Full Text View
Tabular View
Study Results
Related Studies
A Phase III Study of Abatacept (BMS-188667) in Patients With Active Rheumatoid Arthritis and Inadequate Response to Methotrexate
This study has been completed.
Study NCT00048568   Information provided by Bristol-Myers Squibb

First Received on November 2, 2002.   Last Updated on October 26, 2011   History of Changes
Results First Received: March 28, 2011  
Study Type: Interventional
Study Design: Allocation: Randomized;   Endpoint Classification: Safety/Efficacy Study;   Intervention Model: Parallel Assignment;   Masking: Double Blind (Subject, Investigator);   Primary Purpose: Treatment
Condition: Rheumatoid Arthritis
Interventions: Drug: Abatacept
Drug: Methotrexate
Drug: Placebo

  Participant Flow
  Hide Participant Flow

Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
Participants in this evaluation were enrolled 116 sites worldwide: 31 sites in the United States; 32 sites in Europe, 13 sites in Canada; 4 sites in Australia; 7 sites in Argentina; 7 sites in Brazil; 7 sites in Mexico; 3 sites in Peru; 5 sites in South Africa; 3 sites in Taiwan; and 4 sites in Turkey.

Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
Of 1250 participants enrolled, 594 participants were not randomized (519 no longer met study criteria, 37 for unknown reasons, 33 withdrew consent, 3 lost to follow-up, 1 administrative reason by sponsor, and 1 adverse event). Four participants (2 per group) were randomized but never treated; 2 no longer met study criteria and 2 withdrew consent.

Reporting Groups
  Description
Abatacept (ABA) + Methotrexate (MTX) DB Abatacept was dosed intravenously by weight with participants weighing < 60 kg received 500 mg, participants weighing 60 kg to 100 kg received 750 mg, and participants weighing > 100 kg received 1 gram. Study medication was administered on Days 1, 15, 29, and every 28 days thereafter for a total of 14 doses. Each dose was infused intravenously over approximately 30 minutes on Days 1, 15, 29, 57, 85, 113, 141, 169, 197, 225, 253, 281, 309, and 337. Participants also received MTX at a minimum dose of (10-30 mg/wk), although doses of < 10 mg/wk were acceptable if due to toxicity.
MTX + Placebo DB Control group receiving MTX treatment in combination with placebo. Participants received MTX at a minimum dose of (10-30 mg/wk), although doses of < 10 mg/wk were acceptable if due to toxicity. Placebo was administered IV on Days 1, 15, 29, 57, 85, 113, 141, 169, 197, 225, 253, 281, 309, and 337.
ABA + MTX [Open-label (OL)] Abatacept was dosed intravenously by weight at 10 mg/kg in the OL period under tiered dosing such that participants weighing < 60 kg received abatacept 500 mg; participants ≥ 60 kg and ≤ 100 kg received abatacept 750 mg; and participants > 100 kg received abatacept 1 g. MTX was continued at the dose used in the DB period.

Participant Flow for 3 periods

Period 1:   Double-Blind Period Days 1 to 169
    Abatacept (ABA) + Methotrexate (MTX) DB     MTX + Placebo DB     ABA + MTX [Open-label (OL)]  
STARTED     433     219     0  
COMPLETED     401     174     0  
NOT COMPLETED     32     45     0  
Adverse Event                 11                 3                 0  
Lack of Efficacy                 11                 33                 0  
Lost to Follow-up                 1                 1                 0  
Withdrawal by Subject                 7                 4                 0  
Unknown Reasons                 2                 4                 0  

Period 2:   Double-Blind Period Days 170 to 365
    Abatacept (ABA) + Methotrexate (MTX) DB     MTX + Placebo DB     ABA + MTX [Open-label (OL)]  
STARTED     401     174     0  
COMPLETED     385     162     0  
NOT COMPLETED     16     12     0  
Death                 1                 1                 0  
Adverse Event                 7                 1                 0  
Lack of Efficacy                 2                 7                 0  
Withdrawal by Subject                 3                 1                 0  
Poor/Non-Compliance                 0                 1                 0  
Pregnancy                 2                 0                 0  
No Longer Met Study Criteria                 1                 1                 0  

