ClonoSEQ assay receives expanded FDA clearance to assess MRD in CLL

Share on facebook
Share on twitter
Share on linkedin
Share on email
Share on print

The ClonoSEQ assay received expanded FDA clearance to detect and monitor minimal residual disease in blood or bone marrow from patients with chronic lymphocytic leukemia.

To access this subscriber-only content please log in or subscribe.

If your institution has a site license, log in with IP-login or register for a sponsored account.*
*Not all site licenses are enrolled in sponsored accounts.

Login Subscribe
Table of Contents

YOU MAY BE INTERESTED IN

As the chief scientific officer of the Leukemia & Lymphoma Society for the past eleven years, it has been a privilege to lead a group of scientists that has doled out more than $600 million for cutting-edge hematologic oncology research. These dollars went to more than 1,000 research projects through initiatives like our biomedical research grant programs and LLS’s venture philanthropy, the Therapy Acceleration Program (TAP). 

Never miss an issue!

Get alerts for our award-winning coverage in your inbox.

Login