Phase 2 Study to Assess the Safety and Efficacy of ANG003 | MicrobiomeTrials← Back to trialsNCT07450547
Phase 2 Study to Assess the Safety and Efficacy of ANG003
RecruitingPHASE2INTERVENTIONAL
Trial Details
Start: 2026-04-24Est. Completion: 2027-07
Enrollment target: 113 participants Locations- Long Beach Memorial Medical Center, Long Beach, California, United States
- Center for Cystic Fibrosis at Keck Medical Center of USC, Los Angeles, California, United States
- National Jewish Health, Denver, Colorado, United States
- University of Florida, Gainesville, Florida, United States
- Central Florida Pulmonary Group, Orlando, Florida, United States
- The Cystic Fibrosis Institute, Glenview, Illinois, United States
- University of Iowa, Iowa City, Iowa, United States
- University of Kansas Medical Center, Kansas City, Kansas, United States
- University of Kentucky, Lexington, Kentucky, United States
- MaineHealth Pediatric Specialty Care, Portland, Maine, United States
- Massachusetts General Hospital, Boston, Massachusetts, United States
- Boston Children's Hospita, Boston, Massachusetts, United States
- University of Michigan, Michigan Medicine, Ann Arbor, Michigan, United States
- Wayne State University Harper University Hospital, Detroit, Michigan, United States
- Rutgers - Robert Wood Johnson Medical School, New Brunswick, New Jersey, United States
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