Health Equity

To make clinical trials equitable, cancer groups evaluate restrictive eligibility criteria
Guest EditorialHealth Equity

To make clinical trials equitable, cancer groups evaluate restrictive eligibility criteria

Emergent public-private partnerships (PPPs) have risen to the occasion to streamline and coordinate severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines. With these monumental efforts have come important public discussions about equitable access and representation in clinical trials (CTs).
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.