TerminatedPhase 1NCT01644253
Phase 1b Safety and Efficacy Study of TRU-016
Studying T-cell prolymphocytic 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
- Aptevo Therapeutics
- Principal Investigator
- Scott C. Stromatt, M.D.Aptevo Therapeutics
- Intervention
- 20 mg/kg TRU-016 + Rituximab(biological)
- Enrollment
- 87 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2012 – 2021
Study locations (8)
- Augusta, Georgia, United States
- Columbus, Ohio, United States
- Eastern Regional Medical Center, Philadelphia, Pennsylvania, United States
- University of Pittsburgh, Pittsburgh, Pennsylvania, United States
- Greenville Health System, Greenville, South Carolina, United States
- Houston, Texas, United States
- Swedish Cancer Institute,1221 Madison St., Seattle, Washington, United States
- Fred Hutchinson Cancer Research Center, Seattle, Washington, 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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