Clinical Trials Logo

Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01764997
Other study ID # EFC11574
Secondary ID 2012-001984-66U1
Status Terminated
Phase Phase 3
First received January 8, 2013
Last updated November 5, 2015
Start date April 2013
Est. completion date January 2015

Study information

Verified date November 2015
Source Sanofi
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Primary Objective:

To demonstrate the treatment effect of sarilumab and methotrexate (MTX) compared to etanercept and methotrexate (MTX) in patients with rheumatoid arthritis (RA) and an inadequate response to adalimumab and methotrexate by evaluation of the Disease Activity Score for 28 joints (DAS28).

Secondary Objectives:

To assess the signs and symptoms of rheumatoid arthritis (RA) in patients taking sarilumab in combination with methotrexate (MTX).

To assess the quality of life of patients with rheumatoid arthritis (RA) taking sarilumab in combination with methotrexate (MTX).

To assess the safety and tolerability of sarilumab in combination with methotrexate (MTX) in patients with rheumatoid arthritis (RA).


Description:

The maximum study duration per patient enrolled in the Main study is 54 weeks broken down as follows:

- screening/run-in up to a maximum of 24 weeks

- treatment up to a maximum of 24 weeks

- follow-up of 6 weeks after treatment discontinuation.

The maximum study duration per patient enrolled in the Sub-study is 58 weeks broken down as follows:

- treatment up to a maximum of 52 weeks

- follow-up of 6 weeks after treatment discontinuation.


Recruitment information / eligibility

Status Terminated
Enrollment 452
Est. completion date January 2015
Est. primary completion date January 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion criteria:

- Diagnosis of rheumatoid arthritis (RA) >/= 3 months duration.

- Continuous treatment of methotrexate (MTX) 10 - 25 mg/week (or per local labeling requirements if the dose range differs) for at least 12 weeks before screening visit and on a stable dose for 8 weeks before screening visit.

- Active disease defined as: at least 6/66 swollen and 8/68 tender joints and high sensitivity C-reactive protein > 10 mg/L.

Exclusion criteria:

- Age < 18 years.

- Use of parenteral corticosteroids or intra-articular corticosteroids within 4 weeks of the screening visit.

- Use of oral corticosteroids in a dose higher than prednisone 10 mg or equivalent per day, or a change in dosage within 4 weeks of the screening visit.

- Prior treatment with a TNF (tumor necrosis factor)-alpha inhibitor, or other biological disease modifying anti-rheumatoid drug (DMARD) or Janus Kinase inhibitor.

- New treatment with or dose-adjustment of on-going nonsteroidal anti-inflammatory drugs (NSAIDs) or cyclo-oxygenase-2 inhibitors (COX-2 inhibitors within 4 weeks of the screening visit.

- Treatment with traditional oral disease-modifying antirheumatic drugs (DMARD) /immunosuppressive agents other than MTX within 4 weeks or 12 weeks before the screening visit, depending on DMARD.

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Sarilumab SAR153191 (REGN88)
Pharmaceutical form:solution Route of administration: subcutaneous
Etanercept
Pharmaceutical form:solution Route of administration: subcutaneous
Adalimumab
Pharmaceutical form:solution Route of administration: subcutaneous
Methotrexate
Dispensed according to local practice.

