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Phase 2RecruitingPriority 3 · Moderate priorityNCT06151106

Chidamide and Duvalisibon for the Treatment of Refractory/Relapsed Peripheral T-cell Lymphoma

ClinicalTrials.gov

Plain-language summary

This Phase 2 trial is evaluating Chidamide combined with Duvillisib 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 18 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 combined with Duvillisib (DRUG): Specified dose on specified days

Drugs / treatments
Chidamide combined with Duvillisib
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
Overall Response Rate; Complete Response Rate
Ages
18 Years to 75 Years
Start date
2023-11-22
Est. completion
2027-12-25

Locations

0 US sites · 1 total

No US sites currently listed.

Contact

Sponsor
The First Affiliated Hospital of Xiamen University (OTHER)
Contact
Bing Xu | xubingzhangjian@126.com | +8618750918842

Tags

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

Chidamide and Duvalisibon for the Treatment of Refractory/Relapsed Peripheral T-cell Lymphoma

NCT06151106

Phase: Phase 2 | Status: Recruiting | Priority: Medium

Plain-language summary

This Phase 2 trial is evaluating Chidamide combined with Duvillisib 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 18 Years to 75 Years years
  • Newly diagnosed, not yet treated
  • Must be well enough for treatment (adequate performance status)

What's being tested

Chidamide combined with Duvillisib (DRUG): Specified dose on specified days

Drugs / treatments: Chidamide combined with Duvillisib

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: Overall Response Rate; Complete Response Rate

Ages: 18 Years to 75 Years

Start date: 2023-11-22 | Est. completion: 2027-12-25

Locations

0 US sites · 1 total

Contact

Bing Xu | xubingzhangjian@126.com | +8618750918842

Sponsor: The First Affiliated Hospital of Xiamen University (OTHER)

Tags

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

View on ClinicalTrials.gov

https://clinicaltrials.gov/study/NCT06151106

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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