A Study of Baricitinib (LY3009104) in Participants With Systemic Lupus Erythematosus (SLE)

NCT ID: NCT02708095

Last Updated: 2018-11-21

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

314 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-03-24

Study Completion Date

2017-11-09

Brief Summary

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The main purpose of this study is to evaluate the efficacy and safety of the study drug known as baricitinib in participants with systemic lupus erythematosus.

Detailed Description

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Conditions

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Systemic Lupus Erythematosus

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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2 mg Baricitinib

Participants received 2 (milligrams) mg of Baricitinib tablet orally once a day for 24 weeks.

Group Type EXPERIMENTAL

Baricitinib

Intervention Type DRUG

Administered orally

4 mg Baricitinib

Participants received 4 mg of Baricitinib tablet orally once a day for 24 weeks.

Group Type EXPERIMENTAL

Baricitinib

Intervention Type DRUG

Administered orally

Placebo

Participants received Placebo orally once daily (QD) for 24 weeks.

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

Administered orally

Interventions

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Baricitinib

Administered orally

Intervention Type DRUG

Placebo

Administered orally

Intervention Type DRUG

Other Intervention Names

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LY3009104

Eligibility Criteria

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Inclusion Criteria

* Have received a diagnosis of SLE at least 24 weeks prior to screening, meeting the American College of Rheumatology (ACR) 1982 revised criteria OR the 2012 Systemic Lupus Erythematosus International Collaborating Clinics (SLICC) criteria.
* Have a positive antinuclear antibody (ANA) (titer ≥1:80) and/or a positive anti-double-stranded deoxyribonucleic acid (dsDNA) as assessed by a central laboratory at screening.
* Have a SLEDAI-2K score ≥4 based on clinical symptoms (not including lab values) at randomization.
* Have active arthritis and/or active rash as defined by the SLEDAI-2K at randomization.

Exclusion Criteria

* Have active severe lupus nephritis.
* Have active severe central nervous system (CNS) lupus.
* Have a history or presence of cardiovascular, respiratory, hepatic, gastrointestinal, endocrine, hematological, neurological, or neuropsychiatric disorders or any other serious and/or unstable illness that, in the opinion of the investigator, could constitute an unacceptable risk when taking investigational product or interfere with the interpretation of data.
* Have a current or recent clinically serious viral, bacterial, fungal, or parasitic infection.
* Are currently receiving oral corticosteroids at doses \>20-milligrams per day of prednisone (or equivalent) or have adjusted the dose of corticosteroids within 2 weeks of planned randomization.
* Have started treatment with or adjusted the dose of nonsteroidal anti-inflammatory drugs (NSAIDs) (for which the NSAID use is intended for treatment of signs and symptoms of SLE) within 4 weeks of planned randomization.
* Have started treatment with or adjusted the dose of an antimalarial within 12 weeks of planned randomization.
* Have started treatment with or adjusted the dose of an immunosuppressant within 12 weeks of planned randomization.
* Have received cyclophosphamide (or any other cytotoxic agent) within 12 weeks prior to screening.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Eli Lilly and Company

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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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)

Role: STUDY_DIRECTOR

Eli Lilly and Company

Locations

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University of Arizona

Tucson, Arizona, United States

Site Status

Wallace Rheumatic Study Center

Beverly Hills, California, United States

Site Status

Medvin Clinical Research

Covina, California, United States

Site Status

TriWest Research Assocaites

El Cajon, California, United States

Site Status

University of California

La Jolla, California, United States

Site Status

Desert Medical Advances

Palm Desert, California, United States

Site Status

Inlande Rheumatology Clinical Trials

Upland, California, United States

Site Status

Denver Arthritis Center

Denver, Colorado, United States

Site Status

New Horizon Research Center

Miami, Florida, United States

Site Status

West Broward Rheumatology Associates, Inc

Tamarac, Florida, United States

Site Status

Clinical Research of West Florida, Inc.

Tampa, Florida, United States

Site Status

Kansas City Internal Medicine Research

Overland Park, Kansas, United States

Site Status

The Arthritis & Diabetes Clinic Inc.

Monroe, Louisiana, United States

Site Status

Louisiana State University Health Sciences Center

Shreveport, Louisiana, United States

Site Status

University of Michigan

Ann Arbor, Michigan, United States

Site Status

Clayton Medical Research

St Louis, Missouri, United States

Site Status

Arthritis Consultants

St Louis, Missouri, United States

Site Status

Albuquerque Clinical Trials

Albuquerque, New Mexico, United States

Site Status

North Shore University Hospital at Great Neck

Great Neck, New York, United States

Site Status

The Ohio State University

Columbus, Ohio, United States

Site Status

Paramount Medical Research

Middleburg Heights, Ohio, United States

Site Status

Arthritis & Rheumatology Center of Oklahoma PLLC

Oklahoma City, Oklahoma, United States

Site Status

Oklahoma Medical Research Foundation

Oklahoma City, Oklahoma, United States

Site Status

The Oklahoma Center For Arthritis Therapy

Tulsa, Oklahoma, United States

Site Status

East Penn Rheumatology

Bethlehem, Pennsylvania, United States

Site Status

Clinical Research Center of Reading, LLC

Wyomissing, Pennsylvania, United States

Site Status

Accent Clinical Research Professionals, LLC

Allen, Texas, United States

Site Status

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Ciudad Autonoma de Buenos Aire, , Argentina

