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BioWorld - Saturday, April 4, 2026
Home » achondroplasia

Articles Tagged with ''achondroplasia''

Rare disease illustration

TYRA-300 designated rare pediatric disease drug; Tyra collects $200M

Feb. 2, 2024
By Karen Carey
A rare pediatric disease designation for its achondroplasia treatment and a subsequent $200 million private placement boosted shares of Tyra Biosciences Inc. on Feb. 2 by 29.3%.
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Child feet

Biomarin has challengers for treating rare, genetic achondroplasia

Oct. 25, 2023
By Lee Landenberger
Four other companies want to replicate Biomarin Pharmaceuticals Inc.’s recent success as they seek approvals to treat the rare but most prevalent genetic form of dwarfism, achondroplasia. The U.S. FDA approved the sNDA for injectable Voxzogo (vosoritide), fibroblast growth factor receptor 3 (FGFR3) inhibitor from Biomarin on Oct. 20.
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Bridgebio stock grows on phase II achondroplasia data

March 6, 2023
By Lee Landenberger
Positive results from Bridgebio Pharma Inc.’s phase II study of infigratinib in children with achondroplasia, a genetic disease that inhibits bone length and leads to short stature, prompted the company stock to surge. Participants receiving the highest dosage, which was the fifth cohort getting 0.25 mg/kg daily, saw a 3.03-centimeter increase, about 1.19 inch, in their height annually, which produced a “p” value of 0.0022.
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Protein structure illustration of fibroblast growth factor receptor 3.
Endocrine/Metabolic

Tyra to develop FGFR3 inhibitor TYRA-300 for achondroplasia

March 2, 2023
Tyra Biosciences Inc. is expanding development of TYRA-300 into achondroplasia based on promising preclinical results from a study conducted in collaboration with the Imagine Institute. A specific mutation in fibroblast growth factor receptor 3 (FGFR3) causes over 97% of achondroplasia.
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Child feet

Voxzogo counterblow from Bridgebio? ACH therapy could rise to new heights

July 26, 2022
By Randy Osborne
Wall Street apparently wants to see longer-term data from Bridgebio Pharma Inc. with oral infigratinib in children with achondroplasia (ACH) before deciding about the drug’s chances against the approved therapy Voxzogo (vosoritide) from Biomarin Pharmaceutical Inc.
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FDA Approved seal

First drug is approved for achondroplasia

Nov. 19, 2021
By Jennifer Boggs and Lee Landenberger
Biomarin Pharmaceutical Inc.’s data supporting the use of Voxzogo (vosoritide) in children with the most common form of dwarfism proved compelling for the FDA, which cleared the modified C-type natriuretic peptide as the first treatment for the rare genetic disease affecting bone growth.
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Skeletal disorder firm Innoskel launches with $24M

Dec. 14, 2020
By Nuala Moran
LONDON – Innoskel has arrived on the scene with a €20 million (US$24.3 million) series A funding to advance development of gene therapies for type 2 collagenopathies, a group of rare skeletal disorders that affect the structure of connective tissues, leading to short stature.
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