A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Certolizumab Pegol in Combination With Methotrexate in the Treatment of Disease Modifying Antirheumatic Drugs (DMARD)-naïve Adults With Early Active Rheumatoid Arthritis (C-early)

This study is currently recruiting participants.
Verified April 2013 by UCB, Inc.
Sponsor:
Information provided by (Responsible Party):
UCB, Inc. ( UCB Pharma SA )
ClinicalTrials.gov Identifier:
NCT01519791
First received: January 19, 2012
Last updated: April 29, 2013
Last verified: April 2013
  Purpose

This study is intended to evaluate the efficacy and safety of Certolizumab Pegol (CZP) in combination with Methotrexate (MTX) for inducing and sustaining clinical response in the treatment of Disease Modifying Antirheumatic Drug (DMARD)-naïve adults with early active Rheumatoid Arthritis.


Condition Intervention Phase
Rheumatoid Arthritis
Biological: Certolizumab Pegol + Methotrexate (MTX)
Biological: Placebo + Methotrexate (MTX)
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Official Title: A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Certolizumab Pegol in Combination With Methotrexate for Inducing and Sustaining Clinical Response in the Treatment of DMARD-Naïve Adults With Early Active Rheumatoid Arthritis

Resource links provided by NLM:


Further study details as provided by UCB, Inc.:

Primary Outcome Measures:
  • Percentage of subjects in sustained remission at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]
    Sustained remission is defined as a Disease Activity Score [Erythrocyte Sedimentation Rate] (DAS28[ESR]) < 2.6 at both Weeks 40 and 52.


Secondary Outcome Measures:
  • Percentage of subjects in sustained Low Disease Activity (LDA) at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]
    Sustained LDA is defined as a Disease Activity Score [Erythrocyte Sedimentation Rate] (DAS28[ESR]) ≤ 3.2 at both Weeks 40 and 52.

  • Change from Baseline in modified Total Sharp Score (mTSS) to Week 52 [ Time Frame: From Baseline (Week 0) to Week 52 ] [ Designated as safety issue: No ]
    Van der Heijde modified Total Sharp Score (mTSS).

  • Percentage of subjects with radiographic non-progression from Baseline to Week 52 [ Time Frame: From Baseline (Week 0) to Week 52 ] [ Designated as safety issue: No ]
    Radiographic non-progression is defined as change in mTSS ≤ 0.5.

  • Change from Baseline in the joint erosion score to Week 52 [ Time Frame: From Baseline (Week 0) to Week 52 ] [ Designated as safety issue: No ]
  • Change from Baseline in the joint narrowing score to Week 52 [ Time Frame: From Baseline (Week 0) to Week 52 ] [ Designated as safety issue: No ]
  • Percentage of subjects meeting the American College of Rheumatology 20% response criteria (ACR20) at Week 52 [ Time Frame: From Baseline (Week 0) to Week 52 ] [ Designated as safety issue: No ]
    The assessments are based on a 20% or greater improvement from Baseline in the number of tender joints, a 20% or more improvement in the number of swollen joints, and a 20% or greater improvement in 3 of the 5 remaining core set measures: Patient's Global Assessment of Disease Activity (PtGADA), Physician's Global Assessment of Disease Activity (PhGADA), Patient's Assessment of Arthritis Pain (PtAAP), physical function as assessed by the Health Assessment Questionnaire - Disability Index (HAQ-DI) and C-Reactive Protein (CRP).

  • Percentage of subjects meeting the American College of Rheumatology 50% response criteria (ACR50) at Week 52 [ Time Frame: From Baseline (Week 0) to Week 52 ] [ Designated as safety issue: No ]
    The assessments are based on a 50% or greater improvement from Baseline in the number of tender joints, a 50%, or more improvement in the number of swollen joints, and a 50% or greater improvement in 3 of the 5 remaining core set measures: Patient's Global Assessment of Disease Activity (PtGADA), Physician's Global Assessment of Disease Activity (PhGADA), Patient's Assessment of Arthritis Pain (PtAAP), physical function as assessed by the Health Assessment Questionnaire - Disability Index (HAQ-DI) and C-Reactive Protein (CRP).

