ContraVir Pharmaceuticals Receives Positive FDA Response to CRV431 Pre-IND Package for NASH
CONTRAVIR PHARMACEUTICALS INC (CTRV)
US:NASDAQ Investor Relations:
ir.contravir.com/investor-relations
Company Research
Source: GlobeNewswire
EDISON, N.J., June 20, 2019 (GLOBE NEWSWIRE) -- ContraVir Pharmaceuticals, Inc. (NASDAQ:CTRV), a biopharmaceutical company focused on the development of therapeutic drugs for the treatment of liver disease arising from non-alcoholic steatohepatitis (“NASH”) and chronic viral infection, today announced positive feedback from the U.S. Food and Drug Administration (“FDA”) in response to ContraVir’s pre-Investigational New Drug (“pre-IND”) meeting with respect to the development of CRV431 in NASH. The FDA provided positive feedback on ContraVir’s existing preclinical data of CRV431 and supports the study design for the NASH IND opening study. The FDA also concurred with the company’s proposed plan for further preclinical studies to support the development of CRV431. Overall, the FDA supported ContraVir’s clinical development plans for CRV431 in the NASH indication. “We are pleased with the FDA’s positive feedback on the preclinical work we’ve completed to-date, as well their feedback
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