Passage Bio (NASDAQ:PASG – Get Free Report) is projected to post its Q3 2025 results before the market opens on Wednesday, November 12th. Analysts expect Passage Bio to post earnings of ($2.64) per share for the quarter. Parties may review the information on the company’s upcoming Q3 2025 earningreport for the latest details on the call scheduled for Wednesday, November 19, 2025 at 7:00 AM ET.
Passage Bio (NASDAQ:PASG – Get Free Report) last announced its quarterly earnings data on Tuesday, August 12th. The company reported ($2.96) earnings per share (EPS) for the quarter, topping the consensus estimate of ($4.00) by $1.04. On average, analysts expect Passage Bio to post $-1 EPS for the current fiscal year and $-1 EPS for the next fiscal year.
Passage Bio Price Performance
PASG opened at $6.28 on Monday. The company has a market capitalization of $19.97 million, a P/E ratio of -0.35 and a beta of 1.94. The firm’s fifty day moving average price is $7.59 and its two-hundred day moving average price is $7.28. Passage Bio has a fifty-two week low of $5.12 and a fifty-two week high of $26.60.
Analyst Ratings Changes
Get Our Latest Stock Analysis on Passage Bio
Insiders Place Their Bets
In other Passage Bio news, major shareholder Lynx1 Capital Management Lp purchased 19,783 shares of the stock in a transaction on Friday, September 12th. The shares were purchased at an average price of $6.99 per share, with a total value of $138,283.17. Following the completion of the transaction, the insider directly owned 611,804 shares in the company, valued at $4,276,509.96. This represents a 3.34% increase in their ownership of the stock. The acquisition was disclosed in a filing with the Securities & Exchange Commission, which is accessible through the SEC website. Insiders have acquired 32,008 shares of company stock worth $223,726 in the last 90 days. 4.30% of the stock is currently owned by insiders.
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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