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Phase 3RecruitingPriority 1 · Highest priorityNCT06776952

A Randomized, Double-blind, Multicenter Phase III Study of XNW5004 Tablets in Patients With Relapsed or Refractory Peripheral T-cell Lymphoma

ClinicalTrials.gov

Plain-language summary

This Phase 3 trial is comparing XNW5004 ; Chidamide placebo and XNW5004 placebo; Chidamide against other options for people whose T-cell lymphoma has come back or has not responded to previous treatment. 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 Days to 70 Days years
  • Lymphoma came back or did not respond to prior treatment
  • Must be well enough for treatment (adequate performance status)
  • May require specific number of prior treatments

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

What's being tested

XNW5004 ; Chidamide placebo (DRUG): XNW5004 + Chidamide placebo | XNW5004 placebo; Chidamide (DRUG): XNW5004 placebo + Chidamide

Drugs / treatments
XNW5004 ; Chidamide placebo, XNW5004 placebo; Chidamide
Treatment length
Ask the trial team for details
Visit frequency
Ask the trial team for details

At a glance

Phase
Phase 3
Status
Recruiting
Design
Randomized, quadruple blind
Enrollment target
120 patients
Primary endpoint
Progression Free Survival (PFS) assessed by BICR
Ages
18 Days to 70 Days
Start date
2025-04-10
Est. completion
2028-04

Locations

0 US sites · 1 total

No US sites currently listed.

Contact

Sponsor
Evopoint Biosciences Inc. (INDUSTRY)
Contact
Yuqin Song | SongYQ_VIP@163.com | 010-88196118

Tags

All T-cell lymphomasRelapsed/Refractory
TrialCompass — Clinical Trial Summary

A Randomized, Double-blind, Multicenter Phase III Study of XNW5004 Tablets in Patients With Relapsed or Refractory Peripheral T-cell Lymphoma

NCT06776952

Phase: Phase 3 | Status: Recruiting | Priority: Highest

Plain-language summary

This Phase 3 trial is comparing XNW5004 ; Chidamide placebo and XNW5004 placebo; Chidamide against other options for people whose T-cell lymphoma has come back or has not responded to previous treatment. 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 Days to 70 Days years
  • Lymphoma came back or did not respond to prior treatment
  • Must be well enough for treatment (adequate performance status)
  • May require specific number of prior treatments

What's being tested

XNW5004 ; Chidamide placebo (DRUG): XNW5004 + Chidamide placebo | XNW5004 placebo; Chidamide (DRUG): XNW5004 placebo + Chidamide

Drugs / treatments: XNW5004 ; Chidamide placebo, XNW5004 placebo; Chidamide

Treatment length: Ask the trial team for details

Visit frequency: Ask the trial team for details

Trial design

Randomized, quadruple blind

Enrollment target: 120 patients

Primary endpoint: Progression Free Survival (PFS) assessed by BICR

Ages: 18 Days to 70 Days

Start date: 2025-04-10 | Est. completion: 2028-04

Locations

0 US sites · 1 total

Contact

Yuqin Song | SongYQ_VIP@163.com | 010-88196118

Sponsor: Evopoint Biosciences Inc. (INDUSTRY)

Tags

All T-cell lymphomas · Relapsed/Refractory

View on ClinicalTrials.gov

https://clinicaltrials.gov/study/NCT06776952

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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