TerminatedPhase 1NCT05787496
A Safety, Tolerability and Efficacy Study of NC525 in Subjects With Advanced Myeloid Neoplasms
Studying Chronic myelomonocytic leukemia
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
- NextCure, Inc.
- Principal Investigator
- Han Myint, MDNextCure, Inc.
- Intervention
- NC525(drug)
- Enrollment
- 28 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2023 – 2025
Study locations (11)
- City of Hope, Duarte, California, United States
- University of Miami, Miami, Florida, United States
- Massachusetts General Hospital, Boston, Massachusetts, United States
- Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States
- Washington University School of Medicine in St. Louis, St Louis, Missouri, United States
- Roswell Park Cancer Institute, Buffalo, New York, United States
- Weill Cornell Medicine, New York, New York, United States
- University Hospitals Cleveland Medical Center, Cleveland, Ohio, United States
- Cleveland Clinic, Cleveland, Ohio, United States
- Oregon Health & Science University, Portland, Oregon, United States
- MD Anderson Cancer Center, Houston, Texas, United States
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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