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Publications

3 publications

Clinical research

6 studies

Active

2 studies
  • PI
    AN INTERVENTIONAL PHASE 2/3, RANDOMIZED, DOUBLE-BLIND, THIRD PARTY-UNBLINDED, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO INVESTIGATE EFFICACY AND SAFETY OF PF-07275315 IN ADULT PARTICIPANTS WITH MODERATE-TO-SEVERE CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD)
    PHASE2; PHASE3 · Pfizer, Inc. · OPEN TO ACCRUAL (as of 2026)
    Moderate to Severe Chronic Obstructive Pulmonary Disease
    NCT07363694
  • PI
    A Phase 2b/3, randomized, double-blind, placebo-controlled, multicenter study, to investigate the efficacy and safety of lunsekimig in adult participants with inadequately controlled chronic obstructive pulmonary disease (COPD) characterized by an eosinophilic phenotype
    Sanofi S.A. · OPEN TO ACCRUAL (as of 2025)
Completed & closed trials (4)
  • PI
    A 52-week, Randomized, Double-blind, Double-dummy, Placebo- and Active- Controlled (Roflumilast, Daliresp® 500µg), Parallel Group, Study to Evaluate the Efficacy and Safety of Two Doses of CHF6001 DPI add-on to Maintenance Triple Therapy in Subjects With Chronic Obstructive Pulmonary Disease (COPD) and Chronic Bronchitis.
    PHASE3 · Chiesi Farmaceutici S.p.A. · IRB STUDY CLOSURE (as of 2026)
    Chronic Obstructive Pulmonary Disease
    NCT04636814
  • PI
    A Phase III, 52-week, Multinational, Multicenter, Randomized, Double-blind, 2-arm Parallel Group Study Comparing Efficacy, Safety and Tolerability of the Fixed Dose Triple Combination of Beclomethasone Dipropionate Plus Formoterol Fumarate Plus Glycopyrronium Bromide (CHF 5993) With the Fixed Dose Dual Combination of Beclomethasone Dipropionate Plus Formoterol Fumarate (CHF 1535), Both Administered Via pMDI in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
    PHASE3 · Chiesi Farmaceutici S.p.A. · IRB STUDY CLOSURE (as of 2026)
    COPD; COPD Exacerbation
    NCT04320342
  • PI
    Randomized, Double-blind, Placebo-controlled, Parallel-group Phase 3 Study to Evaluate the Efficacy, Safety, and Tolerability of SAR440340/ REGN3500/ Itepekimab (Anti-IL-33 mAb) in Patients With Moderate-to-severe Chronic Obstructive Pulmonary Disease (COPD)
    PHASE3 · Sanofi S.A. · IRB STUDY CLOSURE (as of 2026)
    Chronic Obstructive Pulmonary Disease
    NCT04751487
  • PI
    A Double-blinded Extension Study to Evaluate the Long-term Safety and Tolerability of Itepekimab in Patients With Chronic Obstructive Pulmonary Disease (COPD) Who Participated in Either EFC16750 or EFC16819 Clinical Studies
    PHASE3 · Sanofi S.A. · IRB STUDY CLOSURE (as of 2025)
    Chronic Obstructive Pulmonary Disease
    NCT06208306