It’s easy to test for galactosemia. It’s also simple to treat once it’s diagnosed. And children who have it can live normal lives. Type I occurs in about 1 in every 30,000 to 60,000 people.

Nearly three months after an experimental treatment for classic galactosemia was rejected by the US Food and Drug ...

The US Food and Drug Administration (FDA) has declined to approve Applied Therapeutics’ govorestat for classic galactosemia, ...

Galactosemia is an inherited genetic disorder of metabolism where the body is unable to metabolize a sugar called galactose. Galactose forms half of the sugar lactose, which is found in milk. The ...

Galactosemia is a rare ... Invest alongside the model portfolio or simply access the investment bank-grade financial models and research. I hope to see you there. Analyst’s Disclosure:I/we ...

Galactosemia is a rare genetic disorder that causes an inability to digest galactose, which is a breakdown product of lactose. Lactose is one of the main carbohydrates in milk. In the infant ...

The NDA for govorestat for the galactosemia indication was accepted by the FDA in late February under its Priority Review pathway. A filing designated as a Priority Review reduces the review ...

Galactosemia Foundation Urges FDA to Reconsider on Behalf of Rare Disease Community Facing Devastating Disease ALBANY, N.Y., Nov. 27, 2024 /PRNewswire/ -- The Galactosemia Foundation, a non-profit ...

Galactosemia is a rare genetic disorder that results from the body’s inability to properly metabolize galactose, converting instead to the toxic metabolite, galactitol, which is known to cause ...

Investors reading into the U.S. FDA’s decision to skip an advisory committee meeting to discuss the NDA for Applied Therapeutics Inc.’s govorestat, seeking approval as the first therapy for treating ...