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Phase 2Not yet recruitingPriority 3 · Moderate priorityNCT07457177

Phaes Ⅱ Study of Golidocitinib-Pegaspargase-PD-1 Antibody First-Line for Advanced ENKTL

ClinicalTrials.gov

Plain-language summary

This Phase 2 trial is evaluating Golidocitinib + Pegaspargase + Anti-PD-1 mAb as a treatment for people newly diagnosed with NK/T-cell 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

Golidocitinib + Pegaspargase + Anti-PD-1 mAb (DRUG): * Golidocitinib: 150 mg orally, once daily, continuous administration. * Pegaspargase: 2000-2500 IU/m² intravenously, once every 3 weeks (Day 1 of each cycle). * Anti-PD-1 mAb: Administered per product labeling, once every 3 weeks (Day 1 of each cycle). * Treatment Cycle: 3 weeks per cycle; combined treatment for up to 6 cycles. Patients achieving response may receive maintenance therapy with golidocitinib and/or anti-PD-1 mAb for up to 24 months.

Drugs / treatments
Golidocitinib + Pegaspargase + Anti-PD-1 mAb
Treatment length
Ask the trial team for details
Visit frequency
Ask the trial team for details

At a glance

Phase
Phase 2
Status
Not yet recruiting
Design
Non-randomized, open-label
Enrollment target
40 patients
Primary endpoint
Complete Response Rate (CRR)
Ages
18 Years to —
Start date
2026-02-10
Est. completion
2030-01-30

Locations

0 US sites · 0 total

No US sites currently listed.

Contact

Sponsor
LIANG WANG (OTHER)
Contact
Liang Wang | wangliangtrhos@126.com | +86 15001108693

Tags

ENKTLNewly diagnosedRelapsed/Refractory
TrialCompass — Clinical Trial Summary

Phaes Ⅱ Study of Golidocitinib-Pegaspargase-PD-1 Antibody First-Line for Advanced ENKTL

NCT07457177

Phase: Phase 2 | Status: Not yet recruiting | Priority: Medium

Plain-language summary

This Phase 2 trial is evaluating Golidocitinib + Pegaspargase + Anti-PD-1 mAb as a treatment for people newly diagnosed with NK/T-cell 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

Golidocitinib + Pegaspargase + Anti-PD-1 mAb (DRUG): * Golidocitinib: 150 mg orally, once daily, continuous administration. * Pegaspargase: 2000-2500 IU/m² intravenously, once every 3 weeks (Day 1 of each cycle). * Anti-PD-1 mAb: Administered per product labeling, once every 3 weeks (Day 1 of each cycle). * Treatment Cycle: 3 weeks per cycle; combined treatment for up to 6 cycles. Patients achieving response may receive maintenance therapy with golidocitinib and/or anti-PD-1 mAb for up to 24 months.

Drugs / treatments: Golidocitinib + Pegaspargase + Anti-PD-1 mAb

Treatment length: Ask the trial team for details

Visit frequency: Ask the trial team for details

Trial design

Non-randomized, open-label

Enrollment target: 40 patients

Primary endpoint: Complete Response Rate (CRR)

Ages: 18 Years to —

Start date: 2026-02-10 | Est. completion: 2030-01-30

Locations

0 US sites · 0 total

Contact

Liang Wang | wangliangtrhos@126.com | +86 15001108693

Sponsor: LIANG WANG (OTHER)

Tags

ENKTL · Newly diagnosed · Relapsed/Refractory

View on ClinicalTrials.gov

https://clinicaltrials.gov/study/NCT07457177

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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