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Phase 2RecruitingPriority 3 · Moderate priorityNCT02859402

Allogeneic Stem Cell Transplantation in Relapsed/Refractory T-, NK/T-cell Lymphomas

ClinicalTrials.gov

Plain-language summary

This Phase 2 trial is evaluating Busulfan and Fludarabine 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 19 Years to 65 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

Busulfan (DRUG): intravenous, 3.2 mg/kg + 5% DW (the diluent quantity should be 10 times the volume of Busulfan, so that the final concentration of busulfan becomes approximately 0.5 mg/mL), once daily for 3 hours for 3 days (days -7 to -5) | Fludarabine (DRUG): intravenous, 30 mg/m2 + 5% DW 100㎖, over 1 hour once daily for 6 days (days -8 to -3)

Drugs / treatments
Busulfan, Fludarabine
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
34 patients
Primary endpoint
2-year progression-free survival
Ages
19 Years to 65 Years
Start date
2016-12
Est. completion
2027-12

Locations

0 US sites · 2 total

No US sites currently listed.

Contact

Sponsor
Keimyung University Dongsan Medical Center (OTHER)
Contact
Young Rok Do, MD., Ph.D. | dyr1160@dsmc.or.kr | +82-10-3541-1160

Tags

ENKTLNewly diagnosedRelapsed/Refractory
TrialCompass — Clinical Trial Summary

Allogeneic Stem Cell Transplantation in Relapsed/Refractory T-, NK/T-cell Lymphomas

NCT02859402

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

Plain-language summary

This Phase 2 trial is evaluating Busulfan and Fludarabine 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 19 Years to 65 Years years
  • Newly diagnosed, not yet treated
  • Must be well enough for treatment (adequate performance status)

What's being tested

Busulfan (DRUG): intravenous, 3.2 mg/kg + 5% DW (the diluent quantity should be 10 times the volume of Busulfan, so that the final concentration of busulfan becomes approximately 0.5 mg/mL), once daily for 3 hours for 3 days (days -7 to -5) | Fludarabine (DRUG): intravenous, 30 mg/m2 + 5% DW 100㎖, over 1 hour once daily for 6 days (days -8 to -3)

Drugs / treatments: Busulfan, Fludarabine

Treatment length: Ask the trial team for details

Visit frequency: Ask the trial team for details

Trial design

Non-randomized, open-label

Enrollment target: 34 patients

Primary endpoint: 2-year progression-free survival

Ages: 19 Years to 65 Years

Start date: 2016-12 | Est. completion: 2027-12

Locations

0 US sites · 2 total

Contact

Young Rok Do, MD., Ph.D. | dyr1160@dsmc.or.kr | +82-10-3541-1160

Sponsor: Keimyung University Dongsan Medical Center (OTHER)

Tags

ENKTL · Newly diagnosed · Relapsed/Refractory

View on ClinicalTrials.gov

https://clinicaltrials.gov/study/NCT02859402

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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