Yttrium-90 Anti-CD25 Antibody with BEAM Chemotherapy for Relapsed/Refractory Hodgkin Lymphoma

This study is testing a new treatment for Hodgkin lymphoma that has either come back (relapsed) or didn't respond to previous treatments (refractory). It combines a special antibody called yttrium-90 labeled anti-CD25 with a chemotherapy regimen known as BEAM (carmustine, etoposide, cytarabine, and melphalan). The yttrium-90 labeled anti-CD25 is an antibody (a protein made by your immune system) that has a radioactive substance attached. It's designed to kill cancer cells and shrink tumors. The BEAM chemotherapy drugs work in different ways to stop cancer cells from growing or spreading. We want to see how well this combined treatment prevents the cancer from returning for up to 5 years after treatment. You may be eligible if you are 18 or older with Hodgkin lymphoma that has relapsed or is refractory.

Study design
This is a phase II interventional study aiming to enroll 33 participants. It is testing a specific combination of treatments.
What's involved
You will receive 'cold' basiliximab and yttrium Y 90 basiliximab intravenously (IV) on day -14. You will also receive carmustine, etoposide, cytarabine, and melphalan IV over several days leading up to a stem cell infusion.
Compensation
Not stated in the trial record.
Follow-up
Your progression-free survival will be measured for up to 5 years after the transplant. Overall survival and other outcomes will be tracked for 100 days, 1 year, and 2 years.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT04871607

Yttrium-90 Labeled Anti-CD25 Monoclonal Antibody Combined With BEAM Chemotherapy Conditioning for the Treatment of Primary Refractory or Relapsed Hodgkin Lymphoma

Recruiting
PHASE2Ages 18+InterventionalTreatment
City of Hope Medical Center
~33 participants
Updated 2025-12-04 on ClinicalTrials.gov
What's tested:BasiliximabCarmustineCytarabineEtoposideGenetically Engineered Hematopoietic Stem Progenitor CellsRecombinant Granulocyte Colony-Stimulating Factor

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Progression free survival
Measured over From the start of treatment up to 5 years post transplant
Recurrent Hodgkin Lymphoma
Refractory Hodgkin Lymphoma

NCT04871607

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • City of Hope Medical Center

    Duarte, Californiastudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Alex F Herrera · PRINCIPAL_INVESTIGATOR · City of Hope Medical Center

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Eligibility criteria

Inclusion

B symptoms at relapse
Extranodal disease at relapse
Primary refractory disease'
Relapse \< 1 year after completion of frontline therapy
Not in CR at the time of transplant
Relapse after receiving PD1 blockade or brentuximab vedotin as initial therapy 6. Patients will be enrolled after collection of at least 2.0 x 106 CD34 cells/kg of autologous hematopoietic progenitor cells (HPC-A) by apheresis. 7. Recovery from non-hematologic toxicities of salvage cytoreductive chemotherapy to ≤ grade 2 (CTCAE v5).
Childbearing potential defined as not being surgically sterilized (men and women) or have not been free from menses for \> 1 year (women only).

Exclusion

Eligibility should be confirmed per institutional policies.
  • Progression free survivalFrom the start of treatment up to 5 years post transplant

    Disease relapse or progression, or death from any cause, whichever occurs first. Will be calculated using the Kaplan-Meier method.