Mesothelioma Treatment Moves to Phase III Trial
Merck & Co., Inc announced today its investigational trial of vorinostat (ZOLINZA®), the Company's oral histone deacetylase (HDAC) inhibitor, in patients with advanced malignant pleural mesothelioma has progressed into Phase III investigation and is currently enrolling patients who previously failed or are intolerant to prior therapies such as chemotherapy. The decision to move forward follows the review of currently available safety and efficacy data from the Phase II portion of the trial.
Eric Rubin, M.D., vice president, oncology clinical research, Merck Research Laboratories said "With no currently approved regimens for relapsed or refractory mesothelioma, continued research focused on identifying targeted therapies and differentiated approaches is critical. We are pleased that the investigation of vorinostat for the treatment of advanced mesothelioma has advanced into Phase III development.”
There are several key endpoints of the Phase III trial. They include overall survival as well as characterization of the overall safety and toxicity of ZOLINZA in patients with advanced malignant mesothelioma. Several secondary endpoints include overall objective response, response duration, and progression-free survival.
To Read the entire Press Release, Visit the Mesothelioma Applied Resource Foundation HERE
