RecruitingPhase 2NCT07284459

Study to Evaluate the Efficacy, Safety, and Tolerability of PIPE 791 in Subjects With Idiopathic Pulmonary Fibrosis

Studying Idiopathic pulmonary fibrosis

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Contineum Therapeutics
Principal Investigator
Mudiaga O Sowho, MD, MPH
Contineum Therapeutics
Intervention
PIPE-791 Dose A(drug)
Enrollment
324 enrolled
Eligibility
40 years · All sexes
Timeline
20262028

Study locations (2)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT07284459 on ClinicalTrials.gov

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