Jesus Berdeja, MD
Novel therapeutic strategies presented over the last year shed light not only efficacious outcomes for patients with multiple myeloma, but also on improved supportive care methods, according to Jesus Berdeja, MD.
on Hematologic Malignancies.
FDA Approval of Denosumab
In January 2018, the FDA approved denosumab (Xgeva) for the prevention of skeletal-related events (SRE) in patients with multiple myeloma based on data from the phase III 482 study.1
In this trial, denosumab demonstrated noninferiority to zoledronic acid at delaying the time to the first SRE (HR, 0.98; 95% CI, 0.85-1.14; P
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