  • Percentage of subjects meeting the American College of Rheumatology 70% response criteria (ACR70) at Week 52 [ Time Frame: From Baseline (Week 0) to Week 52 ] [ Designated as safety issue: No ]
    The assessments are based on a 70% or greater improvement from Baseline in the number of tender joints, a 70%, or more improvement in the number of swollen joints, and a 70% or greater improvement in 3 of the 5 remaining core set measures: Patient's Global Assessment of Disease Activity (PtGADA), Physician's Global Assessment of Disease Activity (PhGADA), Patient's Assessment of Arthritis Pain (PtAAP), physical function as assessed by the Health Assessment Questionnaire - Disability Index (HAQ-DI) and C-Reactive Protein (CRP).

  • Percentage of subjects meeting the 2011 American College of Rheumatology/ European League Against Rheumatism (ACR/EULAR) remission criteria at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]

    The ACR/EULAR 2011 remission criteria is defined as:

    Tender Joint Count (TJC) ≤ 1, Swollen Joint Count (SJC) ≤ 1, C-reactive protein (CRP) ≤ 1 mg/dl and Patient's Global Assessment of Disease Activity (PtGADA) ≤ 1.


  • Percentage of subjects with Clinical Disease Activity Index (CDAI) ≤ 2.8 at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]
  • Percentage of subjects with Simplified Disease Activity Index (SDAI) ≤ 3.3 at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]
  • Percentage of subjects with Disease Activity Score 28 [Erythrocyte Sedimentation Rate] (DAS28 [ESR]) < 2.6 at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]
  • Percentage of subjects meeting the 2011 American College of Rheumatology/ European League Against Rheumatism (ACR/EULAR) remission criteria simplified for clinical practice at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]

    The 2011 ACR/EULAR remission criteria simplified for clinical practice is defined as:

    Tender Joint Count (TJC) ≤ 1, Swollen Joint Count (SJC) ≤ 1 and Patient's Global Assessment of Disease Activity (PtGADA) ≤ 1.


  • Percentage of subjects achieving a good or moderate European League Against Rheumatism (EULAR) response at Week 52 [ Time Frame: From Baseline (Week 0) to Week 52 ] [ Designated as safety issue: No ]

    Good response is defined as:

    DAS28[ESR] ≤ 3.2 and decrease from Baseline by > 1.2;

    moderate response is defined as achievement of one of the following:

    • DAS28[ESR] ≤ 3.2 and decrease from Baseline > 0.6 and ≤ 1.2
    • DAS28[ESR] > 3.2 and ≤ 5.1 and decrease from Baseline > 0.6
    • DAS28[ESR] > 5.1 and decrease from Baseline >1.2.

  • Change from Baseline in Disease Activity Score 28 [Erythrocyte Sedimentation Rate] (DAS28 [ESR]) to Week 52 [ Time Frame: From Baseline (Week 0) to Week 52 ] [ Designated as safety issue: No ]
  • Change from Baseline in Clinical Disease Activity Index (CDAI) to Week 52 [ Time Frame: From Baseline (Week 0) to Week 52 ] [ Designated as safety issue: No ]
  • Change from Baseline in Simplified Disease Activity Index (SDAI) to Week 52 [ Time Frame: From Baseline (Week 0) to Week 52 ] [ Designated as safety issue: No ]
  • Percentage of subjects with a Health Assessment Questionnaire- Disability Index (HAQ-DI) ≤ 0.5 at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]

    The domains of the HAQ-DI are dressing and grooming, arising, eating, walking, hygiene, reach, grip and common daily activities.

    The total score ranges from 0 to 3 with lower scores meaning lower disability.


  • Change from Baseline in the Health Assessment Questionnaire - Disability Index (HAQ-DI) to Week 52 [ Time Frame: From Baseline (Week 0) to Week 52 ] [ Designated as safety issue: No ]

    The domains of the HAQ-DI are dressing and grooming, arising, eating, walking, hygiene, reach, grip and common daily activities.

    The total score ranges from 0 to 3 with lower scores meaning lower disability.


  • Change from Baseline in the Bristol Rheumatoid Arthritis Fatigue- Multidimensional Questionnaire (BRAF-MDQ) total score to Week 52 [ Time Frame: From Baseline (Week 0) to Week 52 ] [ Designated as safety issue: No ]
    BRAF-MDQ total score ranges from 0 to 70 (with higher scores indicating worse fatigue).

  • Number of work days missed (Work Productivity Survey - Rheumatoid Arthritis [WPS-RA]) at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]
    Number of work days missed in the last month.

  • Number of work days with reduced productivity (Work Productivity Survey - Rheumatoid Arthritis [WPS-RA]) at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]
    Number of work days with reduced productivity in the last month.

