Passage Bio, Inc. (NASDAQ:PASG – Get Free Report) major shareholder Lynx1 Capital Management Lp acquired 29,300 shares of the stock in a transaction that occurred on Wednesday, November 27th. The stock was purchased at an average price of $0.67 per share, with a total value of $19,631.00. Following the completion of the transaction, the insider now owns 8,883,308 shares of the company’s stock, valued at approximately $5,951,816.36. This trade represents a 0.33 % increase in their ownership of the stock. The purchase was disclosed in a document filed with the Securities & Exchange Commission, which can be accessed through this link. Large shareholders that own 10% or more of a company’s stock are required to disclose their sales and purchases with the SEC.
Lynx1 Capital Management Lp also recently made the following trade(s):
- On Monday, November 25th, Lynx1 Capital Management Lp bought 259,998 shares of Passage Bio stock. The stock was acquired at an average cost of $0.56 per share, for a total transaction of $145,598.88.
Passage Bio Price Performance
Passage Bio stock opened at $0.67 on Friday. The company’s 50 day simple moving average is $0.61 and its 200 day simple moving average is $0.82. Passage Bio, Inc. has a fifty-two week low of $0.45 and a fifty-two week high of $1.79.
Hedge Funds Weigh In On Passage Bio
Wall Street Analyst Weigh In
A number of equities research analysts recently weighed in on the stock. Chardan Capital reissued a “buy” rating and set a $7.00 price target on shares of Passage Bio in a research note on Thursday, November 14th. Canaccord Genuity Group reissued a “buy” rating and issued a $13.00 price target on shares of Passage Bio in a research note on Thursday, November 14th. Finally, Rodman & Renshaw started coverage on Passage Bio in a research report on Tuesday, September 3rd. They issued a “buy” rating and a $7.00 price target on the stock.
Get Our Latest Research Report on Passage Bio
Passage Bio Company Profile
Passage Bio, Inc, a genetic medicines company, develops gene therapies for central nervous system diseases. It develops PBGM01, a functional GLB1 gene encoding ß-galactosidase for infantile GM1; PBFT02, a functional granulin (GRN) and gene encoding progranulin (PGRN) for the treatment of FTD caused by progranulin deficiency; and PBKR03, a functional GALC gene encoding the hydrolytic enzyme galactosylceramidase for infantile Krabbe disease.
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