CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 126 enrolled
Drug / intervention
Ublituximab +1 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/NCT02301156
NCT02301156Phase 3Completed

A Phase 3, Randomized, Study to Assess the Efficacy and Safety of Ublituximab in Combination With Ibrutinib Compared to Ibrutinib Alone, in Patients With Previously Treated High-Risk Chronic Lymphocytic Leukemia (CLL)

TG Therapeutics, Inc.·interventional·Posted Nov 25, 2014·Updated May 20, 2022

In Brief

A Phase 3 clinical trial evaluating Ublituximab and Ibrutinib for Chronic Lymphocytic Leukemia. Completed, enrolled 126 participants across 88 sites in 2 countries.

Detailed Summary

This study evaluates the effect of the addition of ublituximab, a novel monoclonal antibody, to ibrutinib compared to ibrutinib alone on antitumor activity, as measured by the overall response rate (ORR = CR \[complete response\] + PR \[partial response\]) in previously treated Chronic Lymphocytic Leukemia (CLL) participants with high-risk cytogenetic features. Half of the participants will receive ublituximab in combination with ibrutinib, while the other half will receive ibrutinib alone.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesIsrael, United States
Collaborators--

Timeline

Phase 3CompletedFinished
201520162017201820192020202120222023202420252026
First PostedNov 25, 2014
Enrollment StartJan 27, 2015
Primary CompletionApr 1, 2020
TodayJul 2, 2026
Enrollment to primary: 5.2 yearsPosted 11.6 years ago

Interventions

Ublituximabdrug

Administered as an IV infusion

Ibrutinibdrug

Administered orally