drugset / Trial / NCT02457559

Study to Assess the Long-term Safety and Efficacy of Tirabrutinib in Adults With Relapsed/Refractory B-cell Malignancies

NCT02457559

Phase 1 Completed 29 enrolled Gilead Sciences
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is to determine the long-term safety and tolerability of tirabrutinib in adults with relapsed/refractory B-cell malignancy who have tolerated and achieved stable disease or improved with tirabrutinib treatment while enrolled in a prior (parent study) tirabrutinib study (NCT01659255). The dosing regimen will be based on the prior dosing regimen from the parent study.

Timeline

Start
2015-09-10
Primary completion
2020-12-30
Completion
2020-12-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Tirabrutinib Small molecule 40 mg Oral
Subject Tirabrutinib Small molecule 80 mg Oral
Subject Tirabrutinib Small molecule 160 mg Oral
Subject Tirabrutinib Small molecule 300 mg Oral
Subject Tirabrutinib Small molecule 320 mg Oral
Subject Tirabrutinib Small molecule 400 mg Oral
Subject Tirabrutinib Small molecule 480 mg Oral
Subject Tirabrutinib Small molecule 500 mg Oral
Subject Tirabrutinib Small molecule 600 mg Oral

Indications