TrialCompass TCL
Find TrialsAI AssistantLetter GeneratorAbout
Back to results
Early Phase 1RecruitingPriority 4 · Lower priorityNCT07598578

An Open-label, Single-arm, Multicenter Phase II Clinical Study of Azacitidine, Chidamide Combined With PD-1 Monoclonal Antibody in the Treatment of Refractory/Relapsed Peripheral T-cell Lymphoma.

ClinicalTrials.gov

Plain-language summary

This Early Phase 1 trial is evaluating Azacitidine (AZA) as a treatment for people newly diagnosed with T-cell lymphoma. The study starts with lower doses to find the safest effective dose before testing in more people. 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

Azacitidine (AZA) (DRUG): Azacitidine 100 mg is administered subcutaneously once daily from day 1 to day 7. The PD-1 monoclonal antibody 200 mg is administered by intravenous infusion on day 1. Chidamide 20 mg is administered orally twice weekly.

Drugs / treatments
Azacitidine (AZA)
Treatment length
Ask the trial team for details
Visit frequency
Ask the trial team for details

At a glance

Phase
Early Phase 1
Status
Recruiting
Design
Non-randomized, open-label
Enrollment target
30 patients
Primary endpoint
Objective Response Rate (ORR); Complete Response Rate (CRR)
Ages
18 Years to 75 Years
Start date
2026-06-01
Est. completion
2030-01-31

Locations

0 US sites · 1 total

No US sites currently listed.

Contact

Sponsor
Second Affiliated Hospital of Soochow University (OTHER)
Contact
Kang Lu, Master | 15162517756@163.com | 0086-15162517756

Tags

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

An Open-label, Single-arm, Multicenter Phase II Clinical Study of Azacitidine, Chidamide Combined With PD-1 Monoclonal Antibody in the Treatment of Refractory/Relapsed Peripheral T-cell Lymphoma.

NCT07598578

Phase: Early Phase 1 | Status: Recruiting | Priority: Lower

Plain-language summary

This Early Phase 1 trial is evaluating Azacitidine (AZA) as a treatment for people newly diagnosed with T-cell lymphoma. The study starts with lower doses to find the safest effective dose before testing in more people. 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

Azacitidine (AZA) (DRUG): Azacitidine 100 mg is administered subcutaneously once daily from day 1 to day 7. The PD-1 monoclonal antibody 200 mg is administered by intravenous infusion on day 1. Chidamide 20 mg is administered orally twice weekly.

Drugs / treatments: Azacitidine (AZA)

Treatment length: Ask the trial team for details

Visit frequency: Ask the trial team for details

Trial design

Non-randomized, open-label

Enrollment target: 30 patients

Primary endpoint: Objective Response Rate (ORR); Complete Response Rate (CRR)

Ages: 18 Years to 75 Years

Start date: 2026-06-01 | Est. completion: 2030-01-31

Locations

0 US sites · 1 total

Contact

Kang Lu, Master | 15162517756@163.com | 0086-15162517756

Sponsor: Second Affiliated Hospital of Soochow University (OTHER)

Tags

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

View on ClinicalTrials.gov

https://clinicaltrials.gov/study/NCT07598578

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

A free tool to help patients, caregivers, and clinicians find and understand clinical trials for T-cell lymphoma.

Explore

  • Find Trials
  • AI Assistant
  • Letter Generator
  • About
  • Share Your Feedback
  • Terms of Use
  • Privacy Policy

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

Edit with