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OncoMatch/Clinical Trials/NCT07382817

Phase 1 Study of JV-394 Autologous Anti-CD94 CAR T for r/r CD94+ T/NK Cell Neoplasms

Is NCT07382817 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies JV-394 for neoplasms.

Phase 1RecruitingM.D. Anderson Cancer CenterNCT07382817Data as of May 2026

Treatment: JV-394The goal of this clinical research study is to find the highest tolerable dose of JV-394 (a type of autologous CAR-T cell therapy) that can be given to patients who have T/NK cell lymphoma that is relapsed or refractory. The safety and possible side effects of JV-394 will also be studied.

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Extracted eligibility criteria

Biomarker criteria

Required: KLRD1 overexpression (≥50% of tumor cells positive for CD94 by flow cytometry or IHC)

≥50% of tumor cells are positive for CD94 by flow cytometry or IHC. Historical documentation of CD94 expression in the tumor is acceptable if available. If there is no historical documentation of CD94 expression, testing of archival tumor tissue or fresh tumor biopsy is required.

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 1 prior line

Lab requirements

Blood counts

Absolute neutrophil count of ≥1.0×10^9 /L; Absolute lymphocyte count of ≥0.1×10^9 /L; Platelet count of ≥75×10^9 /L

Kidney function

Creatinine clearance (as estimated by Cockcroft Gault) ≥45 mL/min

Liver function

Serum alanine transaminase (ALT) / aspartate transaminase (AST) ≤5 times the upper limit of normal (ULN); Total bilirubin ≤2 mg/dL, except in patients with Gilbert's syndrome

Cardiac function

Cardiac ejection fraction ≥45% with no evidence of clinically significant pericardial effusion

Absolute neutrophil count of ≥1.0×10^9 /L. Absolute lymphocyte count of ≥0.1×10^9 /L. Platelet count of ≥75×10^9 /L. Creatinine clearance (as estimated by Cockcroft Gault) ≥45 mL/min. Serum alanine transaminase (ALT) / aspartate transaminase (AST) ≤5 times the upper limit of normal (ULN). Total bilirubin ≤2 mg/dL, except in patients with Gilbert's syndrome. Cardiac ejection fraction ≥45% with no evidence of clinically significant pericardial effusion. Baseline oxygen saturation ≥92% on room air.

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

US trial sites

  • The University of Texas M. D. Anderson Cancer Center · Houston, Texas

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