Welcome to our dedicated page for Passage Bio SEC filings (Ticker: PASG), a comprehensive resource for investors and traders seeking official regulatory documents including 10-K annual reports, 10-Q quarterly earnings, 8-K material events, and insider trading forms.
The Passage Bio, Inc. (PASG) SEC filings page on Stock Titan provides access to the company’s regulatory disclosures as filed with the U.S. Securities and Exchange Commission. As a clinical stage genetic medicines company listed on the Nasdaq Capital Market, Passage Bio uses SEC filings to report financial results, material corporate events, and key developments in its PBFT02 gene therapy program for neurodegenerative diseases.
Investors can review Form 10-K annual reports and Form 10-Q quarterly reports to see detailed information on research and development and general and administrative expenses, net loss, cash, cash equivalents, and marketable securities, along with risk factor and business discussions. Form 8-K current reports document material events such as quarterly financial press releases, updated corporate presentations, program data updates from the upliFT-D trial, manufacturing and regulatory milestones, board and committee changes, and the implementation of the 1-for-20 reverse stock split and related Nasdaq listing matters.
Where applicable, investors may also consult proxy materials and other governance-related filings for information on board composition and stockholder approvals, including approvals related to capital structure changes. For a company like Passage Bio, which is advancing a gene therapy candidate through early-stage clinical development, these filings help clarify trial status, manufacturing strategy, and the company’s view of its cash runway and operating priorities.
On Stock Titan, Passage Bio filings are supplemented with AI-powered summaries that highlight key points from lengthy documents, helping users quickly understand major changes in financial condition, clinical and regulatory plans, and capital structure. Real-time updates from EDGAR ensure that new PASG filings, including 10-K, 10-Q, and 8-K reports, appear promptly, while structured access to filings supports deeper review of the company’s regulatory and disclosure history.
Passage Bio, Inc. reported updated interim data from its Phase 1/2 upliFT-D trial of PBFT02 for frontotemporal dementia with GRN mutations. Patients earlier in disease progression showed reduced brain atrophy and stabilized plasma NfL levels versus natural history, while more advanced patients did not show similar improvements.
The company completed a Type C meeting where the FDA indicated a randomized controlled registrational trial would be required for PBFT02 in FTD-GRN. Citing ethical, logistical, and financial challenges, Passage Bio is evaluating next steps for PBFT02 and the broader program.
Passage Bio also initiated a review of strategic alternatives that could include mergers, acquisitions, reverse merger, asset sales, partnerships, or licensing, and engaged Wedbush PacGrow as financial advisor. The company does not plan further updates until its board approves a specific action or disclosure is otherwise required.
Passage Bio, Inc. is holding its 2026 Annual Meeting of Stockholders as a virtual-only event on May 19, 2026 at 9:00 a.m. Eastern Time. Holders of 3,207,810 shares of common stock as of March 26, 2026 may vote.
Stockholders will vote on electing two Class III directors, ratifying KPMG LLP as independent auditor for 2026, approving on a non-binding advisory basis the compensation of named executive officers, and choosing how often to hold future advisory pay votes. The board recommends voting for both nominees, for KPMG, for executive pay, and for an annual say-on-pay vote.
The proxy also details governance practices, committee structures, director and executive pay, stock ownership of major holders and management, and change-in-control and severance protections for senior executives.
Passage BIO, Inc. reported that CFO Kathleen Borthwick received an employee stock option grant covering 15,610 shares of common stock. The option has an exercise price of $7.64 per share and expires on March 16, 2035.
The award vests as to 1/48 of the total shares each month beginning on April 16, 2026, so long as she continues providing service on each vesting date. Following this grant, she holds stock options for 15,610 shares directly.
Passage BIO, Inc. reported that President and CEO William Chou received a grant of employee stock options for 58,000 shares of common stock at an exercise price of $7.64 per share. The options vest in equal monthly installments over 48 months beginning on April 16, 2026 and expire on March 16, 2035. This grant is a compensation award, not an open-market purchase or sale, and leaves Chou holding 58,000 options following the transaction.
