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Phase 3RecruitingPriority 1 · Highest priorityNCT07234162

A Phase 3 Multinational Study of Golidocitinib Versus Investigator's Choice in r/r PTCL (JACKPOT19)

ClinicalTrials.gov

Plain-language summary

This Phase 3 trial is comparing Golidocitinib, Chidamide, and other medications 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 Years or older
  • Lymphoma came back or did not respond to prior treatment
  • 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

Golidocitinib (DRUG): 150 mg, orally, once daily, with or without food, in a 21-day cycle | Chidamide (DRUG): 30 mg, orally, twice a week, with an interval of no less than 3 days in a 21-day cycle | Gemcitabine (DRUG): 1000 mg/m2, intravenous infusion, administered on Day 1, Day 8 and Day 15 of a 28-day cycle

Drugs / treatments
Golidocitinib, Chidamide, Gemcitabine
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, open-label
Enrollment target
218 patients
Primary endpoint
Progression-free survival (PFS) assessed by the Independent Review Committee (IRC) according to Lugano 2014
Ages
18 Years to —
Start date
2024-05-13
Est. completion
2028-10-31

Locations

0 US sites · 51 total

No US sites currently listed.

Contact

Sponsor
Dizal Pharmaceuticals (INDUSTRY)
Contact
Ling Zhou | ling.zhou@dizalpharma.com | 021-61095755

Tags

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

A Phase 3 Multinational Study of Golidocitinib Versus Investigator's Choice in r/r PTCL (JACKPOT19)

NCT07234162

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

Plain-language summary

This Phase 3 trial is comparing Golidocitinib, Chidamide, and other medications 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 Years or older
  • Lymphoma came back or did not respond to prior treatment
  • Must be well enough for treatment (adequate performance status)

What's being tested

Golidocitinib (DRUG): 150 mg, orally, once daily, with or without food, in a 21-day cycle | Chidamide (DRUG): 30 mg, orally, twice a week, with an interval of no less than 3 days in a 21-day cycle | Gemcitabine (DRUG): 1000 mg/m2, intravenous infusion, administered on Day 1, Day 8 and Day 15 of a 28-day cycle

Drugs / treatments: Golidocitinib, Chidamide, Gemcitabine

Treatment length: Ask the trial team for details

Visit frequency: Ask the trial team for details

Trial design

Randomized, open-label

Enrollment target: 218 patients

Primary endpoint: Progression-free survival (PFS) assessed by the Independent Review Committee (IRC) according to Lugano 2014

Ages: 18 Years to —

Start date: 2024-05-13 | Est. completion: 2028-10-31

Locations

0 US sites · 51 total

Contact

Ling Zhou | ling.zhou@dizalpharma.com | 021-61095755

Sponsor: Dizal Pharmaceuticals (INDUSTRY)

Tags

All T-cell lymphomas · Relapsed/Refractory

View on ClinicalTrials.gov

https://clinicaltrials.gov/study/NCT07234162

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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