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Brief Title: Talimogene Laherparepvec With Pembrolizumab for Recurrent Metastatic Squamous Cell Carcinoma of the Head and Neck (MASTERKEY232 / KEYNOTE-137)
Official Title: A Phase 1b/3 Multicenter, Randomized, Trial of Talimogene Laherparepvec in Combination With Pembrolizumab for the Treatment of Subjects With Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck
Study ID: NCT02626000
Brief Summary: The primary objective of this study was to evaluate the safety, as assessed by incidence of dose limiting toxicity (DLT), of talimogene laherparepvec in combination with pembrolizumab in adults with recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN).
Detailed Description: This is a phase 1b/3, multicenter, clinical trial conducted in 2 parts (phase 1b and phase 3). In phase 1b talimogene laherparepvec is to be administered in combination with pembrolizumab to adults with recurrent or metastatic squamous cell carcinoma of head and neck (SCCHN). Dose limiting toxicity (DLT) is to be evaluated based on the first 18 DLT-evaluable participants. An expansion cohort of up to an additional 22 treated patients could be enrolled to further evaluate the safety and to estimate the efficacy of the combination of talimogene laherparepvec with pembrolizumab and to support a decision to initiate the phase 3 part of the study. The phase 3 part of the study was designed as a multicenter, randomized, double-blind, placebo-controlled study to evaluate the efficacy, as assessed by overall survival, of treatment with talimogene laherparepvec with pembrolizumab versus placebo with pembrolizumab in adults with recurrent or metastatic SCCHN, however, a decision was made not to proceed to the phase 3 part of the study.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Research Site, Newark, Delaware, United States
Research Site, Chicago, Illinois, United States
Research Site, Chicago, Illinois, United States
Research Site, Louisville, Kentucky, United States
Research Site, Billings, Montana, United States
Research Site, New York, New York, United States
Research Site, New York, New York, United States
Research Site, Canton, Ohio, United States
Research Site, Geelong, Victoria, Australia
Research Site, Melbourne, Victoria, Australia
Research Site, Salzburg, , Austria
Research Site, Bruxelles, , Belgium
Research Site, Wilrijk, , Belgium
Research Site, Toronto, Ontario, Canada
Research Site, Bordeaux, , France
Research Site, Pierre-Benite, , France
Research Site, Toulouse cedex 9, , France
Research Site, Athens, , Greece
Research Site, Ioannina, , Greece
Research Site, Milano, , Italy
Research Site, Sevilla, Andalucía, Spain
Research Site, L'Hospitalet de Llobregat, Cataluña, Spain
Research Site, Madrid, , Spain
Research Site, Madrid, , Spain
Research Site, Bellinzona, , Switzerland
Research Site, Geneva 14, , Switzerland
Research Site, Zurich, , Switzerland
Research Site, Birmingham, , United Kingdom
Research Site, London, , United Kingdom
Research Site, London, , United Kingdom
Research Site, Oxford, , United Kingdom
Research Site, Sutton, , United Kingdom
Research Site, Wirral, , United Kingdom
Name: MD
Affiliation: Amgen
Role: STUDY_DIRECTOR