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Study identifier: NCT07516951 Synced from ClinicalTrials.gov · July 29, 2026
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A Study to Find an Efficacious and Safe Dose of CHF10067 (Zampilimab) in Participants With Idiopathic Pulmonary Fibrosis

Condition: Idiopathic Pulmonary Fibrosis  ·  Sponsor: Chiesi Farmaceutici S.p.A.

PhasePhase 2
Planned participants240
Who can joinAll sexes, 40 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to evaluate the efficacy, safety, and tolerability at Week 24 of 2 doses of CHF10067 (zampilimab) in participants with idiopathic pulmonary fibrosis (IPF). It is a phase IIb, multicentre, randomised, double-blind, placebo-controlled, three-arm parallel-group study. A total of 240 participants with IPF (Idiomatic Pulmonary Fibrosis) will be randomised in approximately 150 investigational sites in North and Latin America, Europe, Asia, and Oceania.

This description comes directly from the study's public registry record.

Talk to the study team

Chiesi Clinical Trial Info  ·  + 39 0521 2791  ·  Clinicaltrials_info@chiesi.com

Always discuss trial participation with your own doctor first.

Locations (1)

PHI University Clinic of Pulmonology and AllergologySkopje, North MacedoniaRecruiting

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Source record: clinicaltrials.gov/study/NCT07516951