Period 3:   Open-Label Period
    Abatacept (ABA) + Methotrexate (MTX) DB     MTX + Placebo DB     ABA + MTX [Open-label (OL)]  
STARTED     0     0     539  
COMPLETED     0     0     379  
NOT COMPLETED     0     0     160  
Death                 0                 0                 13  
Adverse Event                 0                 0                 49  
Lack of Efficacy                 0                 0                 32  
Withdrawal by Subject                 0                 0                 26  
Pregnancy                 0                 0                 5  
No Longer Met Study Criteria                 0                 0                 2  
Administrative Decision By Sponsor                 0                 0                 1  
Unknown Reasons                 0                 0                 25  
Lost to Follow-up                 0                 0                 7  



  Baseline Characteristics
  Hide Baseline Characteristics

Reporting Groups
  Description
ABA + MTX DB Abatacept was dosed by weight with participants weighing < 60 kg received 500 mg, participants weighing 60 kg to 100 kg received 750 mg, and participants weighing > 100 kg received 1 gram. Study medication was administered on Days 1, 15, 29, and every 28 days thereafter for a total of 14 doses. Each dose was infused intravenously over approximately 30 minutes on Days 1, 15, 29, 57, 85, 113, 141, 169, 197, 225, 253, 281, 309, and 337. Participants also received MTX at a minimum dose of (10-30 mg/wk), although doses of < 10 mg/wk were acceptable if due to toxicity. Placebo and MTX were administered IV on Days 1, 15, 29, 57, 85, 113, 141, 169, 197, 225, 253, 281, 309, and 337.
MTX + Placebo DB Control group receiving MTX treatment in combination with placebo. Participants received MTX at a minimum dose of (10-30 mg/wk), although doses of < 10 mg/wk were acceptable if due to toxicity. Placebo was administered IV on Days 1, 15, 29, 57, 85, 113, 141, 169, 197, 225, 253, 281, 309, and 337.

Baseline Measures
    ABA + MTX DB     MTX + Placebo DB     Total  
Number of Participants  
[units: participants]
  433     219     652  
Age  
[units: years]
Mean ± Standard Deviation
  51.5  ± 12.9     50.4  ± 12.4     51.1  ± 12.7  
Gender  
[units: participants]
     
Female     96     40     136  
Male     337     179     516  
Race (NIH/OMB)  
[units: Participants]
     
American Indian or Alaska Native     3     1     4  
Asian     18     10     28  
Native Hawaiian or Other Pacific Islander     0     0     0  
Black or African American     10     4     14  
White     379     193     572  
More than one race     0     0     0  
Unknown or Not Reported     23     11     34  
Duration of Rheumatoid Arthritis (RA) Disease [1]
[units: Participants]
     
<= 2 years     99     45     144  
> 2 years to <= 5 years     93     46     139  
> 5 years to <=10 years     106     54     160  
> 10 years     135     74     209  
[1] Number of participants with RA duration <= 2 years, > 2 years to <= 5 years, > 5 years to <= 10 years, and > 10 years as evaluated at baseline.



  Outcome Measures
  Show All Outcome Measures

1.  Primary:   Number of American College of Rheumatology 20 (ACR 20) Responders at Day 169   [ Time Frame: Day 169 ]

2.  Primary:   Number of Participants Achieving Clinically Meaningful Improvement in Health Assessment Questionnaire (HAQ) at Day 365   [ Time Frame: Day 365 ]

3.  Primary:   Baseline and Mean Change From Baseline (BL) in Radiographic Erosion Score Results at Day 365   [ Time Frame: BL (Day 0), Day 365 ]

