OncoMatch

OncoMatch/Clinical Trials/NCT07202611

DC/NK Cell Therapy

Is NCT07202611 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies In vitro culture of autologous dendritic and natural killer cells for the treatment of patients with non-small cell lung cancer for lung cancer (nsclc).

Phase 2RecruitingNational Taiwan University Clinical Trial CenterNCT07202611Data as of May 2026

Treatment: In vitro culture of autologous dendritic and natural killer cells for the treatment of patients with non-small cell lung cancerPrimary Outcomes The primary objective of this trial is to test the safety of formulations containing dendritic cells (DCs) and natural killer (NK) cells cultured in vitro. By evaluating the reactions following the administration of autologous dendritic cells via axillary lymph node injection and natural killer cells via intravenous injection, the study aims to determine the safety profile of these trial products for human use. Secondary Outcomes To verify the success rate of the cultured cell formulations and assess the cytotoxic capacity of natural killer cells in targeting and killing tumor cells. The evaluation of these secondary objectives involves analyzing specific subcategories, which can be divided into two major components: 1. Validation of Cultured Cell Preparation Success: Assessing the proliferation rate, recovery rate, survival rate, and tumor-killing capacity of the cultured autologous dendritic cells and natural killer cells. 2. Validation of Antitumor Effectiveness: Evaluating the antitumor efficacy of the trial products administered via axillary lymph node injection of autologous dendritic cells and intravenous infusion of autologous natural killer cells.

Check if I qualify

Extracted eligibility criteria

Cancer type

Non-Small Cell Lung Carcinoma

Disease stage

Required: Stage IIIB, IV

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 2 prior lines

Must have received: platinum-based chemotherapy — advanced

Must have received: anti-pd-1 therapy — advanced

Lab requirements

Blood counts

WBC: ≥3000/mm³; Lymphocytes: ≥1000/mm³; Hemoglobin: ≥10 g/dL; Platelets: ≥100,000/mm³

Kidney function

Creatinine: ≤1.25× ULN

Liver function

Total bilirubin: ≤1.5× ULN; SGOT (AST): ≤3× ULN; SGPT (ALT): ≤3× ULN

Normal Blood Count ... Normal Liver and Kidney Function (based on test results within 4 weeks before blood collection for cell preparation)

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

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify