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OncoMatch/Clinical Trials/NCT07072234

Phase I Study of Allogeneic Transforming Growth Factor-beta Receptor Type 2 Knockout CD70 CAR NK Cells in Treatment Refractory Clear Cell Renal Cell Carcinoma

Is NCT07072234 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments for clear cell carcinoma.

Phase 1RecruitingM.D. Anderson Cancer CenterNCT07072234Data as of May 2026

Treatment: Lymphodepleting chemotherapy · Dexamethasone · Fludarabine · Cyclophosphamate · TGFBR-2 KO CD70 CAR NKTesting an investigational cancer therapy called TGFBR-2 KO CD70 CAR NK cell therapy.

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Extracted eligibility criteria

Biomarker criteria

Required: CD70 expression ≥ 10% by immunohistochemistry (≥ 10%)

Confirmation of CD70 expression ≥ 10% by immunohistochemistry staining of the participants primary renal tumor or a metastatic lesion biopsy specimen will be required for enrollment in the study

Disease stage

Metastatic disease required

metastatic or unresectable and for which standard curative or palliative measures do not exist or are no longer effective

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 2 prior lines

Must have received: immune checkpoint inhibitor

Participants must have previously received treatment with at least one ICI...Participants must have had unequivocal disease progression on ICI treatment

Must have received: tyrosine kinase inhibitor

Participants must have previously received treatment with at least one...TKI

Lab requirements

Blood counts

ANC ≥ 1000/mm3, platelet count ≥ 75,000/mm3, hemoglobin ≥ 8 g/dL

Kidney function

Serum creatinine ≤ 1.5 mg/dL or estimated glomerular filtration rate ≥30 ml/min/1.73 m2

Liver function

ALT/AST ≤ 2.5 x ULN or ≤ 5 x ULN if documented liver metastases, total bilirubin ≤ 1.5 mg/dL or ≤ 3.0 mg/dL for Participants with Gilbert's Syndrome. No history of liver cirrhosis.

Cardiac function

Cardiac ejection fraction ≥ 40%, no clinically significant pericardial effusion, no symptomatic cardiac disease or history of serious ventricular arrhythmia, high-grade atrioventricular block, or other cardiac arrhythmias requiring anti-arrhythmic medications (except for atrial fibrillation that is well controlled with anti-arrhythmic medication)

Adequate organ function at screening, as defined by the following: Renal: Serum creatinine ≤ 1.5 mg/dL or estimated glomerular filtration rate ≥30 ml/min/1.73 m2; Hepatic: ALT/AST ≤ 2.5 x ULN or ≤ 5 x ULN if documented liver metastases, total bilirubin ≤ 1.5 mg/dL or ≤ 3.0 mg/dL for Participants with Gilbert's Syndrome. No history of liver cirrhosis; Cardiac: Cardiac ejection fraction ≥ 40%, no clinically significant pericardial effusion as determined by echocardiogram (ECHO) or multigated acquisition (MUGA) scan, and no symptomatic cardiac disease or history of serious ventricular arrhythmia (ie, ventricular tachycardia or ventricular fibrillation), high-grade atrioventricular block, or other cardiac arrhythmias requiring anti-arrhythmic medications (except for atrial fibrillation that is well controlled with anti-arrhythmic medication); Pulmonary: No clinically significant pleural effusion (per principal investigator [PI] judgement), and baseline oxygen saturation ≥ 92% on room air. Subjects with active interstitial lung disease (ILD)/pneumonitis requiring treatment with systemic steroids will be excluded; Hematological: ANC ≥ 1000/mm3, platelet count ≥ 75,000/mm3, and hemoglobin ≥ 8 g/dL; Coagulation: INR ≤ 1.5 ULN and aPTT ≤ 1.5 ULN. Participants on therapeutic doses of anticoagulation medication must have INR and/or aPTT ≤ the upper limit of the therapeutic range for intended use.

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

US trial sites

  • MD Anderson Cancer Center · Houston, Texas

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