Locations

Country Name City State
Argentina Investigational Site Number 032050 Buenos Aires
Argentina Investigational Site Number 032052 Buenos Aires
Argentina Investigational Site Number 032053 La Plata
Argentina Investigational Site Number 032013 Rosario
Argentina Investigational Site Number 032051 San Miguel De Tucumán
Argentina Investigational Site Number 032005 Tucuman
Argentina Investigational Site Number 032009 Zarate
Australia Investigational Site Number 036020 Camperdown
Australia Investigational Site Number 036004 Heidelberg West
Australia Investigational Site Number 036014 Victoria Park
Australia Investigational Site Number 036007 Woodville
Brazil Investigational Site Number 076001 Curitiba
Brazil Investigational Site Number 076016 Curitiba
Brazil Investigational Site Number 076006 Goiania
Brazil Investigational Site Number 076010 Juiz De Fora
Brazil Investigational Site Number 076005 Rio De Janeiro
Brazil Investigational Site Number 076013 Vitoria
Chile Investigational Site Number 152005 Osorno
Chile Investigational Site Number 152001 Santiago
Chile Investigational Site Number 152002 Santiago
Chile Investigational Site Number 152011 Santiago
Chile Investigational Site Number 152018 Santiago
Chile Investigational Site Number 152015 Temuco
Colombia Investigational Site Number 170001 Bogota
Colombia Investigational Site Number 170016 Bogota
Colombia Investigational Site Number 170040 Bogotá
Colombia Investigational Site Number 170007 Bucaramanga
Colombia Investigational Site Number 170009 Bucaramanga
Colombia Investigational Site Number 170041 Medellin
Czech Republic Investigational Site Number 203004 Ostrava
Czech Republic Investigational Site Number 203032 Praha
Czech Republic Investigational Site Number 203001 Praha 2
Czech Republic Investigational Site Number 203030 Praha 4
Czech Republic Investigational Site Number 203031 Praha 4
Czech Republic Investigational Site Number 203033 Praha 4
Czech Republic Investigational Site Number 203002 Uherske Hradiste
Czech Republic Investigational Site Number 203006 Zlin
Ecuador Investigational Site Number 218003 Cuenca
Ecuador Investigational Site Number 218001 Guayaquil
Ecuador Investigational Site Number 218002 Quito
Finland Investigational Site Number 246001 Helsinki
Finland Investigational Site Number 246002 Hyvinkää
Finland Investigational Site Number 246030 Oulu
Finland Investigational Site Number 246003 Pori
Finland Investigational Site Number 246032 Tampere
France Investigational Site Number 250003 Amiens Cedex 1
France Investigational Site Number 250007 Bobigny
France Investigational Site Number 250001 La Roche Sur Yon Cedex 9
France Investigational Site Number 250002 Montpellier
France Investigational Site Number 250005 Paris
France Investigational Site Number 250004 Paris Cedex 4
France Investigational Site Number 250006 Strasbourg
France Investigational Site Number 250008 Toulouse
Germany Investigational Site Number 276007 Berlin
Germany Investigational Site Number 276057 Berlin
Germany Investigational Site Number 276055 Dresden
Germany Investigational Site Number 276056 Dresden
Germany Investigational Site Number 276051 Erlangen
Germany Investigational Site Number 276013 Hamburg
Germany Investigational Site Number 276001 Herne
Germany Investigational Site Number 276058 Koeln
Germany Investigational Site Number 276053 Ludwigsfelde
Germany Investigational Site Number 276050 Rostock
Greece Investigational Site Number 300010 Athens
Greece Investigational Site Number 300002 Heraklion
Greece Investigational Site Number 300014 N. Efkarpia
Greece Investigational Site Number 300012 Patras
Hungary Investigational Site Number 348001 Budapest
Hungary Investigational Site Number 348010 Debrecen
Hungary Investigational Site Number 348021 Esztergom
Hungary Investigational Site Number 348013 Gy?r
Hungary Investigational Site Number 348008 Gyula
Israel Investigational Site Number 376032 Ashkelon
Israel Investigational Site Number 376001 Haifa
Israel Investigational Site Number 376010 Haifa
Israel Investigational Site Number 376031 Haifa
Israel Investigational Site Number 376035 Jerusalem
Israel Investigational Site Number 376030 Ramat Gan
Israel Investigational Site Number 376011 Tel Aviv
Israel Investigational Site Number 376034 Tel Hashomer
Italy Investigational Site Number 380002 Firenze
Italy Investigational Site Number 380004 Genova
Italy Investigational Site Number 380005 Genova
Italy Investigational Site Number 380041 L'Aquila
Italy Investigational Site Number 380042 Valeggio Sul Mincio
Korea, Republic of Investigational Site Number 410006 Busan
Korea, Republic of Investigational Site Number 410020 Busan
Korea, Republic of Investigational Site Number 410013 Daegu
Korea, Republic of Investigational Site Number 410005 Daejeon
