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BioMarin Completes Acquisition of Amicus Therapeutics

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BioMarin (Nasdaq: BMRN) completed its acquisition of Amicus Therapeutics on April 27, 2026, in an all-cash deal at $14.50 per share, valuing the transaction at approximately $4.8 billion. The deal adds commercial therapies Galafold (migalastat) and Pombiliti + Opfolda, plus U.S. rights to Phase 3 candidate DMX-200. BioMarin plans to provide updated FY 2026 guidance on its Q1 earnings call on May 4, 2026.

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AI-generated analysis. Not financial advice.

Positive

  • Acquisition price: $14.50 per share in an all-cash transaction (~$4.8B equity)
  • Adds commercial product Galafold (oral Fabry therapy) approved in >40 countries
  • Adds Pombiliti + Opfolda combination for late-onset Pompe disease to portfolio
  • Acquired U.S. rights to DMX-200, a Phase 3 candidate for FSGS

Negative

  • All-cash purchase implies $4.8B immediate cash outflow and potential near-term financing impact
  • Galafold U.S. approval is accelerated and contingent on confirmatory trials for continued approval
  • Pombiliti carries boxed warnings and contraindication in pregnancy that may affect uptake

News Market Reaction – BMRN

+1.18%
1 alert
+1.18% News Effect

On the day this news was published, BMRN gained 1.18%, reflecting a mild positive market reaction.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Acquisition price per share: $14.50 per share Equity value: $4.8 billion Galafold dose: 123 mg capsules +5 more
8 metrics
Acquisition price per share $14.50 per share Cash consideration for Amicus Therapeutics
Equity value $4.8 billion Total equity value of Amicus acquisition
Galafold dose 123 mg capsules Oral pharmacological chaperone for Fabry disease
Fabry amenable variants 35–50 percent Estimated share of Fabry patients with amenable GLA variants
Galafold countries More than 40 countries Global approvals including U.S., EU, U.K., Japan
Common Galafold AEs ≥10% Threshold for most common adverse reactions in label
Pombiliti + Opfolda weight ≥40 kg Eligible adult late-onset Pompe patients’ body weight
Common Pombiliti AEs ≥5% Incidence threshold for most common adverse reactions

Market Reality Check

Price: $54.23 Vol: Volume 1,080,169 is below...
low vol
$54.23 Last Close
Volume Volume 1,080,169 is below the 20-day average of 1,568,621, suggesting a subdued initial response. low
Technical Shares at $53.18 are trading below the 200-day MA of $56.47, about 19.76% under the 52-week high and 4.77% above the 52-week low.

Peers on Argus

BMRN fell 1.48% while close peers were mixed: BBIO up 2.83%, ASND up 2.31%, and ...
1 Up

BMRN fell 1.48% while close peers were mixed: BBIO up 2.83%, ASND up 2.31%, and IONS, EXEL, SMMT down modestly. With only one peer in momentum scanners and no common headlines, the move appears stock-specific.

Previous Acquisition Reports

3 past events · Latest: Dec 19 (Positive)
Same Type Pattern 3 events
Date Event Sentiment Move Catalyst
Dec 19 Amicus deal announced Positive +17.7% Announced $4.8B Amicus acquisition adding revenue-generating rare disease therapies.
Jul 01 Inozyme deal closed Positive +2.2% Completed $270M Inozyme acquisition adding INZ-701 enzyme therapy program.
May 16 Inozyme deal announced Positive +1.7% Announced acquisition of Inozyme and late-stage ENPP1 Deficiency therapy INZ-701.
Pattern Detected

Recent acquisition announcements and completions for BMRN have coincided with positive share reactions.

Recent Company History

Over the past year, BioMarin has repeatedly used acquisitions to expand its rare disease franchise. The initial Amicus deal announcement on Dec 19, 2025 and both the announcement and completion of the Inozyme transaction in May and July 2025 all saw positive price reactions. Today’s completion of the Amicus acquisition continues this M&A strategy by adding marketed Fabry and Pompe therapies and additional late-stage pipeline assets.

Historical Comparison

+7.2% avg move · In the past year, BMRN’s three acquisition headlines averaged a 7.22% gain. Today’s Amicus deal comp...
acquisition
+7.2%
Average Historical Move acquisition

In the past year, BMRN’s three acquisition headlines averaged a 7.22% gain. Today’s Amicus deal completion with a -1.48% move contrasts with those historically positive M&A reactions.

