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Study identifier: NCT07011056 Synced from ClinicalTrials.gov · July 29, 2026
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A Phase III Clinical Study of Purinostat Mesylate for Injection in Patients With Diffuse Large B-cell Lymphoma

Condition: Recurrent and Refractory Diffuse Large B-cell Lymphoma  ·  Sponsor: Chengdu Zenitar Biomedical Technology Co., Ltd

PhasePhase 3
Planned participants390
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The main objective of this study is to evaluate the differences in objective response rate and overall survival between the Purinostat mesylate for injection and selinexor, as assessed by blinded independent central review (BICR), in patients with relapsed or refractory diffuse large B-cell lymphoma. .The participants in the experimental group will receive treatment with Purinostat mesylate for injection. The dosage is 11.2 mg/m2. Each administration cycle consists of intravenous administration on days 1, 4, 8, and 11. A 21-day period constitutes one treatment cycle, and the total treatment cycle lasts for 6 cycles. .Participants in the control group will receive selinexor treatment. The recommended dose is 60 mg per dose, taken orally on days 1 and 3 of each week (for example, Monday and Wednesday, or Tuesday and Thursday), and a 4-week period constitutes one treatment cycle.

This description comes directly from the study's public registry record.

Talk to the study team

Liangkun Sun  ·  86+15885742617  ·  liangkunsun@zenitar.cn

Always discuss trial participation with your own doctor first.

Locations (1)

West China Hospital Sichuan UniversityChengdu, Sichuan, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07011056