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Novartis Pharma AG: Novartis Cosentyx meets primary and all secondary endpoints in Phase III trial in patients with polymyalgia rheumatica (PMR)
['Globenewswire', 'Europe']
FinanzNachrichten.de: News
Cosentyx demonstrated statistically significant and clinically meaningful sustained remission vs placebo at Week 52 in adults with polymyalgia rheumatica (PMR)1.
Other secondary measures included complete sustained remission at Week 52, and time until patients needed additional treatment3.
Cosentyx® (secukinumab): Summary of Product Characteristics.
"Long-term efficacy and safety of secukinumab in patients with psoriatic arthritis: 5-year (end-of-study) results from the phase III FUTURE 2 study."
Patients were randomized into three treatment arms: Cosentyx 300mg, Cosentyx 150mg, or placebo, all in combination with a 24-week steroid taper regimen.