BioMarin Presents New Data for VOXZOGO® (vosoritide) in Children with Achondroplasia and Other Skeletal Conditions at Two International Endocrinology Meetings

New data in children under 5 years with achondroplasia showed treatment with VOXZOGO was associated with improvement in tibial bowing, a common cause of pain and impaired function Data from the largest retrospective, multi-year observational study of more than 600 children and adults with hypochondroplasia found significantly higher rates of comorbidities, surgeries and overall doctor visits , /PRNewswire/ -- BioMarin Pharmaceutical Inc. (Nasdaq: BMRN) today announced new data from studies of VOXZOGO® (vosoritide), demonstrating meaningful impact on tibial bowing in children with achondroplasia and investigational early efficacy results in other skeletal conditions. The data were presented at the 2025 Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) in Copenhagen, Denmark and will be shared at the Pediatric Endocrine Society Annual Meeting (PES) in National Harbor, Maryland. VOXZOGO Demonstrated Positive Impact on Tibial BowingAn analysis of data presented at PES from the VOXZOGO Phase 2 CANOPY clinical studies in younger children assessed the impact of treatment on tibial bowing, an orthopedic complication and significant cause of pain in children with achondroplasia. Children who received VOXZOGO had a significant reduction in the magnitude of tibial bowing compared to children who received placebo. Furthermore, the researchers found that this improvement was sustained in children who received treatment for several years. "Outcomes beyond height have long been prioritized by the dwarfism community," said Michael Hughes, Chair, Little People of America's (LPA) Biotech Industry Liaison Committee. "Tibial bowing can be a source of pain and surgical intervention for some children with achondroplasia, and this research reflects an encouraging shift toward addressing a meaningful outcome to the community." "In children with achondroplasia, tibial bowing can be painful and often requires surgical intervention," said Klane White, M.D., pediatric orthopedic surgeon and Rose Brown Endowed Chair of Pediatric Orthopedics at Children's Hospital Colorado. "Through my clinical practice, I have observed meaningful improvements that early treatment initiation with VOXZOGO has offered children with achondroplasia, including in proportionality, quality of life and now tibial bowing, which have the potential to improve physical well-being for these children into adulthood." The latest results from the VOXZOGO Phase 3 clinical trial reporting the longest follow-up to date demonstrated that continuous and early treatment was associated with sustained increases in annualized growth velocity (AGV). For the first time, it was possible to model potential final height gain for children with achondroplasia if they were treated early and continuously from 6 months until final adult height (FAH). Modeling indicated that VOXZOGO treatment could result in a height increase of 21.7 centimeters (cm) (95% Cl, 18.7-24.6) in girls and 26.4 cm (95% Cl, 22.9-29.8) in boys compared to untreated children. These data were presented today at ESPE as an oral presentation and add to the totality of evidence demonstrating that early and continuous treatment with VOXZOGO maximizes clinical benefits for children with achondroplasia. Hypochondroplasia Associated with Significant Increase in ComorbiditiesResearchers also presented data shedding light on the comorbidities associated with hypochondroplasia, a genetically defined form of skeletal dysplasia for which VOXZOGO is currently being evaluated in clinical trials. In more than 600 adults and children with hypochondroplasia who were studied using real-world electronic health primary care medical record data in England, comorbidity event rates were more common compared to people without hypochondroplasia. The condition was also associated with an increase in doctor visits, surgeries and orthopedic interventions. "This research is critical to shaping a deeper understanding of hypochondroplasia and underscores the importance of early diagnosis, which allows physicians to begin working with children and their families as soon as possible," said Greg Friberg, M.D., Executive Vice President and Chief Research & Development Officer at BioMarin. "We remain committed to developing new options for skeletal conditions, such as hypochondroplasia and Turner syndrome, and these early data continue to inform our clinical trials." In a prospective, single-center Phase 2 open-label clinical study in girls with Turner syndrome, researchers found that treatment with VOXZOGO was associated with a promising increase in AGV at 6 months compared to their baseline AGV. Importantly, AGV was increased even in children who were previously treated with human growth hormone and discontinued due to suboptimal results prior to enrollment in this study. VOXZOGO was also well-tolerated with safety results consistent with its known profile in achondroplasia. BioMarin continues to advance development across its CANOPY clinical program for VOXZOGO in hypochondroplasia, idiopathic short stature, Noonan syndrome, Turner syndrome and SHOX deficiency. In April, BioMarin completed enrollment in its pivotal Phase 3 study with VOXZOGO in hypochondroplasia, and the company is on track to share topline data in 2026, with potential launch in 2027. Below are key presentations for BioMarin and VOXZOGO at both meetings: ESPE and ESE Design