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Spots Global Cancer Trial Database for Talimogene Laherparepvec With Pembrolizumab for Recurrent Metastatic Squamous Cell Carcinoma of the Head and Neck (MASTERKEY232 / KEYNOTE-137)

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Trial Identification

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

Study Description

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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Contact Details

Name: MD

Affiliation: Amgen

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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