drugset / Trial / NCT03039114

Study Evaluating Safety and Efficacy of INCB050465 Combined With Bendamustine and Obinutuzumab in Relapsed or Refractory Follicular Lymphoma (CITADEL-102)

NCT03039114

Phase 1 Completed 26 enrolled Incyte Corporation
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and efficacy of parsaclisib when combined with bendamustine and obinutuzumab in subjects with relapsed or refractory follicular lymphoma (FL).

Timeline

Start
2017-02-15
Primary completion
2021-03-30
Completion
2021-03-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Parsaclisib Small molecule
Background Bendamustine Small molecule 90 mg/m2 Intravenous
Background Obinutuzumab Monoclonal antibody 1000 mg Intravenous

Indications