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Clinical Trial ● Currently Recruiting Phase II NCT06609239

Long-term Safety and Efficacy Evaluation of Lunsekimig (SAR443765) in Adult Participants With Asthma.

Long-term Safety and Efficacy Evaluation of Lunsekimig (SAR443765) in Adult Participants With Asthma. — Recruiting • Phase II • Respiratory / COPD / Asthma • NCT06609239.

📅 09 Apr 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase II
NCT ID
NCT06609239
Start
2024-09-30
Completion
2031-01-20
ClinicaliQ Trial Snapshot
  • Long-term Safety and Efficacy Evaluation of Lunsekimig (SAR443765) in Adult Participants With Asthma. — Recruiting • Phase II • Respiratory / COPD / Asthma • NCT06609239.
  • Lunsekimig (SAR443765) Long-term Asthma Trial Summary.
  • Long-term safety and effectiveness study of lunsekimig injection for adults with asthma over 96 weeks.

Verify eligibility, endpoints and current status on the original ClinicalTrials.gov registry before acting on this summary.

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What This Trial Is Studying

This is a phase 2, open-label extension study to evaluate the long-term safety and efficacy of lunsekimig in adult participants with asthma who have previously completed the parent studies. After completion of the parent study, eligible participants will be offered the opportunity to participate in the long-term extension (LTE) study with lunsekimig. The study duration will be up to 100 weeks with a treatment duration being up to 96 weeks. Conditions: Asthma Interventions: Lunsekimig Lead Sponsor: Sanofi Planned Enrollment: 900 participants

Full Trial Details
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Eligibility criteria, protocol, and results when available
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