Trial Profile
A Phase III Randomized, Double-blind, Placebo-controlled Multicenter Study of Subcutaneous Secukinumab in Prefilled Syringes to Demonstrate the Efficacy at 24 Weeks and to Assess the Long Term Efficacy, Safety, Tolerability and Usability up to 5 Years in Patients With Active Rheumatoid Arthritis (RA) Who Have an Inadequate Response to anti-TNFalpha Agents
Status:
Discontinued
Phase of Trial:
Phase III
Latest Information Update: 10 Jan 2022
Price :
$35
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At a glance
- Drugs Secukinumab (Primary)
- Indications Rheumatoid arthritis
- Focus Registrational; Therapeutic Use
- Acronyms REASSURE 2
- Sponsors Novartis; Novartis Pharma A.G.; Novartis Pharmaceuticals
- 01 Jul 2018 Primary endpoint (Percentage of Participants Achieving an American College of Rheumatology Response 20 (ACR20)) has not been met, according to results published in the Scandinavian Journal of Rheumatology.
- 01 Jul 2018 Results published in the Scandinavian Journal of Rheumatology.
- 09 Jun 2016 Status changed from completed to discontinued.