An Open-Label, Dose-Finding, and Cohort-Expansion Phase 1 Study Evaluating Safety and Efficacy of INCB050465 in Combination With Bendamustine and Obinutuzumab in Subjects With Relapsed or Refractory Follicular Lymphoma (CITADEL-102)
The purpose of this study is to evaluate the safety and tolerability of INCB050465 when combined with bendamustine and obinutuzumab in relapsed or refractory follicular lymphoma (FL).
For more information, please contact Incyte Corporation at 1.855.463.3463 or visit www.incyteclinicaltrials.com
Condition | Follicular Lymphoma |
---|---|
Clinical Study Identifier | TX151684 |
Sponsor | Incyte Corporation |
Last Modified on | 23 November 2020 |
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