4.  Primary:   Participants With Deaths, Adverse Events (AEs) and SAEs in the Open-Label (OL) Period   [ Time Frame: Day 365 to Day 2,185 ]

5.  Primary:   Participants With Hematology Values Meeting the Marked Abnormality Criteria in the OL Period   [ Time Frame: Day 365 to Day 2,185 ]

6.  Primary:   Participants With Liver and Kidney Function Values Meeting the Marked Abnormality Criteria in the OL Period   [ Time Frame: Day 365 to Day 2,185 ]

7.  Primary:   Participants With Electrolyte Values Meeting the Marked Abnormality Criteria in the OL Period   [ Time Frame: Day 365 to Day 2,185 ]

8.  Primary:   Participants With Glucose, Protein, Metabolites, and Urinalysis Values Meeting the Marked Abnormality Criteria in the OL Period   [ Time Frame: Day 365 to Day 2,185 ]

9.  Primary:   Mean BL Immunoglobulins Over Time in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093 ]

10.  Primary:   Mean Change From BL in Immunoglobulins in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093 ]

11.  Primary:   Participants With Immunogenicity to Abatacept in the Cumulative DB + OL Period   [ Time Frame: Day 1 to Day 1,821 ]

12.  Primary:   Number of Participants Experiencing Clinically Significant Changes in Vital Signs in the OL Period   [ Time Frame: Day 365 to Day 1,821. All changes in participant vital signs were monitored on each day of study drug administration prior to dosing and 60 minutes after dosing. ]

13.  Primary:   Number of Participants Experiencing AEs of Special Interest in the OL Period   [ Time Frame: Day 365 to Day 2,185 ]

14.  Primary:   Mean BL Hematocrit in the OL Period   [ Time Frame: Baseline (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,905, Day 1,989, Day 2,073, Day 2,185 ]

15.  Primary:   Mean Change From BL in Participant Hematocrit in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,905, Day 1,989, Day 2,073, Day 2,185 ]

16.  Primary:   Mean BL Platelet Count in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,905, Day 1,989, Day 2,073, Day 2,185 ]

17.  Primary:   Mean Change From BL in Participant Platelet Count in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,905, Day 1,989, Day 2,073, Day 2,185 ]

18.  Primary:   Mean BL Hemoglobin, Total Protein, and Albumin in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,905, Day 1,989, Day 2,073, Day 2,185 ]

19.  Primary:   Mean Change From BL in Hemoglobin, Total Protein, and Albumin in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,905, Day 1,989, Day 2,073, Day 2,185 ]

20.  Primary:   Mean BL White Blood Cells in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,905, Day 1,989, Day 2,073, Day 2,185 ]

21.  Primary:   Mean Change From BL in White Blood Cells in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,905, Day 1,989, Day 2,073, Day 2,185 ]

22.  Primary:   Mean BL Liver Function Parameters in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,905, Day 1,989, Day 2,073, Day 2,185 ]

23.  Primary:   Mean Change From BL in Liver Function Parameters in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,905, Day 1,989, Day 2,073, Day 2,185 ]

24.  Primary:   Mean BL Select Laboratory Parameters in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,905, Day 1,989, Day 2,073, Day 2,185 ]

25.  Primary:   Mean Change From BL in Select Laboratory Parameters in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,905, Day 1,989, Day 2,073, Day 2,185 ]

26.  Primary:   Mean BL Serum Electrolytes in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,905, Day 1,989, Day 2,073, Day 2,185 ]

27.  Primary:   Mean Change From BL in Serum Electrolytes in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,905, Day 1,989, Day 2,073, Day 2,185 ]

28.  Secondary:   Mean Number of Tender Joints and Swollen Joints at DB BL   [ Time Frame: BL (Day 0) ]

29.  Secondary:   Mean DB BL Participant Physical Pain Assessment, Participant Global Assessment, and Physician Global Assessment   [ Time Frame: BL (Day 0) ]

