AzTrials
AzTrials

Rheumatoid ArthritisPhase 3NCT00095147

Abatacept and Infliximab in Combination With Methotrexate in Subjects With Rheumatoid Arthritis

A Phase 3 study testing Abatacept (ABA) + Methotrexate (MTX), double-blind (DB), Infliximab (INF) + MTX, DB and PLA + MTX switched to ABA+ MTX, DB in people with Rheumatoid Arthritis, run by Bristol-Myers Squibb at 76 sites in 17 countries.

Completed

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

Official record
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Trial summary

The purpose of this clinical research study is to learn if Abatacept or Infliximab in combination with Methotrexate demonstrate a greater reduction in disease activity over placebo. Read more about this study

Who is it for?
Ages 18 to 75 years
Conditions the study is for
Rheumatoid Arthritis
What is being tested?
Abatacept (ABA) + Methotrexate (MTX), double-blind (DB), Infliximab (INF) + MTX, DB and PLA + MTX switched to ABA+ MTX, DB
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
431 participants
Where
76 sitesin 17 countries
Study dates
Feb 2005to Jul 2009
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 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Diagnosis of Rheumatoid Arthritis
  • At least 3 months prior treatment with Methotrexate (MTX)
  • At least 10 swollen joints and 12 tender joints and C-Reactive Protein of at least 1 mg/dl
  • Washout required for other disease modifying anti-rheumatic drugs (DMARDS)

Who cannot join

  • participants who have failed more than 3 DMARDs
  • participants previously treated with an approved biologic drug
  • History of cancer in the last 5 years
  • Severe or recurrent bacterial infection
  • Any previous or current medical conditions that are contraindications to the use of TNF blocking agents
  • Women of Child Bearing Potential

Trial locations and contacts

76 sites in 17 countries.

