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Phase 2RecruitingPriority 2 · High priorityNCT05833724

Chidamide in Patients With Relapsed or Refractory Peripheral T-cell Lymphoma (R/R PTCL)

ClinicalTrials.gov

Plain-language summary

This Phase 2 trial is evaluating Chidamide as a treatment for people newly diagnosed with T-cell lymphoma. The study measures how well this treatment works and monitors for side effects. This trial does not currently list US sites.

Who can join (key eligibility)

  • Age 20 Years to 75 Years years
  • Newly diagnosed, not yet treated
  • Must be well enough for treatment (adequate performance status)

Final eligibility is determined by the trial team. This list is a starting point only.

What's being tested

Chidamide (DRUG): Subjects will receive a single dose of 30 mg chidamide. Twice a week.

Drugs / treatments
Chidamide
Treatment length
Ask the trial team for details
Visit frequency
Ask the trial team for details

At a glance

Phase
Phase 2
Status
Recruiting
Design
Non-randomized, open-label
Enrollment target
33 patients
Primary endpoint
Objective response rate (ORR)
Ages
20 Years to 75 Years
Start date
2024-10-18
Est. completion
2025-12

Locations

0 US sites · 5 total

No US sites currently listed.

Contact

Sponsor
Great Novel Therapeutics Biotech & Medicals Corporation (INDUSTRY)
Contact
Chia-Nan Chen, Ph.D. | alex.chen@gntbm.com.tw | 886-2-2785-1399

Tags

All T-cell lymphomasNewly diagnosedRelapsed/Refractory
TrialCompass — Clinical Trial Summary

Chidamide in Patients With Relapsed or Refractory Peripheral T-cell Lymphoma (R/R PTCL)

NCT05833724

Phase: Phase 2 | Status: Recruiting | Priority: High

Plain-language summary

This Phase 2 trial is evaluating Chidamide as a treatment for people newly diagnosed with T-cell lymphoma. The study measures how well this treatment works and monitors for side effects. This trial does not currently list US sites.

Who can join

  • Age 20 Years to 75 Years years
  • Newly diagnosed, not yet treated
  • Must be well enough for treatment (adequate performance status)

What's being tested

Chidamide (DRUG): Subjects will receive a single dose of 30 mg chidamide. Twice a week.

Drugs / treatments: Chidamide

Treatment length: Ask the trial team for details

Visit frequency: Ask the trial team for details

Trial design

Non-randomized, open-label

Enrollment target: 33 patients

Primary endpoint: Objective response rate (ORR)

Ages: 20 Years to 75 Years

Start date: 2024-10-18 | Est. completion: 2025-12

Locations

0 US sites · 5 total

Contact

Chia-Nan Chen, Ph.D. | alex.chen@gntbm.com.tw | 886-2-2785-1399

Sponsor: Great Novel Therapeutics Biotech & Medicals Corporation (INDUSTRY)

Tags

All T-cell lymphomas · Newly diagnosed · Relapsed/Refractory

View on ClinicalTrials.gov

https://clinicaltrials.gov/study/NCT05833724

Prepared using TrialCompass (trialcompass.com) on June 19, 2026. For informational purposes only. Always discuss with your healthcare team.
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Data sourced from ClinicalTrials.gov.

For informational purposes only. Not medical advice — always consult your healthcare team.

Built with care for the rare cancer community.

Data last updated: June 2026

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