  • Interference with work productivity (Work Productivity Survey - Rheumatoid Arthritis [WPS-RA]) at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]
    The Arthritis interference in the last month with work productivity is measured on a scale that ranges from 0 (no interference) to 10 (complete interference).

  • Number of days with no household work (Work Productivity Survey - Rheumatoid Arthritis [WPS-RA]) at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]
    Number of days with no household work in the last month.

  • Number of days with reduced household work productivity (Work Productivity Survey - Rheumatoid Arthritis [WPS-RA]) at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]
    Number of days with reduced household work productivity in the last month.

  • Number of days with hired outside help (Work Productivity Survey - Rheumatoid Arthritis [WPS-RA]) at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]
    Number of days with hired outside help in the last month.

  • Number of days missed of family/social/leisure activities (Work Productivity Survey - Rheumatoid Arthritis [WPS-RA]) at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]
    Number of days missed of family/social/leisure activities in the last month.

  • Interference with household work productivity (Work Productivity Survey - Rheumatoid Arthritis [WPS-RA]) at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]
    The Arthritis interference in the last month with household work productivity is measured on a scale that ranges from 0 (no interference) to 10 (complete interference).

  • Percentage of subjects achieving Low Disease Activity (LDA) at Week 52 [ Time Frame: Week 52 ] [ Designated as safety issue: No ]
    LDA is defined as achieving a Disease Activity Score 28 [Erythrocyte Sedimentation Rate] (DAS28 [ESR]) ≤ 3.2.


Estimated Enrollment: 800
Study Start Date: January 2012
Estimated Study Completion Date: December 2015
Estimated Primary Completion Date: September 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Certolizumab Pegol + Methotrexate Biological: Certolizumab Pegol + Methotrexate (MTX)

Prefilled syringes containing an injectable volume of 1 ml of solution for injection CZP for single use at a dosage strength of 200 mg/ml.

Injections will be given subcutaneously. CZP 400 mg at Baseline, Week 2 and Week 4, followed by a maintenance dose of 200 mg every 2 Weeks until Week 50.

The MTX treatment is to be initiated at a dose of 10 mg per Week. The MTX dosage should be escalated by 5 mg every 2 Weeks such that the maximum dosage of 25 mg per Week is achieved by Week 6 to Week 8.

Other Names:
  • Cimzia
  • CZP
  • MTX
Placebo Comparator: Placebo + Methotrexate Biological: Placebo + Methotrexate (MTX)

2 syringes Placebo at Baseline, Week 2 and Week 4 + MTX, followed by 1 syringe Placebo every 2 Weeks + MTX.

The MTX treatment is to be initiated at a dose of 10 mg per Week. The MTX dosage should be escalated by 5 mg every 2 Weeks such that the maximum dosage of 25 mg per Week is achieved by Week 6 to Week 8.

Other Name: MTX

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Subjects must have a time since diagnosis of adult-onset Rheumatoid Arthritis (RA) less than 1 year as defined by the 2010 ACR/EULAR classification criteria from Screening Visit
  • Positive Rheumatoid Factor (RF) and/or positive anticyclic Citrullinated Peptide Antibody (anti-CCP)
  • Active RA disease
  • DMARD-naïve
  • Subject is naïve to RA related biologics

Exclusion Criteria:

  • A diagnosis of any other inflammatory Arthritis
  • History of infected joint prosthesis, or other significant infection and other serious medical condition
  • Known Tuberculosis (TB) disease or high risk of acquiring TB infection
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01519791

