Novartis treatment achieves positive results in possible new indication
Novartis announced positive results from its Cosentyx focused PREVENT trial, advancing the drug in potential new indication for patients with axial spondyloarthritis.
The phase III study met its 16-week primary endpoint of ASAS40 in patients with active non-radiographic axial spondyloarthritis (nr-axSpA), showing a considerable and clinically meaningful reduction in disease activity.
Novartis has also submitted to the EMA approval in nr-axSpA, which would be the fourth indication for Cosentyx.
John Tsai, head of global drug development and chief medical officer for Novartis commented on the study results: “build on the company’s long-standing experience in ankylosing spondylitis and are a step toward a new treatment option that could allow patients to realise relief much earlier in axial spondyloarthritis. If approved, this would be the fourth indication for Cosentyx.”
The data added to existing evidence supporting Cosentyx as a rapid and long-lasting comprehensive treatment, backed by evidence from over 100 studies, across axial spondyloarthritis, psoriatic arthritis and psoriatic disease, with over 250,000 patients treated worldwide.
AxSpA is a spectrum of long-term inflammatory disease characterised by chronic inflammatory back pain, including ankylosing spondylitis (AS), in which joint damage is visible on x-ray, and non-radiographic axial spondyloarthritis (nr-axSpA), in which joint damage is not visible on x-ray.