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OncoMatch/Clinical Trials/NCT06839066

A Phase II Study to Evaluate HLX43 in Subjects With Recurrent/Metastatic Nasopharyngeal Carcinoma Failed or Intolerance to Second-line Therapy

Is NCT06839066 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including HLX43 DOSE 1 and HLX43 DOSE 2 for nasopharyngeal carcinoma (npc).

Phase 2RecruitingShanghai Henlius BiotechNCT06839066Data as of May 2026

Treatment: HLX43 DOSE 1 · HLX43 DOSE 2 · HLX43 DOSE 3The study is to explore the reasonable dosage and to evaluate the efficacy, safety and tolerability of HLX43 (Anti-PD-L1 ADC) in patients with recurrent/metastatic Nasopharyngeal Carcinoma (NPC) who failed or are intolerant to second-line herapy.

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Extracted eligibility criteria

Cancer type

Head and Neck Squamous Cell Carcinoma

Biomarker criteria

Required: PD-L1 (CD274) any tested (testing required; no eligibility threshold specified)

Disease stage

Metastatic disease required

recurrent/metastatic nasopharyngeal carcinoma; at least one measurable lesion per RECIST v1.1

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 2 prior lines

Must have received: chemotherapy

failed or are intolerant to at least two prior lines of chemotherapy (including at least one platinum-based regimen)

Must have received: platinum-based chemotherapy

including at least one platinum-based regimen

Must have received: anti-PD-1 therapy

failed or are intolerant to...PD-1/PD-L1 inhibitor therapy

Must have received: anti-PD-L1 therapy

failed or are intolerant to...PD-1/PD-L1 inhibitor therapy

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

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