A Randomized, Double-blind, Parallel-group, Multicenter Study of Secukinumab to Compare 300 mg and 150 mg at Week 52 in Patients With Ankylosing Spondylitis Who Are Randomized to Dose Escalation After Not Achieving Inactive Disease During an Initial 16 Weeks of Open-label Treatment With Secukinumab 150 mg (ASLeap)
Latest Information Update: 19 Aug 2024
At a glance
- Drugs Secukinumab (Primary)
- Indications Ankylosing spondylitis
- Focus Therapeutic Use
- Acronyms ASLeap
- Sponsors Novartis Pharmaceuticals
- 04 Jun 2022 Results presented at the 23rd Annual Congress of the European League Against Rheumatism
- 07 Jul 2021 Status changed from active, no longer recruiting to completed.
- 22 Jul 2020 Status changed from recruiting to active, no longer recruiting.