CompletedPhase 2NCT02998476
A Phase 2 Safety and Efficacy Study of INCB050465 in Subjects With Relapsed or Refractory Diffuse Large B-Cell Lymphoma (CITADEL-202)
Studying B-cell non-Hodgkin lymphoma
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
- Incyte Corporation
- Principal Investigator
- Claudia Corrado, MDIncyte Corporation
- Intervention
- Parsaclisib(drug)
- Enrollment
- 60 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2017 – 2021
Study locations (30)
- University of Alabama at Birmingham, Birmingham, Alabama, United States
- Banner MD Anderson Cancer Center, Gilbert, Arizona, United States
- Arizona Oncology Associates, PC - HAL, Tempe, Arizona, United States
- Sutter Gould Medical Foundation, Modesto, California, United States
- Sharp Memorial Hospital, San Diego, California, United States
- Advanced Pharma CR, LLC, Miami, Florida, United States
- Asclepes Research Centers, Weeki Wachee, Florida, United States
- Advocate Medical Group Niles Milwaukee Ave, Niles, Illinois, United States
- Indiana BMT, Beech Grove, Indiana, United States
- Parkview Research Center, Fort Wayne, Indiana, United States
- University of Kentucky Hospital, Lexington, Kentucky, United States
- St. Agnes Hospital, Baltimore, Maryland, United States
- Karmanos Cancer Institute, Detroit, Michigan, United States
- St. John Hospital and Medical Center, Detroit, Michigan, United States
- CHI Health - St. Francis Medical Center, Grand Island, Nebraska, United States
- +15 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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