A Phase 3 Clinical Trial of Pembrolizumab (MK-3475) in First Line Treatment of Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma.

Merck Sharp & Dohme Corp., a Subsidiary of Merck & Co. Inc.0 个研究点目标入组 750 人开始时间: 2015年6月30日最近更新: 2024年3月12日

试验速览

暂无简介。

•Have histologically or cytologically-confirmed R/M HNSCC that is considered incurable by local therapies.
•Have measurable disease based on RECIST 1.1 as determined by the site.
•Have a performance status of 0 or 1 on the ECOG Performance Scale.
•Have results from local testing of HPV positivity for oropharyngeal cancer defined as p16 IHC testing using CINtec® p16 Histology assay and a 70% cut off point.
•Have provided tissue for PD-L1 biomarker analysis from a core or excisional biopsy.
•Are the trial subjects under 18? no
•Number of subjects for this age range:
•F.1.2 Adults (18-64 years) yes
•F.1.2.1 Number of subjects for this age range 600
•F.1.3 Elderly (>=65 years) yes
•F.1.3.1 Number of subjects for this age range 150

•Has disease that is suitable for local therapy administered with curative intent.
•Has progressive disease within six months of completion of curatively intended treatment for locoregionally advanced HNSCC.
•Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to the first dose of trial treatment.
•Has a known history of prior malignancy with recurrence in the last 5 years.
•Active autoimmune disease that has required systemic treatment in past 2 years.
•Has evidence of active, non-infectious pneumonitis.
•Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent or if the patient has previously participated in Merck MK-3475 clinical trials.
•Has an active infection requiring systemic therapy.

发起方

Merck Sharp & Dohme Corp., a Subsidiary of Merck & Co. Inc.