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Ciudad Autonoma de Buenos Aire, , Argentina

Site Status

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San Juan, , Argentina

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San Miguel de Tucumán, , Argentina

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San Miguel de Tucumán, , Argentina

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Graz, , Austria

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Vienna, , Austria

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Vienna, , Austria

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Bordeaux, , France

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Marseille, , France

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Pessac, , France

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Strasbourg, , France

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Asahikawa, , Japan

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Chūōku, , Japan

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Fukuoka, , Japan

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Hamamatsu, , Japan

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Itabashi-ku, , Japan

Site Status

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Kawagoe, , Japan

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Kita-gun, , Japan

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Kitakyushu, , Japan

Site Status

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Meguro-ku, , Japan

Site Status

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Nagasaki, , Japan

Site Status

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Ōmura, , Japan

Site Status

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Sapporo, , Japan

Site Status

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Sasebo, , Japan

Site Status

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Sendai, , Japan

Site Status

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Guadalajara, , Mexico

Site Status

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Guadalajara, , Mexico

Site Status

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Mexico City, , Mexico

Site Status

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Zapopan, , Mexico

Site Status

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Bydgoszcz, , Poland

Site Status

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Bytom, , Poland

Site Status

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Elblag, , Poland

Site Status

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Gdansk, , Poland

Site Status

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Nadarzyn, , Poland

Site Status

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Świdnik, , Poland

Site Status

Office: Perez-De Jesus, Amarilis

Caguas, , Puerto Rico

Site Status

Mindful Medical Research

San Juan, , Puerto Rico

Site Status

Latin Clinical Trial Center

Santurce, , Puerto Rico

Site Status

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Brasov, , Romania

Site Status

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Bucharest, , Romania

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Galati, , Romania

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Târgu Mureş, , Romania

Site Status

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Gwangju, , South Korea

Site Status

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Incheon, , South Korea

Site Status

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Seoul, , South Korea

Site Status

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Seoul, , South Korea

Site Status

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Suwon, , South Korea

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Badalona, , Spain

Site Status

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Barcelona, , Spain

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Madrid, , Spain

Site Status

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Madrid, , Spain

Site Status

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Vigo, , Spain

Site Status

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Kaohsiung City, , Taiwan

Site Status

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Taichung, , Taiwan

Site Status

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Taichung, , Taiwan

Site Status

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Taipei, , Taiwan

Site Status

Countries

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United States Argentina Austria France Japan Mexico Poland Puerto Rico Romania South Korea Spain Taiwan

References

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Dorner T, Tanaka Y, Dow ER, Koch AE, Silk M, Ross Terres JA, Sims JT, Sun Z, de la Torre I, Petri M. Mechanism of action of baricitinib and identification of biomarkers and key immune pathways in patients with active systemic lupus erythematosus. Ann Rheum Dis. 2022 Aug 11;81(9):1267-1272. doi: 10.1136/annrheumdis-2022-222335.

Reference Type DERIVED
PMID: 35609978 (View on PubMed)

Dorner T, van Vollenhoven RF, Doria A, Jia B, Ross Terres JA, Silk ME, de Bono S, Fischer P, Wallace DJ. Baricitinib decreases anti-dsDNA in patients with systemic lupus erythematosus: results from a phase II double-blind, randomized, placebo-controlled trial. Arthritis Res Ther. 2022 May 16;24(1):112. doi: 10.1186/s13075-022-02794-x.

Reference Type DERIVED
PMID: 35578304 (View on PubMed)

Hannon CW, McCourt C, Lima HC, Chen S, Bennett C. Interventions for cutaneous disease in systemic lupus erythematosus. Cochrane Database Syst Rev. 2021 Mar 9;3(3):CD007478. doi: 10.1002/14651858.CD007478.pub2.

Reference Type DERIVED
PMID: 33687069 (View on PubMed)

Wallace DJ, Furie RA, Tanaka Y, Kalunian KC, Mosca M, Petri MA, Dorner T, Cardiel MH, Bruce IN, Gomez E, Carmack T, DeLozier AM, Janes JM, Linnik MD, de Bono S, Silk ME, Hoffman RW. Baricitinib for systemic lupus erythematosus: a double-blind, randomised, placebo-controlled, phase 2 trial. Lancet. 2018 Jul 21;392(10143):222-231. doi: 10.1016/S0140-6736(18)31363-1.

Reference Type DERIVED
PMID: 30043749 (View on PubMed)

Provided Documents

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Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Related Links

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http://www.lillytrialguide.com/en-US/studies/lupus/JAHH#?postal=

Click here for more information about this study: A Study of Baricitinib (LY3009104) in Participants With Systemic Lupus Erythematosus (SLE)

Other Identifiers

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I4V-MC-JAHH

Identifier Type: OTHER

Identifier Source: secondary_id

2015-004404-35

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

16270

Identifier Type: -

Identifier Source: org_study_id

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