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Spondylitis, AnkylosingPhase 3MEASURE4NCT02159053

16-week Efficacy and 2-year Safety, Tolerability and Efficacy of Secukinumab in Participants With Active Ankylosing Spondylitis

A Phase 3 study testing Secukinumab in people with Spondylitis, Ankylosing, run by Novartis Pharmaceuticals at 90 sites in 19 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The purpose of this study is to provide 16-week efficacy, safety and tolerability data versus placebo to support the use of secukinumab 150 mg by subcutaneous (s.c.) self-administration with or without a loading regimen and maintenance dosing using pre-filled syringe (PFS) and to assess efficacy, safety and… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Spondylitis, Ankylosing
What is being tested?
Secukinumab
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
350 participants
Where
90 sitesin 19 countries
Study dates
18 May 2015to 2 Jan 2018
Phase
Phase 3
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Inclusion criteria: moderate to severe AS, prior radiographic evidence according to the Modified NY Criteria (1984), inadequate response to NSAIDs.

Exclusion criteria: pregnancy or lactation, on-going infectious or malignant process on a chest X-ray or MRI, previous exposure to IL-17 or IL-17R targeting therapies, previous exposure to any biological immunomodulating agent excluding TNF antagonists, previous cell depleting therapy.

Other protocol-defined inclusion/exclusion criteria do apply.

Trial locations and contacts

90 sites in 19 countries.

