Jeffrey Weber, MD, PhD, NYU Langone Health, New York, NY, provides an overview of the Phase III INTerpath-001 trial (NCT05933577), which assesses the efficacy and safety of combining adjuvant pembrolizumab with the individualized neoantigen therapy V940 in patients with resected high-risk stage II-IV melanoma. Eligible patients are stratified by risk and age and will receive pembrolizumab every 6 weeks plus either V940 or placebo every 3 weeks. Primary endpoint is recurrence-free survival, and secondary endpoints including distant metastasis-free survival, overall survival, safety, and quality of life. This interview took place during the 2024 American Society of Clinical Oncology (ASCO) Meeting in Chicago, IL.
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