RecruitingPhase 3NCT06093672
Study on Efficacy and Safety of Givinostat Versus Hydroxyurea in Patients With Polycythemia Vera
Studying Polycythemia vera
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
- Italfarmaco
- Intervention
- Givinostat(drug)
- Enrollment
- 220 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2024 – 2026
Study locations (30)
- University of Alabama at Birmingham, Birmingham, Alabama, United States
- Emad Ibrahim, MD, Inc, Redlands, California, United States
- US Oncology Inc, Englewood, Colorado, United States
- American Oncology Partners of Maryland, PA, Bethesda, Maryland, United States
- Icahn School of Medicine at Mount Sinai, New York, New York, United States
- University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States
- The Cleveland Clinic Foundation, Cleveland, Ohio, United States
- Oncology Associates of Oregon, P.C., Eugene, Oregon, United States
- MD Anderson Cancer Center, Houston, Texas, United States
- Texas Oncology (Webster) - USOR, Houston, Texas, United States
- Texas Oncology-Denison Cancer Center, Sherman, Texas, United States
- University of Utah - Huntsman Cancer Institute - PPDS, Salt Lake City, Utah, United States
- The James Cancer Hospital and Solove Research Institute, Roanoke, Virginia, United States
- VA Puget Sound Health Care System - NAVREF - PPDS, Seattle, Washington, United States
- Landesklinikum Wiener Neustadt, Wiener Neustadt, Lower Austria, Austria
- +15 more locations on ClinicalTrials.gov
Collaborators
PPD Development, LP
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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