Contacts
Contact: UCB Clinical Trial Call Center +1 877 822 9493

  Hide Study Locations
Locations
United States, Alabama
209 Recruiting
Birmingham, Alabama, United States
170 Recruiting
Huntsville, Alabama, United States
180 Recruiting
Mobile, Alabama, United States
United States, Arizona
247 Recruiting
Glendale, Arizona, United States
165 Recruiting
Paradise Valley, Arizona, United States
234 Recruiting
Paradise Valley, Arizona, United States
187 Recruiting
Phoenix, Arizona, United States
243 Recruiting
Phoenix, Arizona, United States
251 Recruiting
Tucson, Arizona, United States
United States, Arkansas
156 Withdrawn
Little Rock, Arkansas, United States
United States, California
160 Recruiting
Covina, California, United States
257 Recruiting
Hemet, California, United States
164 Withdrawn
Huntington Beach, California, United States
159 Recruiting
Los Angeles, California, United States
201 Recruiting
San Leandro, California, United States
202 Recruiting
Upland, California, United States
172 Recruiting
Whittier, California, United States
United States, Florida
190 Recruiting
Fort Lauderdale, Florida, United States
173 Withdrawn
Jacksonville, Florida, United States
196 Recruiting
Jupiter, Florida, United States
238 Recruiting
Lake Mary, Florida, United States
232 Recruiting
Miami, Florida, United States
213 Recruiting
Naples, Florida, United States
214 Recruiting
Ocala, Florida, United States
237 Recruiting
Orange Park, Florida, United States
255 Recruiting
Orlando, Florida, United States
163 Recruiting
Palm Harbor, Florida, United States
166 Recruiting
Plantation, Florida, United States
192 Recruiting
Sarasota, Florida, United States
200 Recruiting
Vero Beach, Florida, United States
United States, Idaho
226 Recruiting
Coeur D'alene, Idaho, United States
United States, Illinois
219 Recruiting
Rock Island, Illinois, United States
244 Recruiting
Springfield, Illinois, United States
United States, Indiana
224 Recruiting
South Bend, Indiana, United States
222 Withdrawn
Terre Haute, Indiana, United States
United States, Iowa
215 Recruiting
Cedar Rapids, Iowa, United States
United States, Kansas
191 Recruiting
Wichita, Kansas, United States
210 Recruiting
Wichita, Kansas, United States
United States, Maryland
218 Recruiting
Baltimore, Maryland, United States
177 Recruiting
Hagerstown, Maryland, United States
United States, Michigan
199 Recruiting
Kalamazoo, Michigan, United States
United States, Minnesota
198 Recruiting
Eagan, Minnesota, United States
253 Recruiting
Rochester, Minnesota, United States
United States, Mississippi
203 Recruiting
Tupelo, Mississippi, United States
United States, Missouri
179 Recruiting
St. Louis, Missouri, United States
United States, Nebraska
181 Recruiting
Lincoln, Nebraska, United States
United States, Nevada
256 Recruiting
Reno, Nevada, United States
United States, New Hampshire
229 Recruiting
Lebanon, New Hampshire, United States
United States, New Jersey
228 Recruiting
Clifton, New Jersey, United States
United States, New Mexico
207 Recruiting
Albuquerque, New Mexico, United States
United States, New York
176 Recruiting
Brooklyn, New York, United States
242 Recruiting
Plainview, New York, United States
227 Recruiting
Rochester, New York, United States
United States, North Carolina
236 Recruiting
Durham, North Carolina, United States
246 Withdrawn
Rocky Mount, North Carolina, United States
United States, North Dakota
182 Withdrawn
Minot, North Dakota, United States
United States, Ohio
231 Recruiting
Cleveland, Ohio, United States
245 Recruiting
Middleburg Heights, Ohio, United States
United States, Oklahoma
241 Recruiting
Oklahoma City, Oklahoma, United States
United States, Oregon
186 Recruiting
Portland, Oregon, United States
United States, Pennsylvania
195 Recruiting
Bethlehem, Pennsylvania, United States
167 Recruiting
Duncansville, Pennsylvania, United States
220 Withdrawn
Willow Grove, Pennsylvania, United States
168 Recruiting
Wyomissing, Pennsylvania, United States
United States, South Carolina
205 Recruiting
Columbia, South Carolina, United States
189 Recruiting
North Charleston, South Carolina, United States
United States, Tennessee
204 Recruiting
Hendersonville, Tennessee, United States
248 Withdrawn
Memphis, Tennessee, United States
United States, Texas
217 Recruiting
Allen, Texas, United States
185 Recruiting
Amarillo, Texas, United States
161 Recruiting
Austin, Texas, United States
178 Recruiting
Corpus Christi, Texas, United States
162 Recruiting
Dallas, Texas, United States
206 Recruiting
Houston, Texas, United States
184 Recruiting
Houston, Texas, United States
158 Recruiting
Mesquite, Texas, United States
175 Recruiting
Nassau Bay, Texas, United States
249 Recruiting
Plano, Texas, United States
197 Recruiting
San Antonio, Texas, United States
223 Recruiting
Sugar Land, Texas, United States
United States, Washington
233 Recruiting
Kennewick, Washington, United States
221 Withdrawn
Seattle, Washington, United States
United States, West Virginia
183 Recruiting
