March 17th 2025, 7:00pm
Bexobrutideg, a bioavailable agent, was granted orphan drug designation by the FDA for Waldenström macroglobulinemia, a type of non-Hodgkin's lymphoma.
December 30th 2024, 2:00pm
NX-5948 has received fast track designation for adults with relapsed or refractory Waldenström macroglobulinemia who received at least two prior lines of therapy.
December 13th 2024, 4:00pm
From Gerry Turner announcing he has cancer to the return of a Chicago Cubs legend’s disease, here’s what’s happening in the cancer space this week.
December 9th 2024, 11:00pm
In patients with certain B-cell blood cancers, heart-related side effects may occur less after receiving second-generation BTK inhibitors.
July 24th 2024, 3:00pm
Eighty percent of patients with relapsed or refractory Waldenstrom’s macroglobulinemia responded to treatment with iopofosine I 131, researchers found.
February 29th 2024, 10:00pm
An oral suspension formula of Imbruvica received the green light from the Food and Drug Administration to be used in all approved indications.
January 15th 2024, 4:00pm
Last week, the FDA provided updates on two cancer therapies. In this episode, we discuss those decisions and more.
January 9th 2024, 4:00pm
A small study of iopofosine I 131 in patients with pretreated Waldenstrom’s macroglobulinemia showed that the disease control rate was 100%.
August 19th 2022, 7:00pm
The FDA has allowed the manufacturer of emavusertib to continue a phase 1/2 study investigating effects of the treatment in patients with lymphoma.
June 27th 2022, 9:00pm
Treatment with the novel CAR-T cell therapy was associated with favorable efficacy and safety results in a group of patients with follicular lymphoma, including a few with Waldenstrom macroglobulinemia, according to findings from a study presented at a recent medical conference.
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