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Constitutive IL7R (C7R) Modified Banked Allogeneic CD30 Chimeric Antigen Receptor Epstein-Barr Virus-Specific T Lymphocytes (CD30.CAR-EBVSTs) in Patients With Relapsed or Refractory CD30-Positive Lymphomas

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

This study involves patients with diffuse large B cell lymphoma (DLBCL), natural killer/T-cell lymphoma (NKTL), or classical Hodgkin lymphoma (cHL) (referred to collectively as lymphoma) whose disease has returned or not responded to treatment. Previous research combined antibodies and T cells to treat cancer. Antibodies bind to foreign substances, and T cells are infection-fighting white blood cells that can kill tumor cells. Both approaches have shown promise but have not been sufficient to cure most patients. In prior studies, an antibody targeting CD30, a protein found on some T cells and cancer cells, was joined to T cells through gene transfer to create CD30.CAR T cells. Another study showed encouraging responses using CD30.CAR T cells made from a patient's own blood and returned to the same patient (autologous cells). In an ongoing study, patients have been treated with CD30.CAR T cells derived from healthy donors (allogeneic cells), allowing use of banked cells without individualized manufacturing. This approach has shown promising clinical activity with no safety concerns to date. In this study, investigators are evaluating CD30.CAR-EBVST cells modified with an additional molecule called C7R, which has been shown in laboratory studies to enhance anti-cancer effects. The study aims to assess the safety and effectiveness of these allogeneic, banked C7R-modified CD30.CAR-EBVST cells and determine whether they may help treat lymphoma. As an added safety measure, the modified T cells include a marker called iC9. If significant side effects occur, patients may receive rimiducid, which can eliminate the infused T cells. Rimiducid is not yet FDA approved but has been tested in patients without significant side effects.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 12
Maximum Age: 75
Healthy Volunteers: f
View:

• Diagnosis and clinical course falling into one of the following categories:

∙ Hodgkin lymphoma

‣ CD30+ aggressive B-cell lymphoma

‣ ALK-negative anaplastic T cell lymphoma or other peripheral T- cell lymphoma

‣ ALK-positive anaplastic T cell lymphoma

• CD30-positive tumor as assayed in a CLIA certified Pathology Laboratory.

• Age 12 to 75.

• Bilirubin less than or equal to 2 times the upper limit of normal (except for Gilbert syndrome, where the criteria will be Bilirubin less than or equal to 3 times the upper limit of normal).

• AST less than 3 times the upper limit of normal.

• Estimated GFR \> 70 mL/min.

• Pulse oximetry of \> 90% on room air

• Karnofsky or Lansky score of \> 60%.

• Recovered from all acute non-hematologic toxic effects of all prior chemotherapy.

⁃ Sexually active patients must be willing to utilize one of the more effective birth control methods during the study and for 6 months after the study is concluded. The male partner should use a condom.

⁃ Informed consent explained to, understood by and signed by patient or guardian. Patient or guardian given a copy of the informed consent form.

Locations
United States
Texas
Houston Methodist Hospital
RECRUITING
Houston
Texas Children's Hospital
NOT_YET_RECRUITING
Houston
Contact Information
Primary
Premal Lulla, MD
lulla@bcm.edu
713-441-1450
Backup
Vicky Torrano, RN
vtorrano@bcm.edu
(832) 824-7821
Time Frame
Start Date: 2025-10-27
Estimated Completion Date: 2043-06-27
Participants
Target number of participants: 90
Treatments
Experimental: Treatment Phase
Four dose levels will be evaluated based on safety data from our current study of CD30 CAR T cells.~Cohorts of three patients will be enrolled at each dose level The dose is based on the number of CD.30 CAR-EBVT-expressing cells administered.~The total number of dose levels evaluated will depend upon toxicities experienced. Dose level cohorts will be numbered sequentially.~* Dose Level 1: 4 × 10\^7 C7R.CD30.CAR-EBVST cells~* Dose Level 2: 1 × 10\^8 C7R.CD30.CAR-EBVST cells~* Dose Level 3: 4 × 10\^8 C7R.CD30.CAR-EBVST cells~* Dose Level 4: 8 × 10\^8 C7R.CD30.CAR-EBVST cells
Sponsors
Collaborators: Center for Cell and Gene Therapy, Baylor College of Medicine, The Methodist Hospital Research Institute
Leads: Baylor College of Medicine

This content was sourced from clinicaltrials.gov

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