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BioMarin to Share Updated Data at 2023 American College of Medical Genetics and Genomics (ACMG) Meeting Demonstrating Commitment to Understanding Long-Term Benefit of VOXZOGO® in Children with Achondroplasia BioMarin Pharmaceutical Inc. (Nasdaq: BMRN), a global biotechnology company dedicated to transforming lives through genetic discovery, will present...

Key Takeaway: BioMarin Pharmaceutical Inc. will present updated findings on VOXZOGO at the 2023 ACMG meeting, emphasizing its long-term benefits in treating children with achondroplasia. Seven-year data indicates sustained improvement in growth velocity compared to untreated peers. VOXZOGO shows continued safety and well-tolerance in patients. This significant presentation aims to enhance understanding of the treatment’s effects as more data becomes available.

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POSITIVE FACTORS

  • The updated data confirms sustained improvements in growth for children with achondroplasia who are treated with VOXZOGO.
  • VOXZOGO remains well tolerated with no change in its adverse event profile over the long term.
  • The presentation at the ACMG meeting includes numerous studies showcasing the efficacy and safety of VOXZOGO.

Full Press Release Details

New Analyses from Phase 2 and Phase 3 Extension Studies Continue to Demonstrate Sustained Improvement in Growth with no Change in Safety Profile
SAN RAFAEL, Calif. , March 14, 2023 /PRNewswire/ -- BioMarin Pharmaceutical Inc. (Nasdaq: BMRN ), a global biotechnology company dedicated to transforming lives through genetic discovery, will present updated data demonstrating the long-term benefit of treatment with VOXZOGO ® (vosoritide) and new observational data on disease burden in children with achondroplasia. These data will be shared this week in an oral presentation and five posters at the 2023 American College of Medical Genetics and Genomics (ACMG) Annual Clinical Genetics Meeting in Salt Lake City, Utah .
The data will include seven-year results from the open-label, Phase 2 extension study in children with achondroplasia, providing further evidence that improvement in growth velocity with VOXZOGO is sustained as children grow older. Mean age- and sex-specific Annualized Growth Velocities (AGVs) in children treated with VOXZOGO were greater than corresponding mean AGVs in untreated children of the same age and sex and at all ages. When looking across all ages for the entire seven-year period, the mean (SD) difference in AGV versus untreated children was 1.90 (0.51) cm/year for boys and 1.36 (0.63) cm/year for girls in this analysis. A trend toward improvement in body proportion (upper:lower body segment ratio) over time continued to be apparent as children grew older.
Results from up to 3.5 years of the open-label extension of BioMarin's Phase 3 pivotal study of VOXZOGO also will be presented. Earlier data from this study supported the drug's approval in the United States , Europe , Brazil , Australia and Japan . In children on VOXZOGO, the mean (standard deviation [SD]) AGV improved from 4.26 (1.54) cm/year at baseline to 5.57 (0.76) cm/year after three years of treatment.
In both studies VOXZOGO remained well tolerated with no change in its adverse event profile.
"We are encouraged to see that as children remain on treatment, the growth promoting effect continues. We are observing sustained increases in growth velocity year on year," said Dr. Melita Irving , MBBS, consultant clinical geneticist at Guy's and St. Thomas' NHS Foundation Trust in London . "The trend toward improving proportionality also has the potential to have an impact on the lives of children with achondroplasia and we look forward to further follow up to better understand that data as they evolve."
"We are grateful to the children and families who continue to participate in the VOXZOGO achondroplasia clinical trials, as we gather longer term data and work toward our goal of providing this therapeutic option to children of all ages," said Hank Fuchs , M.D., president of Worldwide Research and Development at BioMarin.
VOXZOGO addresses the root cause of achondroplasia, the most common form of disproportionate short stature. It is the first U.S. Food and Drug Administration (FDA) and European Medicines Agency (EMA) approved treatment for children with achondroplasia with open epiphyses (bone growth plates). In January, the EMA validated BioMarin's application for extension of indication for VOXZOGO to treat children with achondroplasia under the age of 2 and earlier this month, the FDA accepted the company's Supplemental New Drug Application for children under 5, setting a PDUFA target action date of October 21, 2023 .
BioMarin's presentations at ACMG include:
Oral Presentation:
A Randomized Controlled Trial of Vosoritide in Infants and Toddlers with Achondroplasia Abstract No. O22