30.  Secondary:   BL Rheumatoid Factor (RF) Status for Participants Continuing in the OL Period   [ Time Frame: BL (Day 365) ]

31.  Secondary:   ACR 20 Responders at Day 365   [ Time Frame: Day 365 ]

32.  Secondary:   ACR 20 Responders in the Double-Blind (DB) Period   [ Time Frame: Day 15, Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365 ]

33.  Secondary:   ACR 50 Responders at Day 169   [ Time Frame: Day 169 ]

34.  Secondary:   ACR 50 Responders at Day 365   [ Time Frame: Day 365 ]

35.  Secondary:   ACR 50 Responders in the DB Period   [ Time Frame: Day 15, Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365 ]

36.  Secondary:   ACR 70 Responders at Day 169   [ Time Frame: Day 169 ]

37.  Secondary:   ACR 70 Responders at Day 365   [ Time Frame: Day 365 ]

38.  Secondary:   ACR 70 Responders in the DB Period   [ Time Frame: Day 15, Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365 ]

39.  Secondary:   Number of Participants Achieving Major Clinical Response By Day 365   [ Time Frame: Day 1 to Day 365. Data were collected monthly during the first 6 months and then every other month (with the exception of Day 337) during the second 6 months of the DB period. ]

40.  Secondary:   Mean BL and Disease Activity Score 28 (DAS-28; Erythrocyte Sedimentation Rate [ESR]) at Day 169 and Day 365   [ Time Frame: BL (Day 0), Day 169, Day 365, Day 169, Day 365 ]

41.  Secondary:   Number of Participants With Death, Serious Adverse Events (SAEs), Related SAEs, Discontinuation Due to SAEs, AEs, Related AEs, or Discontinued Due to AEs in the DB Period   [ Time Frame: Day 1 to Day 365 ]

42.  Secondary:   Mean DB BL and Mean Change From BL in Joint Space Narrowing (JSN) and Total Score (TS)   [ Time Frame: BL (Day 0), Day 365 ]

43.  Secondary:   Mean DB BL Physical Component Summary of Health-Related Quality of Life (SF-36)   [ Time Frame: BL (Day 0), Day 169, Day 365 ]

44.  Secondary:   Adjusted Mean Change From BL in the Physical Component Summary of Health-Related Quality of Life (SF-36) in the DB Period   [ Time Frame: BL (Day 0), Day 169, Day 365 ]

45.  Secondary:   Participants in the DB Period Achieving an Extended Major Clinical Response   [ Time Frame: Day 1 to Day 365 ]

46.  Secondary:   Mean BL DAS-28 C-Reactive Protein (CRP) and ESR in the DB Period   [ Time Frame: BL (Day 0), Day 169, Day 365 ]

47.  Secondary:   Adjusted Mean Change From BL in DAS-28 CRP and ESR in the DB Period   [ Time Frame: BL (Day 0), Day 169, Day 365 ]

48.  Secondary:   Mean BL Soluble Interleukin-2 Receptors (sIL2-r) in the DB Period   [ Time Frame: BL (Day 0), Day 169, Day 365 ]

49.  Secondary:   Mean Change From BL in Soluble Interleukin-2 Receptors (sIL2-r) in the DB Period   [ Time Frame: BL (Day 0), Day 169, Day 365 ]

50.  Secondary:   ACR Core Component: Mean Number of Tender Joints at All Post-BL Visits in the DB Period   [ Time Frame: Day 15, Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365 ]

51.  Secondary:   ACR Core Component: Mean Number of Swollen Joints at All Post-BL Visits in the DB Period   [ Time Frame: Day 15, Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365 ]

52.  Secondary:   ACR Core Component: Mean Participant Pain Assessment at All Post-BL Visits in the DB Period   [ Time Frame: Day 15, Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365 ]

53.  Secondary:   ACR Core Component: Mean Participant Physical Function Assessment at All Post-BL Visits in the DB Period   [ Time Frame: Day 15, Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365 ]