76 sites in 17 countries

United States19 sites
  • Local Institution

    Austin, Texas

  • Local Institution

    Bethlehem, Pennsylvania

  • Local Institution

    Boca Raton, Florida

  • Local Institution

    Charlotte, North Carolina

  • Local Institution

    Cincinnati, Ohio

  • Local Institution

    Dallas, Texas

  • Local Institution

    Denver, Colorado

  • Local Institution

    Flowood, Mississippi

  • Local Institution

    Fort Lauderdale, Florida

  • Local Institution

    Huntsville, Alabama

  • Local Institution

    Indianapolis, Indiana

  • Local Institution

    Largo, Florida

  • Local Institution

    New Orleans, Louisiana

  • Local Institution

    Oklahoma City, Oklahoma

  • Local Institution

    Springfield, Massachusetts

  • Local Institution

    Syracuse, New York

  • Local Institution

    Tulsa, Oklahoma

  • Local Institution

    Willow Grove, Pennsylvania

  • Local Institution

    Worcester, Massachusetts

Other trials in United States

Canada11 sites
  • Local Institution

    Calgary, Alberta

  • Local Institution

    Edmonton, Alberta

  • Local Institution

    Hamilton, Ontario

  • Local Institution

    Kitchener, Ontario

  • Local Institution

    Kitchener, ON

  • Local Institution

    Montreal, Quebec

  • Local Institution

    Ottawa, Ontario

  • Local Institution

    Saskatoon, Saskatchewan

  • Local Institution

    St. John's, Newfoundland and Labrador

  • Local Institution

    Ste-Foy, Quebec

  • Local Institution

    Winnipeg, Manitoba

Other trials in Canada

Australia7 sites
  • Local Institution

    Cairns, Queensland

  • Local Institution

    Clayton, Victoria

  • Local Institution

    Cotton Tree, Queensland

  • Local Institution

    Heidelberg, Victoria

  • Local Institution

    Malvern, Victoria

  • Local Institution

    Parkville, Victoria

  • Local Institution

    Perth, Western Australia

Other trials in Australia

Mexico6 sites
  • Local Institution

    Guadalajara, Jalisco

  • Local Institution

    León, Guanajuato

  • Local Institution

    Mexico City, Mexico City

  • Local Institution

    Monterrey, Nuevo León

  • Local Institution

    San Luis Potosí City, San Luis Potosí

  • Local Institution

    Tijuana, Estado de Baja California

Other trials in Mexico

Argentina5 sites
  • Local Institution

    Buenos Aires, Buenos Aires

  • Local Institution

    Capital Federal, Buenos Aires

  • Local Institution

    Córdoba, Córdoba Province

  • Local Institution

    Quilmes, Buenos Aires

  • Local Institution

    San Miguel de Tucumán, Tucumán Province

Other trials in Argentina

Brazil5 sites
  • Local Institution

    Curitiba, Paraná

  • Local Institution

    Porto Alegre, Rio Grande do Sul

  • Local Institution

    Recife, Pernambuco

  • Local Institution

    Rio de Janeiro, Rio de Janeiro

  • Local Institution

    São Paulo, São Paulo

Other trials in Brazil

Sweden5 sites
  • Local Institution

    Falun

  • Local Institution

    Linköping

  • Local Institution

    Lund

  • Local Institution

    Stockholm

  • Local Institution

    Uppsala

Other trials in Sweden

Spain4 sites
  • Local Institution

    A Coruña

  • Local Institution

    Barcelona

  • Local Institution

    Córdoba

  • Local Institution

    Madrid

Other trials in Spain

Poland3 sites
  • Local Institution

    Poznan

  • Local Institution

    Sopot

  • Local Institution

    Warsaw

Other trials in Poland

South Africa3 sites
  • Local Institution

    Berea, KwaZulu-Natal

  • Local Institution

    Muckleneuk, Gauteng

  • Local Institution

    Panorama, Western Cape

Other trials in South Africa

Switzerland2 sites
  • Local Institution

    Bern

  • Local Institution

    Sankt Gallen

Other trials in Switzerland

Czechia1 site
  • Local Institution

    Prague

Other trials in Czechia

Denmark1 site
  • Local Institution

    Copenhagen

Other trials in Denmark

Peru1 site
  • Local Institution

    Lima

Other trials in Peru

Puerto Rico1 site
  • Local Institution

    Rio Piedras

Other trials in Puerto Rico

Russia1 site
  • Local Institution

    Moscow

Other trials in Russia

South Korea1 site
  • Local Institution

    Seoul

Other trials in South Korea

About this study

Official title: A Phase IIIB, Multi-Center, Randomized, Double-Blind, Placebo-Controlled Comparative Study of Abatacept or Infliximab in Combination With Methotrexate in Controlling Disease Activity in Subjects With Rheumatoid Arthritis Having an Inadequate Clinical Response to Methotrexate

The purpose of this clinical research study is to learn if Abatacept or Infliximab in combination with Methotrexate demonstrate a greater reduction in disease activity over placebo.

Being tested
Abatacept (ABA) + Methotrexate (MTX), double-blind (DB), Infliximab (INF) + MTX, DB, Placebo (PLA) + MTX, DB, PLA + MTX switched to ABA+ MTX, DB, ABA, open-label (OL)
Medical subject headings
Arthritis, Rheumatoid

What participants receive

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

  • Abatacept (ABA) + Methotrexate (MTX), double-blind (DB)Drug

    Also called Orencia

    Abatacept, intravenous (IV) Solution, Infusion, Depends on participant weight, Monthly, 12 months.

  • Infliximab (INF) + MTX, DBDrug

    Infliximab, IV Solution, Infusion, Depends on participant weight, Every 2 Months, 12 months.

  • Placebo (PLA) + MTX, DBDrug

    Placebo, IV Solution, Infusion, Depends on participant weight, Monthly, 6 months.

  • PLA + MTX switched to ABA+ MTX, DBDrug

    Also called Orencia

    Placebo=IV Solution, Infusion, Depends on participant weight, Monthly, 6 months. Abatacept=IV Solution, Infusion, Depends on participant weight, Monthly, 6 months

  • ABA, open-label (OL)Drug

    Also called Orencia

    Abatacept, IV solution, Infusion. Depends on participant weight, Monthly, 12+ months

Study groups in NCT00095147
Study groupRoleWhat they receive
Abatacept (ABA) + Methotrexate (MTX) (double-blind [DB])Active comparatorDays 1-365
Receives: Drug: Abatacept (ABA) + Methotrexate (MTX), double-blind (DB)
Infliximab + MTX (DB)Active comparatorDays 1-365
Receives: Drug: Infliximab (INF) + MTX, DB
Placebo + MTX (DB)Placebo comparatorDays 1-197
Receives: Drug: Placebo (PLA) + MTX, DB
Placebo + MTX switched to abatacept + MTX (DB)ExperimentalParticipants received placebo plus methotrexate for days 1-197, and abatacept plus methotrexate for days 198-365
Receives: Drug: PLA + MTX switched to ABA+ MTX, DB
Abatacept (open-label)ExperimentalDays 365 to 729 All participants receive Active Drug
Receives: Drug: ABA, open-label (OL)

What is being measured

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

  1. DB; Adjusted Mean Change From Baseline to Day 197 in Disease Activity Score (DAS) 28 Score (Erythrocyte Sedimentation Rate [ESR]) For ABA Versus PLA (Last Observation Carried Forward [LOCF] Analysis)

    The DAS28 is a continuous disease measure which is a composite of 4 variables: the 28 tender joint count, the 28 swollen joint count, ESR or C-reactive protein (CRP), and participant assessment of disease activity measure on a visual analogue scale. The DAS28 has numeric thresholds that define high disease activity (> 5.1), low disease activity (< 3.2) and remission (< 2.6). A clinically significant response is a decrease in DAS28 score of >1.2 from baseline.

    Measured: Baseline (Day 1), 6 months (Day 197)

  2. OL; Number of Participants With Death, Serious Adverse Events (SAEs), Related SAEs, SAEs Leading to Discontinuation, Adverse Events (AEs), Related AEs, and AEs Leading to Discontinuation

    AE=any new untoward medical occurrence or worsening of a pre-existing medical condition which does not necessarily have a causal relationship with this treatment. SAE=any untoward medical occurrence that at any dose: results in death, is life-threatening, requires inpatient hospitalization or causes prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect, results in development of drug dependency or drug abuse, is an important medical event.

    Measured: From beginning of OL (Day 366) through end of OL (range from 1.9 months to 42.3 months)

  3. OL; Number of Participants With AEs of Special Interest

    AE=any new untoward medical occurrence or worsening of a pre-existing medical condition which does not necessarily have a causal relationship with this treatment. AEs of special interest are those AEs that may be associated with the use of immunomodulatory drugs, including all infections, serious infections, autoimmune disorders; malignancies; and acute infusional AEs (pre-specified AEs occurring within 1 hour of start of infusion).

