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Study identifier: NCT05958719 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Chidamide in Combination With Azacitidine, Liposomal Mitoxantrone, and Prednisone (CAMP Regimen) for the Treatment of Previously Untreated Nodal TFH Cell Lymphoma

Condition: Peripheral T Cell Lymphoma · Epigenetic Repression  ·  Sponsor: Institute of Hematology & Blood Diseases Hospital, China

PhasePhase 2
Planned participants37
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study is investigating the effectiveness (specifically the objective response rate - ORR) of a new combination therapy called CAMP (chidamide, azacitidine, liposomal mitoxantrone, and prednisone) for previously untreated angioimmunoblastic T-cell lymphoma (AITL). It's a single-arm study comparing CAMP's safety and efficacy to standard treatments. Younger patients (≤70) receive the full CAMP regimen, while older patients receive a modified version (CAMP-light). Patients are assessed via PET-CT after 4 cycles. Responders (CR/PR) receive consolidation therapy and then maintenance chidamide for 2 years. Eligible patients achieving CR after 4 cycles can get a transplant, while those with PR need 2 more cycles first. Patients with stable or progressive disease after 4 cycles are withdrawn. Progression at any time leads to study discontinuation.

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

Talk to the study team

Dehui Zou, Dr.  ·  86-022-23909282  ·  zoudehui@ihcams.ac.cn

Huimin Liu, Dr.  ·  86-022-23909282  ·  liuhuimin@ihcams.ac.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Institute of Hematology & Blood Diseases HospitalTianjin, Tianjin Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT05958719