ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

First Study of Secukinumab in Pre-filled Syringes in Subjects With Chronic Plaque-type Psoriasis: Response at 12 Weeks

ClinicalTrials.gov ID: NCT01555125

Public ClinicalTrials.gov record NCT01555125. 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 May 17, 2026, 4:51 AM 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 Randomized, Double-blind, Placebo Controlled, Multicenter Study of Subcutaneous Secukinumab in Prefilled Syringes to Demonstrate Efficacy After Twelve Weeks of Treatment, and to Assess the Safety, Tolerability, Usability and Long-term Efficacy in Subjects With Chronic Plaque-type Psoriasis

Study identification

NCT ID
NCT01555125
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
177 participants

Conditions and interventions

Interventions

  • placebo Drug
  • secukinumab 150 mg Drug
  • secukinumab 300 mg Drug

Drug

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
May 7, 2012
Primary completion
Oct 23, 2016
Completion
Oct 23, 2016
Last update posted
Aug 7, 2018

2012 – 2016

United States locations

U.S. sites
18
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35205
Novartis Investigative Site Mobile Alabama 36608
Novartis Investigative Site Glendale Arizona 85308
Novartis Investigative Site Hot Springs Arkansas 71913
Novartis Investigative Site Los Angeles California 90045
Novartis Investigative Site Atlanta Georgia 30342
Novartis Investigative Site Newnan Georgia 30263
Novartis Investigative Site Skokie Illinois 60077
Novartis Investigative Site Boston Massachusetts 02111
Novartis Investigative Site Fridley Minnesota 55432
Novartis Investigative Site Omaha Nebraska 68131
Novartis Investigative Site Lake Oswego Oregon 97035
Novartis Investigative Site Portland Oregon 97223
Novartis Investigative Site Charleston South Carolina 29407
Novartis Investigative Site Goodlettsville Tennessee 37072-2301
Novartis Investigative Site Austin Texas 78759
Novartis Investigative Site Bryan Texas 77802
Novartis Investigative Site Houston Texas 77030

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 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01555125, 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 Aug 7, 2018 · Synced May 17, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01555125 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →