drugset / Trial / NCT01799889

Study to Evaluate Efficacy, Safety, Tolerability, and Pharmacodynamics of Entospletinib in Adults With Relapsed or Refractory Hematologic Malignancies

NCT01799889

Phase 2 Terminated 326 enrolled Gilead Sciences
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of the study is to evaluate efficacy of entospletinib in participants with relapsed or refractory hematologic malignancies. Participants with the following relapsed or refractory hematologic malignancies will be enrolled into the study: relapsed or refractory chronic lymphocytic leukemia (CLL), mantle cell lymphoma (MCL), diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL), or non-FL indolent non-Hodgkin lymphomas (iNHL; including lymphoplasmacytoid lymphoma/ Waldenström macroglobulinemia \[LPL/WM\], small lymphocytic lymphoma \[SLL\], or marginal zone lymphoma \[MZL\]).

Timeline

Start
2013-03-14
Primary completion
2017-09-14
Completion
2020-01-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Entospletinib Small molecule 100 mg Oral
Subject Entospletinib Small molecule 200 mg Oral
Subject Entospletinib Small molecule 400 mg Oral
Subject Entospletinib Small molecule 800 mg Oral