Berry and colleagues from the Institute for Healthcare Improvement and Henry Ford Health Detroit argue that deep, ...
Recent studies highlight the potential of minimal residual disease (MRD) testing to influence treatment decisions in multiple ...
The FDA has approved the biologics license application (BLA) for the subcutaneous (SC) administration of pembrolizumab ...
In this installment of Chief Insights in Oncology, John M. Burke, MD, co-editor in chief of Targeted Therapies in Oncology, discusses his column from the September II 2025 issue.
Carotuximab (ENV105) plus standard-of-care hormone therapy apalutamide (Erleada) demonstrated a progression-free survival ...
FDA fast track is intended to expedite the development of therapies that fill serious unmet medical needs. With this ...
Following its Type A meeting with the FDA, Replimune reported that a forward pathway “has not been determined” to obtain ...
ADG126 is a novel anti–CTLA-4 agent incorporating protease-cleavable masking technology that enables tumor-specific ...
Sacituzumab govitecan is comprised of a humanized antitrophoblast cell-surface antigen 2 monoclonal antibody coupled to SN-38 ...
Through a search of electronic health records from the IKnowMed clinical oncology database (McKesson, Houston, TX, USA) the ...
The FDA has granted fast track designation to the antibody-drug conjugate (ADC) CRB-701 for the treatment of recurrent or ...
In recognition of September as Prostate Cancer Awareness Month, Daniel Petrylak, MD, professor of oncology and urology at ...
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