    Measured: From beginning of OL (Day 366) through end of OL (range from 1.9 months to 42.3 months)

  4. OL; Number of Participants With Select Hematologic Laboratory Abnormalities

    High=greater than Upper Normal Limit (ULN), Low=lower than Lower Normal Limit (LLN). LLN/ULN= Hemoglobin (HGB): >3 g/dL decrease from Baseline (BL); Hematocrit: <0.75 x BL; Erythrocytes: <0.75 x BL; Platelets (PLT): <0.67 x LLN/>1.5 x ULN; Leukocytes: <0.75 x LLN/ >1.25 x ULN; neutrophils+bands: <1.0 x 10^3 c/uL; lymphocytes: <0.750 x 10^3 c/uL/ >7.50 x 10^3 c/uL; monocytes: >2000 mm3; eosinophils: >0.750 x 10^3 c/uL;

    Measured: From Day 366 through end of OL (range from 1.9 months to 42.3 months)

  5. OL; Number of Participants With Select Blood Chemistry Laboratory Abnormalities

    Low=lower than LLN, High=greater than ULN. LLN/ULN= Alkaline phosphatase (ALP): >2 x ULN; aspartate aminotransferase (AST): >3 x ULN; alanine aminotransferase (ALT): >3 x ULN; G-Glutamyl transferase (GGT): >2 x ULN; Bilirubin: >2 x ULN; blood urea nitrogen (BUN): >2 x BL; creatinine: >4 x BL

    Measured: From Day 366 through end of OL (range from 1.9 months to 42.3 months)

  6. OL; Mean Change From Baseline to Day 365 in Hemoglobin, Total Protein, and Albumin

    Hemoglobin (HGB): >3 g/dL decrease from BL; total protein: < 0.9 x LLN, >1.1 x ULN; albumin:<0.9 x LLN

    Measured: Baseline (Day 1), Day 365

  7. OL; Mean Change From Baseline to Day 365 in Platelets

    Platelets (PLT): <0.67 x LLN, >1.5 x ULN

    Measured: Baseline (Day 1), Day 365

  8. OL; Mean Change From Baseline to Day 365 in Hematocrit

    Hematocrit: <0.75 x BL

    Measured: Baseline (Day 1), Day 365

  9. OL; Mean Change From Baseline to Day 365 in White Blood Cells

    Leukocytes: <0.75 x LLN, >1.25 x ULN; neutrophils+bands: <1.0 x 10^3 c/uL; eosinophils: >0.750 x 10^3 c/uL; basophils: > 400 mm3; monocytes: >2000 mm3; lymphocytes: <0.750 x 10^3 c/uL, >7.50 x 10^3 c/uL.

    Measured: Baseline (Day 1), Day 365

  10. OL; Mean Change From Baseline to Day 365 in Erythrocytes

    Erythrocytes: <0.75 x BL

    Measured: Baseline (Day 1), Day 365

  11. OL; Mean Change From Baseline to Day 365 in Electrolytes

    Sodium (Na): <0.95 x LLN, >1.05 x ULN; potassium (K): <0.9 x LLN, >1.1 x ULN; chloride (Cl): <0.9 x LLN, >1.1 x ULN

    Measured: Baseline (Day 1), Day 365

  12. OL; Mean Change From Baseline to Day 365 in Bilirubin, Blood Urea Nitrogen, Creatinine, Calcium, Phosphorous, Serum Glucose, Fasting Serum Glucose, and Uric Acid

    Bilirubin: >2 x ULN; blood urea nitrogen (BUN): >2 x BL; creatinine: >4 x BL; calcium (Ca): <0.8 x LLN, >1.2 x ULN; phosphorous (P): <0.75 x LLN, >1.2 5 x ULN; serum glucose (Glu): <65 mg/dL, >220 mg/dL; fasting serum Glu: <0.8 x LLN, >1.5 x ULN; uric acid: >1.5 x ULN;

    Measured: Baseline (Day 1), Day 365

  13. OL; Mean Change From Baseline to Day 365 in Alanine Aminotransferase, Aspartate Aminotransferase, G-Glutamyl Transferase, and Alkaline Phosphatase

    alanine aminotransferase (ALT): >3 x ULN; aspartate aminotransferase (AST): >3 x ULN; G-Glutamyl transferase (GGT): >2 x ULN; Alkaline phosphatase (ALP): >2 x ULN

    Measured: Baseline (Day 1), Day 365

  14. OL; Mean Change From Baseline to Day 729 in Hemoglobin, Total Protein, and Albumin

    Hemoglobin (HGB): >3 g/dL decrease from BL; total protein: < 0.9 x LLN, >1.1 x ULN; albumin:<0.9 x LLN

    Measured: Baseline (Day 1), Day 729

  15. OL; Mean Change From Baseline to Day 729 in Platelets

    Platelets (PLT): <0.67 x LLN, >1.5 x ULN

    Measured: Baseline (Day 1), Day 729

  16. OL; Mean Change From Baseline to Day 729 in Hematocrit

    Hematocrit: <0.75 x BL

    Measured: Baseline (Day 1), Day 729

  17. OL; Mean Change From Baseline to Day 729 in White Blood Cells

    Leukocytes: <0.75 x LLN, >1.25 x ULN; neutrophils+bands: <1.0 x 10^3 c/uL; eosinophils: >0.750 x 10^3 c/uL; basophils: > 400 mm3; monocytes: >2000 mm3; lymphocytes: <0.750 x 10^3 c/uL, >7.50 x 10^3 c/uL.

    Measured: Baseline (Day 1), Day 729

  18. OL; Mean Change From Baseline to Day 729 in Erythrocytes

    Erythrocytes: <0.75 x BL

    Measured: Baseline (Day 1), Day 729

  19. OL; Mean Change From Baseline to Day 729 in Electrolytes

    Sodium (Na): <0.95 x LLN, >1.05 x ULN; potassium (K): <0.9 x LLN, >1.1 x ULN; chloride (Cl): <0.9 x LLN, >1.1 x ULN

    Measured: Baseline (Day 1), Day 729

  20. OL; Mean Change From Baseline to Day 729 in Bilirubin, Blood Urea Nitrogen, Creatinine, Calcium, Phosphorous, Serum Glucose, Fasting Serum Glucose, and Uric Acid

