drugset / Trial / NCT02536300

Dose Optimization Study of Idelalisib in Follicular Lymphoma

NCT02536300

Phase 3 Terminated 96 enrolled Gilead Sciences
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is to establish a safe and effective dosing regimen of idelalisib in participants with relapsed or refractory follicular lymphoma (FL) who have no other therapeutic options.

Timeline

Start
2016-01-14
Primary completion
2022-09-27
Completion
2022-09-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Idelalisib Small molecule 100 mg Oral
Subject Idelalisib Small molecule 150 mg Oral

Indications