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OncoMatch/Clinical Trials/NCT06090864

ATLCAR.CD30.CCR4 for CD30+ HL ATLCAR.CD30.CCR4 Cells

Is NCT06090864 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies multiple treatments including Cell infusion and Chemotherapy for hodgkin lymphoma.

Phase 1/2RecruitingUNC Lineberger Comprehensive Cancer CenterNCT06090864Data as of May 2026

Treatment: Chemotherapy · Cell infusionDespite the progress in the therapy, Hodgkin's Lymphoma (HL) remains fatal for more than 15% of patients. Even in patients who are cured, the morbidity of therapy is substantial and long-lasting. New therapeutic agents are required therefore not only to further reduce mortality but also to alleviate morbidity. The majority of HL express the CD30 antigens. CD30 expression is routinely used for the diagnosis of HL. Preclinical observations support CD30 as a viable target of CAR-T therapy. This phase Ib/II study was conducted based on these observations. The purpose of this study is to determine the tolerability of ATLCAR.CD30.CCR4 cells in subjects with Hodgkin's Lymphoma and identify a recommended dose for further. This is a single-center, open-label phase Ib/II trial that uses a 3+3 design to identify a recommended phase 2 dose (RP2D) of ATLCAR.CD30.CCR4 cells in Hodgkin's Lymphoma. The phase II portion is designed to determine the PFS of ATLCAR.CD30.CCR4 in Hodgkin's Lymphoma. Subjects will be enrolled on 1 of 3 dose levels as determined by a 3+3 design. Up to 25 evaluable subjects may then be enrolled in the phase II portion of the study. Subjects may have cells procured to manufacture the ATLCAR.CD30.CCR4 cells if they meet eligibility for procurement. During the time period necessary to manufacture the ATLCAR.CD30.CCR4 cells, Subjects will be allowed to receive standard-of-care bridging therapy at the discretion of their local oncologist. Prior to cell infusion, subjects will undergo additional eligibility evaluations, and then if eligible, will undergo lymphodepletion followed by cell infusion 2-14 days later. Subjects will then be followed for 15 years as is required for studies involving gene transfer experiments.

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Extracted eligibility criteria

Cancer type

Hodgkin Lymphoma

Biomarker criteria

Required: CD30 overexpression

ATLCAR.CD30.CCR4 for CD30+ HL

Prior therapy

Cannot have received: chemotherapy

Subject received chemotherapy or radiation therapy within the previous 3 weeks.

Cannot have received: radiation therapy

Subject received chemotherapy or radiation therapy within the previous 3 weeks.

Cannot have received: investigational agent

Subject received investigational agents or tumor vaccines within 3 weeks.

Cannot have received: tumor vaccine

Subject received investigational agents or tumor vaccines within 3 weeks.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Lineberger Comprehensive Cancer Center · Chapel Hill, North Carolina

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