90 sites in 19 countries

Germany13 sites
  • Novartis Investigative Site

    Bad Doberan, 18209

  • Novartis Investigative Site

    Berlin, 12203

  • Novartis Investigative Site

    Berlin, 13125

  • Novartis Investigative Site

    Chemnitz, 09130

  • Novartis Investigative Site

    Erlangen, 91056

  • Novartis Investigative Site

    Germering, 82110

  • Novartis Investigative Site

    Göttingen, Lower Saxony, 37075

  • Novartis Investigative Site

    Hamburg, 20095

  • Novartis Investigative Site

    Herne, 44649

  • Novartis Investigative Site

    Leipzig, 04103

  • Novartis Investigative Site

    Magdeburg, 39110

  • Novartis Investigative Site

    München, 81541

  • Novartis Investigative Site

    Würzburg, 97080

Other trials in Germany

United States12 sites
  • Novartis Investigative Site

    Anniston, Alabama, 36207-5710

  • Novartis Investigative Site

    Aventura, Florida, 33180

  • Novartis Investigative Site

    Columbia, South Carolina, 29204

  • Novartis Investigative Site

    Duncansville, Pennsylvania, 16635

  • Novartis Investigative Site

    Lincoln, Nebraska, 68516

  • Novartis Investigative Site

    Mesquite, Texas, 75150

  • Novartis Investigative Site

    Oklahoma City, Oklahoma, 73103

  • Novartis Investigative Site

    Peoria, Illinois, 61602

  • Novartis Investigative Site

    Seattle, Washington, 98101

  • Novartis Investigative Site

    Shreveport, Louisiana, 71101

  • Novartis Investigative Site

    Upland, California, 91786

  • Novartis Investigative Site

    Voorhees Township, New Jersey, 08043

Other trials in United States

Spain7 sites
  • Novartis Investigative Site

    A Coruña, Galicia, 15006

  • Novartis Investigative Site

    Barakaldo, Vizcaya, 48903

  • Novartis Investigative Site

    Córdoba, Andalusia, 14004

  • Novartis Investigative Site

    L'Hospitalet de Llobregat, Barcelona, 08907

  • Novartis Investigative Site

    Madrid, 28222

  • Novartis Investigative Site

    Santander, Cantabria, 39008

  • Novartis Investigative Site

    Santiago de Compostela, Galicia, 15706

Other trials in Spain

Poland6 sites
  • Novartis Investigative Site

    Bialystok, 15-351

  • Novartis Investigative Site

    Elblag, 82-300

  • Novartis Investigative Site

    Poznan, 60-218

  • Novartis Investigative Site

    Poznan, 60-702

  • Novartis Investigative Site

    Poznan, 61 113

  • Novartis Investigative Site

    Warsaw, 04 141

Other trials in Poland

Russia6 sites
  • Novartis Investigative Site

    Barnaul, 656024

  • Novartis Investigative Site

    Barnaul, 656050

  • Novartis Investigative Site

    Kemerovo, 650000

  • Novartis Investigative Site

    S.-Petersburg, 192242

  • Novartis Investigative Site

    Saint Petersburg, 197022

  • Novartis Investigative Site

    Saint Petersburg, 197341

Other trials in Russia

Bulgaria5 sites
  • Novartis Investigative Site

    Pleven, 5800

  • Novartis Investigative Site

    Plovdiv, 4000

  • Novartis Investigative Site

    Sofia, 1431

  • Novartis Investigative Site

    Sofia, 1505

  • Novartis Investigative Site

    Targovishte, 7700

Other trials in Bulgaria

Italy5 sites
  • Novartis Investigative Site

    Genova, GE, 16132

  • Novartis Investigative Site

    Milan, MI, 20100

  • Novartis Investigative Site

    Milan, MI, 20132

  • Novartis Investigative Site

    Torino, TO, 10126

  • Novartis Investigative Site

    Verona, VR, 37134

Other trials in Italy

Slovakia5 sites
  • Novartis Investigative Site

    Partizánske, 95801

  • Novartis Investigative Site

    Piešťany, SVK, 921 12

  • Novartis Investigative Site

    Sabinov, 08301

  • Novartis Investigative Site

    Stará Ľubovňa, 06401

  • Novartis Investigative Site

    Topoľčany, 95501

Other trials in Slovakia

Australia4 sites
  • Novartis Investigative Site

    Hobart, Tasmania, 7000

  • Novartis Investigative Site

    Kogarah, New South Wales, 2217

  • Novartis Investigative Site

    Malvern East, Victoria, 3145

  • Novartis Investigative Site

    Maroochydore, Queensland, 4558

Other trials in Australia

Czechia4 sites
  • Novartis Investigative Site

    Ostrava, Czech Republic, 772 00

  • Novartis Investigative Site

    Prague, Czech Republic, 128 50

  • Novartis Investigative Site

    Prague, Czech Republic, 148 00

  • Novartis Investigative Site

    Uherské Hradiště, Czech Republic, 686 01

Other trials in Czechia

Netherlands4 sites
  • Novartis Investigative Site

    Amsterdam, 1105 AZ

  • Novartis Investigative Site

    Heerlen, 6419 PC

  • Novartis Investigative Site

    Leiden, 2333 ZA

  • Novartis Investigative Site

    Rotterdam, 3079 DZ

Other trials in Netherlands

Austria3 sites
  • Novartis Investigative Site

    Graz, 8036

  • Novartis Investigative Site

    Vienna, 1100

  • Novartis Investigative Site

    Vienna, A-1060

Other trials in Austria

Canada3 sites
  • Novartis Investigative Site

    Pointe-Claire, Quebec, H9R 3J1

  • Novartis Investigative Site

    Trois-Rivières, Quebec, G8Z 1Y2

  • Novartis Investigative Site

    Winnipeg, Manitoba, R3A 1M1

Other trials in Canada

Greece3 sites
  • Novartis Investigative Site

    Athens, 12462

  • Novartis Investigative Site

    Athens, 16673

  • Novartis Investigative Site

    Pátrai, 26504

Other trials in Greece

United Kingdom3 sites
  • Novartis Investigative Site

    Doncaster, DN2 5LT

  • Novartis Investigative Site

    Leytonstone, London, E11 1NR

  • Novartis Investigative Site

    Wolverhampton, WV10 0QP

Other trials in United Kingdom

Denmark2 sites
  • Novartis Investigative Site

    Frederiksberg, 2000

  • Novartis Investigative Site

    Odense, 5000 C

Other trials in Denmark

Finland2 sites
  • Novartis Investigative Site

    Hyvinkää, 05800

  • Novartis Investigative Site

    Jyväskylä, FIN-40620

Other trials in Finland

Switzerland2 sites
  • Novartis Investigative Site

    Fribourg, 1708

  • Novartis Investigative Site

    Sankt Gallen, CH 9007

Other trials in Switzerland

Norway1 site
  • Novartis Investigative Site

    Kongsvinger, 2212

Other trials in Norway

About this study

Official title: A Randomized, Double-blind, Placebo-controlled, Phase III Multicenter Study of Subcutaneous Secukinumab (150 mg) With and Without a Subcutaneous Loading Regimen to Assess Efficacy, Safety, and Tolerability up to 2 Years in Patients With Active Ankylosing Spondylitis

The purpose of this study is to provide 16-week efficacy, safety and tolerability data versus placebo to support the use of secukinumab 150 mg by subcutaneous (s.c.) self-administration with or without a loading regimen and maintenance dosing using pre-filled syringe (PFS) and to assess efficacy, safety and tolerability up to 2 years in subjects with active AS despite current or previous NSAID, non-biologic DMARD, or biologic anti-TNFα therapy.