    Bilirubin: >2 x ULN; blood urea nitrogen (BUN): >2 x BL; creatinine: >4 x BL; calcium (Ca): <0.8 x LLN, >1.2 x ULN; phosphorous (P): <0.75 x LLN, >1.2 5 x ULN; serum glucose (Glu): <65 mg/dL, >220 mg/dL; fasting serum Glu: <0.8 x LLN, >1.5 x ULN; uric acid: >1.5 x ULN;

    Measured: Baseline (Day 1), Day 729

  21. OL; Mean Change From Baseline to Day 729 in Alanine Aminotransferase, Aspartate Aminotransferase, G-Glutamyl Transferase, and Alkaline Phosphatase

    alanine aminotransferase (ALT): >3 x ULN; aspartate aminotransferase (AST): >3 x ULN; G-Glutamyl transferase (GGT): >2 x ULN; Alkaline phosphatase (ALP): >2 x ULN

    Measured: Baseline (Day 1), Day 729

  22. OL; Mean Change From Baseline to Day 1121 in Hemoglobin, Total Protein, and Albumin

    Hemoglobin (HGB): >3 g/dL decrease from BL; total protein: < 0.9 x LLN, >1.1 x ULN; albumin:<0.9 x LLN

    Measured: Baseline (Day 1), Day 1121

  23. OL; Mean Change From Baseline to Day 1121 in Platelets

    Platelets (PLT): <0.67 x LLN, >1.5 x ULN

    Measured: Baseline (Day 1), Day 1121

  24. OL; Mean Change From Baseline to Day 1121 in Hematocrit

    Hematocrit: <0.75 x BL

    Measured: Baseline (Day 1), Day 1121

  25. OL; Mean Change From Baseline to Day 1121 in White Blood Cells

    Leukocytes: <0.75 x LLN, >1.25 x ULN; neutrophils+bands: <1.0 x 10^3 c/uL; eosinophils: >0.750 x 10^3 c/uL; basophils: > 400 mm3; monocytes: >2000 mm3; lymphocytes: <0.750 x 10^3 c/uL, >7.50 x 10^3 c/uL.

    Measured: Baseline (Day 1), Day 1121

  26. OL; Mean Change From Baseline to Day 1121 in Erythrocytes

    Erythrocytes: <0.75 x BL

    Measured: Baseline (Day 1), Day 1121

  27. OL; Mean Change From Baseline to Day 1121 in Electrolytes

    Sodium (Na): <0.95 x LLN, >1.05 x ULN; potassium (K): <0.9 x LLN, >1.1 x ULN; chloride (Cl): <0.9 x LLN, >1.1 x ULN

    Measured: Baseline (Day 1), Day 1121

  28. OL; Mean Change From Baseline to Day 1121 in Bilirubin, Blood Urea Nitrogen, Creatinine, Calcium, Phosphorous, Serum Glucose, Fasting Serum Glucose, and Uric Acid

    Bilirubin: >2 x ULN; blood urea nitrogen (BUN): >2 x BL; creatinine: >4 x BL; calcium (Ca): <0.8 x LLN, >1.2 x ULN; phosphorous (P): <0.75 x LLN, >1.2 5 x ULN; serum glucose (Glu): <65 mg/dL, >220 mg/dL; fasting serum Glu: <0.8 x LLN, >1.5 x ULN; uric acid: >1.5 x ULN;

    Measured: Baseline (Day 1), Day 1121

  29. OL; Mean Change From Baseline to Day 1121 in Alanine Aminotransferase, Aspartate Aminotransferase, G-Glutamyl Transferase, and Alkaline Phosphatase

    alanine aminotransferase (ALT): >3 x ULN; aspartate aminotransferase (AST): >3 x ULN; G-Glutamyl transferase (GGT): >2 x ULN; Alkaline phosphatase (ALP): >2 x ULN

    Measured: Baseline (Day 1), Day 1121

  30. OL; Mean Change From Baseline to Day 1513 in Hemoglobin, Total Protein, and Albumin

    Hemoglobin (HGB): >3 g/dL decrease from BL; total protein: < 0.9 x LLN, >1.1 x ULN; albumin:<0.9 x LLN

    Measured: Baseline (Day 1), Day 1513

  31. OL; Mean Change From Baseline to Day 1513 in Platelets

    Platelets (PLT): <0.67 x LLN, >1.5 x ULN

    Measured: Baseline (Day 1), Day 1513

  32. OL; Mean Change From Baseline to Day 1513 in Hematocrit

    Hematocrit: <0.75 x BL

    Measured: Baseline (Day 1), Day 1513

  33. OL; Mean Change From Baseline to Day 1513 in White Blood Cells

    Leukocytes: <0.75 x LLN, >1.25 x ULN; neutrophils+bands: <1.0 x 10^3 c/uL; eosinophils: >0.750 x 10^3 c/uL; basophils: > 400 mm3; monocytes: >2000 mm3; lymphocytes: <0.750 x 10^3 c/uL, >7.50 x 10^3 c/uL.