54.  Secondary:   ACR Core Component: Mean Participant Global Assessment at All Post-BL Visits in the DB Period   [ Time Frame: Day 15, Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365 ]

55.  Secondary:   ACR Core Component: Mean Physician Global Assessment at All Post-BL Visits in the DB Period   [ Time Frame: Day 15, Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365 ]

56.  Secondary:   ACR Core Component: Mean CRP at All Post-BL Visits in the DB Period   [ Time Frame: Day 15, Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365 ]

57.  Secondary:   Number of Participants Discontinuing in the DB Period   [ Time Frame: Day 1 to Day 169, Day 170 to Day 365 ]

58.  Secondary:   Change From BL in Joint Narrowing Score (JSN), Erosion Score (ES), and Total Score (TS) by Category in the DB Period   [ Time Frame: BL (Day 0), Day 365 ]

59.  Secondary:   Participants Experiencing Clinically Significant Changes in Vital Signs in the DB Period   [ Time Frame: Day 1 to Day 365 ]

60.  Secondary:   Participants Experiencing AEs of Special Interest in the DB Period   [ Time Frame: Day 1 to Day 365 ]

61.  Secondary:   Mean BL Individual Components of the HAQ DI at Day 169 and Day 365   [ Time Frame: BL (Day 0), Day 169, Day 365 ]

62.  Secondary:   Adjusted Mean Change From BL in Individual Components of the HAQ DI at Day 169   [ Time Frame: Day 169 ]

63.  Secondary:   Adjusted Mean Change From BL in Individual Components of the HAQ DI at Day 365   [ Time Frame: Day 365 ]

64.  Secondary:   Number of Participants With Immunogenicity to Abatacept in the DB Period   [ Time Frame: Day 1 to Day 365 ]

65.  Secondary:   Number of New Tender Joints and Number of New Swollen Joints in the DB Period   [ Time Frame: Day 169, Day 365 ]

66.  Secondary:   Number of Participants Experiencing a 100% Reduction in Tender Joints or 100% Reduction in Swollen Joints in the DB Period   [ Time Frame: Day 169, Day 365 ]

67.  Secondary:   Number of Participants With Hematology Laboratories Meeting Marked Abnormality Criteria in the DB Period   [ Time Frame: Day 1 to Day 365 ]

68.  Secondary:   Number of Participants With Liver and Kidney Function Tests Meeting Marked Abnormality Criteria in the DB Period   [ Time Frame: Day 1 to Day 365 ]

69.  Secondary:   Mean BL ESR and CRP Levels in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,989, Day 2,185 ]

70.  Secondary:   Mean Change From BL in ESR in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 1,989, Day 2,185 ]

71.  Secondary:   Participant RF Seroconversion in the OL Period   [ Time Frame: Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821, Day 2,185 ]

72.  Secondary:   Number of ACR 20 Responders in the DB and OL Periods   [ Time Frame: Day 15, Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,083, Day 1,177, Day 1,261, Day 1,345, Day 1,497, Day 1,625, Day 1,821 ]

73.  Secondary:   Number of ACR 50 Responders in the DB and OL Periods   [ Time Frame: Day 15, Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,083, Day 1,177, Day 1,261, Day 1,345, Day 1,497, Day 1,625, Day 1,821 ]

74.  Secondary:   Number of ACR 70 Responders in the DB and OL Periods   [ Time Frame: Day 15, Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,083, Day 1,177, Day 1,261, Day 1,345, Day 1,497, Day 1,625, Day 1,821 ]

75.  Secondary:   Number of Participants Continuing in the OL Period With DAS-28 Remission or Low DAS-28 Activity Over Time   [ Time Frame: Day 15, Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,083, Day 1,177, Day 1,261, Day 1,345, Day 1,497, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

76.  Secondary:   Mean BL DAS-28 CRP Over Time for Participants Continuing in the OL Period   [ Time Frame: BL(Day 0), Day 15, Day 29,Day 57,Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,083, Day 1,177, Day 1,261, Day 1,345, Day 1,497, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

