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Phase 2RecruitingPriority 3 · Moderate priorityNCT06716658

JAK1 Inhibitor Golidocitnib for the Treatment of Relapsed/Refractory Indolent T/NK-cell Lymphomas

ClinicalTrials.gov

Plain-language summary

This Phase 2 trial is evaluating JAK1 Inhibitor as a treatment for people newly diagnosed with cutaneous T-cell lymphoma (skin 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 or older
  • 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

JAK1 Inhibitor (DRUG): Golidocitnib 150mg QD orally, with a 28-day cycle. Efficacy will be evaluated once per cycle during the first year, and once every two cycles thereafter. Treatment will continue for up to 24 cycles, or until disease progression, lack of response within the first 6 cycles, or the occurrence of intolerable toxicity, whichever occurs first

Drugs / treatments
JAK1 Inhibitor
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
48 patients
Primary endpoint
Overall response rate
Ages
18 Years to —
Start date
2024-12-25
Est. completion
2028-11-15

Locations

0 US sites · 2 total

No US sites currently listed.

Contact

Sponsor
Institute of Hematology & Blood Diseases Hospital, China (OTHER)
Contact
Shuhua Yi, Doctor | yishuhua@ihcams.ac.cn | 86-22-23909106

Tags

CTCLENKTLNewly diagnosedRelapsed/Refractory
TrialCompass — Clinical Trial Summary

JAK1 Inhibitor Golidocitnib for the Treatment of Relapsed/Refractory Indolent T/NK-cell Lymphomas

NCT06716658

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

Plain-language summary

This Phase 2 trial is evaluating JAK1 Inhibitor as a treatment for people newly diagnosed with cutaneous T-cell lymphoma (skin 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 or older
  • Newly diagnosed, not yet treated
  • Must be well enough for treatment (adequate performance status)

What's being tested

JAK1 Inhibitor (DRUG): Golidocitnib 150mg QD orally, with a 28-day cycle. Efficacy will be evaluated once per cycle during the first year, and once every two cycles thereafter. Treatment will continue for up to 24 cycles, or until disease progression, lack of response within the first 6 cycles, or the occurrence of intolerable toxicity, whichever occurs first

Drugs / treatments: JAK1 Inhibitor

Treatment length: Ask the trial team for details

Visit frequency: Ask the trial team for details

Trial design

Non-randomized, open-label

Enrollment target: 48 patients

Primary endpoint: Overall response rate

Ages: 18 Years to —

Start date: 2024-12-25 | Est. completion: 2028-11-15

Locations

0 US sites · 2 total

Contact

Shuhua Yi, Doctor | yishuhua@ihcams.ac.cn | 86-22-23909106

Sponsor: Institute of Hematology & Blood Diseases Hospital, China (OTHER)

Tags

CTCL · ENKTL · Newly diagnosed · Relapsed/Refractory

View on ClinicalTrials.gov

https://clinicaltrials.gov/study/NCT06716658

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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