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Alumis and ACELYRIN File Joint Definitive Proxy Statement for Proposed Merger

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Alumis Inc.; ACELYRIN, INC.
Alumis Inc.; ACELYRIN, INC.

Stockholders to benefit from differentiated late-stage portfolio of therapies and strong balance sheet

Boards unanimously recommend stockholders vote “FOR” the merger

Transaction expected to be completed in second quarter of 2025

SOUTH SAN FRANCISCO, Calif. and LOS ANGELES, April 04, 2025 (GLOBE NEWSWIRE) -- Alumis Inc. (Nasdaq: ALMS), a clinical-stage biopharmaceutical company developing therapies using a precision approach to optimize clinical outcomes and significantly improve the lives of patients with immune-mediated diseases, and ACELYRIN, INC. (Nasdaq: SLRN), a late-stage clinical biopharma company focused on accelerating the development and delivery of transformative medicines in immunology, have jointly filed a definitive proxy statement/prospectus with the U.S. Securities and Exchange Commission in connection with the proposed merger of the two companies. The joint proxy statement/prospectus are being mailed to all Alumis and ACELYRIN stockholders entitled to vote.

Each company will hold a respective Special Meeting of Stockholders virtually at 12:00 p.m. E.T. on Tuesday, May 13, 2025. The stockholders of record as of the close of business on April 1, 2025, will be entitled to vote at the respective special meetings of stockholders.

With a team that has a successful track-record of developing innovative therapies and an extended financial runway, the transaction will unlock the value of the combined portfolio for current and future investors. Key highlights of the transaction:

  • Creates a late-stage clinical biopharma company dedicated to innovating, developing and commercializing transformative therapies for immune-mediated diseases.

  • Differentiated pipeline with multiple upcoming milestones expected, including:

    • Topline data from Phase 3 ONWARD trials for Alumis’ ESK-001 in moderate-to-severe plaque psoriasis expected for readout in 1Q 2026

    • Topline data from Phase 2b LUMUS trial in systemic lupus erythematosus on track for readout in 2026

    • Phase 2 clinical trial initiation for Alumis’ A-005 in MS

    • Addition of lonigutamab, a subcutaneously delivered anti-IGF-1R for thyroid eye disease, with committed capital for a clinical development plan to evaluate its potential differentiation

  • Pro forma cash of approximately $737 million as of December 31, 2024, provides runway into 2027, beyond multiple expected clinical readouts.

  • Combined company to benefit from world-class leadership team with proven record of operating discipline and capital efficiency. By combining assets, resources and talent, including members of ACELYRIN’s lonigutamab program, the combined company will be well positioned to maximize the value of its pipeline.