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: 21 Aug 2026
At a glance
- Drugs Lunsekimig (Primary)
- Indications Asthma
- Focus Therapeutic Use
- Acronyms AIRLYMPUS
- Sponsors Sanofi; Sanofi-Aventis Recherche & Developpement
Most Recent Events
- 01 Jul 2026 Planned End Date changed from 15 Oct 2027 to 19 Jul 2027.
- 01 Jul 2026 Planned primary completion date changed from 17 Sep 2027 to 21 Jun 2027.
- 01 Jul 2026 Status changed from recruiting to active, no longer recruiting.