RecruitingPhase 2NCT06237335
A Phase 2 Study Evaluating Safety and Tolerability of RCT2100 (CFTR mRNA) in Healthy Participants and in Participants With CF
Studying Cystic 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
- ReCode Therapeutics
- Principal Investigator
- John Matthews, MBBS, MCRP, PhDReCode Therapeutics, Inc.
- Intervention
- RCT2100(drug)
- Enrollment
- 192 enrolled
- Eligibility
- 18-60 years · All sexes
- Timeline
- 2024 – 2026
Study locations (20)
- The University of Alabama at Birmingham, Birmingham, Alabama, United States
- University of Arizona, Tucson, Arizona, United States
- Stanford University, Palo Alto, California, United States
- UCSD, San Diego, California, United States
- National Jewish Health, Denver, Colorado, United States
- Emory University, Atlanta, Georgia, United States
- Boston Children's Hospital, Boston, Massachusetts, United States
- New York Medical College, Valhalla, New York, United States
- The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States
- Oregon Health & Science University, Portland, Oregon, United States
- University of Pittsburgh, Pittsburgh, Pennsylvania, United States
- UT Southwestern Medical Center, Dallas, Texas, United States
- University of Washington, Seattle, Washington, United States
- Centre Hospitalier Régional Universitaire de Montpellier - Hôpital Arnaud de Villeneuve, Montpellier, France
- Hôpital Necker Enfants Malades, Paris, France
- +5 more locations on ClinicalTrials.gov
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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