Personal Stories, Kids, Young Adults, Adults, News, Research, Living with Muscular Dystrophy, Advocacy
Promoting Diversity in Rare Disease Research
Drug companies are developing more therapies for rare disease patients — and doing it faster — than ever before. But when it comes to enrolling minorities in clinical trials, the US track record is lagging behind. That subject was the focus of a March 15 session during the 2022 MDA Clinical & Scientific Conference in . . .
