NCT01870284

Brief Summary

This study will assess the safety and efficacy of ixekizumab (LY2439821) compared to placebo in participants with active AS.

Trial Health

42
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Strong global presence with extensive site network
Timeline
Completed

Started Jul 2014

Typical duration for phase_3

Geographic Reach
15 countries

125 active sites

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 3, 2013

Completed
3 days until next milestone

First Posted

Study publicly available on registry

June 6, 2013

Completed
1.1 years until next milestone

Study Start

First participant enrolled

July 1, 2014

Completed
1.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2016

Completed
2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2018

Completed
Last Updated

September 16, 2014

Status Verified

September 1, 2014

Enrollment Period

1.8 years

First QC Date

June 3, 2013

Last Update Submit

September 15, 2014

Conditions

Outcome Measures

Primary Outcomes (1)

  • Efficacy of Ixekizumab in Participants with Ankylosing Spondylitis (AS). Measure: Assessment of SpondyloArthritis International Society Criteria (ASAS20)

    16 Weeks

Secondary Outcomes (6)

  • Efficacy of Ixekizumab in Participants with AS. Measure: ASAS

    16 Weeks

  • Quality of Life and Outcome Assessments. Measures: Patient Reported Outcomes (PRO)

    Baseline through 16 Weeks

  • Efficacy of Ixekizumab in Participants with AS. Measure: Non-Arthritic Disease Assessments

    Baseline through 16 Weeks

  • Efficacy of Ixekizumab in Participants with AS. Measure: Peripheral Joint Counts

    16 Weeks

  • Efficacy of Ixekizumab in Participants with AS. Measure: Spinal Mobility

    Baseline through 16 Weeks

  • +1 more secondary outcomes

Study Arms (4)

Ixekizumab Dosing Regimen 1

EXPERIMENTAL

Administered by 80 milligram (mg) subcutaneous (SC) injection

Drug: Ixekizumab

Ixekizumab Dosing Regimen 2

EXPERIMENTAL

Administered by 80 mg SC Injection

Drug: Ixekizumab

Placebo

PLACEBO COMPARATOR

Placebo for ixekizumab and placebo for adalimumab administered by SC injection

Drug: Placebo

Adalimumab

ACTIVE COMPARATOR

Administered by 40 mg SC injection

Drug: Adalimumab

Interventions

Administered SC

Also known as: LY2439821
Ixekizumab Dosing Regimen 1Ixekizumab Dosing Regimen 2

Administered SC

Placebo

Administered SC

Adalimumab

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Diagnosis of moderate to severe AS with prior documented radiologic evidence (X-ray) fulfilling the Modified New York criteria for AS (1984)
  • Have active AS defined as Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) ≥4 and the spinal pain (back pain) score ≥4 on a numeric rating scale (NRS)
  • Participants should have been on nonsteroidal anti-inflammatory drugs (NSAIDs) with an inadequate response
  • Participants who are regularly taking NSAIDs or cyclooxygenase-2 (COX-2) inhibitors as part of their AS therapy are required to be on a stable dose
  • Participants who have been on a tumor necrosis factor alpha (TNF) inhibitor (not more than one) must have experienced an inadequate response
  • Total duration of prior therapy (NSAIDs and/or adequate physical therapy) should be at least 12 weeks
  • Men must agree to use a reliable method of birth control or remain abstinent during the study
  • Women must agree to use reliable birth control or remain abstinent during the study and for at least 12 weeks after stopping treatment

You may not qualify if:

  • Participants with a total ankylosis of the spine
  • Prior or current treatment with adalimumab
  • Participants previously treated with any biological or other immunomodulating agents except for those targeting TNF
  • Evidence of active inflammatory arthritic syndromes or spondyloarthropathies other than ankylosing spondylitis
  • Have participated in any study with interleukin 17 (IL-17) antagonists, including ixekizumab
  • Serious disorder or illness other than ankylosing spondylitis
  • Serious infection within the last 3 months
  • Breastfeeding or nursing (lactating) women

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (125)

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Birmingham, Alabama, 35205, United States

Location

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Little Rock, Arkansas, 72205, United States

Location

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Upland, California, 91786, United States

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Denver, Colorado, 80230, United States

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Trumbull, Connecticut, 06611, United States

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Tampa, Florida, 33609, United States

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Atlanta, Georgia, 30342, United States

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Decatur, Georgia, 30033, United States

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Marietta, Georgia, 30060, United States

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Boise, Idaho, 83704, United States

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Idaho Falls, Idaho, 83404, United States

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Cedar Rapids, Iowa, 52401, United States

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Wichita, Kansas, 67207, United States

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Cumberland, Maryland, 21502, United States

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Hagerstown, Maryland, 21740, United States

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Worcester, Massachusetts, 01605, United States

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Ann Arbor, Michigan, 48109, United States

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Albany, New York, 12206, United States

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Brooklyn, New York, 11201, United States

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Mineola, New York, 11501, United States

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Asheville, North Carolina, 28803, United States

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Charlotte, North Carolina, 28210, United States

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Toledo, Ohio, 43606, United States

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Lake Oswego, Oregon, 97035, United States

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Portland, Oregon, 97239, United States

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Charleston, South Carolina, 29407, United States

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Columbia, South Carolina, 29204, United States

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North Charleston, South Carolina, 29406, United States

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Hixon, Tennessee, 37343, United States

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Jackson, Tennessee, 38305, United States

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Dallas, Texas, 75231, United States

