[Source: Research & Innovation]
For patients with rare genetic mutations of the debilitating disease cystic fibrosis, there are few options for effective treatment. EU-funded researchers are working to meet their needs, using new developments in personalised medicine to advance the testing of novel and promising drugs.
19
Jun
Research Headlines – New approach to advance drug pipeline for cystic fibrosis
Leave a Reply
You must be logged in to post a comment.