Korea, Republic of Investigational Site Number 410011 Jeonju
Korea, Republic of Investigational Site Number 410015 Seoul
Korea, Republic of Investigational Site Number 410016 Seoul
Korea, Republic of Investigational Site Number 410021 Seoul
Korea, Republic of Investigational Site Number 410022 Seoul
Korea, Republic of Investigational Site Number 410023 Seoul
Korea, Republic of Investigational Site Number 410008 Suwon
Latvia Investigational Site Number 428002 Liepaja
Latvia Investigational Site Number 428001 Riga
Latvia Investigational Site Number 428003 Ventspils
Lithuania Investigational Site Number 440005 Kaunas
Lithuania Investigational Site Number 440006 Klaipeda
Lithuania Investigational Site Number 440010 Panevezys
Lithuania Investigational Site Number 440011 Vilnius
Malaysia Investigational Site Number 458012 Batu Caves
Malaysia Investigational Site Number 458014 Georgetown
Malaysia Investigational Site Number 458001 Ipoh
Malaysia Investigational Site Number 458013 Kota Bharu
Malaysia Investigational Site Number 458002 Kuching
Malaysia Investigational Site Number 458010 Melaka
Malaysia Investigational Site Number 458011 Seremban
Mexico Investigational Site Number 484027 Cd. Obregon
Mexico Investigational Site Number 484023 Chihuahua
Mexico Investigational Site Number 484029 Deleg. Benito Juárez
Mexico Investigational Site Number 484013 Guadalajara
Mexico Investigational Site Number 484018 Guadalajara
Mexico Investigational Site Number 484004 Merida
Mexico Investigational Site Number 484010 Mexicali
Mexico Investigational Site Number 484026 Mexicali
Mexico Investigational Site Number 484017 México
Mexico Investigational Site Number 484052 Mexico City
Mexico Investigational Site Number 484025 San Luis
Mexico Investigational Site Number 484051 Tijuana
New Zealand Investigational Site Number 554007 Auckland
New Zealand Investigational Site Number 554010 Dunedin
New Zealand Investigational Site Number 554005 Hamilton
New Zealand Investigational Site Number 554011 Nelson
Peru Investigational Site Number 604001 Lima
Peru Investigational Site Number 604005 Lima
Peru Investigational Site Number 604007 Lima
Peru Investigational Site Number 604009 Lima
Peru Investigational Site Number 604010 Lima
Peru Investigational Site Number 604012 Lima
Peru Investigational Site Number 604020 Lima
Poland Investigational Site Number 616019 Bydgoszcz
Poland Investigational Site Number 616054 Bytom
Poland Investigational Site Number 616052 Dzialdowo
Poland Investigational Site Number 616015 Elblag
Poland Investigational Site Number 616057 Krakow
Poland Investigational Site Number 616059 Krakow
Poland Investigational Site Number 616061 Krakow
Poland Investigational Site Number 616005 Lublin
Poland Investigational Site Number 616063 Myslenice
Poland Investigational Site Number 616018 Poznan
Poland Investigational Site Number 616013 Sosnowiec
Poland Investigational Site Number 616056 Starachowice
Poland Investigational Site Number 616016 Szczecin
Poland Investigational Site Number 616058 Ustron
Poland Investigational Site Number 616051 Warszawa
Poland Investigational Site Number 616053 Zyrardow
Romania Investigational Site Number 642041 Bacau
Romania Investigational Site Number 642004 Bucharest
Romania Investigational Site Number 642012 Bucharest
Romania Investigational Site Number 642023 Bucharest
Romania Investigational Site Number 642001 Bucuresti
Romania Investigational Site Number 642002 Bucuresti
Romania Investigational Site Number 642040 Bucuresti
Romania Investigational Site Number 642042 Bucuresti
Romania Investigational Site Number 642005 Galati
Romania Investigational Site Number 642013 Iasi
Romania Investigational Site Number 642014 Iasi
Romania Investigational Site Number 642022 Targoviste
Russian Federation Investigational Site Number 643006 Kemerovo
Russian Federation Investigational Site Number 643056 Krasnoyarsk
Russian Federation Investigational Site Number 643021 Moscow
Russian Federation Investigational Site Number 643030 Moscow
Russian Federation Investigational Site Number 643031 Moscow
Russian Federation Investigational Site Number 643052 Moscow
Russian Federation Investigational Site Number 643022 Novosibirsk
Russian Federation Investigational Site Number 643010 Samara
Russian Federation Investigational Site Number 643011 Saratov
Russian Federation Investigational Site Number 643059 Smolensk
Russian Federation Investigational Site Number 643008 St-Petersburg
Russian Federation Investigational Site Number 643058 St. Peterburg
Russian Federation Investigational Site Number 643013 Ufa
Russian Federation Investigational Site Number 643050 Voronezh
Russian Federation Investigational Site Number 643051 Yaroslavl