    Measured: Baseline (Day 1), Day 1513

  34. OL; Mean Change From Baseline to Day 1513 in Erythrocytes

    Erythrocytes: <0.75 x BL

    Measured: Baseline (Day 1), Day 1513

  35. OL; Mean Change From Baseline to Day 1513 in Electrolytes

    Sodium (Na): <0.95 x LLN, >1.05 x ULN; potassium (K): <0.9 x LLN, >1.1 x ULN; chloride (Cl): <0.9 x LLN, >1.1 x ULN

    Measured: Baseline (Day 1), Day 1513

  36. OL; Mean Change From Baseline to Day 1513 in Bilirubin, Blood Urea Nitrogen, Creatinine, Calcium, Phosphorous, Serum Glucose, Fasting Serum Glucose, and Uric Acid

    Bilirubin: >2 x ULN; blood urea nitrogen (BUN): >2 x BL; creatinine: >4 x BL; calcium (Ca): <0.8 x LLN, >1.2 x ULN; phosphorous (P): <0.75 x LLN, >1.2 5 x ULN; serum glucose (Glu): <65 mg/dL, >220 mg/dL; fasting serum Glu: <0.8 x LLN, >1.5 x ULN; uric acid: >1.5 x ULN;

    Measured: Baseline (Day 1), Day 1513

  37. OL; Mean Change From Baseline to Day 1513 in Alanine Aminotransferase, Aspartate Aminotransferase, G-Glutamyl Transferase, and Alkaline Phosphatase

    alanine aminotransferase (ALT): >3 x ULN; aspartate aminotransferase (AST): >3 x ULN; G-Glutamyl transferase (GGT): >2 x ULN; Alkaline phosphatase (ALP): >2 x ULN

    Measured: Baseline (Day 1), Day 1513

  38. OL; Mean Systolic (SBP) and Diastolic (DBP) Blood Pressure During Open Label Period

    Seated Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP), units=mm mercury (Hg)

    Measured: Days 365, 729, 1121, and 1513

  39. OL; Mean Heart Rate (HR) During Open Label Period

    Heart Rate (HR), units=beats per minute (bpm)

    Measured: Days 365, 729, 1121, and 1513

  40. OL; Mean Temperature (T) During Open Label Period

    Temperature (T), units=degrees Celcius

    Measured: Days 365, 729, 1121, and 1513

Secondary outcomes (31)
  1. DB; Adjusted Mean Change From Baseline to Day 197 in DAS 28 Score (ESR) For INF Versus PLA (LOCF Analysis)

    The DAS28 is a continuous disease measure which is a composite of 4 variables: the 28 tender joint count, the 28 swollen joint count, ESR or CRP, and participant assessment of disease activity measure on a visual analogue scale. The DAS28 has numeric thresholds that define high disease activity (> 5.1), low disease activity (< 3.2) and remission (< 2.6). A clinically significant response is a decrease in DAS28 score of >1.2 from baseline.

    Measured: Baseline (Day 1), 6 months (Day 197)

  2. DB; DAS 28 (ESR) Area Under The Curve (AUC) Over 12 Months For ABA Versus INF

    The DAS28 is a continuous disease measure which is a composite of 4 variables: the 28 tender joint count, the 28 swollen joint count, ESR or CRP, and participant assessment of disease activity measure on a visual analogue scale. The DAS28 has numeric thresholds that define high disease activity (> 5.1), low disease activity (< 3.2) and remission (< 2.6). Clinically significant response= decrease in DAS28 score of >1.2 from baseline. DAS28 AUC can be calculated from the DAS28 score versus time curve, which provides an assessment of changes in disease activity over time.

    Measured: From Day 1 through Day 365 (12 months)

  3. DB; Percentage of Participants With Clinically Meaningful Health Assessment Questionnaire-Disability Index (HAQ-DI) Response at Day 197

    The disability section of the full HAQ includes 20 questions to assess physical functions in 8 domains: dressing, arising, eating, walking, hygiene, reach, grip and common activities. The questions are evaluated on a 4-point scale: 0=without any difficulty, 1= with some difficulty, 2= with much difficulty, and 3= unable to do. Higher scores= greater dysfunction. A disability index was calculated by summing the worst scores in each domain and dividing by the number of domains answered. Clinically meaningful HAQ response=an improvement of at least 0.3 units from baseline in HAQ disability Index.

    Measured: DB Day 197

  4. DB; Percentage of Participants With Clinically Meaningful Health Assessment Questionnaire-Disability Index (HAQ-DI) Response at Day 365

    The disability section of the full HAQ includes 20 questions to assess physical functions in 8 domains: dressing, arising, eating, walking, hygiene, reach, grip and common activities. The questions are evaluated on a 4-point scale: 0=without any difficulty, 1= with some difficulty, 2= with much difficulty, and 3= unable to do. Higher scores= greater dysfunction. A disability index was calculated by summing the worst scores in each domain and dividing by the number of domains answered. Clinically meaningful HAQ response=an improvement of at least 0.3 units from baseline in HAQ disability Index.

    Measured: DB Day 365

  5. DB; Adjusted Mean Change From Baseline to Day 197 in HAQ-DI (LOCF Analysis)

    The disability section of the full HAQ includes 20 questions to assess physical functions in 8 domains: dressing, arising, eating, walking, hygiene, reach, grip and common activities. The questions are evaluated on a 4-point scale: 0=without any difficulty, 1= with some difficulty, 2= with much difficulty, and 3= unable to do. Higher scores= greater dysfunction. A disability index was calculated by summing the worst scores in each domain and dividing by the number of domains answered. Clinically meaningful HAQ response=an improvement of at least 0.3 units from baseline in HAQ disability Index.

    Measured: Baseline (Day 1), 6 months (Day 197)

  6. DB; Adjusted Mean Change From Baseline to Day 365 in HAQ-DI (LOCF Analysis)

    The disability section of the full HAQ includes 20 questions to assess physical functions in 8 domains: dressing, arising, eating, walking, hygiene, reach, grip and common activities. The questions are evaluated on a 4-point scale: 0=without any difficulty, 1= with some difficulty, 2= with much difficulty, and 3= unable to do. Higher scores= greater dysfunction. A disability index was calculated by summing the worst scores in each domain and dividing by the number of domains answered. Clinically meaningful HAQ response=an improvement of at least 0.3 units from baseline in HAQ disability Index.

