Minorities in clinical trials
This article was originally published in The Tan Sheet
Executive SummaryEvening meeting to examine role of FDA, institutional review boards, other stakeholders "in the protection of human subjects in clinical trials as it relates to minority participation" slated for Aug. 22. Meeting will take place from 7:30 p.m.-9:30 p.m. at Meharry Medical School in Nashville, Tenn. For more information, contact FDA's Sandra Baxter at 615-781-5385...
You may also be interested in...
ICER president Steve Pearson is ‘cautiously optimistic’ that net pricing for acute migraine treatments will align with benefits once discounts are factored in.
Almost 50 novel agents are already under review at FDA for potential 2020 approval. Candidates are notably diverse, with concentrations in established strongholds (oncology, neuroscience), popular programs (breakthrough), and powerhouse sponsors (keep an eye on Bristol-Myers Squibb right out of the gate).
CBER is starting the year with four novel gene and cell therapy applications under review and rolling submissions underway for more.