Clarksburg, West Virginia, United States
United States, Wisconsin
174 Recruiting
Glendale, Wisconsin, United States
Argentina
276 Recruiting
Buenos Aires, Argentina
279 Recruiting
San Juan, Argentina
291 Recruiting
Tucuman, Argentina
Australia, New South Wales
6 Recruiting
Coffs Harbour, New South Wales, Australia
Australia, Queensland
2 Recruiting
Herson, Queensland, Australia
1 Recruiting
Maroochydore, Queensland, Australia
Australia, South Australia
8 Recruiting
Woodville South, South Australia, Australia
Australia, Victoria
5 Recruiting
Fitzroy, Victoria, Australia
4 Recruiting
Geelong, Victoria, Australia
3 Recruiting
Malvern, Victoria, Australia
Australia, Western Australia
7 Recruiting
Perth, Western Australia, Australia
Austria
50 Recruiting
Wien, Austria
Belgium
51 Recruiting
Brussels, Belgium
31 Recruiting
Gent, Belgium
126 Recruiting
Gilly, Belgium
36 Recruiting
Kortrijk, Belgium
30 Recruiting
Leuven, Belgium
65 Recruiting
Yvoir, Belgium
Canada, British Columbia
240 Recruiting
Kelowna, British Columbia, Canada
Canada, Ontario
235 Recruiting
Hamilton, Ontario, Canada
Canada, Quebec
188 Recruiting
Montreal, Quebec, Canada
194 Recruiting
Trois-rivieres, Quebec, Canada
Colombia
303 Recruiting
Barranquilla, Colombia
293 Recruiting
Bogota, Colombia
299 Recruiting
Bogota, Colombia
272 Recruiting
Bogota, Colombia
297 Recruiting
Bucaramanga, Colombia
288 Recruiting
Chia, Colombia
298 Recruiting
Medellin, Colombia
271 Recruiting
Medellin, Colombia
Czech Republic
108 Recruiting
Brno, Czech Republic
124 Recruiting
Bruntal, Czech Republic
38 Recruiting
Hradec Kralove, Czech Republic
37 Recruiting
Praha, Czech Republic
France
95 Recruiting
Clermont Ferrand, France
16 Recruiting
Le Kremlin Bicetre, France
85 Recruiting
Le Mans, France
48 Recruiting
Marseille, France
88 Recruiting
Montpellier Cedex 5, France
34 Recruiting
Orleans, France
79 Recruiting
Strasbourg, France
Germany
52 Recruiting
Bad Doberan, Germany
17 Recruiting
Bayreuth, Germany
113 Recruiting
Berlin, Germany
120 Recruiting
Berlin, Germany
89 Recruiting
Erfurt, Germany
70 Recruiting
Frankfurt, Germany
28 Withdrawn
Goslar, Germany
71 Recruiting
Hamburg, Germany
81 Recruiting
Hildesheim, Germany
127 Recruiting
Lingen, Germany
61 Recruiting
München, Germany
53 Recruiting
Planegg, Germany
132 Recruiting
Ratingen, Germany
49 Recruiting
Rendsburg, Germany
69 Recruiting
Rheine, Germany
114 Recruiting
Würzburg, Germany
59 Recruiting
Zerbst, Germany
Hungary
18 Recruiting
Budapest, Hungary
21 Recruiting
Budapest, Hungary
86 Recruiting
Eger, Hungary
20 Recruiting
Gyula, Hungary
112 Recruiting
Heviz, Hungary
131 Recruiting
Szolnok, Hungary
110 Recruiting
Szombathely, Hungary
19 Recruiting
Veszprem, Hungary
Ireland
33 Recruiting
Cork, Ireland
54 Recruiting
Dublin, Ireland
104 Recruiting
Dublin, Ireland
32 Recruiting
Limerick, Ireland
Italy
115 Recruiting
Ferrara, Italy
122 Recruiting
Milano, Italy
29 Recruiting
Padova, Italy
91 Withdrawn
Prato, Italy
40 Recruiting
Reggio Emilia, Italy
72 Recruiting
Roma, Italy
116 Recruiting
Roma, Italy
41 Recruiting
Valeggio, Italy
Mexico
281 Recruiting
Durango, Mexico
286 Recruiting
Guadalajara, Mexico
302 Recruiting
Merida, Mexico
292 Recruiting
Mexico City, Mexico
280 Recruiting
Monterrey, Mexico
294 Recruiting
San Luis Potosi, Mexico
Monaco
78 Recruiting
Monaco, Monaco
Netherlands
43 Recruiting
Den Haag, Netherlands
66 Recruiting
Den Haag, Netherlands
90 Recruiting
Gouda, Netherlands
42 Recruiting
Leiden, Netherlands
Poland
128 Recruiting
Bydgoszcz, Poland
67 Recruiting
Elblag, Poland
46 Recruiting
Katowice, Poland
99 Recruiting
Krakow, Poland
92 Recruiting
Poznan, Poland
74 Recruiting
Torun, Poland
62 Recruiting
Ustron, Poland
100 Recruiting
Warszawa, Poland
44 Recruiting
Wroclaw, Poland
Romania
58 Recruiting
Brasov, Romania
26 Recruiting
Bucharest, Romania
111 Recruiting
Bucharest, Romania
22 Recruiting
Bucharest, Romania
25 Recruiting
Bucharest, Romania
23 Recruiting
Cluj-napoca, Romania
24 Recruiting
Iasi, Romania
57 Recruiting
Iasi, Romania
Spain
93 Recruiting
A Coruna, Spain
47 Recruiting
Madrid, Spain
64 Recruiting
Madrid, Spain
63 Active, not recruiting
Santiago de Compostela, Spain
103 Withdrawn
Sevilla, Spain
Sweden
102 Recruiting
Falun, Sweden
76 Recruiting
Göteborg, Sweden
82 Recruiting
Huddinge, Sweden
106 Recruiting
Lund, Sweden
123 Recruiting
Malmö, Sweden
77 Recruiting
Stockholm, Sweden
75 Recruiting
Uppsala, Sweden
Switzerland
107 Recruiting
Aarau, Switzerland
118 Recruiting
Fribourg, Switzerland
87 Recruiting
Lausanne, Switzerland
68 Recruiting
St. Gallen, Switzerland
United Kingdom
55 Recruiting
Bury-st-edmunds, United Kingdom
125 Recruiting
Cannock, United Kingdom
105 Recruiting
Dudley, United Kingdom
56 Recruiting
Leeds, United Kingdom
27 Recruiting
London, United Kingdom
121 Recruiting
London, United Kingdom
80 Recruiting
Sheffield, United Kingdom
119 Recruiting
York, United Kingdom
Sponsors and Collaborators
UCB Pharma SA
Investigators
Study Director: UCB Clinical Trial Call Center +1 877 822 9493 (UCB)
  More Information