The Amicus transaction progressed from announcement in Dec 2025 to expected close in Q2 2026, while the Inozyme deal moved from signing to completion in 2025, reflecting a pattern of executing acquisitions to expand BioMarin’s rare disease portfolio.

Market Pulse Summary

This announcement confirms completion of the Amicus acquisition, adding marketed therapies for Fabry...
Analysis

This announcement confirms completion of the Amicus acquisition, adding marketed therapies for Fabry and Pompe diseases plus a Phase 3 asset in focal segmental glomerulosclerosis. Historically, BioMarin’s acquisition news produced average moves of about 7.22%, reflecting the strategic importance of M&A. Investors may track upcoming FY 2026 guidance, integration progress, and performance of Galafold and Pombiliti + Opfolda within the broader rare disease portfolio.

Key Terms

fabry disease, pompe disease, lysosomal storage diseases, alpha-galactosidase a, +4 more
8 terms
fabry disease medical
"Galafold® (migalastat) for Fabry Disease and Pombiliti®..."
Fabry disease is a rare inherited disorder caused by a missing or nonworking enzyme that lets certain fatty substances build up inside cells, like a clogged drain causing damage over time. It matters to investors because developing, approving, or improving treatments can create significant market opportunities and affect the value of companies focused on therapies, diagnostics, or long-term care for affected patients.
pompe disease medical
"Pombiliti® (cipaglucosidase alfa-atga) + Opfolda® (miglustat) for Pompe Disease..."
Pompe disease is a rare inherited disorder caused by a missing enzyme that normally breaks down sugar inside muscle cells, so those cells gradually weaken and organs like the heart and lungs can be affected. It matters to investors because treatments are expensive, require long development and regulatory approval, and successful therapies can create sizable markets and influence valuation and partnership decisions for companies working on gene therapies, enzyme replacement or other cures — think of it as a small but high‑value customer base for specialized medical products.
lysosomal storage diseases medical
"medicines that target lysosomal storage diseases: Galafold®..."
Lysosomal storage diseases are a group of rare inherited conditions where cells lose the ability to break down and recycle specific materials, causing those materials to accumulate like a trash compactor that’s jammed. For investors, they matter because the small, well-defined patient groups and urgent unmet needs create opportunities and risks around drug development, pricing, regulatory approval, and long-term treatment demand — factors that can greatly affect a company’s value.
alpha-galactosidase a medical
"oral pharmacological chaperone of alpha-Galactosidase A (alpha-Gal A)..."
Alpha-galactosidase A is an enzyme the body uses to break down certain fatty sugar molecules inside cells; a deficiency causes a genetic disorder where those molecules build up and damage organs. Investors care because restoring or replacing this enzyme is the goal of several therapies, so tests, treatments, manufacturing and regulatory approvals for products targeting this enzyme can drive clinical and commercial value—think of it as fixing a clogged filter in a costly machine.
focal segmental glomerulosclerosis medical
"DMX-200, a potential first-in-class... for the treatment of focal segmental glomerulosclerosis (FSGS)..."
Focal segmental glomerulosclerosis is a chronic kidney disease in which some of the tiny filters in the kidneys (glomeruli) become scarred in parts, reducing the organ’s ability to remove waste and control fluid balance. For investors, it matters because the condition can drive sustained demand for specialized drugs, diagnostic tests, and treatment services, influence healthcare spending and reimbursement dynamics, and affect the commercial prospects of companies developing therapies or diagnostics for rare kidney disorders.
phase 3 medical
"a rare and fatal kidney disease in Phase 3 development."
Phase 3 is the late-stage clinical testing step for a new drug or medical treatment, where the product is given to large groups of patients to confirm effectiveness, monitor side effects, and compare it to standard care. Successful Phase 3 results are often the final scientific hurdle before regulators decide on approval and market launch—like passing a final exam before graduation—and can sharply change a company's valuation and future revenue prospects.
enzyme replacement therapy medical
"who are not improving on their current enzyme replacement therapy (ERT)."
Enzyme replacement therapy is a medical treatment that involves providing patients with artificial versions of natural enzymes their bodies are missing or not producing enough of. This approach can help manage certain health conditions by restoring essential functions, similar to replacing a faulty part in a machine to keep it running smoothly. For investors, advancements or approvals in this therapy can signal progress in biotech innovation and potential market growth.
anaphylaxis medical
"HYPERSENSITIVITY REACTIONS INCLUDING ANAPHYLAXIS: Appropriate medical support..."
Anaphylaxis is a sudden, severe allergic reaction in which the body's defense system overreacts to a trigger (like a drug, food, or insect sting), causing widespread symptoms such as difficulty breathing, low blood pressure, and shock; it can be life‑threatening without prompt treatment. Investors care because anaphylaxis risks can affect a drug or product's safety profile, regulatory approval, liability exposure and market acceptance—similar to a sprinkler system going off and damaging the whole house rather than just one room.

