Extension Study of Secukinumab Prefilled Syringes in Subjects With Moderate to Severe Chronic Plaque-type Psoriasis Completing Preceding Psoriasis Phase III Studies With Secukinumab
Completed · Phase 3 · Has a placebo group
Conditions studied: Moderate to Severe Plaque-type Psoriasis
In brief
This was an extension study of secukinumab prefilled syringes in subjects with moderate to severe chronic plaque-type psoriasis completing preceding psoriasis phase III studies with secukinumab. Subjects on secukinumab at the end of treatment period in phase III studies (e.g., ongoing CAIN457A2302 and CAIN457A2303 and potentially other secukinumab phase III studies) were eligible to join this extension study. This extension study was planned to collect an additional 2 years of long-term efficacy, safety, and tolerability data of secukinumab in either continuous or interrupted therapy (randomized withdrawal period) in subjects showing at least partial response to secukinumab and completing treatment period on secukinumab in previous phase III studies. In this extension study, the prefilled syringe (PFS) liquid formulation of secukinumab were used.
Key facts
- Study ID
- NCT01544595
- Run by
- Novartis Pharmaceuticals
- People needed
- 1147
- Starts
- 2012-06-19
- Expected to finish
- 2017-06-26
- Last updated by the study team
- 2018-12-20
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Novartis Investigative Site — Birmingham, Alabama, United States
- Novartis Investigative Site — Phoenix, Arizona, United States
- Novartis Investigative Site — Phoenix, Arizona, United States
- Novartis Investigative Site — Los Angeles, California, United States
- Novartis Investigative Site — Oceanside, California, United States
- Novartis Investigative Site — Pasadena, California, United States
- Novartis Investigative Site — San Diego, California, United States
- Novartis Investigative Site — San Diego, California, United States
- Novartis Investigative Site — Colorado Springs, Colorado, United States
- Novartis Investigative Site — Snellville, Georgia, United States
- Novartis Investigative Site — Indianapolis, Indiana, United States
- Novartis Investigative Site — Topeka, Kansas, United States
- Novartis Investigative Site — Louisville, Kentucky, United States
- Novartis Investigative Site — Louisville, Kentucky, United States
- Novartis Investigative Site — Ann Arbor, Michigan, United States
- Novartis Investigative Site — Omaha, Nebraska, United States
- Novartis Investigative Site — New York, New York, United States
- Novartis Investigative Site — Rochester, New York, United States
- Novartis Investigative Site — High Point, North Carolina, United States
- Novartis Investigative Site — Warren, Ohio, United States
- Novartis Investigative Site — Oregon City, Oregon, United States
- Novartis Investigative Site — Portland, Oregon, United States
- Novartis Investigative Site — Portland, Oregon, United States
- Novartis Investigative Site — Duncansville, Pennsylvania, United States
- Novartis Investigative Site — Birmingham, Alabama, United States
Full record on ClinicalTrials.gov
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