California’s recent decision to create a Rare Disease Advisory Council is a milestone that brings new hope to people living ...
Cherokees deserve help, treatment and hope – especially those who’ve long felt unseen by the health care system due to their ...
In a new study, researchers at McMaster University have identified a potential treatment for Sandhoff and Tay-Sachs ...
Are you battling a rare disease or think you might be suffering from one? If so, there are resources to get help from ...
Recruiting patients for rare disease trials is akin to finding a needle in a haystack, with challenges such as geographical ...
Karl Fitzpatrick has described his frightening ordeal after being diagnosed with potentially life-threatening Guillain–Barré ...
“Receiving rare pediatric disease designation from the FDA underscores the urgent need for new treatment options for patients with EWS and recognizes elraglusib’s transformative potential,” said ...
A new treatment that could prevent blindness in children with the CLN2 type Batten disease has been trialed by clinicians and ...
In the wake of an unfavorable advisory committee meeting in September, Intercept Pharmaceuticals’ bid to win full approval ...
Intercept’s US president Vivek Devaraj said the pharma company still believes in the evidence supporting the liver disease ...
to use its artificial intelligence to identify novel rare disease indications for a discontinued drug asset. Under the terms of the agreement, Sanofi will provide data related to the unnamed drug ...
Actuate Therapeutics (ACTU) announced that the U.S. Food and Drug Administration, FDA, has granted rare pediatric disease designation to ...