BMRN

Prezzo BioMarin Pharmaceutical Inc

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BMRN
$54,70
+$0,62(+1,14%)

*Data last updated: 2026-05-10 21:22 (UTC+8)

As of 2026-05-10 21:22, BioMarin Pharmaceutical Inc (BMRN) is priced at $54,70, with a total market cap of $10,39B, a P/E ratio of 32,66, and a dividend yield of 0,00%. Today, the stock price fluctuated between $53,21 and $55,21. The current price is 2,80% above the day's low and 0,92% below the day's high, with a trading volume of 1,97M. Over the past 52 weeks, BMRN has traded between $52,00 to $57,44, and the current price is -4,77% away from the 52-week high.

BMRN Key Stats

Yesterday's Close$54,12
Market Cap$10,39B
Volume1,97M
P/E Ratio32,66
Dividend Yield (TTM)0,00%
Diluted EPS (TTM)1,39
Net Income (FY)$348,90M
Revenue (FY)$3,22B
Earnings Date2026-08-03
EPS Estimate0,97
Revenue Estimate$914,64M
Shares Outstanding192,10M
Beta (1Y)0.229

About BMRN

BioMarin Pharmaceutical Inc. develops and commercializes therapies for people with serious and life-threatening rare diseases and medical conditions. Its commercial products include Vimizim, an enzyme replacement therapy for the treatment of mucopolysaccharidosis (MPS) IV type A, a lysosomal storage disorder; Naglazyme, a recombinant form of N-acetylgalactosamine 4-sulfatase for patients with MPS VI; and Kuvan, a proprietary synthetic oral form of 6R-BH4 that is used to treat patients with phenylketonuria (PKU), an inherited metabolic disease. The company's commercial products also comprise Palynziq, a PEGylated recombinant phenylalanine ammonia lyase enzyme, which is delivered through subcutaneous injection to reduce blood Phe concentrations; Brineura, a recombinant human tripeptidyl peptidase 1 for the treatment of patients with ceroid lipofuscinosis type 2, a form of Batten disease; Voxzogo, a once daily injection analog of c-type natriuretic peptide for the treatment of achondroplasia; and Aldurazyme, a purified protein designed to be identical to a naturally occurring form of the human enzyme alpha-L-iduronidase. In addition, it develops valoctocogene roxaparvovec, an adeno associated virus vector, which is in Phase III clinical trial for the treatment of patients with severe hemophilia A; BMN 307, an AAV5 mediated gene therapy, which is in Phase 1/2 clinical trial to normalize blood Phe concentration levels in patients with PKU; and BMN 255 that is in Phase 1/2 clinical trial for treating primary hyperoxaluria. The company serves specialty pharmacies, hospitals, and non-U.S. government agencies, as well as distributors and pharmaceutical wholesalers in the United States, Europe, Latin America, and internationally. BioMarin Pharmaceutical Inc. has license and collaboration agreements with Sarepta Therapeutics, Ares Trading S.A., Catalyst Pharmaceutical Partners, Inc., and Asubio Pharma Co., Ltd. The company was incorporated in 1996 and is headquartered in San Rafael, California.
SectorHealthcare
IndustryBiotechnology
CEOAlexander Hardy
HeadquartersSan Rafael,CA,US
Official Websitehttps://www.biomarin.com
Employees (FY)3,22K
Average Revenue (1Y)$1,00M
Net Income per Employee$108,32K

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BioMarin Pharmaceutical Inc (BMRN) Latest News

2026-02-11 08:56Tom Lee看好MrBeast进军金融,或成新一代Robinhood与“数字银行入口”财资公司BitMine Immersion(BMRN)董事长Tom Lee在香港共识大会上表示,下一代具有颠覆力的金融平台,可能并非来自华尔街,而是诞生于YouTube生态。Lee认为,全球顶级内容创作者MrBeast进军金融服务领域,或将成为Z世代与Alpha世代的“主流金融入口”,并在未来承担类似Robinhood与嘉信理财的角色。 本月早些时候,MrBeast旗下公司同意收购新银行Step,而BitMine已向该公司投资约2亿美元。Lee指出,这并非一次短期资本运作,而是面向年轻人金融需求变化的长期布局。“Beast有机会成为他们这一代的金融机构,”他说。 Lee将这一趋势与以往世代的金融平台更替作类比:嘉信理财服务于婴儿潮一代,BlackRock和Blackstone吸引X世代资本,而Robinhood赢得了千禧一代。如今,Z世代与Alpha世代正在形成自己的金融消费路径。仅在美国,这两代人规模约1.2亿,而MrBeast在全球拥有超过10亿粉丝,具备天然的用户基础和信任优势。 “这些年轻用户现在或许尚未积累大量财富,但未来十年,他们将经历一次大规模的代际财富转移,”Lee表示。他认为,如果Step成为他们日常使用的金融平台,那么围绕MrBeast构建的金融生态,将自然成为这一代人接触数字资产和新型金融工具的重要渠道。 在Lee看来,年轻群体对数字化资产与线上金融服务的接受度更高,内容平台与金融基础设施的结合,可能重塑未来的金融格局。随着创作者经济与加密金融的融合加速,MrBeast的金融布局,正在被视为通往下一代资本市场的关键通道之一。