Being tested
Secukinumab, Placebo
Keywords
AIN457, ankylosing spondylitis, chronic inflammatory disease, inflammatory back pain, secukinumab, self-injection
Medical subject headings
Spondylitis, Ankylosing

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • SecukinumabBiological

    Also called Secukinumab (AIN457) 150 mg s.c.

    Eligible subjects are randomized to each of the three treatment arms in a 1:1:1 ratio

  • SecukinumabBiological

    Also called Secukinumab (AIN457) 150 mg s.c.

    Eligible subjects are randomized to each of the three treatment arms in 1:1:1 ratio

  • PlaceboBiological

    Eligible subjects are randomized to each of the three treatment arms in a 1:1:1 ratio

Study groups in NCT02159053
Study groupRoleWhat they receive
Secukinumab 150 mg s.c. with loadingExperimentalSecukinumab 150 mg at Baseline, Weeks 1, 2, and 3, followed by dosing every four weeks starting at Week 4.
Receives: Biological: Secukinumab
Secukinumab 150 mg s.c. without loadingExperimentalSecukinumab 150 mg at Baseline, followed by dosing every four weeks starting at Week 4, with Placebo at Weeks 1, 2, and 3.
Receives: Biological: Secukinumab
PlaceboPlacebo comparatorPlacebo at Baseline, Weeks 1, 2, 3, 4, 8, and 12, followed by dosing with Secukinumab 150 mg every four weeks starting at Week 16.
Receives: Biological: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Percentage of Participants Responded for Assessment of Spondyloarthritis International Society 20 Criteria (ASAS20) at 16 Weeks

    ASAS 20 response is a validated composite assessment, defined as an improvement of at least 20 percent (%) and 1 unit on a scale of 10 in three main domains and no worsening of at least 20% and 1 unit on a scale of 10 in the fourth domain within a defined time frame. Four main ASAS domains include: 1. Patient's global assessment of disease activity measured on a 100 mm VAS ranging from not severe to very severe 2. Patient's assessment of back pain, measured on a 100 mm VAS ranging from no pain to unbearable pain 3. Function represented by Bath Ankylosing Spondylitis Functional Index (BASFI) average of 10 questions regarding ability to perform specific tasks as measured by a 0-10 VAS scale 4. Inflammation represented by average of duration and severity of morning stiffness for last 2 questions on BASDAI scale (0 - no problem, 10 - worst problem)

    Measured: 16 Weeks

Secondary outcomes (9)
  1. Percentage of Participants Responded for ASAS 40 Response at 16 Weeks

    ASAS 20 response is a validated composite assessment, defined as an improvement of at least 40% and 2 unit on a scale of 10 in three main domains and no worsening at all in the remaining domain within a defined time frame. Four main ASAS domains include:

    1. Patient's global assessment of disease activity measured on a 100 mm VAS ranging from not severe to very severe
    2. Patient's assessment of back pain, measured on a 100 mm VAS ranging from no pain to unbearable pain
    3. Function represented by Bath Ankylosing Spondylitis Functional Index (BASFI) average of 10 questions regarding ability to perform specific tasks as measured by a 0-10 VAS scale
    4. Inflammation represented by average of duration and severity of morning stiffness for last 2 questions on BASDAI scale (0 - no problem, 10 - worst problem).

    Measured: 16 Weeks

  2. Change From Baseline in Serum High Sensitivity C-reactive Protein (hsCRP) at 16 Weeks

    Blood levels of C-reactive protein (CRP) is an acute phase reactant, which are indicative of inflammation and of its severity, and can be used to monitor treatment response. A hsCRP test is implemented to assess the efficacy of secukinumab (with or without load) versus placebo in reducing ankylosing spondylitis elicited systemic inflammation over the time.

    Measured: Baseline, 16 Weeks

  3. Percentage of Participants Responded for ASAS 5/6 Response at 16 Weeks

    ASAS 5/6 response is a validated composite assessment, defined as an improvement of at least 20% in score in at least 5 of 6 clinical domains relevant to ankylosing spondylitis and no worsening in the remaining domain. ASAS domains includes:

    1. Patient's global assessment of disease activity measured on a 100 mm VAS ranging from not severe to very severe
    2. Patient's assessment of back pain, measured on a 100 mm VAS ranging from no pain to unbearable pain
    3. Function represented by BASFI average of 10 questions regarding ability to perform specific tasks as measured by a 0-10 VAS scale
    4. Inflammation represented by average of duration and severity of morning stiffness for last 2 questions on BASDAI scale (0 - no problem, 10 - worst problem)
    5. Spinal mobility represented by the Bath Ankylosing Spondylitis Metrology Index (BASMI) lateral spinal flexion assessment
    6. C-reactive protein (CRP, acute phase reactant).

