Last updated on May 2019

Dose Optimization Study of Idelalisib in Follicular Lymphoma


Brief description of study

This study will optimize the safety and efficacy of chronic administration of idelalisib in participants with follicular lymphoma (FL) and evaluate the overall safety profile of idelalisib and the overall response rate (ORR) by Week 24.

Clinical Study Identifier: NCT02536300

Recruitment Status: Closed


Brief Description Eligibility Contact Research Team


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