of a Phase 2, Randomized, Controlled, Multicentre Study of Vosoritide Treatment in Children with Idiopathic Short StatureePoster P647Saturday, May 10 Design of a Randomized, Multicentre, Phase 2 Study of Vosoritide in Children with Turner Syndrome, Noonan Syndrome, or Short Stature Homeobox-Containing Gene (SHOX) DeficiencyePoster EP840Saturday, May 10 The Medical Impact of Hypochondroplasia Among Children in England Between 1998 and 2019: A Matched Cohort Study Using Electronic Medical Records from the Clinical Practice Research DatalinkePoster P617Saturday, May 10 The Medical Impact of Hypochondroplasia by Age Among Adults in England between 1998 and 2019: A Matched Cohort Study Using Electronic Medical Records from the Clinical Practice Research Datalink ePoster P603Saturday, May 10 The Achondroplasia Roadmap ePoster EP202Saturday, May 10 Long-Term Height Gain and Maintenance of Treatment Effect in Children with Achondroplasia Receiving VosoritideOral Presentation OC7.4Monday, May 12, 3:05 – 3:15 p.m. Central European Summer Time (CEST) PES (all times in Eastern Daylight Time [EDT]) IGF-1 Values in Hypochondroplasia and Effects of VosoritidePoster P9Thursday, May 15, 6:30 – 8:30 p.m. Medical Impact of Hypochondroplasia Among Children and Adults in England: A 22-Year Retrospective StudyPoster P42Friday, May 16, 12:00 – 12:30 p.m. Vosoritide Improves Tibial Bowing in Infants and Toddlers with AchondroplasiaPoster P28Friday, May 16, 12:00 – 12:30 p.m. Preliminary Assessment of Vosoritide for Short Stature in Turner Syndrome: 6-Month Data from a Clinical TrialPoster P39Saturday, May 17, 12:45 – 2:30 p.m. About Achondroplasia Achondroplasia, the most common form of skeletal dysplasia, is characterized by impaired bone growth caused by a change in the FGFR3 gene. Bone growth is regulated by multiple biological processes including signaling pathways through fibroblast growth factor (FGF, which slows bone growth) and C-type natriuretic peptide (CNP, which increases bone growth). In achondroplasia, these signals are out of balance, resulting in a slowing of endochondral ossification, and causing disproportionate short stature and disordered architecture in the long bones, spine, face and base of the skull. More than 80% of children with achondroplasia have parents of average stature and have the condition as a result of a spontaneous gene mutation. The worldwide incidence rate of achondroplasia is about one in 25,000 live births. VOXZOGO is being evaluated in children whose growth plates are still "open," typically those under 18 years of age. Approximately 25% of people with achondroplasia fall into this category. About VOXZOGO In children with achondroplasia, endochondral bone growth, an essential process by which bone tissue is created, is negatively regulated due to a gain of function mutation in FGFR3. VOXZOGO, a C-type natriuretic peptide (CNP) analog, acts as a positive regulator of the signaling pathway downstream of FGFR3 to promote endochondral bone growth. VOXZOGO is approved in the U.S., Japan and Australia to increase linear growth in children of all ages with achondroplasia with open epiphyses, and VOXZOGO is indicated in the EU for the treatment of achondroplasia in children 4 months of age and older whose epiphyses are not closed, as confirmed by appropriate genetic testing. In the U.S., this indication is approved under accelerated approval based on an improvement in annualized growth velocity. Continued approval may be contingent upon verification and description of clinical benefit in confirmatory trial(s). To fulfill this post-marketing requirement, BioMarin intends to use the ongoing open-label extension studies compared to available natural history. Patient Support Accessing VOXZOGO To reach a BioMarin RareConnections® Case Manager, please call, toll-free, 1-833-VOXZOGO (1-833-869-9646) or e-mail [email protected]. For more information about VOXZOGO, please visit www.voxzogo.com. For additional information regarding this product, please contact BioMarin Medical Information at [email protected]. VOXZOGO U.S. Important Safety Information What is VOXZOGO used for? VOXZOGO is a prescription medicine used to increase linear growth in children with achondroplasia and open growth plates (epiphyses). VOXZOGO is approved under accelerated approval based on an improvement in annualized growth velocity. Continued approval may be contingent upon verification and description of clinical benefit in confirmatory trials. What is the most important safety information about VOXZOGO? VOXZOGO may cause serious side effects including a temporary decrease in blood pressure in some patients. To reduce the risk of a decrease in blood pressure and associated symptoms (dizziness, feeling tired, or nausea), patients should eat a meal and drink 8 to 10 ounces of fluid within 1 hour before receiving VOXZOGO. What are the most common side effects of VOXZOGO? The most common side effects of VOXZOGO include injection site reactions (including redness, itching, swelling, bruising, rash, hives, and injection site pain), high levels of blood alkaline phosphatase shown in blood tests, vomiting, joint pain, decreased blood pressure, and stomachache. These are not all the possible side effects of VOXZOGO. Ask your healthcare provider for medical advice about side effects, and about any side effects that bother the patient or that do not go away. How is VOXZOGO taken? VOXZOGO is taken daily as an injection given under the skin, administered by a caregiver after a healthcare provider