Australia markets open in 50 minutes

Passage Bio, Inc. (PASG)

NasdaqGS - NasdaqGS Real-time price. Currency in USD
Add to watchlist
1.19000.0000 (0.00%)
At close: 04:00PM EDT
1.1900 0.00 (0.00%)
After hours: 04:10PM EDT
Full screen
Trade prices are not sourced from all markets
Previous close1.1900
Open1.1700
Bid1.1300 x 100
Ask1.2200 x 100
Day's range1.1201 - 1.2325
52-week range0.5750 - 1.7900
Volume42,853
Avg. volume301,932
Market cap73.352M
Beta (5Y monthly)1.27
PE ratio (TTM)N/A
EPS (TTM)-1.5300
Earnings date05 Aug 2024 - 09 Aug 2024
Forward dividend & yieldN/A (N/A)
Ex-dividend dateN/A
1y target est6.75
  • GlobeNewswire

    Passage Bio Announces Recipient of Third Annual Tachi Yamada Scholarship Award

    PHILADELPHIA, May 21, 2024 (GLOBE NEWSWIRE) -- Passage Bio, Inc. (Nasdaq: PASG), a clinical stage genetic medicines company focused on improving the lives of patients with neurodegenerative diseases, today announced Carrie Gordon, a sophomore at Drexel University, as the third recipient of its Tachi Yamada Scholarship award. The scholarship honors the legacy of Dr. Tachi Yamada, co-founder and former Chairman of the Passage Bio Board of Directors and is open to students enrolled in life sciences

  • Zacks

    All You Need to Know About Passage Bio (PASG) Rating Upgrade to Buy

    Passage Bio (PASG) has been upgraded to a Zacks Rank #2 (Buy), reflecting growing optimism about the company's earnings prospects. This might drive the stock higher in the near term.

  • GlobeNewswire

    Passage Bio Reports First Quarter 2024 Financial Results and Provides Recent Business Highlights

    Updated interim data from the upliFT-D trial in FTD-GRN demonstrated that Dose 1 PBFT02 achieved consistent elevation of CSF progranulin at six months post-treatment in the two patients with longest follow-upCompleted dosing of Cohort 1 (n=5) in upliFT-D trial; on track to deliver 6-month safety and biomarker data from Cohort 1 in 2H 2024Plan to continue studying Dose 1 in Cohort 2 of upliFT-D trial; expect to initiate dosing by the end of 1H 2024, as plannedInitiated regulatory process with FDA