    Measured: Baseline (Day 1), 12 months (Day 365)

  7. DB; Adjusted Mean Change From Baseline to Day 197 in SF-36 Physical Component Summary (PCS) and Mental Component Summary (MCS)

    The SF-36 is a validated instrument measuring health-related quality of life across multiple disease states. It has 36 questions with 8 subscale scores and 2 summary scores (1) physical component summary=physical functioning, role-physical, bodily pain, and general health; (2) mental component summary=vitality, social functioning, role-emotional, and mental health. There is no total overall score; scoring is done for both subscores and summary scores. For subscores and summary scores, 0 =worst score (or quality of life) and 100=best score. Change from Baseline= post-Baseline - Baseline value.

    Measured: Baseline (Day 1), 6 months (Day 197)

  8. DB; Adjusted Mean Change From Baseline to Day 365 in SF-36 Physical Component Summary (PCS) and Mental Component Summary (MCS)

    The SF-36 is a validated instrument measuring health-related quality of life across multiple disease states. It has 36 questions with 8 subscale scores and 2 summary scores (1) physical component summary=physical functioning, role-physical, bodily pain, and general health; (2) mental component summary=vitality, social functioning, role-emotional, and mental health. There is no total overall score; scoring is done for both subscores and summary scores. For subscores and summary scores, 0 =worst score (or quality of life) and 100=best score. Change from Baseline= post-Baseline - Baseline value.

    Measured: Baseline (Day 1), 12 months (Day 365)

  9. DB; Percentage of Participants With Good, Moderate, or No Response According to European League Against Rheumatism (EULAR) at Day 365

    The DAS28 is a continuous disease measure composite of 4 variables: 28 tender joint count, 28 swollen joint count, ESR or CRP, and participant assessment of disease activity measure on a visual analogue scale. High disease activity= > 5.1, low disease activity= < 3.2, and remission= < 2.6. Clinically significant response= decrease of >1.2 from baseline. Utilizing EULAR response criteria, DAS28 categorical responses define a good (absolute: <3.2 or >1.2 improvement from baseline [BL]), moderate (absolute: 3.2-5.1 or 0.6-1.2 change from BL), or no response (absolute: >5.1 or <0.6 change from BL)

    Measured: DB Day 365

  10. DB; Percentage of Participants With American College of Rheumatology (ACR) Responses at Day 197

    The ACR 20 definition of improvement is a 20% improvement from baseline in the number of tender and swollen joint counts, and a 20% improvement from baseline in 3 of the remaining 5 core set measures: participant global assessment of pain, participant global assessment of disease activity, physician global assessment of disease activity, participant assessment of physical function and acute phase reactant value (C-reactive protein [CRP]). The evaluation for 50% improvement (ACR 50) and 70% improvement (ACR 70) follow similarly.

    Measured: DB Day 197

  11. DB; Percentage of Participants With American College of Rheumatology (ACR) Responses at Day 365

    The ACR 20 definition of improvement is a 20% improvement from baseline in the number of tender and swollen joint counts, and a 20% improvement from baseline in 3 of the remaining 5 core set measures: participant global assessment of pain, participant global assessment of disease activity, physician global assessment of disease activity, participant assessment of physical function and acute phase reactant value (C-reactive protein [CRP]). The evaluation for 50% improvement (ACR 50) and 70% improvement (ACR 70) follow similarly.

    Measured: DB Day 365

  12. DB; Number of Participants With Death, Serious Adverse Events (SAEs), Related SAEs, SAEs Leading to Discontinuation, AEs, Related AEs, and AEs Leading to Discontinuation From Day 1 Through Day 197

    AE=any new untoward medical occurrence or worsening of a pre-existing medical condition which does not necessarily have a causal relationship with this treatment. SAE=any untoward medical occurrence that at any dose: results in death, is life-threatening, requires inpatient hospitalization or causes prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect, results in development of drug dependency or drug abuse, is an important medical event.

    Measured: From Baseline (Day 1) through Day 197, and up to 56 days after last dose if occurring on-study

  13. DB; Number of Participants With AEs of Special Interest From Day 1 Through Day 197

    AE=any new untoward medical occurrence or worsening of a pre-existing medical condition which does not necessarily have a causal relationship with this treatment. AEs of special interest are those AEs that may be associated with the use of immunomodulatory drugs, including all infections, serious infections, autoimmune disorders; malignancies; and acute infusional AEs (pre-specified AEs occurring within 1 hour of start of infusion).

    Measured: From Baseline (Day 1) through Day 197, and up to 56 days after last dose if occurring on-study

  14. DB; Number of Participants With Death, Serious Adverse Events (SAEs), Related SAEs, SAEs Leading to Discontinuation, AEs, Related AEs, and AEs Leading to Discontinuation From Day 1 Through Day 365

    AE=any new untoward medical occurrence or worsening of a pre-existing medical condition which does not necessarily have a causal relationship with this treatment. SAE=any untoward medical occurrence that at any dose: results in death, is life-threatening, requires inpatient hospitalization or causes prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect, results in development of drug dependency or drug abuse, is an important medical event.

    Measured: From Baseline (Day 1) through Day 365, and up to 56 days after last dose if occurring on-study

  15. DB; Number of Participants With Death, Serious Adverse Events (SAEs), Related SAEs, SAEs Leading to Discontinuation, AEs, Related AEs, and AEs Leading to Discontinuation From Day 198 Through Day 365 in Participants Receiving Placebo Switched to Abatacept

    AE=any new untoward medical occurrence or worsening of a pre-existing medical condition which does not necessarily have a causal relationship with this treatment. SAE=any untoward medical occurrence that at any dose: results in death, is life-threatening, requires inpatient hospitalization or causes prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect, results in development of drug dependency or drug abuse, is an important medical event.