AI-generated analysis. Not financial advice.

Acquisition Adds Galafold® (migalastat) for Fabry Disease and Pombiliti® (cipaglucosidase alfa-atga) + Opfolda® (miglustat) for Pompe Disease to BioMarin's Commercial Portfolio

BioMarin Expects to Provide Updated FY 2026 Guidance During its First Quarter Earnings Call, May 4, 2026

SAN RAFAEL, Calif., April 27, 2026 /PRNewswire/ -- BioMarin Pharmaceutical Inc. (Nasdaq: BMRN) said today that it completed the previously announced agreement to acquire Amicus Therapeutics for $14.50 per share in an all-cash transaction for a total equity value of approximately $4.8 billion. The acquisition will strengthen BioMarin's commercial portfolio, adding two new treatments to the company's existing portfolio of medicines that target lysosomal storage diseases: Galafold® (migalastat), the first oral treatment for Fabry disease, and Pombiliti® (cipaglucosidase alfa-atga) + Opfolda® (miglustat), a two-component therapy for Pompe disease. BioMarin also now has U.S. rights to DMX-200, a potential first-in-class investigational small molecule for the treatment of focal segmental glomerulosclerosis (FSGS), a rare and fatal kidney disease in Phase 3 development.

"The completion of the Amicus acquisition advances BioMarin's strategy to strengthen and diversify our growth profile while furthering our mission to deliver medicines for people living with rare diseases," said Alexander Hardy, President and Chief Executive Officer of BioMarin. "BioMarin's global scale, established commercial infrastructure, and advanced in‑house manufacturing capabilities build on Amicus' legacy and position us to bring Galafold and Pombiliti + Opfolda to more patients around the world."

About Galafold
Galafold® (migalastat) 123 mg capsules is an oral pharmacological chaperone of alpha-Galactosidase A (alpha-Gal A) for the treatment of Fabry disease in adults who have amenable galactosidase alpha gene (GLA) variants. In these patients, Galafold works by stabilizing the body's own dysfunctional enzyme so that it can clear the accumulation of disease substrate. Globally, Amicus Therapeutics estimates that approximately 35 to 50 percent of people living with Fabry disease may have amenable GLA variants, though amenability rates within this range vary by geography. Galafold is approved in more than 40 countries around the world, including the U.S., EU, U.K., and Japan.

U.S. INDICATIONS AND USAGE
Galafold is indicated for the treatment of adults with a confirmed diagnosis of Fabry disease and an amenable GLA variant based on in vitro assay data.

This indication is approved under accelerated approval based on reduction in kidney interstitial capillary cell globotriaosylceramide (KIC GL-3) substrate. Continued approval for this indication may be contingent upon verification and description of clinical benefit in confirmatory trials.

U.S. IMPORTANT SAFETY INFORMATION

ADVERSE REACTIONS: The most common adverse reactions reported with Galafold (≥10%) were headache, nasopharyngitis, urinary tract infection, nausea and pyrexia.

USE IN SPECIFIC POPULATIONS: There is insufficient clinical data on Galafold use in pregnant women to inform a drug-associated risk for major birth defects and miscarriage. Advise women of the potential risk to a fetus. It is not known if Galafold is present in human milk. Therefore, the developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for Galafold and any potential adverse effects on the breastfed child from Galafold or from the underlying maternal condition. Galafold is not recommended for use in patients with severe renal impairment or end-stage renal disease requiring dialysis. The safety and effectiveness of Galafold have not been established in pediatric patients. To report Suspected Adverse Reactions, contact Amicus Therapeutics at 1-877-4AMICUS or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. For additional information about Galafold, including the full U.S. Prescribing Information, please visit https://www.amicusrx.com/pi/Galafold.pdf.

