drugset / Trial / NCT04224493

A Study to Assess the Efficacy, Safety, Pharmacodynamics, and Pharmacokinetics of Tazemetostat in Combination With Lenalidomide Plus Rituximab Versus Placebo in Combination With Lenalidomide Plus Rituximab in Adult Patients at Least 18 Years of Age With Relapsed/Refractory Follicular Lymphoma.

NCT04224493

Phase 3 Active not recruiting 599 enrolled Epizyme, Inc.
RandomizedSequentialQuadruple-blindTreatment

Summary

The participants of this study would have relapsed/refractory follicular lymphoma. Follicular lymphoma is a type of blood cancer. It is referred to as 'relapsed' when the disease has come back after a period of improvement after that follows a treatment regimen and 'refractory' when treatment no longer works. Stage 1 of this trial will study the safety and the level that adverse effects of each of the study drug combinations can be tolerated (known as tolerability). It is also designed to establish a recommended study drug dosage for stage 2 and 3. Stage 1 of the study is completed. Stages 2 and 3 will evaluate and compare how long participants live without their disease getting worse when receiving the study drug in combination with other drug treatment versus the placebo (dummy drug) in combination with other drug treatment.

Timeline

Start
2020-06-11
Primary completion
2027-02-13
Completion
2029-03-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Tazemetostat Small molecule 400 mg Oral
Subject Tazemetostat Small molecule 600 mg Oral
Subject Tazemetostat Small molecule 800 mg Oral
Background Lenalidomide Other / unclassified 10 mg Oral
Background Lenalidomide Other / unclassified 20 mg Oral
Background Rituximab Monoclonal antibody 375 mg/m2 Intravenous

Indications