    Measured: 16 Weeks

  4. Change From Baseline in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) at 16 Weeks

    BASDAI is a validated assessment tool using 0 through 10 scales (0 indicating "no problem" and 10 indicating "worst problem" on continuous VAS), to answer 6 questions (clinical domains) pertaining to 5 major symptoms of ankylosing spondylitis. Computed composite scores of 4 or greater indicate suboptimal disease control. BASDAI questions includes:

    1. Fatigue
    2. Spinal pain
    3. Joint pain / swelling
    4. Areas of localized tenderness (called enthesitis, or inflammation of tendons and ligaments)
    5. Morning stiffness duration
    6. Morning stiffness severity. Each symptom has equal weighting, the mean of two scores related to morning stiffness was taken (questions 5 and 6). The resulting 0 to 10 score was added to the scores from questions 1-4. The resulting 0 to 50 score was divided by 5 to give a final 0-10 BASDAI score. BASDAI was a quick and simple index taking between 30 seconds and 2 minutes for completion.

    Measured: Baseline, 16 Weeks

  5. Change From Baseline in Physical Function Component Summary (PCS) of the Medical Outcomes Study Questionnaire Short-form Health Survey (SF-36)

    SF-36 is a 36 item questionnaire which measures Quality of Life across eight subscales that were scored individually: physical functioning, role- physical, bodily pain, general health, vitality, social functioning, role-emotional, and mental health. Scores are weighted sums of the questions in each section. Scores range from 0-100. Lower scores = more disability, higher scores = less disability. The overall summary scores, SF-36 physical Component Summary (PCS) was used to assess improvement from baseline in the Health-Related Quality Of Life of subjects. The change in SF-36 scores were evaluated using MMRM.

    Measured: Baseline, 16 Weeks

  6. Change From Baseline in Ankylosing Spondylitis Quality of Life Questionnaire (ASQoL) at 16 Weeks

    ASQoL is a self-administered 18 item questionnaire that assesses disease-specific quality of life (QoL), consisting of statements that are relevant to the physical and mental conditions for a subject with ankylosing spondylitis: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each statement is answered as a 'Yes' (scored as 1) or 'No' (scored as 0). All item scores are summed to give a total score. Total score ranges from 0 (good QoL) to 18 (poor QoL). The change in ASQoL scores was evaluated using a mixed effect repeated measures model (MMRM).

    Measured: Baseline, 16 Weeks

  7. Number of Participants With Adverse Events (AEs), Deaths, Serious Adverse Events (SAEs) and Related Discontinuations at 104 Weeks

    AEs were defined as any unfavorable and unintended diagnosis, symptom, sign (including an abnormal laboratory finding), syndrome or disease which either occurs during study, having been absent at baseline, or, if present at baseline, appears to worsen. SAEs were defined as any untoward medical occurrences that result in death, are life threatening, require (or prolong) hospitalization, cause persistent or significant disability/incapacity, result in congenital anomalies or birth defects, or are other conditions which in judgement of investigators represent significant hazards.

    Measured: 104 Weeks

  8. Percentage of Participants Responded for ASAS 20 at Week 4

    ASAS 20 response is a validated composite assessment, defined as an improvement of at least 20% and 1 unit on a scale of 10 in three main domains and no worsening of at least 20% and 1 unit on a scale of 10 in the fourth domain within a defined time frame. Four main ASAS domains include:

    1. Patient's global assessment of disease activity measured on a 100 mm VAS ranging from not severe to very severe
    2. Patient's assessment of back pain, measured on a 100 mm VAS ranging from no pain to unbearable pain
    3. Function represented by Bath Ankylosing Spondylitis Functional Index (BASFI) average of 10 questions regarding ability to perform specific tasks as measured by a 0-10 VAS scale
    4. Inflammation represented by average of duration and severity of morning stiffness for last 2 questions on BASDAI scale (0 - no problem, 10 - worst problem).

    Measured: Week 4

  9. Percentage of Participants Responded for ASAS 40 Response at Week 4

    ASAS 20 response is a validated composite assessment, defined as an improvement of at least 40% and 2 unit on a scale of 10 in three main domains and no worsening at all in the remaining domain within a defined time frame. Four main ASAS domains include:

    1. Patient's global assessment of disease activity measured on a 100 mm VAS ranging from not severe to very severe
    2. Patient's assessment of back pain, measured on a 100 mm VAS ranging from no pain to unbearable pain
    3. Function represented by Bath Ankylosing Spondylitis Functional Index (BASFI) average of 10 questions regarding ability to perform specific tasks as measured by a 0-10 VAS scale
    4. Inflammation represented by average of duration and severity of morning stiffness for last 2 questions on BASDAI scale (0 - no problem, 10 - worst problem).

