Prader-Willi syndrome is a rare genetic disease that causes poor feeding in infancy but later triggers insatiable hunger.

DelveInsight Business Research LLP The Prader–Willi syndrome market is experiencing growth due to increasing in diagnosis rate owing to an increase in genetic testing, more and more ...

Prader-Willi syndrome (PWS) is a rare, complicated condition that affects many parts of your body. It stems from a problem with one of your chromosomes (a strand of DNA that carries your genes).

The rare disease that Aardvark aims to treat is Prader-Willi syndrome (PWS), a genetic disorder that manifests as hyperphagia, a constant feeling of hunger that can’t be satisfied by any amount ...

This rare disease, Prader-Willi syndrome, has been described in medical literature for nearly 70 years. But even as medical understanding of the disorder grew, efforts to develop a drug to treat i ...

Harvey, 22, has a rare genetic condition called Prader-Willi syndrome, which means he's always hungry. As a consequence of his uncontrollable hunger, he is now battling life-threatening obesity.

Aardvark Therapeutics has raised $94.2m in an initial public offering (IPO) to support the development of its hunger-suppressing drug ARD-101 for the rare disease Prader-Willi syndrome.

The mum-of-five candidly shared that due to his genetic disorder, Prader-Willi syndrome, Harvey isn't getting smaller at present. Speaking to the Sun, Katie said: "He’s putting on weight.

The Food and Drug Administration approved a medication this week known as VYKAT XR to treat hyperphagia — or an incessant feeling of hunger — in kids and adults with Prader-Willi syndrome. The ...

The FDA approved extended-release diazoxide choline (Vykat XR) to treat the intense persistent sensation of hunger in patients 4 years of age and older with Prader-Willi syndrome, maker Soleno ...