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NARecruitingPriority 4 · Lower priorityNCT07074457

Chidamide Combined With Brentuximab Vedotin Regimen for CD30+ PTCL Patients

ClinicalTrials.gov

Plain-language summary

This NA trial is comparing different first-line treatment approaches for people newly diagnosed with T-cell lymphoma. Patients are randomly assigned to different treatment groups to see which approach works best. 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

Induction therapy-3 cycles of BvC (Brentuximab vedotin plus Chidamide) (DRUG): 3 cycles of BvC treatment for all enrolled patients. Brentuximab vedotin; Specification: 50mg per vial; 1.8mg/kg qd d1 every 3 weeks, ivgtt.; Chidamide; Specification: 5mg per tablet; 20mg biw for 2 weeks every 3 weeks, po.; | Consolidation therapy- 3 or 6 cycles of BvC(Brentuximab vedotin plus chidamide) (DRUG): Consolidation therapy( For patients who achieved CR after induction therapy, 3 cycles of additional BvC treatment; For patients who achieved PR after induction therapy, 6 cycles of additional BvC treatment). Brentuximab vedotin; Specification: 50mg per vial; 1.8mg/kg qd d1 every 3 weeks, ivgtt.; Chidamide; Specification: 5mg per tablet; 20mg biw for 2 weeks every 3 weeks, po.; Maintenance therapy chidamide (20mg biw for 2 weeks every 3 weeks, po.) for ≥2 years | Maintenance therapy-chidamide (DRUG): Chidamide (20mg biw for 2 weeks every 3 weeks, po.) for ≥2 years

Drugs / treatments
Induction therapy-3 cycles of BvC (Brentuximab vedotin plus Chidamide), Consolidation therapy- 3 or 6 cycles of BvC(Brentuximab vedotin plus chidamide), Maintenance therapy-chidamide
Treatment length
Ask the trial team for details
Visit frequency
Ask the trial team for details

At a glance

Phase
NA
Status
Recruiting
Design
Non-randomized, open-label
Enrollment target
47 patients
Primary endpoint
Complete response rate(CRR)
Ages
18 Years to 75 Years
Start date
2024-11-01
Est. completion
2028-11-01

Locations

0 US sites · 1 total

No US sites currently listed.

Contact

Sponsor
The First Affiliated Hospital of Soochow University (OTHER)
Contact
Zhengming Jin | jinzhengming519519@163.com | 67781856

Tags

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

Chidamide Combined With Brentuximab Vedotin Regimen for CD30+ PTCL Patients

NCT07074457

Phase: NA | Status: Recruiting | Priority: Lower

Plain-language summary

This NA trial is comparing different first-line treatment approaches for people newly diagnosed with T-cell lymphoma. Patients are randomly assigned to different treatment groups to see which approach works best. 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

Induction therapy-3 cycles of BvC (Brentuximab vedotin plus Chidamide) (DRUG): 3 cycles of BvC treatment for all enrolled patients. Brentuximab vedotin; Specification: 50mg per vial; 1.8mg/kg qd d1 every 3 weeks, ivgtt.; Chidamide; Specification: 5mg per tablet; 20mg biw for 2 weeks every 3 weeks, po.; | Consolidation therapy- 3 or 6 cycles of BvC(Brentuximab vedotin plus chidamide) (DRUG): Consolidation therapy( For patients who achieved CR after induction therapy, 3 cycles of additional BvC treatment; For patients who achieved PR after induction therapy, 6 cycles of additional BvC treatment). Brentuximab vedotin; Specification: 50mg per vial; 1.8mg/kg qd d1 every 3 weeks, ivgtt.; Chidamide; Specification: 5mg per tablet; 20mg biw for 2 weeks every 3 weeks, po.; Maintenance therapy chidamide (20mg biw for 2 weeks every 3 weeks, po.) for ≥2 years | Maintenance therapy-chidamide (DRUG): Chidamide (20mg biw for 2 weeks every 3 weeks, po.) for ≥2 years

Drugs / treatments: Induction therapy-3 cycles of BvC (Brentuximab vedotin plus Chidamide), Consolidation therapy- 3 or 6 cycles of BvC(Brentuximab vedotin plus chidamide), Maintenance therapy-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: 47 patients

Primary endpoint: Complete response rate(CRR)

Ages: 18 Years to 75 Years

Start date: 2024-11-01 | Est. completion: 2028-11-01

Locations

0 US sites · 1 total

Contact

Zhengming Jin | jinzhengming519519@163.com | 67781856

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

Tags

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

View on ClinicalTrials.gov

https://clinicaltrials.gov/study/NCT07074457

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.

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Data last updated: June 2026

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