    Measured: From Day 198 through Day 365, and up to 56 days after last dose if occurring on-study

  16. DB; Number of Participants With AEs of Special Interest From Day 1 Through Day 365

    AE=any new untoward medical occurrence or worsening of a pre-existing medical condition which does not necessarily have a causal relationship with this treatment. AEs of special interest are those AEs that may be associated with the use of immunomodulatory drugs, including all infections, serious infections, autoimmune disorders; malignancies; and acute infusional AEs (pre-specified AEs occurring within 1 hour of start of infusion).

    Measured: From Baseline (Day 1) through Day 365, and up to 56 days after last dose if occurring on-study

  17. DB; Number of Participants With AEs of Special Interest From Day 198 Through Day 365 in Participants Receiving Placebo Switched to Abatacept

    AE=any new untoward medical occurrence or worsening of a pre-existing medical condition which does not necessarily have a causal relationship with this treatment. AEs of special interest are those AEs that may be associated with the use of immunomodulatory drugs, including all infections, serious infections, autoimmune disorders; malignancies; and acute infusional AEs (pre-specified AEs occurring within 1 hour of start of infusion).

    Measured: From Day 198 through Day 365, and up to 56 days after last dose if occurring on-study

  18. DB; Number of Participants With Significant Changes in Mean Systolic and Diastolic Blood Pressure During Days 1 Through 197 and Days 1 Through 365

    Seated Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP) were assessed as clinically significant or relevant at the discretion of the Clinical Investigator. Criteria may have varied between institutions.

    Measured: From Baseline (Day 1) through Day 197, or Day 1 through Day 365, and up to 56 days after last dose if occurring on-study

  19. DB; Number of Participants With Significant Changes in Mean Heart Rate During Days 1 Through 197 and Days 1 Through 365

    Heart Rate (HR) was assessed as clinically significant or relevant at the discretion of the Clinical Investigator. Criteria may have varied between institutions.

    Measured: From Baseline (Day 1) through Day 197, or Day 1 through Day 365, and up to 56 days after last dose if occurring on-study

  20. DB; Number of Participants With Significant Changes in Mean Temperature During Days 1 Through 197 and Days 1 Through 365

    Temperature (T) was assessed as clinically significant or relevant at the discretion of the Clinical Investigator. Criteria may have varied between institutions.

    Measured: From Baseline (Day 1) through Day 197, and up to 56 days after last dose if occurring on-study

  21. DB; Number of Participants With Select Hematologic and Blood Chemistry Laboratory Abnormalities on Days 1 Through 197

    High=greater than Upper Normal Limit (ULN), Low=lower than Lower Normal Limit (LLN). LLN/ULN= Hemoglobin (HGB): >3 g/dL decrease from Baseline (BL); Hematocrit: <0.75 x BL; Platelets (PLT): <0.67 x LLN/>1.5 x ULN; Leukocytes: <0.75 x LLN/ >1.25 x ULN; neutrophils+bands: <1.0 x 10^3 c/uL; aspartate aminotransferase (AST): >3 x ULN; alanine aminotransferase (ALT): >3 x ULN; creatinine: >4 x BL

    Measured: From Baseline (Day 1) through Day 197, and up to 56 days after last dose if occurring on-study

  22. DB; Number of Participants With Select Hematologic and Blood Chemistry Laboratory Abnormalities on Days 1 Through 365

    High=greater than Upper Normal Limit (ULN), Low=lower than Lower Normal Limit (LLN). LLN/ULN= Hemoglobin (HGB): >3 g/dL decrease from Baseline (BL); Hematocrit: <0.75 x BL; Platelets (PLT): <0.67 x LLN/>1.5 x ULN; Leukocytes: <0.75 x LLN/ >1.25 x ULN; neutrophils+bands: <1.0 x 10^3 c/uL; aspartate aminotransferase (AST): >3 x ULN; alanine aminotransferase (ALT): >3 x ULN; creatinine: >4 x BL

    Measured: From Baseline (Day 1) through Day 365, and up to 56 days after last dose if occurring on-study

  23. DB; Number of Participants With Anti-Abatacept Antibodies From Day 1 Through Day 365 (Electrochemiluminescent [ECL] Immunoassay)

    ECL screened sera for drug-specific antibodies, immunocompetition was used to identify specific anti-Abatacept reactivity. Cytotoxic leukocyte antigen 4 (CTLA4) and Possibly Immunoglobulin (Ig) Category=reactivity against extracellular domain of human CTLA4, constant regions of human IgG1, or both (CTLA4Ig; Abatacept molecule). Ig and/or Junction Category=reactivity against constant regions and/or hinge region of human IgG1. Drug-induced seropositivity was defined as a post-baseline titer higher than Baseline, or any post-baseline positivity if Baseline value was missing.

    Measured: Day 1 through day 365

  24. DB; Percentage of Participants With Antibodies Against Infliximab (Human Anti-chimeric Antibody [HACA]) From Day 1 Through Day 365

    Infliximab levels were measured using a microplate enzyme-linked immunosorbant assay (ELISA) with infliximab bound to immobilized recombinant tumor necrosis factor (TNF)-alpha. Bound infliximab is detected utilizing a horseradish peroxidase-conjugated anti-human IgG Fc(fragment, crystallizable region)-specific). The enzyme turns over the substrate O-phenlenediamine to a chromogenic product that is measured at 490 nm. The cut-off value was 1.40 ug/mL; this was based on the mean (+ 3 SD) value in serum samples from 40 participants who had never received infliximab.

    Measured: Day 1 through day 365

  25. OL; Mean Change From Baseline Over Time in DAS 28 (ESR) Score

    The DAS28 is a continuous disease measure which is a composite of 4 variables: the 28 tender joint count, the 28 swollen joint count, ESR or CRP, and participant assessment of disease activity measure on a visual analogue scale. The DAS28 has numeric thresholds that define high disease activity (> 5.1), low disease activity (< 3.2) and remission (< 2.6). A clinically significant response is a decrease in DAS28 score of >1.2 from baseline.