determines the caregiver is able to administer VOXZOGO. Do not try to inject VOXZOGO until you have been shown the right way by your healthcare provider. VOXZOGO is supplied with Instructions for Use that describe the steps for preparing, injecting, and disposing VOXZOGO. Caregivers should review the Instructions for Use for guidance and any time they receive a refill of VOXZOGO in case any changes have been made. Inject VOXZOGO 1 time every day, at about the same time each day. If a dose of VOXZOGO is missed, it can be given within 12 hours from the missed dose. After 12 hours, skip the missed dose and administer the next daily dose as usual. The dose of VOXZOGO is based on body weight. Your healthcare provider will adjust the dose based on changes in weight following regular check-ups. Your healthcare provider will monitor the patient's growth and tell you when to stop taking VOXZOGO if they determine the patient is no longer able to grow. Stop administering VOXZOGO if instructed by your healthcare provider. What should you tell the doctor before or during taking VOXZOGO? Tell your doctor about all of the patient's medical conditions including If the patient has heart disease (cardiac or vascular disease), or if the patient is on blood pressure medicine (anti-hypertensive medicine). If the patient has kidney problems or renal impairment. If the patient is pregnant or plans to become pregnant. It is not known if VOXZOGO will harm the unborn baby. If the patient is breastfeeding or plans to breastfeed. It is not known if VOXZOGO passes into breast milk. Tell your doctor about all of the medicines the patient takes, including prescription and over-the-counter medicines, vitamins, and herbal supplements. You may report side effects to BioMarin at 1-866-906-6100. You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088. Please see additional safety information in the full Prescribing Information and Patient Information. About BioMarin BioMarin is a global biotechnology company dedicated to translating the promise of genetic discovery into medicines that make a profound impact on the life of each patient. The San Rafael, California-based company, founded in 1997, has a proven track record of innovation with eight 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 offer new possibilities for people living with genetically defined conditions around the world. To learn more, please visit www.biomarin.com. Forward-Looking Statements This press release contains forward-looking statements about the business prospects of BioMarin Pharmaceutical Inc. (BioMarin), including without limitation, statements about: data presented at the 2025 Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) and data to be shared at the Pediatric Endocrine Society Annual Meeting (PES), including the oral and poster presentations; VOXZOGO's efficacy, safety and impact on children with achondroplasia, including the potential benefits of early treatment with VOXZOGO on height increase, proportionality, quality of life and tibial bowing and potential to improve physical well-being for children into adulthood; VOXZOGO's potential benefits, safety and impact on children with hypochondroplasia and Turner syndrome, including potential increase in annualized growth velocity (AGV); BioMarin's commitment to develop new options for skeletal conditions; and BioMarin's CANOPY clinical development program for achondroplasia, hypochondroplasia, idiopathic short stature, Noonan syndrome, Turner syndrome and SHOX deficiency, including BioMarin's plans and expectations to share topline data for its pivotal Phase 3 study with VOXZOGO in hypochondroplasia in 2026, with potential launch in 2027. These forward-looking statements are predictions and involve risks and uncertainties such that actual results may differ materially from these statements. These risks and uncertainties include, among others: results and timing of current and planned pre-clinical studies and clinical trials of VOXZOGO; any potential adverse events observed in the continuing monitoring of the patients in the clinical trials; the content and timing of decisions by the U.S. Food and Drug Administration, the European Medicines Agency, the European Commission and other regulatory authorities; and those factors detailed in BioMarin's filings with the Securities and Exchange Commission, including, without limitation, the factors contained under the caption "Risk Factors" in BioMarin's Quarterly Report on Form 10-Q for the quarter ended March 31, 2025, as such factors may be updated by any subsequent reports. Stockholders are urged not to place undue reliance on forward-looking statements, which speak only as of the date hereof. BioMarin is under no obligation, and expressly disclaims any obligation to update or alter any forward-looking statement, whether as a result of new information, future events or otherwise. BioMarin®, BioMarin RareConnections® and VOXZOGO® are registered trademarks of BioMarin Pharmaceutical Inc. Contacts: Investors MediaTraci McCarty Andrew VillaniBioMarin Pharmaceutical Inc. BioMarin Pharmaceutical Inc.(415) 455-7558 (628) 269-7393 SOURCE BioMarin Pharmaceutical Inc. WANT YOUR COMPANY'S NEWS FEATURED ON PRNEWSWIRE.COM? 440k+ Newsrooms & Influencers 9k+ Digital Media Outlets 270k+ Journalists Opted In

BioMarin Presents New Data for VOXZOGO® (vosoritide) in Children with Achondroplasia and Other Skeletal Conditions at Two International Endocrinology Meetings

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