A DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, SINGLE AND MULTIPLE ASCENDING DOSE PHASE 1 STUDY TO INVESTIGATE THE SAFETY, TOLERABILITY, PHARMACOKINETIC, AND PHARMACODYNAMIC PROFILE OF RES-010 IN HEALTHY, OVERWEIGHT, AND MODERATELY OBESE SUBJECTS
Latest Information Update: 04 Dec 2024
At a glance
- Drugs RES-010 (Primary)
- Indications Obesity
- Focus Adverse reactions; First in man
- Sponsors Resalis Therapeutics
Most Recent Events
- 04 Dec 2024 Status changed from planning to recruiting.
- 03 Dec 2024 According to a Resalis Therapeutics media release, company will share data from the combined SAD/MAD study, which involves multiple phases of dose escalation and extensive safety evaluation, are expected by mid-2026.
- 04 Jan 2024 According to a Resalis Therapeutics media release, company plans to initiate this Phase 1 clinical study evaluating the safety and efficacy of RES-010 in the first half of 2024.