Active, not recruitingPhase 1NCT05195918
Study of Oral Epigallocatechin-3-gallate (EGCG) in IPF Patients
Studying Idiopathic pulmonary fibrosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Hal Chapman
- Principal Investigator
- Harold Chapman, MDUniversity of California, San Francisco
- Intervention
- EGCG 300 mg + Nintedanib(combination_product)
- Enrollment
- 50 target
- Eligibility
- 40-85 years · All sexes
- Timeline
- 2023 – 2026
Study locations (7)
- UCSF Parnassus, San Francisco, California, United States
- Massachusetts General Hospital, Boston, Massachusetts, United States
- University of Michigan, Ann Arbor, Michigan, United States
- Weill Cornell Medicine, New York, New York, United States
- Temple University, Philadelphia, Pennsylvania, United States
- University of Virginia, Charlottesville, Virginia, United States
- University of Washington, Seattle, Washington, United States
Collaborators
University of Michigan · Cornell University · Massachusetts General Hospital · Temple University · University of Washington · University of Virginia
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.
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