A Phase 1, Multicenter, Randomized, Placebo-Controlled, Double-Blind Trial of LY3885125 to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of a Single Ascending Dose in Participants with Dyslipidemia and Repeat-Doses in Participants with NAFLD
Latest Information Update: 13 Mar 2025
At a glance
- Drugs LY 3885125 (Primary)
- Indications Dyslipidaemias; Non-alcoholic fatty liver disease
- Focus Adverse reactions
- Sponsors Eli Lilly and Company
- 06 Mar 2025 Status changed from active, no longer recruiting to discontinued as participants were not dosed in Part B as per the protocol, the patient population will be refined and new outcome measures will be applied in a separate study.
- 20 Dec 2024 Status changed from recruiting to active, no longer recruiting.
- 26 Jun 2024 Planned End Date changed from 15 Apr 2025 to 1 Apr 2025.