Treatment tolerability in mHSPC and nmCRPC
Expert Insights Videos

Discover these expert opinions on the management and treatment of patients prescribed NUBEQA in clinical practice. These two informative videos feature leading oncologists,
Stay informed and enhance your clinical practice with these expert insights:
ARASENS trial. Men with mHSPC. NUBEQA + ADT + docetaxel (n=651) vs. placebo + ADT + docetaxel (n=654). Primary endpoint was OS. The most frequently observed adverse reactions in patients with mHSPC receiving NUBEQA are hypertension, rash, blood bilirubin increased, ALT increased, AST increased (≥1/10). The most common serious adverse reactions in patients receiving darolutamide in combination with docetaxel were febrile neutropenia (6.1%), neutrophil count decreased (2.8%) and pneumonia (2.5%).
ARAMIS trial. Men with high-risk nmCRPC. NUBEQA + ADT (n=955) vs. placebo + ADT (n=554). Primary endpoint was median metastasis free survival (MFS), secondary endpoint was overall survival (OS). Number of patients with events 148/955 (15.5%) vs. 106/554 (19.1%) with placebo + ADT. Final analysis for OS was conducted after 254 deaths.
The most frequently observed adverse reactions in patients with nmCRPC receiving NUBEQA were fatigue/asthenic conditions, neutrophil count decreased, blood bilirubin increased and AST increased (≥1/10), and rash, pain in the extremity, musculoskeletal pain, fractures, ischaemic heart disease and heart failure (≥1/100).
Speakers
PP-NUB-GB-2036 | January 2025


