Oral administration of AMC6156 in tablet form at a dose of 0.3 mg once daily for 12 weeks. |
| DRUG | AMC6156 1.0mg | Oral administration of AMC6156 in tablet form at a dose of 1.0 mg once daily for 12 weeks. |
| DRUG | Placebo | Oral administration of placebo tablets matching AMC6156 in appearance, once daily for 12 weeks. |
Timeline
- Start date
- 2025-07-01
- Primary completion
- 2026-03-01
- Completion
- 2026-06-01
- First posted
- 2025-07-18
- Last updated
- 2025-07-29
Locations
4 sites across 1 country: South Korea
Source: ClinicalTrials.gov record NCT07072195. Inclusion in this directory is not an endorsement.