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Priya Life Science Compound trial record
Compound · clinical trials

Tucidinostat clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 6 trials in our China and Taiwan registers that name Tucidinostat as an intervention. Synced 9 Nov 2026
6Current trials
5Recruiting now
4Lead sponsors
2Country registers
At a glance

Tucidinostat is named as an intervention in 6 current clinical trials in our China and Taiwan registers. 5 are recruiting patients now. The most common phase is Phase 2. The sponsor with the most trials is Ou Bai, MD/PHD (2). The most-studied condition is Diffuse Large B-Cell Lymphoma (DLBCL).

How Tucidinostat works

All drug targets →
  • Inhibits HDAC1 Primary target
    Target: HDAC1 histone deacetylase 1
    Guide to Pharmacology only
Diseases it has been tested for in clinical trials, by furthest phase
  • Acute myeloid leukemiaPhase 3
  • Breast cancerPhase 3
  • Colorectal cancerPhase 3
  • Diffuse large B-cell lymphomaPhase 3
  • Mature T-cell and NK-cell non-Hodgkin lymphomaPhase 3
  • MelanomaPhase 3
  • Peripheral T-cell lymphoma, not otherwise specifiedPhase 3
  • HIV infectious diseasePhase 2/3
  • T-lymphoblastic lymphomaPhase 2/3
  • Acute lymphoblastic leukemiaPhase 2/3
67 diseases in all

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL3621988, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3.1), ligand 8305, CC BY-SA 4.0. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

Patient leaflets for Tucidinostat

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Reference identifiers for Tucidinostat

ChEMBL
CHEMBL3621988
DrugBank
DB06334
PubChem CID
12136798
CAS number
1616493-44-7
FDA UNII
87CIC980Y0
Wikidata
Q19903814
Wikipedia
Tucidinostat

Codes that identify this medicine in other databases, from Wikidata (CC0), matched by its ChEMBL ID. The ATC code is the WHO classification of what the medicine is used for.

Trials by status

  • Recruiting583%
  • Not yet open117%

Trials by phase

  • Phase 2350%
  • Phase 3350%
01

Clinical trials of Tucidinostat

6 trials
StudyPhaseStatusLead sponsorRegisters
A Study of Tucidinostat in Combination With Sintilimab and Bevacizumab in MSS/pMMR Colorectal Cancer Patients
NCT06497985 · ClinicalTrials.gov ↗ · Colorectal Cancer
Phase 3 Recruiting Chipscreen Biosciences, Ltd China
Tucidinostat in Combination With CHOP in Newly Diagnosed Peripheral T-Cell Lymphoma With Follicular Helper of T Cell Phenotype
NCT06947967 · ClinicalTrials.gov ↗ · Lymphoma, T-Cell, Peripheral
Phase 3 Recruiting Chipscreen Biosciences, Ltd China
Chidamide for Maintenance Treatment of HBV-infected Diffuse DLBCL in Patients Initially Treated With R-CHOP
NCT07493109 · ClinicalTrials.gov ↗ · Diffuse Large B-Cell Lymphoma (DLBCL)
Phase 3 Recruiting Ou Bai, MD/PHD China
Chidamide in Patients With Relapsed or Refractory Peripheral T-cell Lymphoma (R/R PTCL)
NCT05833724 · ClinicalTrials.gov ↗ · Relapsed or Refractory Peripheral T-cell Lymphoma
Phase 2 Recruiting Great Novel Therapeutics Biotech & Medicals Corporation Taiwan
Chidamide Combination With R-mini CHOP Followed by Chidamide+CD20 Maintenance in Elderly Newly Diagnosed MYC/BCL2+ DLBCL
NCT07493148 · ClinicalTrials.gov ↗ · Diffuse Large B-Cell Lymphoma (DLBCL)
Phase 2 Recruiting Ou Bai, MD/PHD China
Chidamide Monotherapy for Intermediate-to-High-Risk Myelodysplastic Syndromes
NCT07616336 · ClinicalTrials.gov ↗ · Myelodysplastic Syndromes
Phase 2 Not yet open Zhongshan Hospital (Xiamen), Fudan University China

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with Tucidinostat

5 conditions
Diffuse Large B-Cell Lymphoma (DLBCL)2Colorectal Cancer1Myelodysplastic Syndromes1Lymphoma, T-Cell, Peripheral1Relapsed or Refractory Peripheral T-cell Lymphoma1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Ou Bai, MD/PHD2
Chipscreen Biosciences, Ltd2
Zhongshan Hospital (Xiamen), Fudan University1
Great Novel Therapeutics Biotech & Medicals Corporation1
04

By country register

RegisterTrialsRecruiting
Clinical trials in China54
Clinical trials in Taiwan11

A trial with sites in more than one country appears in each of those registers.

05

Related compounds

06

Questions about Tucidinostat trials

How many clinical trials are testing Tucidinostat?

6 current trials in our China and Taiwan registers name Tucidinostat as a drug or biological intervention, as of the registry sync on 9 November 2026. Completed and withdrawn studies are not counted.

Are Tucidinostat trials recruiting patients?

Yes. 5 of the 6 trials are recruiting: 4 with sites in China and 1 with sites in Taiwan. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Tucidinostat clinical trials?

Ou Bai, MD/PHD (2), Chipscreen Biosciences, Ltd (2), Zhongshan Hospital (Xiamen), Fudan University (1) and Great Novel Therapeutics Biotech & Medicals Corporation (1). The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Tucidinostat works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how Tucidinostat works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Tucidinostat (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 9 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.