No publications provided

Responsible Party: UCB, Inc. ( UCB Pharma SA )
ClinicalTrials.gov Identifier: NCT01519791     History of Changes
Other Study ID Numbers: RA0055A, 2011-001729-25
Study First Received: January 19, 2012
Last Updated: April 29, 2013
Health Authority: United States: Food and Drug Administration
Argentina: Administracion Nacional de Medicamentos, Alimentos y Tecnologia Medica
Australia: Department of Health and Ageing Therapeutic Goods Administration
Austria: Federal Office for Safety in Health Care
Belgium: Federal Agency for Medicinal Products and Health Products
Canada: Health Canada
Colombia: INVIMA Instituto Nacional de Vigilancia de Medicamentos y Alimentos
Czech Republic: State Institute for Drug Control
France: L’Agence nationale de sécurité du médicament et des produits de santé
Germany: Federal Institute for Drugs and Medical Devices
Hungary: National Institute of Pharmacy
Ireland: Irish Medicines Board
Italy: The Italian Medicines Agency
Mexico: Ministry of Health
Poland: Office for Registration of Medicinal Products, Medical Devices and Biocidal Products
Romania: National Medicines Agency
Spain: Agencia Española de Medicamentos y Productos Sanitarios
Sweden: Medical Products Agency
Switzerland: Swissmedic
Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
United Kingdom: Medicines and Healthcare Products Regulatory Agency

Keywords provided by UCB, Inc.:
Certolizumab Pegol - Cimzia
Methotrexate
Rheumatoid Arthritis

Additional relevant MeSH terms:
Arthritis
Arthritis, Rheumatoid
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases
Connective Tissue Diseases
Autoimmune Diseases
Immune System Diseases
Antirheumatic Agents
Methotrexate
Immunoglobulin Fab Fragments
Therapeutic Uses
Pharmacologic Actions
Abortifacient Agents, Nonsteroidal
Abortifacient Agents
Reproductive Control Agents
Physiological Effects of Drugs
Antimetabolites, Antineoplastic
Antimetabolites
Molecular Mechanisms of Pharmacological Action
Antineoplastic Agents
Dermatologic Agents
Enzyme Inhibitors
Folic Acid Antagonists
Immunosuppressive Agents
Immunologic Factors
Nucleic Acid Synthesis Inhibitors

ClinicalTrials.gov processed this record on May 22, 2013