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Completed Phase 3 Interventional Results available

Extension Study of Secukinumab Prefilled Syringes in Subjects With Moderate to Severe Chronic Plaque-type Psoriasis Completing Preceding Psoriasis Phase III Studies With Secukinumab

ClinicalTrials.gov ID: NCT01544595

Public ClinicalTrials.gov record NCT01544595. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 2:29 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Double-blind, Randomized Withdrawal Extension Study of Subcutaneous Secukinumab in Prefilled Syringes to Demonstrate Long-term Efficacy, Safety, and Tolerability up to 4 Years in Subjects With Moderate to Severe Chronic Plaque-type Psoriasis Completing Preceding Psoriasis Phase III Studies With Secukinumab

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT01544595
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
1,147 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 19, 2012 (Actual)
Primary completion
Jun 26, 2017 (Actual)
Completion
Jun 26, 2017 (Actual)
Last update posted
Dec 20, 2018

2012 – 2017

United States locations

U.S. sites
37
U.S. states
21
U.S. cities
31
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35205 —
Novartis Investigative Site Birmingham Alabama 35233 —
Novartis Investigative Site Phoenix Arizona 85013 —
Novartis Investigative Site Phoenix Arizona 85032 —
Novartis Investigative Site Los Angeles California 90045 —
Novartis Investigative Site Oceanside California 92056 —
Novartis Investigative Site Pasadena California 91105 —
Novartis Investigative Site San Diego California 92103 —
Novartis Investigative Site San Diego California 92123 —
Novartis Investigative Site Colorado Springs Colorado 80915 —
Novartis Investigative Site Snellville Georgia 30078 —
Novartis Investigative Site Indianapolis Indiana 46256 —
Novartis Investigative Site Topeka Kansas 66606 —
Novartis Investigative Site Louisville Kentucky 40241 —
Novartis Investigative Site Louisville Kentucky 40291 —
Novartis Investigative Site Ann Arbor Michigan 48109 —
Novartis Investigative Site Omaha Nebraska 68144 —
Novartis Investigative Site New York New York 10029 —
Novartis Investigative Site Rochester New York 14623 —
Novartis Investigative Site High Point North Carolina 27262 —
Novartis Investigative Site Warren Ohio 44483 —
Novartis Investigative Site Oregon City Oregon 97045 —
Novartis Investigative Site Portland Oregon 97210 —
Novartis Investigative Site Portland Oregon 97223 —
Novartis Investigative Site Duncansville Pennsylvania 16635 —
Novartis Investigative Site Philadelphia Pennsylvania 19104 —
Novartis Investigative Site Johnston Rhode Island 02919 —
Novartis Investigative Site Charleston South Carolina 29407 —
Novartis Investigative Site Kingsport Tennessee 37660 —
Novartis Investigative Site Nashville Tennessee 37203 —
Novartis Investigative Site Austin Texas 78759 —
Novartis Investigative Site Dallas Texas 75231 —
Novartis Investigative Site Dallas Texas 75246-1613 —
Novartis Investigative Site Houston Texas 77030 —
Novartis Investigative Site San Antonio Texas 78229 —
Novartis Investigative Site Salt Lake City Utah 84117 —
Novartis Investigative Site Norfolk Virginia 23507 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 145 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01544595, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 20, 2018 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01544595 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →