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Study identifier: NCT04025450 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Comparation of Chidamide Plus VRD (Bortezomib, Lenalidomide, Dexamethasone) With VRD Regimen for Primary High-Risk Multiple Myeloma Patients

Condition: Multiple Myeloma  ·  Sponsor: The First Affiliated Hospital of Soochow University

PhasePhase 1/Phase 2
Planned participants50
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

In the phase I trial, dose escalation of chidamide will be performed at 4 different dosages (15mg, 20mg, 25mg, 30mg) for optimal dosage, in the phase II trial, the safety and efficacy of chidamide+VRD will be compared with that of VRD regimen.

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

Talk to the study team

Chengcheng Fu, PhD  ·  13962191404  ·  fuzhengzheng@suda.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

First Affiliated Hospital, Soochow UniversitySuzhou, Jiangsu, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT04025450