    Measured: Week 4

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Jun 2014 (estimated)
  2. Study start18 May 2015
  3. Primary completion23 Feb 2016
  4. Study completion2 Jan 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
350 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02159053
Sponsor's protocol ID
CAIN457F2320
Other IDs
2013-005575-41
Acronym
MEASURE4
Status last verified
Nov 2018
First submitted
28 Feb 2014
Last updated
10 Apr 2019
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Undecided: Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations. This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com

Publications

  • Ramiro S, Gaillez C, Kiltz U, Gensler LS, Pisal C, Braun J, Ogdie A. No major effect of age (< 40 vs. >/= 40 years) on response to secukinumab in patients with axSpA: a post hoc analysis of six phase 3 trials. Arthritis Res Ther. 2026 Apr 11;28(1):112. doi: 10.1186/s13075-026-03804-y.

    PubMed 41965705
  • Merola JF, McInnes IB, Deodhar AA, Dey AK, Adamstein NH, Quebe-Fehling E, Aassi M, Peine M, Mehta NN. Effect of Secukinumab on Traditional Cardiovascular Risk Factors and Inflammatory Biomarkers: Post Hoc Analyses of Pooled Data Across Three Indications. Rheumatol Ther. 2022 Jun;9(3):935-955. doi: 10.1007/s40744-022-00434-z. Epub 2022 Mar 19.

    PubMed 35305260
  • Dougados M, Kiltz U, Kivitz A, Pavelka K, Rohrer S, McCreddin S, Quebe-Fehling E, Porter B, Talloczy Z. Nonsteroidal anti-inflammatory drug-sparing effect of secukinumab in patients with radiographic axial spondyloarthritis: 4-year results from the MEASURE 2, 3 and 4 phase III trials. Rheumatol Int. 2022 Feb;42(2):205-213. doi: 10.1007/s00296-021-05044-6. Epub 2021 Nov 13.

    PubMed 34773130
  • van der Horst-Bruinsma I, Miceli-Richard C, Braun J, Marzo-Ortega H, Pavelka K, Kivitz AJ, Deodhar A, Bao W, Porter B, Pournara E. A Pooled Analysis Reporting the Efficacy and Safety of Secukinumab in Male and Female Patients with Ankylosing Spondylitis. Rheumatol Ther. 2021 Dec;8(4):1775-1787. doi: 10.1007/s40744-021-00380-2. Epub 2021 Oct 7.

    PubMed 34618347
  • Schett G, Baraliakos X, Van den Bosch F, Deodhar A, Ostergaard M, Gupta AD, Mpofu S, Fox T, Winseck A, Porter B, Shete A, Gensler LS. Secukinumab Efficacy on Enthesitis in Patients With Ankylosing Spondylitis: Pooled Analysis of Four Pivotal Phase III Studies. J Rheumatol. 2021 Aug;48(8):1251-1258. doi: 10.3899/jrheum.201111. Epub 2021 Mar 15.

    PubMed 33722947
  • Deodhar A, Gladman DD, McInnes IB, Spindeldreher S, Martin R, Pricop L, Porter B, Safi J Jr, Shete A, Bruin G. Secukinumab Immunogenicity over 52 Weeks in Patients with Psoriatic Arthritis and Ankylosing Spondylitis. J Rheumatol. 2020 Apr;47(4):539-547. doi: 10.3899/jrheum.190116. Epub 2019 Jun 15.

    PubMed 31203228
  • Kivitz AJ, Wagner U, Dokoupilova E, Supronik J, Martin R, Talloczy Z, Richards HB, Porter B. Efficacy and Safety of Secukinumab 150 mg with and Without Loading Regimen in Ankylosing Spondylitis: 104-week Results from MEASURE 4 Study. Rheumatol Ther. 2018 Dec;5(2):447-462. doi: 10.1007/s40744-018-0123-5. Epub 2018 Aug 18.

    PubMed 30121827

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Secukinumab in people with Spondylitis, Ankylosing, run by Novartis Pharmaceuticals at 90 sites in 19 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 10 Apr 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 90 sites in Germany, United States, Spain, Poland, Russia and 14 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 10 Apr 2019). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Percentage of Participants Responded for Assessment of Spondyloarthritis International Society 20 Criteria (ASAS20) at 16 Weeks (time frame: 16 Weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02159053, which also lists 7 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Apr 2019.

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