BioMarin Reports Strong 2025 Earnings Growth
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Feb 24 2026
0mins
Should l Buy BMRN?
Source: seekingalpha
- Significant Revenue Growth: BioMarin's total revenue for 2025 reached $3.22 billion, reflecting a 13% year-over-year increase, with enzyme therapies growing by 9% and Voxzogo revenues soaring by 26%, indicating strong performance and heightened market demand in the biopharmaceutical sector.
- Strategic Acquisition Progress: The company completed its acquisition of Inozyme and expects to finalize the acquisition of Amicus next quarter, which will enhance its enzyme therapy portfolio and further solidify BioMarin's leadership position in the rare disease treatment market.
- Optimistic Future Outlook: The CFO projected total revenues for 2026 to be between $3.325 billion and $3.425 billion, with enzyme therapies and Voxzogo revenues expected to be between $2.225 billion to $2.275 billion and $975 million to $1.025 billion respectively, demonstrating the company's confidence in future growth.
- Robust Cash Flow: BioMarin reported a non-GAAP diluted EPS of $3.15 for 2025, with operating cash flow reaching $828 million, a 45% increase year-over-year, providing strong financial support for future investments and acquisitions.
Trade with 70% Backtested Accuracy
Stop guessing "Should I Buy BMRN?" and start using high-conviction signals backed by rigorous historical data.
Sign up today to access powerful investing tools and make smarter, data-driven decisions.
Analyst Views on BMRN
Wall Street analysts forecast BMRN stock price to rise
19 Analyst Rating
14 Buy
5 Hold
0 Sell
Moderate Buy
Current: 58.530
Low
60.00
Averages
87.35
High
120.00
Current: 58.530
Low
60.00
Averages
87.35
High
120.00
About BMRN
BioMarin Pharmaceutical Inc. is a global biotechnology company engaged in the development of genetic discovery into medicines that make an impact on the life of each patient. The Company has eight commercial therapies and a clinical and preclinical pipeline. Its commercial products include Vimizim (elosulfase alpha), Naglazyme (galsulfase), Palynziq (pegvaliase-pqpz), Brineura (cerliponase alfa), Aldurazyme (laronidase), Roctavian (valoctocogene roxaparvovec), Kuvan (sapropterin dihydrochloride), and Voxzogo (vosoritide). Vimizim is an enzyme replacement therapy for the treatment of MPS IVA, a lysosomal storage disorder. The Roctavian is an adeno-associated virus (AAV5) vector gene therapy designed to restore factor VIII plasma concentrations in patients with severe hemophilia A. Its key clinical programs include Vosoritide, BMN 333, BMN 390, BMN 351, BMN 349, and INZ-701. Its late-stage enzyme replacement therapy, INZ-701, is being developed for the treatment of ENPP1 deficiency.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
FDA Faces Criticism Amid Innovation Challenges
- Regulatory Standards Controversy: Congressman Jake Auchincloss criticized FDA Commissioner Marty Makary for replacing standards of safety and efficacy with fear and favoritism, undermining patient confidence in new therapies and impacting the market launch of innovative drugs.
- Staffing Losses: The FDA has experienced significant staff reductions in its Center for Drug Evaluation and Research, with oncology review staff dropping from about 100 to below 60, which may lead to approval delays and incomplete response letters.
- Decline in Accelerated Approvals: In 2024, the FDA approved 20 drugs through the accelerated approval process, down from 9 the previous year, indicating a direct impact on drug approval efficiency due to the loss of experienced reviewers.
- New Therapy Approval Pathways: The FDA proposed a new system for approving personalized drugs aimed at rare diseases, intending to provide more flexible approval pathways, but this change has sparked widespread controversy, affecting the agency's core mission.
See More
BioMarin's Drug Approved by FDA for PKU Treatment
- FDA Approval: The U.S. FDA has approved BioMarin's supplemental application for Palynziq (pegvaliase-pqpz), making it the only enzyme substitution therapy approved for managing phenylketonuria (PKU) in adolescents aged 12 and older, marking a significant advancement for the company in the rare disease sector.
- Clinical Study Results: The approval is based on the Phase 3 PEGASUS study, which demonstrated statistically significant reductions in blood phenylalanine levels at Week 72 for individuals on Palynziq compared to those on diet alone, indicating the drug's effectiveness in improving patient health outcomes.
- Market Performance Analysis: BioMarin's stock is currently trading at $59.30, which is 4.5% below its 20-day simple moving average and 8.2% below its 100-day simple moving average, reflecting short-term market weakness, with shares down approximately 19% over the past 12 months.