Hot Posts su BioMarin Pharmaceutical Inc (BMRN)

DeFi_Dad_Jokes

DeFi_Dad_Jokes

2025-12-26 05:46
Ascendis Pharma A/S (ASND) announced that the U.S. Food and Drug Administration has postponed its review completion date for TransCon CNP by three months, with the new target set for February 28, 2026. Originally scheduled for November 30, 2025, the regulatory delay stems from the FDA's need to conduct a thorough assessment of additional post-marketing requirement materials submitted by the company on November 5, 2025. ## Understanding Achondroplasia And Current Treatment Gaps Achondroplasia represents a significant genetic disorder affecting more than a quarter million individuals globally. This skeletal dysplasia condition extends far beyond disproportionate short stature—it frequently triggers serious complications affecting muscle function, neurological systems, and cardiorespiratory health. The rarity and severity of achondroplasia underscores the critical need for safe, effective therapeutic options. Current treatment landscape remains limited. Voxzogo, marketed by BioMarin Pharmaceutical Inc. (BMRN), holds the distinction of being the sole FDA-approved therapy for pediatric achondroplasia patients, requiring daily subcutaneous injections. This once-daily dosing regimen, while effective, presents adherence challenges for families managing long-term treatment protocols. ## TransCon CNP: A Potential Game-Changer For Dosing Convenience Ascendis Pharma's investigational candidate, known as Navepegritide or TransCon CNP, operates as an experimental prodrug of C-type natriuretic peptide (CNP). The medication's distinguishing feature lies in its administration schedule: once-weekly subcutaneous injection instead of daily dosing. If approved by the FDA, TransCon CNP could reshape treatment paradigms for pediatric achondroplasia by offering superior convenience without compromising safety or efficacy. The reduced injection frequency addresses a fundamental patient care challenge inherent in daily regimens, potentially improving long-term medication adherence and quality of life for affected children. ## Market Outlook And Investor Perspective The three-month regulatory extension reflects standard FDA procedures when additional information requires careful evaluation rather than indicating approval challenges. This timeline adjustment provides Ascendis Pharma with continued opportunity to present comprehensive safety and efficacy data supporting the product's potential benefits. ASND shares have demonstrated volatility throughout the current trading period. On the day of this announcement, the stock declined 2.38%, closing at $206.65, reflecting typical market responses to regulatory timeline adjustments in the biopharmaceutical sector.
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TokenTherapist

TokenTherapist

2025-10-28 11:09
BioMarin Pharmaceutical Inc. (BMRN) has announced a groundbreaking agreement to acquire Inozyme Pharma, Inc. (INZY) for approximately $270 million, or $4 per share, in cash. This strategic move, expected to conclude in the third quarter of 2025, marks a significant development in the biotechnology sector, potentially reshaping the landscape of rare genetic disorder treatments. ## Key Acquisition Details and Strategic Implications - **Expansion of BioMarin's Portfolio**: The acquisition introduces INZ-701, a Phase 3 enzyme replacement therapy, to BioMarin's pipeline. - **Target Condition**: INZ-701 is under evaluation for the treatment of ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) Deficiency, a rare genetic disorder affecting blood vessels, soft tissues, and bones. - **Clinical Timeline**: Data from the first Phase 3 pivotal study of INZ-701 in pediatric patients is anticipated in early 2026. - **Financial Position**: BioMarin's robust financial standing enables the pursuit of external innovation alongside internal research and development efforts. ## Market Impact Analysis The acquisition of Inozyme by BioMarin represents a strategic consolidation within the biotechnology sector, particularly in the realm of rare genetic disorders. This move could potentially: 1. **Accelerate Drug Development**: By combining resources and expertise, the development timeline for INZ-701 and other pipeline products may be expedited. 2. **Enhance Market Competitiveness**: BioMarin's expanded portfolio strengthens its position in the rare disease therapeutics market. 3. **Drive Innovation**: The merger of two specialized entities may foster increased innovation in enzyme replacement therapies and related fields. ## Technology Innovation Outlook This acquisition highlights the growing trend of leveraging advanced technologies in biotechnology: - **Precision Medicine**: The focus on ENPP1 Deficiency underscores the move towards highly targeted therapies for rare genetic conditions. - **Data-Driven Research**: The emphasis on Phase 3 clinical data indicates the critical role of robust, data-centric approaches in drug development. - **Potential for Digitalization**: As the biotech sector evolves, there may be increased integration of digital technologies for research, development, and patient care. Alexander Hardy, President and Chief Executive Officer of BioMarin, emphasized the company's strategic vision: "As BioMarin continues our transformation and delivers on our corporate strategy, we will continue to evaluate external innovation alongside internal innovation. We are in a strong financial position to bring in additional assets as we accelerate the development of medicines for patients with significant unmet need." This acquisition not only expands BioMarin's therapeutic offerings but also signals a broader trend of strategic consolidations in the biotechnology industry, aimed at accelerating the development of cutting-edge treatments for rare genetic disorders.
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