BioMarin to Acquire Amicus Therapeutics for $4.8 Billion, Expanding Position as a Leader in Rare Diseases, Accelerating Revenue Growth and Strengthening Financial Outlook
Prnewswire·2025-12-19 12:45

Core Viewpoint - BioMarin Pharmaceutical Inc. has announced a definitive agreement to acquire Amicus Therapeutics for $14.50 per share in an all-cash transaction valued at approximately $4.8 billion, which is expected to enhance BioMarin's revenue growth and diversify its product portfolio in the rare disease market [2][3][4]. Group 1: Acquisition Details - The acquisition will add two marketed high-growth products, Galafold and Pombiliti + Opfolda, which generated combined revenues of $599 million over the past four quarters [1][4]. - The transaction has been unanimously approved by the Boards of Directors of both companies and is expected to close in the second quarter of 2026, pending regulatory clearances and stockholder approval [2][3]. - BioMarin intends to finance the acquisition through cash on hand and approximately $3.7 billion of non-convertible debt financing [8]. Group 2: Financial Impact - The acquisition is expected to be accretive to Non-GAAP Diluted Earnings Per Share (EPS) in the first 12 months post-close and substantially accretive beginning in 2027 [1][4][5]. - BioMarin is targeting a gross leverage of less than 2.5x within two years after the close of the transaction, demonstrating a commitment to deleveraging [5][8]. Group 3: Strategic Fit - The combination of BioMarin and Amicus is seen as a strategic fit due to both companies' dedication to transforming care for patients with rare diseases [3][4]. - The acquisition will strengthen BioMarin's commercial portfolio and provide opportunities to expand access to Galafold and Pombiliti + Opfolda across its global footprint [1][4][5]. Group 4: Product Information - Galafold is the first oral treatment for Fabry disease, while Pombiliti + Opfolda is a two-component therapy for Pompe disease, both targeting lysosomal storage disorders [4][15]. - Amicus also holds U.S. rights to DMX-200, an investigational small molecule for treating focal segmental glomerulosclerosis, which is in Phase 3 development [4].