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

Sanofi
NCT IDNCT06609239ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

900

Study length

about 6.3 years

Ages

18+

Locations

24 sites in AZ, CO, FL +7

What this study is about

Researchers are testing the safety and effectiveness of lunsekimig over a long period in adults with asthma. The trial will last up to 100 weeks, with treatment lasting up to 96 weeks. Participants who have previously completed other studies on this medication are eligible.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Lunsekimig

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Number of participants having any treatmentemergent adverse event (TEAE), including adverse events of special interest (AESI), and serious adverse event (SAE)

Secondary: Change from parent study baseline in Asthma Quality of Life Questionnaire Standardized Activites for 12 years and older (AQLQ[S] +12) domain and total scores, Change from parent study baseline in Asthma Quality of Life Questionnaire Standardized Activities for 12 years and older (AQLQ[S] +12) domain and total scores, Change from parent study baseline in pre bronchodilator (BD) FEV1, Change from parent study baseline in prebronchodilator (BD) forced expiratory volume in 1 second (FEV1)

Body systems

Respiratory