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Phase 3RecruitingPriority 1 · Highest priorityNCT06724237

Testing Whether High Dose Chemotherapy and Infusion of the Patients' Own Stem Cells Improves Survival in Patients With Peripheral T-cell Lymphoma Who Achieved a Complete Response at the End of the Initial Chemotherapy

ClinicalTrials.gov

Plain-language summary

This Phase 3 trial is comparing different first-line treatment approaches for people newly diagnosed with a type of T-cell lymphoma called AITL. Patients are randomly assigned to different treatment groups to see which approach works best. It is widely available at 158 US locations.

Who can join (key eligibility)

  • Age 18 Years to 75 Years years
  • Newly diagnosed, not yet treated
  • Must be well enough for treatment (adequate performance status)
  • May require specific number of prior treatments

Final eligibility is determined by the trial team. This list is a starting point only.

What's being tested

Autologous Hematopoietic Stem Cell Transplantation (PROCEDURE): Undergo ASCT | Best Practice (OTHER): Receive standard of care observation | Biospecimen Collection (PROCEDURE): Undergo blood sample collection | Bone Marrow Aspiration (PROCEDURE): Undergo bone marrow aspiration and biopsy | Bone Marrow Biopsy (PROCEDURE): Undergo bone marrow aspiration and biopsy | Computed Tomography (PROCEDURE): Undergo CT or PET/CT | High Dose Chemotherapy (DRUG): Receive high dose chemotherapy | Leukapheresis (PROCEDURE): Undergo leukapheresis | Positron Emission Tomography (PROCEDURE): Undergo PET/CT | Stem Cell Mobilization Therapy (DRUG): Receive stem cell mobilization therapy

Drugs / treatments
Autologous Hematopoietic Stem Cell Transplantation, Best Practice, Biospecimen Collection, Bone Marrow Aspiration, Bone Marrow Biopsy, Computed Tomography, High Dose Chemotherapy, Leukapheresis, Positron Emission Tomography, Stem Cell Mobilization Therapy
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
294 patients
Primary endpoint
Progression-free survival (PFS)
Ages
18 Years to 75 Years
Start date
2025-01-30
Est. completion
2033-12-01

Locations

158 US sites · 158 total

AlabamaAlaskaArizonaCaliforniaColoradoDelawareFloridaGeorgiaIdahoIndianaIowaKansasKentuckyLouisianaMarylandMichiganMinnesotaMissouriMontanaNew YorkNorth CarolinaOhioOklahomaOregonPennsylvaniaSouth CarolinaUtahVirginiaWashingtonWisconsin

Contact

Sponsor
Eastern Cooperative Oncology Group (NETWORK)
Contact
Pamela Cogliano | ecog.rss@jimmy.harvard.edu | 857-504-2900

Tags

AITL/TFHALCL ALK−PTCL-NOSNewly diagnosed
TrialCompass — Clinical Trial Summary

Testing Whether High Dose Chemotherapy and Infusion of the Patients' Own Stem Cells Improves Survival in Patients With Peripheral T-cell Lymphoma Who Achieved a Complete Response at the End of the Initial Chemotherapy

NCT06724237

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

Plain-language summary

This Phase 3 trial is comparing different first-line treatment approaches for people newly diagnosed with a type of T-cell lymphoma called AITL. Patients are randomly assigned to different treatment groups to see which approach works best. It is widely available at 158 US locations.

Who can join

  • Age 18 Years to 75 Years years
  • Newly diagnosed, not yet treated
  • Must be well enough for treatment (adequate performance status)
  • May require specific number of prior treatments

What's being tested

Autologous Hematopoietic Stem Cell Transplantation (PROCEDURE): Undergo ASCT | Best Practice (OTHER): Receive standard of care observation | Biospecimen Collection (PROCEDURE): Undergo blood sample collection | Bone Marrow Aspiration (PROCEDURE): Undergo bone marrow aspiration and biopsy | Bone Marrow Biopsy (PROCEDURE): Undergo bone marrow aspiration and biopsy | Computed Tomography (PROCEDURE): Undergo CT or PET/CT | High Dose Chemotherapy (DRUG): Receive high dose chemotherapy | Leukapheresis (PROCEDURE): Undergo leukapheresis | Positron Emission Tomography (PROCEDURE): Undergo PET/CT | Stem Cell Mobilization Therapy (DRUG): Receive stem cell mobilization therapy

Drugs / treatments: Autologous Hematopoietic Stem Cell Transplantation, Best Practice, Biospecimen Collection, Bone Marrow Aspiration, Bone Marrow Biopsy, Computed Tomography, High Dose Chemotherapy, Leukapheresis, Positron Emission Tomography, Stem Cell Mobilization Therapy

Treatment length: Ask the trial team for details

Visit frequency: Ask the trial team for details

Trial design

Randomized, open-label

Enrollment target: 294 patients

Primary endpoint: Progression-free survival (PFS)

Ages: 18 Years to 75 Years

Start date: 2025-01-30 | Est. completion: 2033-12-01

Locations

158 US sites · 158 total

Alabama, Alaska, Arizona, California, Colorado, Delaware, Florida, Georgia, Idaho, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maryland, Michigan, Minnesota, Missouri, Montana, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Utah, Virginia, Washington, Wisconsin

Contact

Pamela Cogliano | ecog.rss@jimmy.harvard.edu | 857-504-2900

Sponsor: Eastern Cooperative Oncology Group (NETWORK)

Tags

AITL/TFH · ALCL ALK− · PTCL-NOS · Newly diagnosed

View on ClinicalTrials.gov

https://clinicaltrials.gov/study/NCT06724237

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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