A Randomized, Phase 2, Double-blind, Placebo-controlled, Parallel-group, 2-arm Study to Investigate the Efficacy, Safety, and Tolerability of Subcutaneous Lunsekimig (SAR443765) in Adult Participants With High-risk Asthma Who Are Not Currently Eligible for Biologic Treatment
Latest Information Update: 16 Feb 2026
At a glance
- Drugs Lunsekimig (Primary)
- Indications Asthma
- Focus Therapeutic Use
- Acronyms AIRLYMPUS
- Sponsors Sanofi
Most Recent Events
- 22 Jan 2026 Planned number of patients changed from 1000 to 1147.
- 13 Jan 2026 Planned End Date changed from 12 Nov 2027 to 15 Oct 2027.
- 13 Jan 2026 Planned primary completion date changed from 12 Oct 2027 to 17 Sep 2027.