Passage Bio, Inc. entered into a lease termination agreement with Hopewell Campus Owner LLC on March 4, 2026, ending its lease for about 62,000 square feet of laboratory space in Hopewell. The lease, originally signed in December 2020, carried a 15‑year term starting in March 2021.
Under the termination agreement, Passage Bio will pay the landlord a termination fee of approximately $4.8 million plus accrued rent through February 14, 2026. The company had already ceased all operations at the Hopewell facilities following a restructuring in January 2025.
After this agreement, Passage Bio states it expects its cash and cash equivalents to fund operations through the first quarter of 2027, while cautioning that this estimate is based on assumptions that may change and could result in capital being used faster than anticipated.
Passage Bio files its annual report describing progress on PBFT02, a gene therapy for frontotemporal dementia caused by progranulin deficiency (FTD-GRN) and related neurodegenerative diseases. In a Phase 1/2 trial, Dose 1 of PBFT02 raised cerebrospinal fluid progranulin from below 3.0 ng/mL at baseline to means of 12.4 ng/mL at one month, 19.4 ng/mL at six months, 25.9 ng/mL at 12 months and 23.8 ng/mL at 18 months, above healthy control ranges. Plasma neurofilament light chain, a marker of neurodegeneration, increased 4% at 12 months versus natural-history increases of about 28–29%. Safety data showed treatment-related venous sinus thrombosis and hepatotoxicity at the higher dose, which were asymptomatic and responsive to treatment. The company is now enrolling a lower-dose Cohort 3, extending PBFT02 development into FTD with C9orf72 mutations, and positioning a higher-yield suspension manufacturing process with Catalent for late-stage trials. Passage Bio also highlights an HD program with Gemma Biotherapeutics targeting MSH3 to reduce somatic instability, plus orphan and Fast Track designations for PBFT02 in FTD.
Passage Bio reported fourth-quarter and full-year 2025 results and highlighted progress in its PBFT02 gene therapy program for frontotemporal dementia. The company enrolled the first three FTD-GRN patients in Cohort 3 and treated the first FTD-C9orf72 patient with Dose 2 PBFT02 in Cohort 4 of the upliFT-D study.
Net loss for 2025 was $45,522 thousand, narrowing from $64,767 thousand in 2024, as research and development expenses fell to $23,276 thousand from $40,179 thousand and general and administrative expenses declined to $19,875 thousand from $24,988 thousand. Cash and cash equivalents were $46,303 thousand at December 31, 2025, and the company projects a cash runway through the first quarter of 2027.
The upliFT-D Phase 1/2 trial continues to enroll FTD-GRN and FTD-C9orf72 patients, focusing primarily on safety and tolerability, with biomarker and clinical outcomes as secondary measures. Passage Bio plans updated interim safety and biomarker data and regulatory feedback on an FTD-GRN registrational trial design in the first half of 2026, and expects to select a clinical candidate for its Huntington’s program in the second half of 2026.
Passage BIO, Inc. reported an insider equity transaction by President and CEO William Chou. On January 8, 2026, 10,000 restricted stock units converted into an equal number of common shares at an exercise price of $0. In connection with this vesting, 4,076 common shares were sold at a weighted average price of $18.4394 per share as part of an issuer-mandated "sell to cover" transaction to satisfy tax withholding obligations, rather than a discretionary sale.
After these transactions, Chou directly held 6,524 common shares and 10,000 RSUs. The RSUs vest in two equal installments, with 50% scheduled to vest on January 8, 2026 and the remaining 50% on January 8, 2027, subject to continued service with Passage BIO.
Passage BIO, Inc. CFO Kathleen Borthwick reported the vesting of equity awards and an associated tax sale. On January 8, 2026, 5,000 restricted stock units converted into common stock at an exercise price of $0, reflecting previously granted compensation.
On the same date, she sold 2,062 shares of common stock at a weighted average price of $18.4394 per share, in an issuer-mandated “sell to cover” transaction to satisfy tax withholding obligations tied to the RSU vesting. The price for these shares came from multiple trades between $18.13 and $19.3061 per share. After these transactions, she directly held 5,402 shares of common stock and 5,000 RSUs.