Russian Federation Investigational Site Number 643057 Yaroslavl
South Africa Investigational Site Number 710007 Cape Town
South Africa Investigational Site Number 710011 Cape Town
South Africa Investigational Site Number 710006 Pretoria
South Africa Investigational Site Number 710008 Pretoria
South Africa Investigational Site Number 710010 Stellenbsoch
Spain Investigational Site Number 724043 Córdoba
Spain Investigational Site Number 724009 La Coruña
Spain Investigational Site Number 724040 Madrid
Spain Investigational Site Number 724041 Madrid
Spain Investigational Site Number 724042 Madrid
Spain Investigational Site Number 724001 Málaga
Spain Investigational Site Number 724011 Sabadell
Spain Investigational Site Number 724012 Santiago De Compostela
Taiwan Investigational Site Number 158010 Changhua
Taiwan Investigational Site Number 158004 Chia-Yi
Taiwan Investigational Site Number 158011 Kaohsiung
Taiwan Investigational Site Number 158012 Kaohsiung
Taiwan Investigational Site Number 158006 Taipei
Thailand Investigational Site Number 764002 Bangkok
Thailand Investigational Site Number 764010 Bangkok
Thailand Investigational Site Number 764003 Bangkok-Noi
Thailand Investigational Site Number 764011 Khon Kaen
Ukraine Investigational Site Number 804003 Dnipropetrovsk
Ukraine Investigational Site Number 804002 Donetsk
Ukraine Investigational Site Number 804024 Donetsk
Ukraine Investigational Site Number 804029 Ivano-Frankivsk
Ukraine Investigational Site Number 804010 Kharkiv
Ukraine Investigational Site Number 804001 Kharkov
Ukraine Investigational Site Number 804025 Kiev
Ukraine Investigational Site Number 804011 Kyiv
Ukraine Investigational Site Number 804014 Kyiv
Ukraine Investigational Site Number 804023 Kyiv
Ukraine Investigational Site Number 804027 Kyiv
Ukraine Investigational Site Number 804030 Lutsk
Ukraine Investigational Site Number 804005 Lviv
Ukraine Investigational Site Number 804020 Lviv
Ukraine Investigational Site Number 804033 Lviv
Ukraine Investigational Site Number 804022 Odesa
Ukraine Investigational Site Number 804032 Odesa
Ukraine Investigational Site Number 804012 Odessa
Ukraine Investigational Site Number 804021 Simferopol
Ukraine Investigational Site Number 804028 Zaporozhye
Ukraine Investigational Site Number 804031 Zhytomyr
United Kingdom Investigational Site Number 826023 Barnsley
United Kingdom Investigational Site Number 826022 Birmingham
United Kingdom Investigational Site Number 826021 Dudley
United Kingdom Investigational Site Number 826026 Durham
United Kingdom Investigational Site Number 826027 Durham
United Kingdom Investigational Site Number 826020 Harlow
United Kingdom Investigational Site Number 826025 Wigan
United States Investigational Site Number 840204 Battle Creek Michigan
United States Investigational Site Number 840004 Birmingham Alabama
United States Investigational Site Number 840124 Clarksburg West Virginia
United States Investigational Site Number 840210 Clearwater Florida
United States Investigational Site Number 840073 Cumberland Maryland
United States Investigational Site Number 840209 Danbury Connecticut
United States Investigational Site Number 840201 Denver Colorado
United States Investigational Site Number 840212 Glendale California
United States Investigational Site Number 840202 Hagerstown Maryland
United States Investigational Site Number 840018 Idaho Falls Idaho
United States Investigational Site Number 840213 Indianapolis Indiana
United States Investigational Site Number 840025 Jackson Tennessee
United States Investigational Site Number 840200 Jackson Mississippi
United States Investigational Site Number 840109 Lake Charles Louisiana
United States Investigational Site Number 840150 Lansing Michigan
United States Investigational Site Number 840112 Lincoln Nebraska
United States Investigational Site Number 840074 Mesquite Texas
United States Investigational Site Number 840056 New York New York
United States Investigational Site Number 840016 North Charleston South Carolina
United States Investigational Site Number 840128 Ormond Beach Florida
United States Investigational Site Number 840063 Palm Harbor Florida
United States Investigational Site Number 840117 Pittsburgh Pennsylvania
United States Investigational Site Number 840060 Sarasota Florida
United States Investigational Site Number 840061 Tacoma Washington
United States Investigational Site Number 840207 Tampa Florida
United States Investigational Site Number 840211 Thousand Oaks California
United States Investigational Site Number 840037 Tupelo Mississippi
United States Investigational Site Number 840049 Upland California
United States Investigational Site Number 840205 Victorville California
United States Investigational Site Number 840203 Washington District of Columbia

