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Study identifier: NCT05881265 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Treatment of Chidamide and Venetoclax for Retinoic Acid and Arsenic Resistant Acute Promyelocytic Leukemia

Condition: APL  ·  Sponsor: Shanghai Jiao Tong University School of Medicine

PhasePhase 2
Planned participants30
Who can joinAll sexes, 16 Years to 70 Years
Healthy volunteersNo

About this study

Based on the current treatment with retinoic acid (ATRA) and arsenic (As), most patients with APL achieved long-term survival. There are few patients relapsed and became refractory to the RA and As treatment. In our pre-clinical study, we found that targeting histone deacetylase inhibitor 3 (HDAC3)degraded PML-RARa oncoprotein and induced differentiation and apoptosis of RA and As resistant APL in vitro and in vivo. In this study, we evaluate the efficacy and feasibility of combination therapy for HDAC3 inhibitor and venetoclax in patients with refractory APL.

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

Talk to the study team

Chun Wang, M.D.,  ·  8613386259777  ·  wangchunsh@medmail.com.cn

Always discuss trial participation with your own doctor first.

Locations (5)

The Affiliated Huai An No 1 Perople's Hospital of NanJing UniversityHuai'an, Jiangsu, ChinaNot Yet Recruiting
The First Affiliated Hospital of Nanchang UniversityNanchang, Jiangxi, ChinaNot Yet Recruiting
Jiong HUShanghai, Shanghai Municipality, ChinaRecruiting
Zhaxin Hospital, Go Broad Health CareShanghai, Shanghai Municipality, ChinaActive Not Recruiting
NanFang HospitalGuangzhou, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT05881265