The Phase I study of ASC30 once-monthly subcutaneous injection is a randomized, double-blind, placebo-controlled, single ascending dose (5 cohorts) study to evaluate the safety, tolerability, PK and efficacy of ASC30 in participants with obesity over 16 weeks
Latest Information Update: 24 Sep 2024
At a glance
- Drugs ASC 30 (Primary)
- Indications Obesity
- Focus Adverse reactions; Pharmacokinetics; Therapeutic Use
- 24 Sep 2024 New trial record
- 17 Sep 2024 According to Ascletis media release, the Company expects topline data from the study in the first quarter of 2025.
- 17 Sep 2024 Results from cohort 1 (n=2 ) presented in an Ascletis media release.