Persistent Growth-Promoting Effects of Vosoritide in Children with Achondroplasia for up to 3.5 years: Update from Phase 3 Extension Study Abstract No. P193
Health-Related Quality of Life (HRQoL) in Achondroplasia: Findings from LISA (Life Impact Study on Achondroplasia), a Multinational and Observational Study in Latin America Abstract No. P233
Vosoritide Therapy in Patients with Achondroplasia: Early Experience and Practical Considerations for Clinical Practice Abstract No. P339
Persistence of Growth Promoting Effects in Children with Achondroplasia Over Seven Years: Update from Phase 2 Extension Study with Vosoritide Abstract No. P194
Objectives and Design of the Acorn Study: A Non-Interventional Study Evaluating Long-term Safety in Achondroplasia Patients Treated with Vosoritide Abstract No. P338
About VOXZOGO ® (vosoritide) for Injection
In patients 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 fibroblast growth factor receptor 3 gene ( FGFR3 ). VOXZOGO, a C-type natriuretic peptide (CNP) analog, represents a new class of therapy, which acts as a positive regulator of the signaling pathway downstream of FGFR3 to promote endochondral bone growth.
Through BioMarin's broad clinical development program, the company has enrolled 250 children with achondroplasia from eight countries in seven clinical studies evaluating the safety and efficacy of VOXZOGO.
VOXZOGO is approved in the U.S. and indicated to increase linear growth in pediatric patients with achondroplasia who are 5 years of age and older with open epiphyses. This indication is approved under accelerated approval based on an improvement in annualized growth velocity. Continued approval for this indication 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.
VOXZOGO is also approved in the EU, Brazil, and Australia in children with achondroplasia who are 2 years of age and older with open growth plates. It is also approved in Japan in children from birth who have achondroplasia with open growth plates.
About Achondroplasia
Achondroplasia, the most common form of skeletal dysplasia leading to disproportionate short stature in humans, is characterized by slowing of endochondral ossification, which results in disproportionate short stature and disordered architecture in the long bones, spine, face, and base of the skull. This condition is caused by a change in the fibroblast growth factor receptor 3 gene (FGFR3), a negative regulator of bone growth.
More than 80% of children with achondroplasia have parents of average stature and have the condition as the result of a spontaneous gene mutation. The worldwide incidence rate of achondroplasia is about one in 25,000 live births. VOXZOGO is being tested 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.
VOXZOGO U.S. Important Safety Information
What is VOXZOGO used for?
What is the most important safety information about VOXZOGO?
What are the most common side effects of VOXZOGO?
How is VOXZOGO taken?
What should you tell the doctor before or during taking VOXZOGO?
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 .
Founded in 1997, BioMarin is a global biotechnology company dedicated to transforming lives through genetic discovery. The company develops and commercializes targeted therapies that address the root cause of the genetic conditions. BioMarin's unparalleled research and development capabilities have resulted in eight transformational commercial therapies for patients with rare genetic disorders. The company's distinctive approach to drug discovery has produced a diverse pipeline of commercial, clinical, and pre-clinical candidates that address a significant unmet medical need, have well-understood biology, and provide an opportunity to be first-to-market or offer a substantial benefit over existing treatment options. For additional information, please visit www.biomarin.com .
Forward-Looking Statements
BioMarin ® and VOXZOGO ® are registered trademarks of BioMarin Pharmaceutical Inc.
Contacts:
Investors Media
Traci McCarty Marni Kottle
BioMarin Pharmaceutical Inc. BioMarin Pharmaceutical Inc.
(415) 455-7558 (415) 218-7111
SOURCE BioMarin Pharmaceutical Inc.

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Frequently Asked Questions

What are the benefits of VOXZOGO treatment?

VOXZOGO has shown sustained improvements in growth velocity in children with achondroplasia.

Is VOXZOGO safe for long-term use?

Yes, VOXZOGO remains well tolerated with no change in its adverse event profile.

How long has VOXZOGO been studied in children?

VOXZOGO has been studied for up to seven years in children with achondroplasia.

What is the mechanism of VOXZOGO?

VOXZOGO is a CNP analog that positively regulates bone growth pathways.

At what age is VOXZOGO approved for use?

VOXZOGO is approved for children aged 5 years and older with open epiphyses.

Last updated: Mar 14, 2023