As FDA weighs another myeloma endpoint for accelerated approvals, experts say timely access is at stake

As FDA weighs another myeloma endpoint for accelerated approvals, experts say timely access is at stake

Source: 
Fierce Pharma
snippet: 

Now, after nearly a decade of work, Landgren and other researchers will share research that aims to substantiate a link between MRD negativity and improved clinical outcomes such as delayed tumor progression or death in multiple myeloma. A team led by Landgren, now with the Sylvester Comprehensive Cancer Center, and another International Myeloma Foundation-backed group known as i2TEAMM, will present their separate meta-analysis studies of MRD in myeloma at an FDA advisory committee meeting this Friday.