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Completed Phase 4 Interventional Results available

Study Estimating the Clinical Difference Between 300 mg and 150 mg of Secukinumab Following Dose Escalation to 300 mg in Patients With Ankylosing Spondylitis

ClinicalTrials.gov ID: NCT03350815

Public ClinicalTrials.gov record NCT03350815. 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 25, 2026, 9:56 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 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)

Brief summary

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

This was a study estimating the clinical difference between 300 mg and 150 mg of secukinumab following dose escalation to 300 mg in patients with ankylosing spondylitis

Study identification

NCT ID
NCT03350815
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
322 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
Mar 13, 2018 (Actual)
Primary completion
Mar 11, 2021 (Actual)
Completion
May 29, 2021 (Actual)
Last update posted
Apr 29, 2022

2018 – 2021

United States locations

U.S. sites
65
U.S. states
27
U.S. cities
63
Facility City State ZIP Site status
Novartis Investigative Site Jonesboro Arkansas 72401 —
Novartis Investigative Site Fullerton California 92835 —
Novartis Investigative Site Loma Linda California 92354 —
Novartis Investigative Site Palm Desert California 92260 —
Novartis Investigative Site Tustin California 92780 —
Novartis Investigative Site Upland California 91786 —
Novartis Investigative Site Aventura Florida 33180 —
Novartis Investigative Site Boca Raton Florida 33486 —
Novartis Investigative Site Brandon Florida 33511 —
Novartis Investigative Site DeLand Florida 32720 —
Novartis Investigative Site Gainesville Florida 32608 —
Novartis Investigative Site Orlando Florida 32810 —
Novartis Investigative Site Plantation Florida 33324 —
Novartis Investigative Site St. Petersburg Florida 33705 —
Novartis Investigative Site Tamarac Florida 33321 —
Novartis Investigative Site Tampa Florida 33609 —
Novartis Investigative Site Zephyrhills Florida 33542 —
Novartis Investigative Site Duluth Georgia 30096 —
Novartis Investigative Site Springfield Illinois 62703 —
Novartis Investigative Site Vernon Hills Illinois 60061 —
Novartis Investigative Site Evansville Indiana 47715 —
Novartis Investigative Site Monroe Louisiana 71203 —
Novartis Investigative Site Cumberland Maryland 21740 —
Novartis Investigative Site Hagerstown Maryland 21740 —
Novartis Investigative Site Wheaton Maryland 20902 —
Novartis Investigative Site Boston Massachusetts 02111 —
Novartis Investigative Site Worcester Massachusetts 01655 —
Novartis Investigative Site Ann Arbor Michigan 48109 5271 —
Novartis Investigative Site Saint Clair Shores Michigan 48081 —
Novartis Investigative Site Edina Minnesota 55435 —
Novartis Investigative Site Springfield Missouri 65810 —
Novartis Investigative Site Midland Park New Jersey 07432 —
Novartis Investigative Site Voorhees Township New Jersey 08043 —
Novartis Investigative Site Albuquerque New Mexico 87102 —
Novartis Investigative Site Santa Fe New Mexico 87505 —
Novartis Investigative Site Brooklyn New York 11201 —
Novartis Investigative Site New York New York 10016 —
Novartis Investigative Site Orchard Park New York 14127 —
Novartis Investigative Site Potsdam New York 13676 —
Novartis Investigative Site Minot North Dakota 58701 —
Novartis Investigative Site Cincinnati Ohio 45219 —
Novartis Investigative Site Dayton Ohio 45402 —
Novartis Investigative Site Middleburg Heights Ohio 44130 —
Novartis Investigative Site Oklahoma City Oklahoma 73103 —
Novartis Investigative Site Corvallis Oregon 97330 —
Novartis Investigative Site Portland Oregon 97239 —
Novartis Investigative Site Duncansville Pennsylvania 16635 —
Novartis Investigative Site Wexford Pennsylvania 15090 —
Novartis Investigative Site Charleston South Carolina 29460 —
Novartis Investigative Site Columbia South Carolina 29204 —
Novartis Investigative Site Jackson Tennessee 38305 —
Novartis Investigative Site Memphis Tennessee 38119 —
Novartis Investigative Site Beaumont Texas 77701 —
Novartis Investigative Site Colleyville Texas 76034 —
Novartis Investigative Site Dallas Texas 75231 —
Novartis Investigative Site Houston Texas 77025 —
Novartis Investigative Site Houston Texas 77089 —
Novartis Investigative Site Mesquite Texas 75150 —
Novartis Investigative Site Salt Lake City Utah 84132 —
Novartis Investigative Site Seattle Washington 98104 —
Novartis Investigative Site Seattle Washington 98195 —
Novartis Investigative Site Spokane Washington 99204 —
Novartis Investigative Site Charleston West Virginia 25304 —
Novartis Investigative Site Manitowoc Wisconsin 54220 —
Novartis Investigative Site Onalaska Wisconsin 54650 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03350815, 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 Apr 29, 2022 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03350815 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →