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Study identifier: NCT07074470 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Combination Regimen of Teniposide, PD-1 Monoclonal Antibody and Selinixor for Patients With Relapsed or Refractory PCNSL

Condition: Primary Central Nervous System Lymphoma (PCNSL)  ·  Sponsor: The First Affiliated Hospital of Soochow University

PhaseNA
Planned participants40
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

This study aims to evaluate the efficacy and safety of the VPX regimen, a novel combination of teniposide, PD-1 monoclonal antibody and selinexor, in patients with relapsed/refractory (R/R) primary central nervous system lymphoma (PCNSL) who have progressed after high-dose methotrexate (HD-MTX)-based systemic therapy. By investigating this therapeutic approach, we seek to establish a new treatment paradigm that may improve clinical outcomes of this high-risk population.

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

Talk to the study team

Zhengming Jin  ·  67781856  ·  jinzhengming519519@163.com

Changju Qu  ·  67781856  ·  qcj310@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

The First Affiliated Hospital of Soochow UniversitySuzhou, Jiangsu, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07074470