Shares of Passage Bio, Inc. (NASDAQ:PASG – Get Free Report) have earned an average recommendation of “Hold” from the seven ratings firms that are covering the company, Marketbeat.com reports. One analyst has rated the stock with a sell rating, four have given a hold rating and two have assigned a buy rating to the company. The average twelve-month price target among brokers that have issued a report on the stock in the last year is $13.25.
A number of equities analysts recently commented on PASG shares. Oppenheimer lowered their target price on shares of Passage Bio from $30.00 to $15.00 and set an “outperform” rating for the company in a research note on Tuesday, April 21st. Wall Street Zen upgraded shares of Passage Bio from a “strong sell” rating to a “sell” rating in a research note on Sunday, May 3rd. Lucid Cap Mkts downgraded shares of Passage Bio from a “strong-buy” rating to a “hold” rating in a research note on Monday, April 20th. Chardan Capital set a $7.00 price objective on shares of Passage Bio and gave the company a “neutral” rating in a research note on Tuesday, April 21st. Finally, TD Cowen downgraded shares of Passage Bio from a “buy” rating to a “hold” rating in a research note on Tuesday, April 21st.
Check Out Our Latest Analysis on Passage Bio
Hedge Funds Weigh In On Passage Bio
Passage Bio Trading Up 2.4%
Shares of PASG stock opened at $5.20 on Friday. The firm has a fifty day moving average price of $7.11 and a 200 day moving average price of $9.14. The company has a market cap of $16.69 million, a P/E ratio of -0.44 and a beta of 1.38. Passage Bio has a 12 month low of $3.93 and a 12 month high of $20.00.
Passage Bio (NASDAQ:PASG – Get Free Report) last issued its earnings results on Tuesday, May 12th. The company reported ($2.36) EPS for the quarter, topping analysts’ consensus estimates of ($2.76) by $0.40. On average, equities analysts forecast that Passage Bio will post -8.62 EPS 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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