CI

At a glance

ClinicalIndex Comparison Record
Phase 2Not Yet Recruiting· 22 target
Drug / intervention
Pirtobrutinib +2 moredrug
Likely dose
Pirtobrutinib 200mgfrom 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/NCT07122609
NCT07122609Phase 2Not Yet Recruiting

A Study of Pirtobrutinib in Combination With Rituximab, Gemcitabine, Oxaliplatin With or Without Polatuzumab Vedotin (Pirto-R-GemOx±Pola) in Covalent BTK Inhibitor-Pretreated Relapsed/Refractory Diffuse Large B-Cell Lymphoma (DLBCL)

Ruijin Hospital·interventional·Posted Aug 14, 2025·Updated Aug 14, 2025

In Brief

A Phase 2 clinical trial evaluating Pirtobrutinib, R-GemOx, and 1 other intervention for Relapsed and Refractory DLBCL. Not yet recruiting, targeting 22 participants across 1 site.

Detailed Summary

This is a prospective, single arm trial in patients with ≥ 18 years with relapsed and refractory DLBCL. Aim of this study is to evaluate the efficacy and safety of pirtobrutinib in combination with rituximab, gemcitabine, and oxaliplatin with or without polatuzumab vedotin (Pirto-R-GemOx±pola) in patients with relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL) previously treated with covalent BTK inhibitors.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 2Not Yet Recruiting
20262027
First PostedAug 14, 2025
Enrollment StartAug 5, 2025
Primary CompletionAug 15, 2026
Study CompletionAug 15, 2027
TodayJul 1, 2026
Enrollment to primary: 1.0 yearsPosted 11 months agoPrimary completion in 1 month

Interventions

Pirtobrutinibdrug

Dose:200mg,d1-21

R-GemOxdrug

Dose: Rituximab: 375mg/m2, d1; Gemcitabine: 1000mg/m2, d2; Oxaliplatin:100mg/m2, d2

Polatuzumab Vedotindrug

Dose: 1.8mg/kg,iv,d1 (For patient who is CD79b positive and has not previously received polatuzumab Vedotin)