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Stock impact report

HOOKIPA Announces FDA Clearance of IND Application for HB-201 Clinical Trial to Treat HPV-Positive Cancers

HOOKIPA Pharma Inc. (HOOK) 
Last hookipa pharma inc. earnings: 3/19 07:00 am Check Earnings Report
Company Research Source: GlobeNewswire
New York and VIENNA, Austria, July 11, 2019 (GLOBE NEWSWIRE) -- HOOKIPA Pharma Inc. (NASDAQ: HOOK), a company developing a new class of immunotherapeutics targeting infectious diseases and cancers based on its proprietary arenavirus platform, today announced that its Investigational New Drug (IND) Application for a Phase 1/2 clinical trial of HB-201, a TheraT®*-based immunotherapy, for the treatment of Human Papilloma Virus (HPV)-positive cancers is now effective following the clearance by the U.S. Food and Drug Administration (FDA). HB-201 (LCMV) is a TheraT®-based product candidate expressing a non-oncogenic but highly antigenic E6/E7 fusion protein derived from HPV16. In animal models, HB-201 was observed to induce strong immunogenicity, resulting in a robust E6 and E7 antigen specific CD8+ T cell response. HOOKIPA will now start a clinical trial with the goal to provide therapeutic benefit to patients with HPV16+ cancers. Based on the magnitude of response shown in pre-clinical Show less Read more
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