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Passage Bio agrees to reverse merger with Remix; Remix equity value $226M; $100M concurrent financing
Remix ascribed equity value of $226M; Passage Bio's equity value ~$20M, subject to net cash adjustment at closing.
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Passage Bio cuts ~75% of workforce, expects $3.3M in severance costs
Workforce reduction of approximately 75%; substantial completion expected in Q2 and Q3 2026.
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PBFT02 cuts brain atrophy 64% vs natural history; FDA demands randomized trial; strategic review begun
PBFT02 patients with global CDR 1 at baseline showed 64% less whole brain atrophy (3.1% vs 8.7%) at 12 months vs ALLFTD natural history.
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Passage Bio terminates Hopewell lease; pays $4.8M fee, cash runway to Q1 2027
Terminated 62,000 sq ft lab lease (15-year term from March 2021) via Termination Agreement dated March 4, 2026.
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Passage Bio reports 2025 net loss of $45.5M; cash runway through Q1 2027; advances FTD clinical program
Cash and cash equivalents $46.3M at Dec 31, 2025; funding expected through Q1 2027.
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Passage Bio reports preliminary cash ~$46M as of Dec 31, 2025; runway into Q1 2027
Preliminary unaudited cash, cash equivalents and marketable securities of approximately $46 million as of December 31, 2025.
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Passage Bio Q3 net loss $7.7M; cash runway into 1Q 2027; FTD trial enrollment ongoing
Cash and marketable securities $52.8M as of Sep 30, 2025; expected to fund operations into 1Q 2027.
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Passage Bio Q2 net loss narrows to $9.4M; cash runway into Q1 2027
Cash, cash equivalents and marketable securities: $57.6M as of June 30, 2025 vs $91.8M a year ago; runway into Q1 2027.
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PBFT02 Phase 1/2 data: durable PGRN boost; new pulmonary embolism SAE, protocol to add anticoagulation
Dose 1 PBFT02 increased CSF PGRN from <3 ng/mL to mean 25.9 ng/mL at 12 months (n=4); Dose 2 patient rose to 7.6 ng/mL at 1 month.
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Passage Bio Q1 2025 net loss $15.4M; cash runway into Q1 2027; first FTD-GRN patient dosed at Dose 2
Net loss of $15.4M ($0.25 per share) vs $16.7M ($0.30 per share) in Q1 2024.
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Passage Bio reports FY2024 net loss $64.8M, cash $76.8M; PBFT02 shows durable PGRN elevation in FTD-GRN
Cash, cash equivalents and marketable securities $76.8M as of Dec 31, 2024, down from $114.3M; runway extended into 1Q 2027.
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Passage Bio transfers listing to Nasdaq Capital Market; granted 180-day extension to meet $1.00 bid price
Received Nasdaq deficiency notice on Aug 1, 2024 for bid price below $1.00 for 30 consecutive days.
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Passage Bio cuts workforce 55%, extends cash runway into Q1 2027; updates PBFT02 data
Preliminary cash $76.8M as of Dec 31, 2024; expected runway into Q1 2027 after restructuring.
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Passage Bio Q3 net loss $19.3M; 4 patients enrolled in FTD-GRN Cohort 2; cash to Q2 2026
Net loss $19.3M ($0.31/share) vs $27.1M loss a year ago; R&D expenses fell to $8.7M from $15.1M.
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PBFT02 delivers superior CSF progranulin with AAV1 vector; interim safety and biomarker data promising
Capsid comparison in NHPs: AAV1 vector achieved superior human PGRN levels in CSF versus AAV5 and AAVhu68 after ICM administration.
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PBFT02 shows robust CSF progranulin increase; well-tolerated with enhanced immunosuppression
CSF PGRN up to 6-fold at month 1 (10.7-17.3 ng/mL) and up to 10-fold at month 6 (21.7-27.3 ng/mL), exceeding healthy controls (3.3-8.2 ng/mL).
