A Phase 1, Randomized, Placebo-controlled, Investigator and Participant Blinded, Single-ascending Dose and Multiple-ascending Dose Study to Evaluate Safety, Tolerability, and Pharmacokinetics of LY4005130 in Healthy Participants
Latest Information Update: 13 Nov 2025
At a glance
- Drugs LY 4005130 (Primary) ; LY 4005130 (Primary)
- Indications Unspecified
- Focus Adverse reactions
- Acronyms FPAB
- Sponsors Eli Lilly and Company
Most Recent Events
- 10 Nov 2025 Planned number of patients changed from 140 to 118.
- 10 Nov 2025 Planned End Date changed from 1 Jan 2026 to 1 Apr 2026.
- 10 Nov 2025 Planned primary completion date changed from 1 Jan 2026 to 1 Apr 2026.