Conversation with The Cancer Letter

Conversation with The Cancer Letter

FDA’s Lola Fashoyin-Aje: Stop getting stuck on the “risks” of diversity in drug development, it’s time to fix disparities in access
Conversation with The Cancer LetterFreeHealth Equity

FDA’s Lola Fashoyin-Aje: Stop getting stuck on the “risks” of diversity in drug development, it’s time to fix disparities in access

There’s a cultural perception in drug development that enrolling a diverse, heterogeneous patient cohort can be “risky” for detecting drug effects—a perception that needs to go away, said Lola Fashoyin-Aje, associate director of the Science & Policy Program to Address Disparities at the FDA’s Oncology Center of Excellence and a deputy division director in the agency’s Office of Oncologic Diseases.
NCTN group chairs, experts: Diverse representation of minorities in clinical trials and drug development saves lives
Conversation with The Cancer LetterFreeHealth Equity

NCTN group chairs, experts: Diverse representation of minorities in clinical trials and drug development saves lives

Drug manufacturers and researchers have a moral obligation to design clinical trials that adequately represent the target population for the investigational agent—and these medical products need to be safe and effective for everyone, leading clinical trial experts in oncology say.
Danny Milner: mRNA vaccines may become a viable treatment for cancer because of COVID-19 pandemic
Conversation with The Cancer Letter

Danny Milner: mRNA vaccines may become a viable treatment for cancer because of COVID-19 pandemic

The pandemic has accelerated the development of mRNA vaccines, which could have significant implications for cancer research, said Danny Milner, chief medical officer of the American Society for Clinical Pathology, and adjunct associate professor of immunology and infectious diseases in the Department of Immunology and Infectious Diseases at the Harvard T.H. Chan School of Public Health.