Benitec Biopharma’s BB-301 Receives FDA Clearance of the IND for the Treatment of Oculopharyngeal Muscular Dystrophy
(24/7 MARKET NEWS) – Benitec Biopharma Inc. (NASDAQ:BNTC) reported, this morning, that the U.S. Food and Drug Administration (FDA) cleared its Investigational New Drug (IND) application for BB-301, its silence and replace gene therapy for the treatment of Oculopharyngeal Muscular Dystrophy-related Dysphagia.
Benitec Biopharma is trading at $0.238, up $0.039 (+19.60%), on 3.06M premarket shares traded.
Its 52-week range is $0.1309 to 2.10. It’s above its 2=23 high and can now set its sights on its 2022 trading levels.
24/7 MARKET NEWS, INC Disclaimer
24/7 MARKET NEWS (“24/7 MN”) is dedicated to covering various underreported segments of the stock markets. Our goal is to help you to better understand these markets, but 24/7 MN is neither an investment advisor nor a financial advisor, and no information provided here is to be interpreted as a suggestion to buy or sell stocks or other investment products. All opinions, news, research, analysis, prices or other information contained on 247marketnews.com, its press releases, or other services are provided for educational purposes only and do not constitute investment advice. You are solely responsible for the investment decisions you make.
Please go to 247marketnews.com or https://247marketnews.com/terms-disclaimer/