77.  Secondary:   Mean Change From BL in DAS-28 CRP Over Time for Participants Continuing in the OL Period   [ Time Frame: BL(Day 0),Day 15,Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,083, Day 1,177, Day 1,261, Day 1,345, Day 1,497, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

78.  Secondary:   Mean BL DAS-28 ESR Over Time in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,083, Day 1,177, Day 1,261, Day 1,345, Day 1,497, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

79.  Secondary:   Mean Change From BL in DAS-28 ESR Over Time in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,083, Day 1,177, Day 1,261, Day 1,345, Day 1,497, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

80.  Secondary:   Number of Participants Achieving HAQ Response Over Time for Participants Continuing in the OL Period   [ Time Frame: Day 15, Day 29, Day 57, Day 85, Day 113, Day 141, Day 169, Day 225, Day 281, Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,083, Day 1,177, Day 1,261, Day 1,345, Day 1,497, Day 1,625, Day 1,821 ]

81.  Secondary:   BL and Mean Change From BL in Radiographic Erosion, Joint Space Narrowing (JSN), and Total Scores (TS) in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 729, Day 1,093, Day 1,457, Day 1,821 ]

82.  Secondary:   Mean BL Physical Component Summary of the SF-36 by Visit in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 14,57, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

83.  Secondary:   Mean Change From BL by Visit in the Physical Component Summary of the SF-36 in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 14,57, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

84.  Secondary:   Mean BL Mental Component Summary of the SF-36 by Visit in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

85.  Secondary:   Mean Change From BL by Visit in the Mental Component Summary of the SF-36 in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

86.  Secondary:   Mean BL Physical Function Component of the SF-36 by Visit in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

87.  Secondary:   Mean Change From BL by Visit in the Physical Function Component of the SF-36 in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

88.  Secondary:   Mean BL Role-Physical Component of the SF-36 by Visit in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

89.  Secondary:   Mean Change From BL by Visit in the Role-Physical Component of the SF-36 in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

90.  Secondary:   Mean BL Bodily Pain Component of the SF-36 by Visit in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

91.  Secondary:   Mean Change From BL by Visit in the Bodily Pain Component of the SF-36 in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

92.  Secondary:   Mean BL General Health Component of the SF-36 by Visit in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

93.  Secondary:   Mean Change From BL by Visit in the General Health Component of the SF-36 in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

94.  Secondary:   Mean BL Social Functioning Component of the SF-36 by Visit in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

95.  Secondary:   Mean Change From BL by Visit in the Social Functioning Component of the SF-36 in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

96.  Secondary:   Mean BL Role-Emotional Component of the SF-36 by Visit in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

97.  Secondary:   Mean Change From BL by Visit in the Role-Emotional Component of the SF-36 in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

98.  Secondary:   Mean BL Vitality Component of the SF-36 by Visit in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

99.  Secondary:   Mean Change From BL by Visit in the Vitality Component of the SF-36 in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

100.  Secondary:   Mean BL Mental Health Component of the SF-36 by Visit in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

101.  Secondary:   Mean Change From BL by Visit in the Mental Health Component of the SF-36 in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

102.  Secondary:   Mean BL Fatigue in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

103.  Secondary:   Mean Change From BL in Fatigue in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

104.  Secondary:   Mean BL Sleep Quality in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

105.  Secondary:   Mean Change From BL in Sleep Quality in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 617, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457, Day 1,625, Day 1,821, Day 1,989, Day 2,185 ]

106.  Secondary:   Mean BL Limitations on Activities of Daily Living in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457 ]

107.  Secondary:   Mean Change From BL in Limitations on Activities of Daily Living in the OL Period   [ Time Frame: BL (Day 0), Day 365, Day 449, Day 533, Day 729, Day 813, Day 897, Day 981, Day 1,093, Day 1,177, Day 1,261, Day 1,345, Day 1,457 ]