    Measured: Baseline (Day 1), Day 365, Day 533, Day 729

  26. OL; Percentage of Participants With DAS28 (ESR) Remission and Low Disease Activity (LDAS) Over Time

    The DAS28 is a continuous disease measure which is a composite of 4 variables: the 28 tender joint count, the 28 swollen joint count, ESR or CRP, and participant assessment of disease activity measure on a visual analogue scale. The DAS28 has numeric thresholds that define high disease activity (> 5.1), low disease activity (< 3.2) and remission (< 2.6). A clinically significant response is a decrease in DAS28 score of >1.2 from baseline.

    Measured: Baseline (Day 1), Day 365, Day 533, Day 729

  27. OL; Percentage of Participants With Good, Moderate, or No Response According to European League Against Rheumatism (EULAR) Over Time

    The DAS28 is a continuous disease measure composite of 4 variables: 28 tender joint count, 28 swollen joint count, ESR or CRP, and participant assessment of disease activity measure on a visual analogue scale. High disease activity= > 5.1, low disease activity= < 3.2, and remission= < 2.6. Clinically significant response= decrease of >1.2 from baseline. Utilizing EULAR response criteria, DAS28 categorical responses define a good (absolute <3.2 or >1.2 improvement from baseline [BL]), moderate (absolute 3.2-5.1 or 0.6-1.2 change from BL), or no response (absolute >5.1 or <0.6 change from BL)

    Measured: DB Days 365, 533, and 729

  28. OL; Percentage of Participants With American College of Rheumatology (ACR) Responses Over Time

    The ACR 20 definition of improvement is a 20% improvement from baseline in the number of tender and swollen joint counts, and a 20% improvement from baseline in 3 of the remaining 5 core set measures: participant global assessment of pain, participant global assessment of disease activity, physician global assessment of disease activity, participant assessment of physical function and acute phase reactant value (C-reactive protein [CRP]). The evaluation for 50% improvement (ACR 50) and 70% improvement (ACR 70) follow similarly.

    Measured: DB Day 197, Day 365, Day 533, Day 729

  29. OL; Percentage of Participants Who Achieved Major Clinical Response

    Major Clinical Response was defined as a continuous ACR 70 for six months.

    Measured: Defined from the date of achieving ACR 70 response to 6 months post response

  30. OL; Percentage of Participants With Clinically Meaningful Health Assessment Questionnaire-Disability Index (HAQ-DI) Response Over Time

    The disability section of the full HAQ includes 20 questions to assess physical functions in 8 domains: dressing, arising, eating, walking, hygiene, reach, grip and common activities. The questions are evaluated on a 4-point scale: 0=without any difficulty, 1= with some difficulty, 2= with much difficulty, and 3= unable to do. Higher scores= greater dysfunction. A disability index was calculated by summing the worst scores in each domain and dividing by the number of domains answered. Clinically meaningful HAQ response=an improvement of at least 0.3 units from baseline in HAQ disability Index.

    Measured: OL Days 197, 253, 281, 309, 337, 365, 449, 533, 617, and 729

  31. OL; Adjusted Mean Change From Baseline to Day 729 in HAQ-DI

    The disability section of the full HAQ includes 20 questions to assess physical functions in 8 domains: dressing, arising, eating, walking, hygiene, reach, grip and common activities. The questions are evaluated on a 4-point scale: 0=without any difficulty, 1= with some difficulty, 2= with much difficulty, and 3= unable to do. Higher scores= greater dysfunction. A disability index was calculated by summing the worst scores in each domain and dividing by the number of domains answered. Clinically meaningful HAQ response=an improvement of at least 0.3 units from baseline in HAQ disability Index.

    Measured: Day 1 (Baseline), Day 729

Timeline

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

  1. First posted2 Nov 2004 (estimated)
  2. Study startFeb 2005
  3. Primary completionJul 2009
  4. Study completionJul 2009

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
431 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00095147
Sponsor's protocol ID
IM101-043
Status last verified
Mar 2015
First submitted
1 Nov 2004
Last updated
24 Mar 2015

Publications

  • Schiff M, Keiserman M, Codding C, Songcharoen S, Berman A, Nayiager S, Saldate C, Li T, Aranda R, Becker JC, Lin C, Cornet PL, Dougados M. Efficacy and safety of abatacept or infliximab vs placebo in ATTEST: a phase III, multi-centre, randomised, double-blind, placebo-controlled study in patients with rheumatoid arthritis and an inadequate response to methotrexate. Ann Rheum Dis. 2008 Aug;67(8):1096-103. doi: 10.1136/ard.2007.080002. Epub 2007 Nov 29.

    PubMed 18055472

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Abatacept (ABA) + Methotrexate (MTX), double-blind (DB), Infliximab (INF) + MTX, DB and PLA + MTX switched to ABA+ MTX, DB in people with Rheumatoid Arthritis, run by Bristol-Myers Squibb at 76 sites in 17 countries.

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

Who may be eligible to take part?

The sponsor lists 4 inclusion and 6 exclusion criteria. 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 24 Mar 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 76 sites in United States, Canada, Australia, Mexico, Argentina and 12 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 21 Jan 2011). 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?

DB; Adjusted Mean Change From Baseline to Day 197 in Disease Activity Score (DAS) 28 Score (Erythrocyte Sedimentation Rate [ESR]) For ABA Versus PLA (Last Observation Carried Forward [LOCF] Analysis) (time frame: Baseline (Day 1), 6 months (Day 197)). The study lists 40 primary outcomes in all. 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 NCT00095147, which also lists 1 linked publication.

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 24 Mar 2015.

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