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OncoMatch/Clinical Trials/NCT04875611

Nivolumab in Nasopharyngeal Cancer With Progression During or After Platinum-based Treatment

Is NCT04875611 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Opdivo for nasopharyngeal cancer.

Phase 2RecruitingMaria Sklodowska-Curie National Research Institute of OncologyNCT04875611Data as of Jun 2026Location: Poland

Treatment: OpdivoMulticentre , non-randomized, prospective clinical trial to assess efficacy of Nivolumab in treatment of nasopharyngeal cancer who progressed during or after platinum-based chemotherapy . Patients disqualified from radical therapy . The total number of patients was estimated for 32.

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Opdivo

Cancer type

Head and Neck Squamous Cell Carcinoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 1 prior line

Must have received: platinum-based chemotherapy

Previous, documented failure on platinum-based chemotherapy or progression of the disease during platinum-based chemotherapy

Cannot have received: anti-PD-1/PD-L1/PD-L2 or anti-ICOS directed agent

Prior therapy with an anti-PD-1/L1/L2 and/or anti-ICOS directed agent

Cannot have received: bone marrow or solid organ transplantation

Patient with prior bone marrow or solid organ transplantation.

Lab requirements

Blood counts

hemoglobin < 9 g/dl, platelets < 100 x 10^9 /L, ANC < 1.0 x 10^9 /L

Kidney function

eGFR < 30 ml/min/m2

Liver function

AST and/or ALT > 2.5 x ULN (> 5 x ULN in patients with documented liver metastases); total bilirubin > 1.5 x ULN (acceptable if direct bilirubin < 35%); albumin < 2.5 g/dL

Cardiac function

ejection fraction in echocardiography < 50%

Presence of renal insufficiency defined as eGFR < 30 ml/min/m2; Presence of liver disfunction, defined as level of AST and/or ALT > 2.5 x ULN (> 5 x ULN in patients with documented liver metastases); total bilirubin > 1.5 x ULN (acceptable if direct bilirubin < 35%) or albumin < 2.5 g/dL; Abnormalities in blood count such as: hemoglobin < 9 g/dl, platelets < 100 x 10^9 /L, ANC <1.0 x 10^9 /L; Ejection fraction in echocardiography < 50%

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

Frequently asked questions

Is NCT04875611 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior anti-PD-1/PD-L1/PD-L2 or anti-ICOS directed agent, bone marrow or solid organ transplantation disqualifies patients from enrollment.

Could you qualify for this trial?

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

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