108.  Secondary:   Mean BL Interleukin-6 (IL-6), SIL-2R, and Tumor Necrosis Alpha (TNF-Alpha) in the DB Period   [ Time Frame: BL (Day 0), Day 169, Day 365 ]

109.  Secondary:   Mean Change From BL in Interleukin-6 (IL-6), SIL-2R, and Tumor Necrosis Alpha (TNF-Alpha) in the DB Period   [ Time Frame: BL (Day 0), Day 169, Day 365 ]

110.  Secondary:   Mean Change From BL in RF in the DB Period   [ Time Frame: BL (Day 0), Day 169, Day 365 ]

111.  Secondary:   Mean BL E-Selectin, SICAM-1, and MMP3 in the DB Period   [ Time Frame: BL (Day 0), Day 169, Day 365 ]

112.  Secondary:   Mean Change From BL in E-Selectin, SICAM-1, and MMP3 in the DB Period   [ Time Frame: BL (Day 0), Day 169, Day 365 ]

113.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) for the Day 365 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 365 ]

114.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 365 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 365 ]

115.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) for the Day 449 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 449 ]

116.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 449 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 449 ]

117.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) for the Day 533 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 533 ]

118.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 533 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 533 ]

119.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) of the Day 617 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 617 ]

120.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 617 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 617 ]

121.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) of the Day 729 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 729 ]

122.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 729 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 729 ]

123.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) of the Day 813 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 813 ]

124.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 813 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 813 ]

125.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) of the Day 897 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 897 ]

126.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 897 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 897 ]

127.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) of the Day 981 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 981 ]

128.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 981 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 981 ]

129.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) of the Day 1,093 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,093 ]

130.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 1,093 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,093 ]

131.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) of the Day 1,177 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,177 ]

132.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 1,177 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,177 ]

133.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) of the Day 1,261 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,261 ]

134.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 1,261 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,261 ]

135.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) of the Day 1,345 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,345 ]

136.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 1,345 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,345 ]

137.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) of the Day 1,457 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,457 ]

138.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 1,457 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,457 ]

139.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) of the Day 1,625 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,625 ]

140.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 1,625 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,625 ]

141.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) of the Day 1,821 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,821 ]

142.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 1,821 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,821 ]

143.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) of the Day 1,989 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,989 ]

144.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 1,989 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 1,989 ]

145.  Secondary:   Mean BL HAQ-DI Score and HAQ-DI Individual Component Scores at BL (Day 0) of the Day 2,185 Cohort of Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 2,185 ]

146.  Secondary:   Mean Change From BL in HAQ-DI Score and HAQ-DI Individual Component Scores at Day 2,185 for Participants Continuing in the OL Period   [ Time Frame: BL (Day 0), Day 2,185 ]


  Serious Adverse Events
  Show Serious Adverse Events


  Other Adverse Events
  Show Other Adverse Events


  More Information
  Hide More Information

Certain Agreements:  
Principal Investigators are NOT employed by the organization sponsoring the study.
There IS an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.
The agreement is:
unchecked The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is less than or equal to 60 days. The sponsor cannot require changes to the communication and cannot extend the embargo.
unchecked The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is more than 60 days but less than or equal to 180 days. The sponsor cannot require changes to the communication and cannot extend the embargo.


Limitations and Caveats
Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
No text entered.  


Results Point of Contact:  
Name/Title: BMS Study Director
Organization: Bristol Myers-Squibb
e-mail: clinical.trials@bms.com


Publications of Results:
Publications automatically indexed to this study:

Responsible Party: Bristol-Myers Squibb
ClinicalTrials.gov Identifier: NCT00048568     History of Changes
Other Study ID Numbers: IM101-102
Study First Received: November 2, 2002
Results First Received: March 28, 2011
Last Updated: October 26, 2011
Health Authority: United States: Food and Drug Administration