drugset / Trial / NCT03552692

Use of Venetoclax as Single Agent in Patients With Relapsed/Refractory BCL-2 Positive Peripheral T Cell Lymphoma

NCT03552692 ↗

Phase 2 Terminated 22 enrolled Fondazione Italiana Linfomi - ETS
NaSingle-groupOpen-labelTreatment

Summary

The FIL\_VERT study is a phase II, open label, multicenter clinical trial. The primary of objective of the Study is to evaluate the efficacy of Venetoclax ABT-199/GDC-0199) in terms of overall response rate (ORR) in patients with relapsed/refractory BCL-2 positive peripheral T cell lymphoma not otherwise specified (PTCL-NOS), angioimmunoblastic T-cell lymphoma (AITL) and other nodal T-cell lymphomas of T-follicular helper origin (TFH)

Timeline

Start
2018-09-25
Primary completion
2020-03-04
Completion
2023-02-17

Outcome

Outcome not reported

Stopped: “efficacy lower than expected”

Drugs

EvaluationDrugModalityDoseRoute
Subject Venetoclax Small molecule 800 mg Oral