About Pombiliti + Opfolda
Pombiliti + Opfolda, is a two-component therapy that consists of cipaglucosidase alfa-atga, a bis-M6P-enriched rhGAA that facilitates high-affinity uptake through the M6P receptor while retaining its capacity for processing into the most active form of the enzyme, and the oral enzyme stabilizer, miglustat, that's designed to reduce loss of enzyme activity in the blood.

U.S. INDICATIONS AND USAGE
POMBILITI in combination with OPFOLDA is indicated for the treatment of adult patients with late-onset Pompe disease (lysosomal acid alpha-glucosidase (GAA) deficiency) weighing ≥40 kg and who are not improving on their current enzyme replacement therapy (ERT).

SAFETY INFORMATION
HYPERSENSITIVITY REACTIONS INCLUDING ANAPHYLAXIS: Appropriate medical support measures, including cardiopulmonary resuscitation equipment, should be readily available. If a severe hypersensitivity reaction occurs, POMBILITI should be discontinued immediately and appropriate medical treatment should be initiated. INFUSION-ASSOCIATED REACTIONS (IARs): If severe IARs occur, immediately discontinue POMBILITI and initiate appropriate medical treatment. RISK OF ACUTE CARDIORESPIRATORY FAILURE IN SUSCEPTIBLE PATIENTS: Patients susceptible to fluid volume overload, or those with acute underlying respiratory illness or compromised cardiac or respiratory function, may be at risk of serious exacerbation of their cardiac or respiratory status during POMBILITI infusion. See the full U.S. Prescribing Information for complete Boxed Warning. CONTRAINDICATION: POMBILITI in combination with Opfolda is contraindicated in pregnancy. EMBRYO-FETAL TOXICITY: May cause embryo-fetal harm. Advise females of reproductive potential of the potential risk to a fetus and to use effective contraception during treatment and for at least 60 days after the last dose. Adverse Reactions: Most common adverse reactions ≥ 5% are headache, diarrhea, fatigue, nausea, abdominal pain, and pyrexia. Please see U.S. full PRESCRIBING INFORMATION, including BOXED WARNING, for POMBILITI (cipaglucosidase alfa-atga) and full PRESCRIBING INFORMATION for OPFOLDA (miglustat).

About BioMarin
BioMarin is a leading, global rare disease biotechnology company focused on delivering medicines for people living with genetically defined conditions. Founded in 1997, the San Rafael, California-based company has a proven track record of innovation, with a portfolio of commercial therapies and a strong clinical and preclinical pipeline. Using a distinctive approach to drug discovery and development, BioMarin seeks to unleash the full potential of genetic science by pursuing category-defining medicines that have a profound impact on patients. To learn more, please visit www.biomarin.com.

Forward-Looking Statements
This press release contains forward-looking statements about, among other things, the business prospects of Amicus Therapeutics (Amicus) and BioMarin Pharmaceutical Inc. (BioMarin), including, without limitation, statements about: the prospective benefits of the acquisition; expectations regarding Amicus' products, Galafold and Pombiliti + Opfolda; expectations regarding Amicus' product candidate, DMX-200, and its ongoing development; BioMarin's capital allocation strategy to leverage its financial strength to diversify its pipeline and add innovative new therapies for patients; BioMarin's plans for external innovation, including BioMarin's ability to execute additional transactions in future quarters; statements about BioMarin's future performance; and other statements that are not historical facts. Actual results could differ materially from those anticipated in these forward-looking statements. Except as required by law, each of BioMarin and Amicus assume no obligation to update these forward-looking statements, whether as a result of new information, future events or otherwise. These statements, which represent each of BioMarin's and Amicus' current expectations or beliefs concerning various future events that are subject to significant risks and uncertainties, may contain words such as "may," "will," "would," "could," "expect," "anticipate," "intend," "plan," "believe," "estimate," "project," "seek," "should," "strategy," "future," "opportunity," "potential" or other similar words and expressions indicating future results.

