Passage Bio, Inc. (NASDAQ:PASG – Get Free Report) has been given an average rating of “Hold” by the nine ratings firms that are presently covering the company, Marketbeat.com reports. One research analyst has rated the stock with a sell recommendation, six have assigned a hold recommendation and two have given a buy recommendation to the company. The average 1-year target price among brokerages that have covered the stock in the last year is $13.25.
PASG has been the topic of a number of recent research reports. Wall Street Zen raised Passage Bio from a “strong sell” rating to a “sell” rating in a research note on Sunday, May 3rd. Weiss Ratings reissued a “sell (d-)” rating on shares of Passage Bio in a research note on Friday, March 27th. Canaccord Genuity Group cut their price target on shares of Passage Bio from $67.00 to $23.00 and set a “buy” rating on the stock in a report on Wednesday, March 4th. Chardan Capital set a $7.00 price objective on shares of Passage Bio and gave the stock a “neutral” rating in a report on Tuesday, April 21st. Finally, UBS Group lowered Passage Bio to a “neutral” rating in a research note on Wednesday.
Read Our Latest Research Report on PASG
Hedge Funds Weigh In On Passage Bio
Passage Bio Stock Performance
PASG opened at $5.81 on Wednesday. Passage Bio has a 1-year low of $3.93 and a 1-year high of $20.00. The stock’s fifty day simple moving average is $6.51 and its 200 day simple moving average is $8.89. The stock has a market cap of $18.65 million, a PE ratio of -0.49 and a beta of 1.41.
Passage Bio (NASDAQ:PASG – Get Free Report) last posted its quarterly earnings results on Tuesday, May 12th. The company reported ($2.36) earnings per share for the quarter, beating analysts’ consensus estimates of ($2.76) by $0.40. Equities analysts forecast that Passage Bio will post -8.62 earnings per share for the current year.
Passage Bio Company Profile
Passage Bio is a clinical-stage biotechnology company focused on the development of gene therapies to treat rare, monogenic central nervous system and neuromuscular disorders. The company applies its in-house gene therapy platform to design and engineer adeno-associated virus (AAV)–based vectors that restore or replace defective genes, aiming to deliver durable treatments with a single administration.
The company’s lead programs include PBGM01, an AAV9-based therapy for GM2 gangliosidoses (Tay–Sachs and Sandhoff diseases), which is conducting a first-in-human study to assess safety and potential therapeutic benefit.
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