CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 97 enrolled
Drug / intervention
BGB-10188 +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/NCT04282018
NCT04282018Phase 2Completed

A Phase 1/2, Dose Escalation and Expansion Study of BGB-10188, a Phosphatidylinositol 3-Kinase Delta (PI3Kδ) Inhibitor, Combined With Zanubrutinib in Patients With Mature B-Cell Malignancies and Combined With Tislelizumab in Patients With Solid Tumors

BeiGene·interventional·Posted Feb 24, 2020·Updated Feb 20, 2026

In Brief

A Phase 2 clinical trial evaluating BGB-10188, Zanubrutinib, and 1 other intervention for Chronic Lymphocytic Leukemia and 6 related conditions. Completed, enrolled 97 participants across 24 sites in 2 countries.

Detailed Summary

The purpose of this study was to determine the maximum tolerated dose (MTD), recommended dose for expansion (RDFE), safety and tolerability of BGB-10188 as monotherapy in participants with relapsed/refractory (R/R) mature B-cell malignancies; in combination with zanubrutinib in participants with R/R follicular lymphoma (FL), R/R mantle cell lymphoma (MCL) or R/R diffuse large B-cell lymphoma (DLBCL); and in combination with tislelizumab in participants with advanced solid tumors.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, China
Collaborators--

Timeline

Phase 2CompletedFinished
2020202120222023202420252026
First PostedFeb 24, 2020
Enrollment StartApr 29, 2020
Primary CompletionAug 28, 2024
TodayJul 2, 2026
Enrollment to primary: 4.3 yearsPosted 6.4 years ago

Interventions

BGB-10188drug

Administered as specified in the treatment arm

Zanubrutinibdrug

Administered as specified in the treatment arm

Tislelizumabdrug

Administered as specified in the treatment arm