The World of Health & Medicine News

BridgeBio’s oral drug boosts growth in children with dwarfism in late-stage trial

BridgeBio’s oral drug boosts growth in children with dwarfism in late-stage trial

 BridgeBio Pharma said its experimental therapy boosted growth rates in children with a rare genetic disorder that causes dwarfism, sending the company’s shares 7% higher on Thursday.

The company said it plans to seek regulatory approval in the U.S. and Europe in the second half of 2026, and if approved, infigratinib would be the first oral therapy for achondroplasia.

In the late-stage trial, the therapy improved growth rate by 1.74 cm, on average, compared with placebo after 52 weeks in children with achondroplasia, a condition that causes disproportionate short stature.

In a pre-specified analysis of children aged 3 to 8 years, the therapy also showed statistically significant improvement in body proportions compared with placebo.

“We think these results clearly hit and exceed the bar hoped for by investors and make infigratinib highly competitive in the achondroplasia landscape as an oral with superior efficacy and clean safety,” said Barclays analyst Eliana Merle.

Currently, BioMarin Pharmaceutical’s  injection, Voxzogo, is the only approved drug for the condition. Ascendis’  TransCon CNP is currently under review by the U.S. FDA.

A safe daily oral option is “always going to be the preferred way of administering medicine for young children,” which potentially is a “game changer” in this space, BridgeBio executive Justin To said.

The drug’s results outperformed Voxzogo and TransCon CNP, which showed mean annualized growth increases of 1.57 cm and 1.49 cm versus placebo, respectively, according to TD Cowen analyst Tyler Van Buren.

Achondroplasia affects about 55,000 people in the U.S. and the European Union, BridgeBio said.

The data positions infigratinib as a potential blockbuster, said Cantor analyst Josh Schimmer, who estimated the drug could generate nearly $2 billion in peak annual sales in achondroplasia.

The company is also testing the drug in another related condition called hypochondroplasia, a milder form of achondroplasia with less severe growth issues.

spot_img

Explore more

spot_img

GSK enters lung cancer drug market with early FDA nod for...

GSK enters lung cancer drug market with early FDA nod for Jideytro GSK (GSK.L), opens new tab said on Wednesday the U.S. FDA approved its drug ​to...

Working from home could be harming your health, warns Chris Whitty

Working from home could be harming your health, warns Chris Whitty England’s chief medical officer has issued a warning about the health dangers of prolonged sitting, coinciding...

Popular sugar substitutes linked to faster brain aging

Popular sugar substitutes linked to faster brain aging Several popular sugar substitutes may not be as harmless as they seem. Adults who consumed the most...

 The Best Time to Eat Peaches for Energy, According to a...

The Best Time to Eat Peaches for Energy, According to a Dietitian Peaches are a juicy, naturally sweet, nutritious, and refreshing fruit. While there’s no...

FDA approves at-home starter dose of Eisai-Biogen Alzheimer’s drug

FDA approves at-home starter dose of Eisai-Biogen Alzheimer's drug The U.S. FDA on Monday approved an at-home starting dose of Eisai's (4523.T), opens new tab and Biogen's (BIIB.O),...

The One Healthy Food That Might be Spiking Your ‘Bad’ Cholesterol

The One Healthy Food That Might be Spiking Your 'Bad' Cholesterol Coconut oil has enjoyed a long run as a wellness favorite. It's been blended...

US FDA approves Vertex’s gene therapy for sickle cell disease in...

US FDA approves Vertex's gene therapy for sickle cell disease in children as young as two The U.S. Food and Drug Administration approved expanded use...

FDA clears Orca’s blood cancer therapy to reduce stem cell transplant...

FDA clears Orca's blood cancer therapy to reduce stem cell transplant complications The U.S. Food and Drug Administration said on ​Tuesday it has approved Orca...