- Analyst Ratings: Despite the challenging market environment, BioMarin's stock carries a Buy rating with an average price target of $88.80, with recent target increases from analysts like Canaccord Genuity and Bernstein, indicating confidence in the company's future potential.
See More
BioMarin Receives FDA Approval for PALYNZIQ in Pediatric Patients
- FDA Approval: BioMarin Pharmaceutical Inc. announced that its PALYNZIQ (pegvaliase-pqpz) has received approval from the U.S. FDA for use in pediatric patients aged 12 and older with phenylketonuria, marking a significant advancement in treatment options.
- Unique Therapy: PALYNZIQ is the only approved enzyme substitution therapy that effectively reduces blood phenylalanine (Phe) concentrations, helping patients with phenylketonuria improve their health outcomes and overall quality of life.
- European Market Expansion: BioMarin is also seeking approval from the European Medicines Agency to expand PALYNZIQ's indication to adolescents aged 12 and older in the European Union, further broadening its market reach.
- Market Reaction: Although BioMarin's stock rose by 1.01% to $61.73 during regular trading on Friday, it fell by 3.92% to $59.31 in after-hours trading, indicating mixed market reactions to the new approval.
See More
FDA Approves PALYNZIQ for Pediatric PKU Treatment in Adolescents
- FDA Approval for New Indication: BioMarin announced that PALYNZIQ has received FDA approval for use in adolescents aged 12 and older with PKU, marking an expansion of the drug's application in the adolescent population and is expected to improve their daily management.
- Significant Clinical Study Results: In the PEGASUS study, the PALYNZIQ group showed an average reduction of 473 μmol/L in blood phenylalanine (Phe) levels at Week 72, compared to only 19 μmol/L in the control group, demonstrating PALYNZIQ's significant advantage in controlling Phe levels.
- Benefits for Adolescent Patients: The study revealed that 44.4% of participants reached Phe levels below guideline recommendations after treatment, with 75% of patients achieving levels below 120 μmol/L and an average Phe reduction of 828 μmol/L, indicating PALYNZIQ's potential benefits for adolescents.
- Safety and Tolerability: While common side effects in adolescents included injection site reactions and headaches, PALYNZIQ's safety profile was well managed in clinical trials, particularly during the maintenance phase, where the incidence of adverse reactions significantly decreased.
See More
FDA Approves PALYNZIQ for Adolescent PKU Treatment
- FDA Approval: BioMarin announced that the FDA has approved PALYNZIQ for adolescents aged 12 and older with PKU, marking an expansion of the drug's application in the adolescent population and is expected to improve their daily management.
- Clinical Trial Results: In the PEGASUS study, the PALYNZIQ group showed an average reduction of 473 μmol/L in blood phenylalanine (Phe) levels at Week 72, compared to a mere -19 μmol/L in the diet-only group, indicating a significant efficacy difference that could transform treatment for adolescent PKU patients.
- Increased Dietary Freedom: As the only enzyme substitution therapy, PALYNZIQ allows patients to manage Phe levels without dietary restrictions, helping adolescents alleviate the burdens of dietary limitations while facing academic and independence challenges.
- Safety and Side Effects: While PALYNZIQ's side effects include injection site reactions and hypersensitivity, most adverse reactions occurred during the induction phase in clinical trials, with a significant decrease in frequency during maintenance, indicating a favorable long-term safety profile.
See More
FDA Grants Approval for Biomarin's Palynziq® (Pegvaliase-PQPZ) for Adolescents Aged 12 and Up with Phenylketonuria (PKU)
- FDA Approval: The U.S. Food and Drug Administration has approved Biomarin's Palynziq (pegvaliase-pqpz) for adolescents aged 12 years and older.
- Indication: This medication is specifically indicated for the treatment of phenylketonuria (PKU), a genetic disorder that affects the metabolism of phenylalanine.
See More
FDA Faces Criticism Amid Innovation Challenges
- Regulatory Standards Controversy: Congressman Jake Auchincloss criticized FDA Commissioner Marty Makary for replacing standards of safety and efficacy with fear and favoritism, undermining patient confidence in new therapies and impacting the market launch of innovative drugs.
- Staffing Losses: The FDA has experienced significant staff reductions in its Center for Drug Evaluation and Research, with oncology review staff dropping from about 100 to below 60, which may lead to approval delays and incomplete response letters.
- Decline in Accelerated Approvals: In 2024, the FDA approved 20 drugs through the accelerated approval process, down from 9 the previous year, indicating a direct impact on drug approval efficiency due to the loss of experienced reviewers.
- New Therapy Approval Pathways: The FDA proposed a new system for approving personalized drugs aimed at rare diseases, intending to provide more flexible approval pathways, but this change has sparked widespread controversy, affecting the agency's core mission.
