Achondroplasia Market to Evolve Rapidly Over the Next Decade by 2034, DelveInsight Observes

DelveInsight's "Achondroplasia Market Insights, Epidemiology, and Market Forecast-2034′′ report offers an in-depth understanding of the Achondroplasia, historical and forecasted epidemiology as well as the Achondroplasia market trends in the United States, EU4 (Germany, Spain, Italy, France) the United Kingdom and Japan.

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Some of the key facts of the Achondroplasia Market Report:
• The Achondroplasia market size is anticipated to grow with a significant CAGR during the study period (2020-2034).
• In June 2025, Ascendis Pharma reported the week 26 interim results from its ongoing Phase II COACH Trial, which is assessing the combination of TransCon CNP (navepegritide) and TransCon hGH (lonapegsomatropin) in children with achondroplasia, a rare genetic disorder. The data indicate that TransCon hGH enhances the effects of TransCon CNP, leading to greater growth and improved body proportions after 26 weeks of treatment. The combination's safety and tolerability were consistent with what has been observed for each therapy individually.
• In March 2025, Ascendis Pharma A/S (Nasdaq: ASND) has filed a New Drug Application (NDA) with the U.S. FDA for TransCon CNP (navepegritide), intended for the treatment of children with achondroplasia. This investigational prodrug, administered once weekly, is based on C-type natriuretic peptide (CNP) and is engineered to deliver prolonged CNP exposure to receptors across the body-particularly in growth plates and skeletal muscles-targeting the underlying cause of achondroplasia.
• In January 2025, The FDA has approved the Investigational New Drug (IND) application for TYRA-300, an oral FGFR3-selective inhibitor, for the treatment of low-grade, intermediate-risk non-muscle invasive bladder cancer (NMIBC). This approval enables the initiation of a Phase 2 clinical trial targeting this patient group. TYRA-300 is an experimental oral therapy being developed to treat cancers and skeletal dysplasias, such as achondroplasia and hypochondroplasia.
• In September 2024, BridgeBio Pharma, Inc. (Nasdaq: BBIO), a biopharmaceutical company specializing in genetic disorders, announced today that the FDA has granted Breakthrough Therapy Designation to oral infigratinib, which is being developed for pediatric achondroplasia. This designation aims to accelerate the development and regulatory review of drugs in the U.S. that meet strict criteria. To qualify, a drug must show initial clinical evidence of potentially significant improvement on clinically meaningful endpoints compared to existing treatments.
• In the United States, achondroplasia impacts a slightly higher percentage of females (51.2%) compared to males (48.8%). This slight difference may be attributed to genetic or biological factors that contribute to its somewhat greater prevalence in females.
• In 2023, the total number of diagnosed prevalent cases of achondroplasia in Japan and the US was approximately 18,000, with expectations for this number to increase in the coming years.
• In 2023, Japan had around 3,000 diagnosed prevalent cases of achondroplasia.
• The epidemiology model categorizes age-specific cases into nine groups: 0-4, 5-10, 11-15, 16-20, 21-30, 31-40, 41-50, 51-60, and over 60. DelveInsight's estimates indicate that the 5-10 age group was the most affected in the US, with around 4,000 cases reported in 2023.
• Achondroplasia is estimated to occur in 1 out of every 15,000 to 40,000 live births, making it one of the most prevalent types of skeletal dysplasia.
• Key Achondroplasia Companies: BioMarin Pharmaceuticals, RIBOMIC Inc., Sanofi, Black Diamond Therapeutics, Ribomic, Tyra Biosciences, QED Therapeutics, and others
• Key Achondroplasia Therapies: VOXZOGO (vosoritide), RBM-007, SAR-442501, BDTX 4876, RBM-007, TYRA 300, Infigratinib, and others
• The Achondroplasia market is expected to surge due to the disease's increasing prevalence and awareness during the forecast period. Furthermore, launching various multiple-stage Achondroplasia pipeline products will significantly revolutionize the Achondroplasia market dynamics.

Achondroplasia Overview
Achondroplasia is a genetic disorder and the most common form of dwarfism, characterized by abnormal bone growth that results in short stature with disproportionately short arms and legs, a larger head, and distinctive facial features. It is caused by mutations in the *FGFR3* gene, which affects cartilage formation and bone growth. This condition is typically inherited in an autosomal dominant pattern, meaning that only one copy of the altered gene is sufficient to cause the disorder. While people with achondroplasia often have normal intelligence and lifespan, they may experience certain health challenges such as spinal stenosis, ear infections, and respiratory issues.

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Achondroplasia Epidemiology
The epidemiology section provides insights into the historical, current, and forecasted epidemiology trends in the seven major countries (7MM) from 2020 to 2034. It helps to recognize the causes of current and forecasted trends by exploring numerous studies and views of key opinion leaders. The epidemiology section also provides a detailed analysis of the diagnosed patient pool and future trends.

Achondroplasia Epidemiology Segmentation:
The Achondroplasia market report proffers epidemiological analysis for the study period 2020-2034 in the 7MM segmented into:
• Total Prevalence of Achondroplasia
• Prevalent Cases of Achondroplasia by severity
• Gender-specific Prevalence of Achondroplasia
• Diagnosed Cases of Episodic and Chronic Achondroplasia

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Achondroplasia Drugs Uptake and Pipeline Development Activities
The drugs uptake section focuses on the rate of uptake of the potential drugs recently launched in the Achondroplasia market or expected to get launched during the study period. The analysis covers Achondroplasia market uptake by drugs, patient uptake by therapies, and sales of each drug.
Moreover, the therapeutics assessment section helps understand the drugs with the most rapid uptake and the reasons behind the maximal use of the drugs. Additionally, it compares the drugs based on market share.
The report also covers the Achondroplasia Pipeline Development Activities. It provides valuable insights about different therapeutic candidates in various stages and the key companies involved in developing targeted therapeutics. It also analyzes recent developments such as collaborations, acquisitions, mergers, licensing patent details, and other information for emerging therapies.

Achondroplasia Therapies and Key Companies
• VOXZOGO (vosoritide): BioMarin Pharmaceuticals
• RBM-007: RIBOMIC Inc.
• SAR-442501: Sanofi
• BDTX 4876: Black Diamond Therapeutics
• RBM-007: Ribomic
• TYRA 300: Tyra Biosciences
• Infigratinib: QED Therapeutics

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Scope of the Achondroplasia Market Report
• Study Period: 2020-2034
• Coverage: 7MM [The United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan]
• Key Achondroplasia Companies: BioMarin Pharmaceuticals, RIBOMIC Inc., Sanofi, Black Diamond Therapeutics, Ribomic, Tyra Biosciences, QED Therapeutics, and others
• Key Achondroplasia Therapies: VOXZOGO (vosoritide), RBM-007, SAR-442501, BDTX 4876, RBM-007, TYRA 300, Infigratinib, and others
• Achondroplasia Therapeutic Assessment: Achondroplasia current marketed and Achondroplasia emerging therapies
• Achondroplasia Market Dynamics: Achondroplasia market drivers and Achondroplasia market barriers
• Competitive Intelligence Analysis: SWOT analysis, PESTLE analysis, Porter's five forces, BCG Matrix, Market entry strategies
• Achondroplasia Unmet Needs, KOL's views, Analyst's views, Achondroplasia Market Access and Reimbursement

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About DelveInsight
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It also offers Healthcare Consulting Services, which benefits in market analysis to accelerate the business growth and overcome challenges with a practical approach.

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