Immunotherapy for Solid Tumor Malignancies in Pediatrics Using Interleukin-15 and -21 Armored Glypican-3-specific Chimeric Antigen Receptor T Cells

Phase

Condition

Hepatoblastoma

Carcinoma

Hepatic Fibrosis

Treatment

SC-CAR.GPC3xIL15.21 CAR T cells

Clinical Study ID

NCT07148050

IMPACT

Ages 1-26
All Genders

Study Summary

This Phase 1, open-label, non-randomized study will enroll pediatric and young adult subjects with relapsed or refractory non-central nervous system (CNS) malignant solid tumors expressing glypican-3 (GPC3) to examine the safety, feasibility, and efficacy of administering T cell products derived from peripheral blood mononuclear cells (PBMC) that have been genetically modified to co-express a GPC3-specific chimeric antigen receptor (CAR), interleukin (IL)-15 and IL-21 as well as the inducible caspase 9 (iC9) suicide gene (SC-CAR.GPC3xIL15.21 T cells).

A child or young adult meeting all eligibility criteria and meeting none of the exclusion criteria will have a blood sample collected, which will be used to bioengineer the CAR T cells targeting their tumor.

Eligibility Criteria

Inclusion

Procurement Eligibility Inclusion Criteria:

Diagnosis of a solid tumor expressing GPC3
Lansky or Karnofsky score of >=60%
Life expectancy of >16 weeks
Informed consent explained to, understood by and signed by patient/guardian. For patients with hepatocellular carcinoma only:
Barcelona Liver Cancer Stage A, B or C
Child-Pugh Turcotte Score <7

Exclusion

Exclusion Criteria:

History of hypersensitivity reactions to murine protein-containing products ORpresence of human anti-mouse antibody (HAMA) prior to enrollment for patientswho have received prior therapy with murine antibodies.
History of organ transplantation
Known HIV positivity
Active bacterial, fungal, or viral infection (except Hepatitis B orHepatitis C virus infections)

Treatment eligibility

Inclusion Criteria:

Lansky or Karnofsky score of >=60%
Life expectancy of >16 weeks
Informed consent explained to, understood by and signed by patient/guardian.
Adequate organ function
Adequate laboratory values
Refractory or relapsed disease after treatment with up- front therapy and at leastone salvage treatment cycle
Recovered from acute toxic effects of all prior chemotherapy and investigationalagents before entering this study
Sexually active patients must be willing to utilize one of the more effective birthcontrol methods for 12 months after the T-cell infusion.
Informed consent explained to, understood by and signed by patient/guardian.

For patients with hepatocellular carcinoma only:

Barcelona Liver Cancer Stage A, B or C
Child-Pugh Turcotte Score <7

Exclusion Criteria:

History of hypersensitivity reactions to murine protein-containing products ORpresence of human anti-mouse antibody (HAMA) prior to enrollment for patients whohave received prior therapy with murine antibodies.
History of organ transplantation
Known HIV positivity
Active autoimmune or inflammatory disorder
Live vaccines within 30 days prior to enrollment

• Active bacterial, fungal, or viral infection (except Hepatitis B or Hepatitis Cvirus infections)

Pregnancy or lactation
Uncontrolled infection
Systemic steroid treatment (≥ 0.5 mg prednisone equivalent/kg/day, dose adjustmentor discontinuation of medication must occur at least 24hrs prior to CAR T cellinfusion)
Congestive heart failure (as defined by New York Heart Association FunctionalClassification III or IV), unstable angina, serious uncontrolled cardiac arrhythmia,a myocardial infarction within 6 months prior to study entry or a history ofmyocarditis.

Study Design

SC-CAR.GPC3xIL15.21 CAR T cells

December 22, 2025

April 22, 2044

Study Description

Study Overview

This study is testing a different treatment which uses the body's own immune system to recognize and kill the cancer cells, called chimeric antigen receptor (CAR) T cells. Some solid tumors express a specific type of molecule called glypican-3 or GPC3. We are able to insert a new gene (a piece of DNA that contains a set of instructions for the body) into T cells which are a type of immune system cell. This is how we make CAR T cells: We will insert a gene that will program the CAR T cell to recognize GPC3 to make GPC3-CAR T cells. To make GPC3-CAR T cells more effective against tumor cells, we also added two genes called IL15 and IL21 which help CAR T cells grow better and stay in the blood longer. We think that this will kill tumors better. When we did this in the laboratory, we found that this mixture of GPC3-CAR, IL15, and IL21 in T cells killed tumor cells better when compared with GPC3-CAR T cells that did not have IL15 and IL21. This research study will use these cells (named GPC3xIL15.21) to treat patients with solid tumors that express GPC3 on their surface. The GPC3xIL15.21 CAR T cells are an investigational product and have not been approved by the Food and Drug Administration.

We also wanted to make sure that we could stop the GPC3xIL15.21 CAR T cells from growing in the blood if there are any bad or severe side effects. To do so, we inserted a gene called iCasp9 into the GPC3xIL15.21 CAR T cells. This allows us to eliminate the GPC3xIL15.21 CAR T cells in the blood when we give a medicine called AP1903 (also known as rimiducid). Rimiducid is an experimental medicine that has been tested in humans, with no known bad side effects. We only intend to use this medicine to get rid of the GPC3xIL15.21 CAR T cells if you develop dangerous side effects. Approximately 21 people will participate in this study.

Treatment plan

We would first confirm that the participant tumor expresses GPC3. Upon confirmation, a maximum of approximately 6 tablespoons (or 90 mL) of blood will be drawn and sent to Seattle Children's Therapeutics (SCTx) to make the CAR T cells.

After the CAR T cells are made and treatment eligibility has been verified, participants will come to Seattle Children's Hospital for treatment and close monitoring for about one month. Participants will be given lymphodepleting chemotherapy for 3 days, using cyclophosphamide and fludarabine to make room for the CAR T cells, followed by CAR T cell infusion IV.

This is a dose escalation study, which means that the investigators do not know the highest safe dose of CAR T cells. The dose each patient gets depends on how many participants get the agent before that patient and how they react. Since the treatment is experimental, what is likely to happen at any dose is not known.

All of the treatments will be given at Seattle Children's Hospital.

After treatment, participants will be monitored closely for a month to monitor for side effects and response to treatment. After this month, participants would continue to be followed for 15 years after they receive your CAR T cells, with visits becoming less frequent the longer it has been since CAR T cell infusion.

Connect with a study center

Seattle Children's Hospital
Seattle 5809844, Washington 5815135 98105
United States
Active - Recruiting

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