One of Cathie Wood's Ark Invest funds sold over 675,000 shares of Galileo Acquisition on June 17.
Sarepta Therapeutics, Inc. (NASDAQ: SRPT) saw its shares make a handy gain on Monday after the firm received an upgrade from Morgan Stanley. The driving force behind this upgrade is Sarepta’s...
Sarepta shares jumped last week on news that the company reached a licensing deal with Roche. While investors saw about a five-point bump from this news, one analyst sees much more upside for this...
One of Cathie Wood's Ark Invest funds sold over 40,000 shares of Baidu on August 18.
This report was sent to Briefing.com subscribers earlier today. Upgrades: > Coupang (CPNG) upgraded to Buy from Hold at Deutsche Bank; tgt $20 > Empire State Realty Trust (ESRT) upgraded to Buy...
One of Cathie Wood's Ark Invest funds sold over 225,000 shares of Takeda Pharma on June 15.
One of Cathie Wood's Ark Invest funds sold over 350,000 shares of Takeda Pharmaceutical on June 16.
Selecta Biosciences and Sarepta Therapeutics have announced that they had entered into a research license and option agreement.
Sarepta Therapeutics plunged early on Friday as the result of a failed clinical trial by BioMarin Pharmaceutical.
Source: Photo by Spencer Platt/Getty ImagesThe stock market is up slightly Wednesday, with the Dow Jones Industrial Average up 0.07%, the Nasdaq up 0.24% and the S&P 500 up 0.13%. Today’s winners...
Catabasis Pharmaceuticals shares skyrocketed on Thursday following an announcement that it would be partnering with Sarepta Therapeutics for a joint research collaboration.
One of Cathie Wood's ARK Invest exchange-traded funds sold nearly 24,000 shares of Boeing on September 7.
Sarepta Therapeutics shares skyrocketed on Tuesday after the firm presented positive preliminary results from its midstage Duchenne muscular dystrophy trial.
Sarepta Therapeutics closed out Wednesday with its shares up over 25% following positive developments surrounding eteplirsen, its treatment of Duchenne muscular dystrophy.
Pfizer released initial clinical data from its Phase 1b gene therapy study for Duchenne muscular dystrophy. While these results did not necessarily live up to expectations, there is a winner in this.