See More
BioMarin's Drug Approved by FDA for PKU Treatment
- FDA Approval: The U.S. FDA has approved BioMarin's supplemental application for Palynziq (pegvaliase-pqpz), making it the only enzyme substitution therapy approved for managing phenylketonuria (PKU) in adolescents aged 12 and older, marking a significant advancement for the company in the rare disease sector.
- Clinical Study Results: The approval is based on the Phase 3 PEGASUS study, which demonstrated statistically significant reductions in blood phenylalanine levels at Week 72 for individuals on Palynziq compared to those on diet alone, indicating the drug's effectiveness in improving patient health outcomes.
- Market Performance Analysis: BioMarin's stock is currently trading at $59.30, which is 4.5% below its 20-day simple moving average and 8.2% below its 100-day simple moving average, reflecting short-term market weakness, with shares down approximately 19% over the past 12 months.
- Analyst Ratings: Despite the challenging market environment, BioMarin's stock carries a Buy rating with an average price target of $88.80, with recent target increases from analysts like Canaccord Genuity and Bernstein, indicating confidence in the company's future potential.
See More
BioMarin Receives FDA Approval for PALYNZIQ in Pediatric Patients
- FDA Approval: BioMarin Pharmaceutical Inc. announced that its PALYNZIQ (pegvaliase-pqpz) has received approval from the U.S. FDA for use in pediatric patients aged 12 and older with phenylketonuria, marking a significant advancement in treatment options.
- Unique Therapy: PALYNZIQ is the only approved enzyme substitution therapy that effectively reduces blood phenylalanine (Phe) concentrations, helping patients with phenylketonuria improve their health outcomes and overall quality of life.
- European Market Expansion: BioMarin is also seeking approval from the European Medicines Agency to expand PALYNZIQ's indication to adolescents aged 12 and older in the European Union, further broadening its market reach.
- Market Reaction: Although BioMarin's stock rose by 1.01% to $61.73 during regular trading on Friday, it fell by 3.92% to $59.31 in after-hours trading, indicating mixed market reactions to the new approval.
See More
FDA Approves PALYNZIQ for Pediatric PKU Treatment in Adolescents
- FDA Approval for New Indication: BioMarin announced that PALYNZIQ has received FDA approval for use in adolescents aged 12 and older with PKU, marking an expansion of the drug's application in the adolescent population and is expected to improve their daily management.
- Significant Clinical Study Results: In the PEGASUS study, the PALYNZIQ group showed an average reduction of 473 μmol/L in blood phenylalanine (Phe) levels at Week 72, compared to only 19 μmol/L in the control group, demonstrating PALYNZIQ's significant advantage in controlling Phe levels.
- Benefits for Adolescent Patients: The study revealed that 44.4% of participants reached Phe levels below guideline recommendations after treatment, with 75% of patients achieving levels below 120 μmol/L and an average Phe reduction of 828 μmol/L, indicating PALYNZIQ's potential benefits for adolescents.
- Safety and Tolerability: While common side effects in adolescents included injection site reactions and headaches, PALYNZIQ's safety profile was well managed in clinical trials, particularly during the maintenance phase, where the incidence of adverse reactions significantly decreased.
See More
FDA Approves PALYNZIQ for Adolescent PKU Treatment
- FDA Approval: BioMarin announced that the FDA has approved PALYNZIQ for adolescents aged 12 and older with PKU, marking an expansion of the drug's application in the adolescent population and is expected to improve their daily management.
- Clinical Trial Results: In the PEGASUS study, the PALYNZIQ group showed an average reduction of 473 μmol/L in blood phenylalanine (Phe) levels at Week 72, compared to a mere -19 μmol/L in the diet-only group, indicating a significant efficacy difference that could transform treatment for adolescent PKU patients.
- Increased Dietary Freedom: As the only enzyme substitution therapy, PALYNZIQ allows patients to manage Phe levels without dietary restrictions, helping adolescents alleviate the burdens of dietary limitations while facing academic and independence challenges.
- Safety and Side Effects: While PALYNZIQ's side effects include injection site reactions and hypersensitivity, most adverse reactions occurred during the induction phase in clinical trials, with a significant decrease in frequency during maintenance, indicating a favorable long-term safety profile.
See More
FDA Grants Approval for Biomarin's Palynziq® (Pegvaliase-PQPZ) for Adolescents Aged 12 and Up with Phenylketonuria (PKU)
- FDA Approval: The U.S. Food and Drug Administration has approved Biomarin's Palynziq (pegvaliase-pqpz) for adolescents aged 12 years and older.
- Indication: This medication is specifically indicated for the treatment of phenylketonuria (PKU), a genetic disorder that affects the metabolism of phenylalanine.
See More
