FDA approves first-in-class therapy for polycythemia vera
The approval was supported by results from the global randomized phase 3 VERIFY trial involving 293 patients, which showed that patients receiving rusfertide
The approval was supported by results from the global randomized phase 3 VERIFY trial involving 293 patients, which showed that patients receiving rusfertide
In this SOHO Insider video interview, Elias Jabbour, MD, professor of medicine in the department of leukemia at The University of Texas MD
Clinical investigators are actively evaluating these novel agents across several strategic combinations and settings, Prof. Weisel explained. "We have very interesting maintenance trials,"
The approval is based on the Phase 2/3 ENERGY study, the full results of which were presented at the European Hematology Association 2026
The China National Medical Products Administration (NMPA) has approved felzartamab (Jingfei), a human monoclonal antibody targeting CD38, in combination with lenalidomide and dexamethasone
He explains how this in vivo lentiviral vector infusion aims to eliminate traditional manufacturing barriers by shifting the cell engineering process directly into
To date, the initiative has enabled access to the treatment for more than 300 patients across Armenia, Ethiopia, and Nepal, exceeding its original
...the approval is based on results from the Phase 3 EXCALIBER-RRMM trial, which showed iberdomide significantly improved minimal residual disease (MRD)-negative complete response
The results showed a 30% spleen response rate and a 47% symptom response rate among evaluable patients. Overall survival reached around 37 months,
The draft guidance expands frontline options for patients who are ineligible for stem cell transplants or who require oral therapies.