ADQUEY’s approval opens the door to a new alternative for millions of Americans struggling with atopic dermatitis
KEYTRUDA QLEX is contraindicated in patients with known hypersensitivity to its components
The milestone means more than 1,000 men are now enrolled across both Phase 3 programs
These results were consistent across all clinically relevant patient subgroups regardless of key patient characteristics like age or sex, the cause of stroke or the severity of the stroke
Nucala is the first and only monthly biologic in the EU evaluated in a wide COPD population with an eosinophilic phenotype
This Orphan Drug Designation from the USFDA underlines the urgent medical need to develop a therapy for sickle cell disease
The approval follows the pivotal Phase III ARANOTE trial, which demonstrated that darolutamide plus ADT cut the risk of radiological progression or death by 46% compared to placebo plus ADT
The study tested whether PF’3944 could maintain efficacy when switching from weekly to monthly injections and remain safe and well-tolerated
The Phase III programme, Enith1 and Enith2, is expected to launch this quarter
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