Clinical trial
A Two-part, Phase 2a Randomized, Part Parallel-group, Double-blind Placebo-controlled Cross-over Multi-center Study to Evaluate the Effect of Two Dose Levels of (S)-Pindolol Benzoate (ACM-001.1) on Lean Body Mass in Obese Patients During (PROACT 1), and Post-semaglutide Therapy (PROACT 2)
NCT07101939 is registered in ClinicalTrials.gov with Actimed Therapeutics Ltd as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Two-part, Phase 2a Randomized, Part Parallel-group, Double-blind Placebo-controlled Cross-over Multi-center Study to Evaluate the Effect of Two Dose Levels of (S)-Pindolol Benzoate (ACM-001.1) on Lean Body Mass in Obese Patients During (PROACT 1), and Post-semaglutide Therapy (PROACT 2)
- Lead sponsor
- Actimed Therapeutics Ltd
- Phase
- Phase 2
- Overall status
- Recruiting
- Start date
- June 23, 2025
- Completion date
- March 31, 2027
- Enrollment
- 120 (estimated)
- Sites
- 7
Conditions
As the registry lists them; a condition with its own page is linked.
muscle loss, obesity