Active, not recruitingPhase 1NCT03952078
A Dose Escalation Study Evaluating CPI-818 in Relapsed/Refractory T-Cell Lymphoma
Studying Aggressive primary cutaneous T-cell 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
- Corvus Pharmaceuticals, Inc.
- Principal Investigator
- Suresh Mahabhashyam, MD, MPHCorvus Pharmaceuticals
- Intervention
- CPI-818(drug)
- Enrollment
- 151 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2019 – 2026
Study locations (22)
- Stanford University, Palo Alto, California, United States
- University of Michigan, Ann Arbor, Michigan, United States
- Washington University, St Louis, Missouri, United States
- Hackensack University Medical Center, Hackensack, New Jersey, United States
- Ohio State University, Columbus, Ohio, United States
- University of Pittsburgh, Pittsburgh, Pennsylvania, United States
- Concord Repatriation General Hospital, Concord, New South Wales, Australia
- Liverpool Hospital, Liverpool, New South Wales, Australia
- Royal Adelaide Hospital, Adelaide, South Australia, Australia
- Epworth Healthcare, Melbourne, Victoria, Australia
- Beijing Friendship Hospital, Beijing, Beijing Municipality, China
- Beijing Boren Hospital, Beijing, Beijing Municipality, China
- Beijing Cancer Hospital, Beijing, Beijing Municipality, China
- Shanghai East Hospital, Pudong, Shanghai Municipality, China
- Henan Cancer Hospital, Henan, Zhengzhou, China
- +7 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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