A Single-Ascending and Repeated Subcutaneous Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3849891 in Participants With Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) Who Have the PNPLA3 I148M Genotype
Latest Information Update: 23 May 2025
At a glance
- Drugs LY 3849891 (Primary)
- Indications Non-alcoholic fatty liver disease
- Focus Adverse reactions; Pharmacodynamics
- Sponsors Eli Lilly and Company
Most Recent Events
- 03 Mar 2025 Planned End Date changed from 1 Sep 2026 to 1 Oct 2026.
- 03 Mar 2025 Planned primary completion date changed from 1 Sep 2026 to 1 Oct 2026.
- 03 Dec 2024 Planned End Date changed from 1 Dec 2025 to 1 Sep 2026.