Sponsors (2)

Lead Sponsor Collaborator
Sanofi Regeneron Pharmaceuticals

Countries where clinical trial is conducted

United States,  Argentina,  Australia,  Brazil,  Chile,  Colombia,  Czech Republic,  Ecuador,  Finland,  France,  Germany,  Greece,  Hungary,  Israel,  Italy,  Korea, Republic of,  Latvia,  Lithuania,  Malaysia,  Mexico,  New Zealand,  Peru,  Poland,  Romania,  Russian Federation,  South Africa,  Spain,  Taiwan,  Thailand,  Ukraine,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Disease Activity Score for 28 joints - C-reactive protein (DAS28-CRP score) score change from baseline (randomized treatment phase) Week 24 No
Secondary Number of patients with American College of Rheumatology (ACR) efficacy response rates of 20%, 50% and 70% Week 24 No
Secondary Disease Activity Score for 28 joints - C-reactive protein (DAS28-CRP) remission score (<2.6) incidence rate Week 24 No
Secondary Change from baseline in Disease Activity Score for 28 joints - C-reactive protein (DAS28-CRP) score Week 12 No
See also
  Status Clinical Trial Phase
Completed NCT04226131 - MusculRA: The Effects of Rheumatoid Arthritis on Skeletal Muscle Biomechanics N/A
Completed NCT04171414 - A Study to Evaluate Usability of Subcutaneous Auto-injector of CT-P17 in Patients With Active Rheumatoid Arthritis Phase 3
Completed NCT02833350 - Safety and Efficacy Study of GDC-0853 Compared With Placebo and Adalimumab in Participants With Rheumatoid Arthritis (RA) Phase 2
Completed NCT04255134 - Biologics for Rheumatoid Arthritis Pain (BIORA-PAIN) Phase 4
Recruiting NCT05615246 - Exactech Humeral Reconstruction Prosthesis of Shoulder Arthroplasty PMCF (HRP)
Completed NCT03248518 - Lessening the Impact of Fatigue in Inflammatory Rheumatic Diseases N/A
Completed NCT03514355 - MBSR in Rheumatoid Arthritis Patients With Controlled Disease But Persistent Depressive Symptoms N/A
Recruiting NCT06005220 - SBD121, a Synbiotic Medical Food for RA Management N/A
Recruiting NCT05451615 - Efficacy and Safety of Abatacept Combined With JAK Inhibitor for Refractory Rheumatoid Arthritis Phase 3
Completed NCT05054920 - Eccentric Versus Concentric Exercises for Rotator Cuff Tendinopathy in Patients With Rheumatoid Arthritis N/A
Completed NCT02037737 - Impact and Use of Abatacept IV for Rheumatoid Arthritis in Real Life Setting N/A
Recruiting NCT04079374 - Comparative Efficacy, Safety and Immunogenicity Study of Etanercept and Enbrel Phase 3
Completed NCT02504268 - Effects of Abatacept in Patients With Early Rheumatoid Arthritis Phase 3
Recruiting NCT05496855 - Remote Care in People With Rheumatoid Arthritis N/A
Completed NCT05051943 - A Study of the Real-world Use of an Adalimumab Biosimilar and Evaluation of Nutritional Status on the Therapeutic Response
Recruiting NCT06103773 - A Study of Single and Multiple Oral Doses of TollB-001 Phase 1
Recruiting NCT06031415 - Study of GS-0272 in Participants With Rheumatoid Arthritis Phase 1
Completed NCT05999266 - The Cartilage and Muscle Thickness on Knee Pain in Patients With Rheumatoid Arthritis
Recruiting NCT05302934 - Evaluation of the PHENO4U Data Platform in Patients Undergoing Total Knee Arthroplasty
Recruiting NCT04169100 - Novel Form of Acquired Long QT Syndrome Phase 4