A Phase 1, Randomized, Double-blind, Placebo-controlled, Integrated Single Ascending Dose, Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AMG 691 in Healthy Participants and Participants With Mild-to-Moderate Asthma
Latest Information Update: 21 Jun 2025
At a glance
- Drugs AMG 691 (Primary)
- Indications Asthma
- Focus Adverse reactions
- Sponsors Amgen
Most Recent Events
- 13 Jun 2025 Planned End Date changed from 3 Aug 2026 to 24 Sep 2026.
- 13 Jun 2025 Planned primary completion date changed from 23 Mar 2026 to 13 Aug 2026.
- 08 Jun 2025 Timeframe for primary endpoint changed from aprx 7 months to aprx 8 months.