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BridgeBio Pharma's New Drug Application for Genetic Short Stature Condition Accepted by US FDA

BridgeBio Pharma's New Drug Application for Genetic Short Stature Condition Accepted by US FDA

MT newswireMT newswire2026/10/06 12:25

08:25 AM EDT, 10/06/2026 (MT Newswires) -- BridgeBio Pharma (BBIO) oral version of Infigratinib's new drug application has been accepted by the US Food and Drug Administration as a treatment for children with achondroplasia, the company said Tuesday. The treatment has also been granted priority review with a target action date of Feb. 4, the company said. Achondroplasia is a genetic disorder which is the most common cause of disproportionate short stature. The FDA's acceptance was based on a phase 3 study that met its primary and key secondary endpoints, showing statistically significant improvement in both body proportionality and arm span in comparison with a placebo, the company said. BridgeBio plans to submit a marketing authorization application for achondroplasia to the European Medicines Agency in Q4 2026, it said. Shares of the company were up 2.1% in recent premarket trading.

08:25 AM EDT, 10/06/2026 (MT Newswires) -- BridgeBio Pharma (BBIO) oral version of Infigratinib's new drug application has been accepted by the US Food and Drug Administration as a treatment for children with achondroplasia, the company said Tuesday. The treatment has also been granted priority review with a target action date of Feb. 4, the company said. Achondroplasia is a genetic disorder which is the most common cause of disproportionate short stature. The FDA's acceptance was based on a phase 3 study that met its primary and key secondary endpoints, showing statistically significant improvement in both body proportionality and arm span in comparison with a placebo, the company said. BridgeBio plans to submit a marketing authorization application for achondroplasia to the European Medicines Agency in Q4 2026, it said. Shares of the company were up 2.1% in recent premarket trading.
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