CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 35 enrolled
Drug / intervention
Tirabrutinib +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02968563
NCT02968563Phase 2Completed

A Prospective, Open-Label, Multicenter, Phase 2 Trial to Evaluate the Safety and Efficacy of the Combination of Tirabrutinib (GS-4059) and Idelalisib With and Without Obinutuzumab in Subjects With Chronic Lymphocytic Leukemia

Gilead Sciences·interventional·Posted Nov 18, 2016·Updated Jan 21, 2022

In Brief

A Phase 2 clinical trial evaluating Tirabrutinib, Idelalisib, and 1 other intervention for Chronic Lymphocytic Leukemia. Completed, enrolled 35 participants across 14 sites.

Detailed Summary

The primary objective of this study is to determine the preliminary efficacy of the combination of tirabrutinib and idelalisib with obinutuzumab in adults with relapsed or refractory chronic lymphocytic leukemia (CLL). The study has a 6 participant per arm safety run-in to evaluate safety prior to the enrollment of subsequent participants. The treatment period is adaptive, with a duration of active treatment up to two years and a total follow-up on study for up to 30 days post end of treatment, or up to Week 25 should a participant discontinue treatment prior to Week 25 for reasons other than disease progression.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesGermany

Timeline

Phase 2CompletedFinished
2017201820192020202120222023202420252026
First PostedNov 18, 2016
Enrollment StartDec 13, 2016
Primary CompletionJun 17, 2019
Study CompletionJan 14, 2021
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 9.6 years ago

Interventions

Tirabrutinibdrug

Tablets administered orally

Idelalisibdrug

Tablets administered orally

Obinutuzumabdrug

Administered intravenously