drugset / Trial / NCT02953652

Efficacy and Safety of Oral HBI-8000 in Patients With Relapsed or Refractory Peripheral T-cell Lymphoma (PTCL)

NCT02953652 ↗

NaSingle-groupOpen-labelTreatment

Summary

Phase 2b, open-label, non-randomized, single arm study to evaluate the safety, efficacy, and pharmacokinetics of HBI-8000 40 mg BIW in patients with relapsed or refractory PTCL (R/R PTCL).

Timeline

Start
2016-11
Primary completion
2022-02-17
Completion
2022-02-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Tucidinostat Small molecule 40 mg Oral