RecruitingPHASE1, PHASE2NCT06315738
Study to Assess the Safety, Tolerability, and Preliminary Efficacy of ST266 in Infants With Necrotizing Enterocolitis
Studying Necrotizing enterocolitis
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
- Noveome Biotherapeutics, formerly Stemnion
- Intervention
- ST266(biological)
- Enrollment
- 36 target
- Eligibility
- All sexes
- Timeline
- 2024 – 2029
Study locations (7)
- Yale-New Haven Hospital, New Haven, Connecticut, United States
- Orlando Health, Inc. Winnie Palmer Hospital for Women and Babies, Orlando, Florida, United States
- BayCare Health System-St. Joseph's Women's Hospital, Tampa, Florida, United States
- NorthShore University-Evanston Hospital, Evanston, Illinois, United States
- Duke University Medical Center (DUMC), Durham, North Carolina, United States
- Oklahoma Children's Hospital, Oklahoma City, Oklahoma, United States
- University of Pittsburgh Medical Center Magee Womens Hospital, Pittsburgh, Pennsylvania, United States
Collaborators
Parexel
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 NCT06315738 on ClinicalTrials.govOther trials for Necrotizing enterocolitis
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