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Phase 3Not yet recruitingPriority 1 · Highest priorityNCT07178457

Brentuximab Vedotin in CutAneous T-cell Lymphomas (CTCL): Post-allogeneic Hematopoietic Stem Cell Transplant Maintenance

ClinicalTrials.gov

Plain-language summary

This Phase 3 trial is comparing Brentuximab Vedotin (Bv) and Placebo against other options for people whose cutaneous T-cell lymphoma (skin 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 to 70 Years years
  • 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

Brentuximab Vedotin (Bv) (DRUG): 1.8 mg/kg in 100 mlof NaCl 0.9%, Q3W with a maximum of 16 cycles | Placebo (DRUG): NaCl 0.9% 100 ml IV Q3W with a maximum of 16 cycles

Drugs / treatments
Brentuximab Vedotin (Bv), Placebo
Treatment length
Ask the trial team for details
Visit frequency
Ask the trial team for details

At a glance

Phase
Phase 3
Status
Not yet recruiting
Design
Randomized, triple blind
Enrollment target
84 patients
Primary endpoint
Progression Free Survival
Ages
18 Years to 70 Years
Start date
2025-11-01
Est. completion
2032-11-01

Locations

0 US sites · 0 total

No US sites currently listed.

Contact

Sponsor
Assistance Publique - Hôpitaux de Paris (OTHER)
Contact
Adèle de Masson, MD PhD | adele.demasson@aphp.fr | +33 (0)1 71 20 75 01

Tags

CTCLMaintenanceRelapsed/Refractory
TrialCompass — Clinical Trial Summary

Brentuximab Vedotin in CutAneous T-cell Lymphomas (CTCL): Post-allogeneic Hematopoietic Stem Cell Transplant Maintenance

NCT07178457

Phase: Phase 3 | Status: Not yet recruiting | Priority: Highest

Plain-language summary

This Phase 3 trial is comparing Brentuximab Vedotin (Bv) and Placebo against other options for people whose cutaneous T-cell lymphoma (skin 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 to 70 Years years
  • Lymphoma came back or did not respond to prior treatment
  • Must be well enough for treatment (adequate performance status)

What's being tested

Brentuximab Vedotin (Bv) (DRUG): 1.8 mg/kg in 100 mlof NaCl 0.9%, Q3W with a maximum of 16 cycles | Placebo (DRUG): NaCl 0.9% 100 ml IV Q3W with a maximum of 16 cycles

Drugs / treatments: Brentuximab Vedotin (Bv), Placebo

Treatment length: Ask the trial team for details

Visit frequency: Ask the trial team for details

Trial design

Randomized, triple blind

Enrollment target: 84 patients

Primary endpoint: Progression Free Survival

Ages: 18 Years to 70 Years

Start date: 2025-11-01 | Est. completion: 2032-11-01

Locations

0 US sites · 0 total

Contact

Adèle de Masson, MD PhD | adele.demasson@aphp.fr | +33 (0)1 71 20 75 01

Sponsor: Assistance Publique - Hôpitaux de Paris (OTHER)

Tags

CTCL · Maintenance · Relapsed/Refractory

View on ClinicalTrials.gov

https://clinicaltrials.gov/study/NCT07178457

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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