Shares of Passage Bio, Inc. (NASDAQ:PASG – Get Free Report) have been assigned an average rating of “Hold” from the nine research firms that are presently covering the company, Marketbeat reports. One equities 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 price target among analysts that have issued ratings on the stock in the last year is $13.25.
PASG has been the subject of a number of recent analyst reports. Wedbush reiterated a “neutral” rating and set a $8.00 target price (down from $32.00) on shares of Passage Bio in a research report on Tuesday, April 21st. TD Cowen downgraded Passage Bio from a “buy” rating to a “hold” rating in a research report on Tuesday, April 21st. Wall Street Zen upgraded Passage Bio from a “strong sell” rating to a “sell” rating in a research report on Sunday, May 3rd. Weiss Ratings reiterated a “sell (d-)” rating on shares of Passage Bio in a research report on Friday, March 27th. Finally, Guggenheim cut Passage Bio from a “buy” rating to a “neutral” rating in a report on Wednesday.
View Our Latest Report on PASG
Institutional Investors Weigh In On Passage Bio
Passage Bio Trading Up 3.8%
PASG stock opened at $5.81 on Wednesday. The firm has a market capitalization of $18.65 million, a PE ratio of -0.49 and a beta of 1.41. Passage Bio has a 1-year low of $3.93 and a 1-year high of $20.00. The business’s 50 day simple moving average is $6.51 and its 200 day simple moving average is $8.89.
Passage Bio (NASDAQ:PASG – Get Free Report) last released its quarterly earnings results on Tuesday, May 12th. The company reported ($2.36) earnings per share (EPS) for the quarter, beating the consensus estimate of ($2.76) by $0.40. As a group, sell-side analysts predict that Passage Bio will post -8.62 EPS for the current fiscal 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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