Status:
ACTIVE_NOT_RECRUITING
Dose Ranging Study of Lunsekimig Compared With Placebo-control in Adult Participants With Moderate-to-severe Asthma
Lead Sponsor:
Sanofi
Conditions:
Asthma
Eligibility:
All Genders
18-80 years
Phase:
PHASE2
Brief Summary
This is a Phase 2b, global, multicenter, randomized, double-blind, placebo-controlled, parallel group, dose ranging study to assess the efficacy, safety, and tolerability of add-on therapy with SC lun...
Eligibility Criteria
Inclusion
- A physician-diagnosed moderate-to-severe asthma for ≥12 months based on GINA guidelines Steps 4 and 5
- Participants with existing treatment with moderate-to-high doses of ICS therapy for in combination with at least 1 but no more than 2 additional controller medications at least 3 months with a stable dose ≥1 month prior to Visit 1
- At least 1 asthma exacerbation in the past year, with at least one exacerbation occurring while on treatment with moderate to high doses of ICS therapy
- ACQ-5 score more than 1.5 at Screening (Visit 1)
Exclusion
- Chronic obstructive or other lung diseases (eg, COPD, idiopathic pulmonary fibrosis, etc) which may impair lung function, or another diagnosed pulmonary or systemic disease.
- Current smoker or former smoker with cessation within 6 months of Screening or history of \>10 pack-years. Active vaping of any products and/or marijuana smoking within 6 months of Screening.
- Participants who experience a deterioration of asthma that results in emergency treatment or hospitalization, or treatment with systemic steroids within 1 month prior to the Screening
- Participants who have experienced an upper or lower respiratory tract infection within the 4 weeks prior to Screening
- For participants on chronic OCS use for the maintenance treatment of asthma: history of a serious infection requiring hospitalization within the past 12 months prior to Randomization (Visit 2).
- Participants with active tuberculosis (TB), latent TB, a history of incompletely treated TB, suspected extrapulmonary TB infection, or who are at high risk of contracting TB (such as close contact with individuals with active or latent TB) or received Bacillus Calmette-Guérin (BCG)-vaccination within 12 weeks prior to Screening
- Severe concomitant illness that would in the Investigator's opinion inhibit the participant's participation in the study, including for example, but not limited to, hypertension, renal disease, neurological conditions, heart failure and pulmonary disease
- The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial
Key Trial Info
Start Date :
October 16 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 23 2026
Estimated Enrollment :
685 Patients enrolled
Trial Details
Trial ID
NCT06102005
Start Date
October 16 2023
End Date
March 23 2026
Last Update
May 28 2025
Active Locations (156)
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1
Allergy, Asthma & Immunology Associates- Site Number : 8400009
Scottsdale, Arizona, United States, 85251
2
Yuma Pulmonary & Sleep Research, LLC- Site Number : 8400072
Yuma, Arizona, United States, 85364
3
Antelope Valley Clinical Trials- Site Number : 8400020
Lancaster, California, United States, 93534
4
Amicis Research Center - Northridge - Nordhoff Street- Site Number : 8400032
Northridge, California, United States, 91324