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Passage Bio expects $3.5M-$5.5M impairment charge on sublease of lab space
Subleased 3,200 sq ft (5% of 62,000 sq ft lab) in Hopewell, NJ; term Sept 2024 to Sept 2029, option to extend to 2032.
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Passage Bio reports Q2 net loss $16M; advances upliFT-D trial, out-licenses programs to GEMMABio
Enrolled first FTD-GRN patient in Cohort 2 of upliFT-D trial; FDA agreed to expand trial to FTD-C9orf72 patients.
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Passage Bio receives Nasdaq delisting notice for bid price below $1.00
Notice received Aug 1, 2024; closing bid price below $1.00 for 30 consecutive days.
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Passage Bio out-licenses three pediatric gene therapy programs to GEMMABio, extends cash runway to Q2 2026
Out-licensed PBGM01, PBKR03, PBML04 to GEMMABio; initial $10M + up to $124M milestones + royalties.
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Passage Bio gets FDA green light to add FTD-C9orf72 arm to PBFT02 trial
Positive Type C meeting feedback from FDA supports evaluating PBFT02 in FTD-C9orf72 patients.
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Passage Bio Q1 net loss $16.7M, cash $104.5M; PBFT02 shows sustained CSF PGRN in 2 patients
Net loss of $16.7M ($0.30/shr) vs $34.3M a year ago; cash $104.5M, runway through Q4 2025.
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Passage Bio reports FY2023 net loss of $102.1M, appoints Kathleen Borthwick as CFO; cash runway into Q4 2025
Cash, cash equivalents and marketable securities $114.3M as of Dec 31, 2023; cash runway expected into Q4 2025.
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Passage Bio reports promising Phase 1/2 data for PBFT02 in FTD-GRN; shifts strategy to adult neurodegenerative diseases
Dose 1 of PBFT02 achieved 3.6-6.6-fold increase in CSF PGRN at day 30, reaching supraphysiologic levels of 10.7-17.3 ng/mL.
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Passage Bio reports Q3 net loss of $27.1M; cash runway into Q4 2025, clinical data on track
Cash, equivalents and marketable securities of $132.8M as of Sept 30, 2023; cash runway extended into Q4 2025.
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Passage Bio receives Nasdaq delisting notice for bid price below $1.00
Notice received Aug 31, 2023; closing bid price below $1/share for 30 consecutive days.
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Passage Bio Q2 net loss $23.9M; GM1 gene therapy shows biomarker normalization at Dose 2; cash runway extended
Net loss $23.9M ($0.44/sh) vs $39.5M ($0.73) in Q2 2022.
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Passage Bio announces CFO/CTO departures, 26% workforce reduction, extends cash runway into Q4 2025
CFO Simona King and CTO Alex Fotopoulos to depart July 28, 2023; Fotopoulos may consult through July 2024.
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Passage Bio reports Q1 2023 net loss of $34.3M; cash runway into H1 2025
Cash, cash equivalents and marketable securities $167.8M as of March 31, 2023, down from $267.1M a year ago; expected to fund operations into first half 2025.
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Passage Bio amends Catalent agreements, eliminates $10.6M annual minimum purchase obligation
Eliminated $10.6M/year minimum purchase obligation and Clean Room Suite fee through Nov 2025.
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Passage Bio reports FY2022 net loss of $136.1M; cash runway into H1 2025; clinical updates for GM1 and FTD
Cash and marketable securities $189.6M at Dec 31, 2022, down from $315.8M; runway into first half of 2025.
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Passage Bio reports PBGM01 interim data: MRI stabilization, biomarker decreases in GM1 gangliosidosis trial
All six treated patients showed stabilization of MRI severity scores over 6-12 months follow-up.
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Passage Bio reports positive interim Phase 1/2 data for PBGM01 in GM1 gangliosidosis
No treatment-related SAEs; all AEs mild-moderate; no DRG toxicity or ICM administration complications.
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Passage Bio reports Q3 net loss $26.7M; cuts workforce 23%, halts Krabbe program
Net loss of $26.7M ($0.49 per share) vs $46.9M in Q3 2021; R&D expenses fell to $15.4M.