A Phase 3 Open-Label Randomized Parallel Group Study to Evaluate the Efficacy and Safety of Intrapleural Administration of Adenovirus-Delivered Interferon Alpha-2b (rAd-IFN) in Combination with Celecoxib and Gemcitabine in Patients with Malignant Pleural Mesothelioma

Brief description of study

The purpose of this study involves research and is being conducted to determine the safety and efficacy of the investigational agent, rAd-IFN, when given with Celecoxib and Gemcitabine. The sponsor believes that rAd-IFN in combination with Celecoxib and Gemcitabine may help inhibit your tumor growth.

Clinical Study Identifier: s17-01785

ClinicalTrials.gov Identifier: NCT03710876

Principal Investigator: Daniel H. Sterman.

Other Investigators: Virginia M Ferreira, Elaine Shum, Natalia Cherkassky, Bedros Taslakian, David Mendoza, William H. Moore, Anissa Lajean Walker, Jamie L. Bessich, Joshua K Sabari, Abraham Chachoua, Jonathan Gross, Gaetane C. Michaud, Samaan Rafeq, Harvey I Pass, Vamsidhar Velcheti, Melissa L Martinez.

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Perlmutter Cancer Center

Clinical Trials & Research Studies