RecruitingPHASE1, PHASE2NCT05019716
Testing the Safety and Efficacy of the Addition of a New Anti-cancer Drug, ZEN003694, to Chemotherapy Treatment (Cisplatin and Etoposide or Carboplatin and Paclitaxel) for Adult and Pediatric Patients (12-17 Years) With NUT Carcinoma
Studying NUT midline carcinoma
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
- National Cancer Institute (NCI)
- Principal Investigator
- Jia LuoDana-Farber - Harvard Cancer Center LAO
- Intervention
- BET Bromodomain Inhibitor ZEN-3694(drug)
- Enrollment
- 36 target
- Eligibility
- 12 years · All sexes
- Timeline
- 2022 – 2026
Study locations (5)
- Los Angeles General Medical Center, Los Angeles, California, United States
- USC / Norris Comprehensive Cancer Center, Los Angeles, California, United States
- Dana-Farber Cancer Institute, Boston, Massachusetts, United States
- University of Pittsburgh Cancer Institute (UPCI), Pittsburgh, Pennsylvania, United States
- M D 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.
Open NCT05019716 on ClinicalTrials.govOther trials for NUT midline carcinoma
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