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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Key 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
20122021

Study locations (8)

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 NCT01644253 on ClinicalTrials.gov

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