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 that have a cancer called diffuse large B cell lymphoma (DLBCL), Natural killer/T-cell lymphoma (NKTL), or classical Hodgkin lymphoma (cHL) (referred to collectively as lymphoma). Patients' lymphoma has come back or not gone away after treatment. A previous research study at Baylor combined two ways of fighting disease: antibodies and T cells. Antibodies are proteins that bind to bacteria, viruses and other foreign substances to prevent disease. T-cells are special infection-fighting white blood cells that can kill tumor cells or cells infected with bacteria and viruses. Both have shown promise treating cancer, but neither has been strong enough to cure most patients. In the previous study, an antibody called anti-CD30 which is found on the surface of some T-cells and cancer cells, and had been used to treat lymphoma with limited success, was joined to the T-cells through a process called gene transfer, resulting in CD30.CAR T cells. Another study saw encouraging responses using CD30.CAR T cells made in a lab from a patients' own blood then injected back into the same patient to treat their lymphoma. These cells are termed 'autologous' because they're given back to the original patient. In an ongoing study, patients were treated with allogeneic CD30.CAR T cells, which are made from healthy donors instead of the patients. The use of allogenic cells avoids a lengthy manufacture time since the products are stored as a bank and available on demand. This ongoing trial has preliminarily shown promising clinical activity with no safety concerns. With the current study, investigators plan to extend the anti-cancer effects of the CD30.CAR T cell by attaching another molecule called C7R, which has made CAR T cells have deeper and longer anticancer effects in the laboratory. The aim is to study the safety and effectiveness of allogeneic banked CD30.CAR-EBVST cells that also carry the C7R molecule, to learn the side effects of C7R modified CD30.CAR-EBVST cells in lymphoma patients, and to see whether this therapy may help them. As an extra safety step, the C7R containing T cells will also have a marker called iC9. If a patient experiences intolerable side effects from the C7R T cells, they could receive a medication called 'rimiducid' that can eliminate the C7R containing T cells by binding iC9, thereby potentially resolving the side effects. While not yet FDA approved, rimiducid has been tested in patients before without bad 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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