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Houston, Texas, 77036, United States

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Kennewick, Washington, 99336, United States

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Seattle, Washington, 98104, United States

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Buenos Aires, C1428DQG, Argentina

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Caba, 1181, Argentina

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Córdoba, X5004BAL, Argentina

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San Miguel de Tucumán, T4000AXL, Argentina

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Genk, 3600, Belgium

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Ghent, 9000, Belgium

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Liège, 4000, Belgium

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Mons, 7000, Belgium

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Edmonton, Alberta, T6G 2R7, Canada

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Winnipeg, Manitoba, R3N 0K6, Canada

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Toronto, Ontario, M5T 2S8, Canada

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Québec, Quebec, G1W 4R4, Canada

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Rimouski, Quebec, G5L 8W1, Canada

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Sainte-Foy, Quebec, G1V 3M7, Canada

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Brno, 638 00, Czechia

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Bruntál, 79201, Czechia

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Kladno, 272 01, Czechia

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Ostrava - Trebovice, 722 00, Czechia

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Prague, 140 00, Czechia

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Zlín, 760 01, Czechia

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Amiens, 80054, France

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Bordeaux, 33076, France

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Montpellier, 34295, France

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Nantes, 44093, France

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Orléans, 45032, France

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Paris, 75679, France

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Rennes, 35202, France

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Strasbourg, 67098, France

Location

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Bad Doberan, 18209, Germany

Location

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Berlin, 12203, Germany

Location

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Halle, 06108, Germany

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Heidelberg, 69121, Germany

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Ratingen, 40882, Germany

Location

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Balatonfüred, 8230, Hungary

Location

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Budapest, 1036, Hungary

Location

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Debrecen, 4032, Hungary

Location

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Kalocsa, H-6300, Hungary

Location

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Nyíregyháza, 4400, Hungary

Location

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Veszprém, 8200, Hungary

Location

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Guadalajara, 45040, Mexico

Location

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Mexico City, 06700, Mexico

Location

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Monterrey, 64000, Mexico

Location

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Morelia, 58249, Mexico

Location

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San Luis, 78200, Mexico

Location

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Amsterdam, 1105 AZ, Netherlands

Location

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Breda, 4818 CK, Netherlands

Location

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Leiden, 2333 ZA, Netherlands

Location

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Maastricht, 6229 HX, Netherlands

Location

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Nijmegen, 6522 JV, Netherlands

Location

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Rotterdam, 3079 DZ, Netherlands

Location

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Sneek, 8601 ZK, Netherlands

Location

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Katowice, 40-635, Poland

Location

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Krakow, 31-501, Poland

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Lublin, 20582, Poland

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Poznan, 60-539, Poland

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Warsaw, 02-118, Poland

Location

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Wroclaw, 51-124, Poland

Location

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Barnaul, 656024, Russia

Location

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Kazan', 420097, Russia

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Krasnoyarsk, 660022, Russia

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Moscow, Russia

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Novosibirsk, 630099, Russia

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Petrozavodsk, 185019, Russia

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Ryazan, 390026, Russia

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Saint Petersburg, 194291, Russia

Location

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Yekaterinburg, 620102, Russia

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A Coruña, 15006, Spain

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Barcelona, 08034, Spain

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Bilbao, 48013, Spain

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Córdoba, 14004, Spain

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Madrid, 28007, Spain

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Málaga, 29009, Spain

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Oviedo, 33012, Spain

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Santander, 39008, Spain

Location

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Seville, 41009, Spain

Location

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Dnipropetrovsk, 49044, Ukraine

Location

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Donetsk, 83045, Ukraine

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Ivano-Frankivsk, 76018, Ukraine

Location

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Kharkiv, 61039, Ukraine

Location

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Kyiv, 1601, Ukraine

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Lutsk, 43024, Ukraine

Location

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Odesa, 65026, Ukraine

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Vinnytsia, 21018, Ukraine

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Zaporizhzhia, 69600, Ukraine

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London, Greater London, E11 1NR, United Kingdom

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Southampton, Hants, SO16 6YD, United Kingdom

Location

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Norwich, Norfolk, NR4 7UY, United Kingdom

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Coventry, West Midlands, CV2 2DX, United Kingdom

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Wolverhampton, West Midlands, WV10 0QP, United Kingdom

Location

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Bradford, West Yorkshire, BD5 0NA, United Kingdom

Location

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Leeds, West Yorkshire, LS7 4SA, United Kingdom

Location

MeSH Terms

Conditions

Spondylitis, Ankylosing

Interventions

ixekizumabAdalimumab

Condition Hierarchy (Ancestors)

Axial SpondyloarthritisSpondylarthropathiesSpondylarthritisSpondylitisSpinal DiseasesBone DiseasesMusculoskeletal DiseasesAnkylosisJoint DiseasesArthritis

Intervention Hierarchy (Ancestors)

Antibodies, Monoclonal, HumanizedAntibodies, MonoclonalAntibodiesImmunoglobulinsImmunoproteinsBlood ProteinsProteinsAmino Acids, Peptides, and ProteinsSerum GlobulinsGlobulins

Study Officials

  • Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)

    Eli Lilly and Company

    STUDY DIRECTOR
0

Study Design

Study Type
interventional
Phase
phase 3
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 3, 2013

First Posted

June 6, 2013

Study Start

July 1, 2014

Primary Completion

April 1, 2016

Study Completion

April 1, 2018

Last Updated

September 16, 2014

Record last verified: 2014-09

Locations