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NCT07565389PHASE2NOT_YET_RECRUITING

Evaluating Ivonescimab in PD-1 Resistant Recurrent or Metastatic Nasopharyngeal Carcinoma

Phase II Open-label Study Evaluating Ivonescimab in PD-1 Resistant Recurrent or Metastatic Nasopharyngeal Carcinoma

Sponsor: National University Hospital, Singapore

No open prediction endpoints

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Key Facts

Study type
INTERVENTIONAL
Conditions
Nasopharyngeal Carcinoma (NPC)
Interventions
Ivonescimab 20 mg/kg
Enrollment
42 participants
Primary completion
May 2031
Study completion
May 2031
First posted
May 2026
Last updated
May 2026

Primary Endpoints (CT.gov)

Objective Response Rate (ORR)

Time frame: Best response at 1 year

Secondary Endpoints

Progression-Free Survival (PFS)

Overall Survival (OS)

Duration of Response (DoR)

Eligibility Criteria

Inclusion Criteria: * Participant is eligible to be included in the study only if all the following criteria are met: 1. The participant (or legally acceptable representative if applicable) provides written consent for the trial. 2. Participant is at least 21 years of age on the day of signing informed consent 3. Has a locally or centrally determined histologically or cytologically confirmed diagnosis of Epstein Barr Virus (EBV)-positive nasopharyngeal carcinoma Note: The EBV status is to be determined by the EBV-encoded small RNA in situ hybridization (EBER in situ hybridization \[ISH\]) assay. If EBV-positive status has been previously determined by EBER ISH assay, then no re-testing is required. If EBV status by EBER ISH assay has not been previously determined, tumour tissue from archival tissue may be submitted for EBV determination. 4. Has recurrent or metastatic (R/M) disease not amenable to curative local therapy (surgery or radiation) 5. Must have seen at least 1 p

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✦ Analyst Commentary

Expert commentary on why this trial matters and what to watch for.

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Source

Open on ClinicalTrials.gov