USFDA accepts dupilumab for priority review in adults with prurigo nodularis
Dupixent would be the first and only medicine specifically indicated to treat prurigo nodularis in the U.S., if approved
Dupixent would be the first and only medicine specifically indicated to treat prurigo nodularis in the U.S., if approved
JADE DARE trial met co-primary and key secondary endpoints and demonstrated a safety profile consistent with previous studies for moderate to severe atopic dermatitis
It's a development that marks a major step forward for patients struggling with moderate-to-severe chronic spontaneous urticaria
The deal reinforces GSK’s leadership in respiratory care and builds upon the company’s expanding COPD portfolio
Dupixent (dupilumab) approved as the first-ever biologic medicine in Japan for patients with Chronic Obstructive Pulmonary Disease (COPD)
Dupixent is indicated for the approximately 300,000 adults in the US with inadequately controlled COPD and an eosinophilic phenotype
Data support the potential of Dupixent as the first new treatment approach in more than a decade and first-ever targeted therapy for COPD
Accelerating FDA submission and confirming potential to become first approved biologic for this serious disease
68% of children on a higher dose of Dupixent achieved histological disease remission at week 16
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