However, no definitive conclusions can be drawn from the Company’s early data about the potential efficacy profile of this investigational therapy. Further research is required, and these results must be confirmed in a well-controlled Phase III clinical trial of this investigational therapy that is currently in progress. Subject to completion of that Phase III trial and FDA’s review of our entire data set on this investigational therapy, CEL-SCI believes that these early-stage clinical trial results indicate the potential for this investigational therapy to be a benefit in the treatment of advanced primary head and neck cancer. The U.S. Food and Drug Administration also granted orphan drug status to Multikine (Leukocyte Interleukin, Injection) in the neoadjuvant therapy of patients with squamous cell carcinoma of the head and neck.About CEL-SCI Corporation
CEL-SCI’s Taiwanese Partner Orient Europharma Presents Development Strategies In Taiwan For Investigational Cancer Therapy Multikine (Leukocyte Interleukin, Injection) At World Orphan Drug Conference Today In Seoul, Korea
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