These forward-looking statements are predictions and involve risks and uncertainties such that actual results may differ materially from these statements. Forward-looking statements reflect current beliefs and expectations; however, these statements involve inherent risks and uncertainties, including, without limitation, with respect to: the effects of the acquisition on Amicus' or BioMarin's stock price and/or Amicus' or BioMarin's operating results; unknown or inestimable liabilities; the development, launch and commercialization of products and product candidates; the parties' ability to realize the anticipated benefits of the acquisition, including the possibility that the expected benefits from the acquisition will not be realized or will not be realized within the expected time period and that BioMarin and Amicus will not be integrated successfully or that such integration may be more difficult, time-consuming or costly than expected; obtaining and maintaining adequate coverage and reimbursement for BioMarin's or Amicus' products; the time-consuming and uncertain regulatory approval process; the costly and time-consuming pharmaceutical product development process and the uncertainty of clinical success, including risks related to failure or delays in successfully initiating or completing clinical trials and assessing patients, including with respect to current and planned future clinical trials; global economic, financial, and healthcare system disruptions and the current and potential future negative impacts to BioMarin's or Amicus' business operations and financial results; the sufficiency of BioMarin's or Amicus' cash flows and capital resources; BioMarin's evaluation of the potential impact of the transaction on its financial results and financial guidance; BioMarin's or Amicus' ability to achieve targeted or expected future financial performance and results and the uncertainty of future tax, accounting and other provisions and estimates; the effects of the transaction on relationships with key third parties, including employees, customers, suppliers, other business partners or governmental entities, including the risk that the acquisition adversely affects employee retention; risks that the acquisition disrupts current plans and operations; any legal proceedings related to the acquisition; and other risks and uncertainties affecting BioMarin and Amicus, including those risk factors detailed in BioMarin's and Amicus' filings with the Securities and Exchange Commission (SEC), including, without limitation, the risk factors contained under the caption "Risk Factors" in BioMarin's Annual Report on Form 10-K for the fiscal year ended December 31, 2025 and Amicus' Annual Report on Form 10-K for the fiscal year ended December 31, 2025, as such risk factors may be updated by any subsequent reports, as well as the Proxy Statement on Schedule 14A filed by Amicus (as amended and/or supplemented). Stockholders of BioMarin and Amicus are urged not to place undue reliance on forward-looking statements, which speak only as of the date hereof. BioMarin and Amicus are under no obligation, and expressly disclaim any obligation, to update (publicly or otherwise) or alter any forward-looking statement, including without limitation any financial projection or guidance, whether as a result of new information, future events or otherwise.

BioMarin® is a registered trademark of BioMarin Pharmaceutical Inc. or its affiliates.

Contacts:
Investors
Traci McCarty
BioMarin Pharmaceutical Inc.
(415) 455-7558

Media
Marni Kottle
BioMarin Pharmaceutical Inc.
(415) 218-7111

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/biomarin-completes-acquisition-of-amicus-therapeutics-302754256.html

SOURCE BioMarin Pharmaceutical Inc.

FAQ

What did BioMarin (BMRN) announce in the Amicus acquisition on April 27, 2026?

BioMarin completed an all-cash acquisition of Amicus at $14.50 per share, valuing the deal at ~$4.8 billion. According to the company, the purchase adds Galafold, Pombiliti + Opfolda, and U.S. rights to DMX-200 to BioMarin's portfolio.

How will the Amicus assets change BioMarin's commercial portfolio and pipeline (BMRN)?

The acquisition adds two marketed rare-disease therapies and a Phase 3 asset, expanding rare-disease coverage. According to the company, Galafold and Pombiliti + Opfolda broaden offerings for Fabry and Pompe diseases while DMX-200 advances the kidney disease pipeline.

When will BioMarin (BMRN) update 2026 guidance after the Amicus deal?

BioMarin expects to provide updated FY 2026 guidance on its Q1 earnings call on May 4, 2026. According to the company, the guidance update will reflect the completed acquisition and its expected financial effects.

What regulatory or safety considerations from Amicus products affect BioMarin shareholders (BMRN)?

Galafold's U.S. approval is under accelerated approval and requires confirmatory trials for continued approval. According to the company, Pombiliti carries boxed warnings, infusion risks, and a pregnancy contraindication that could affect clinical use and uptake.

Does the Amicus acquisition include any late-stage investigational drugs for BioMarin (BMRN)?

Yes. The transaction conveys U.S. rights to DMX-200, a potential first-in-class small molecule in Phase 3 for FSGS. According to the company, DMX-200 represents a late-stage pipeline addition targeting a rare kidney disease.