A study to evaluate efficacy, tolerability and safety of Adalimumab (Zydus) and Adalimumab (Reference) in patients with Rheumatoid Arthritis.â??
- Conditions
- Health Condition 1: M069- Rheumatoid arthritis, unspecifiedHealth Condition 2: null- Rheumatoid arthritis.
- Registration Number
- CTRI/2013/10/004040
- Lead Sponsor
- Cadila Healthcare Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 120
1.Adults subjects of either gender in age group of >= 18 year and <=65 years.
2.History of rheumatoid arthritis, as defined by the American College of Rheumatology (ACR) Classification1, for atleast 6 months.
3.Moderate to severe active seropositive disease.
4.History of treatment with Methotrexate (MTX) 10-25mg per week for atleast 12 weeks with last 4 weeks at the stable dose before screening.
5.If female and of childbearing potential, she shall have a negative pregnancy test at the time of screening and agrees to use adequate contraception throughout the study period.
6.Able and willing to give written informed consent and comply with the requirements of the study protocol.
1.Patients with significant systemic manifestations of RA.
2.Female nursing patients.
3.Rheumatic autoimmune disease other than RA.
4.History of diagnosis of juvenile idiopathic arthritis (JIA) (also known as juvenile rheumatoid arthritis [JRA]) and/or RA before age 16.
5.History of inflammatory arthritis other than RA (e.g., inflammatory bowel disease (IBD), systemic lupus erythematosus (SLE), or psoriatic arthritis).
6.Any surgical procedure, including bone/joint surgery or planned surgery within 8 weeks prior to screening or during the study period.
7.Functional Class IV as defined by the American College of Rheumatology (ACR) classification of functional status in RA2.
8.History of use of disease-modifying anti-rheumatic drugs (DMARDs) other than MTX within 4 weeks prior to randomization (8 weeks prior for leflunomide).
9.Treatment with any investigational agent within 4 weeks of screening or 5 half-lives of the investigational drug (whichever is longer).
10.Preceding treatment with any tumor necrosis factor (TNF) antagonist, including adalimumab.
11.Use of intra-articular or parenteral corticosteroids within 4 weeks prior to screening visit. Inhaled corticosteroids for stable medical conditions are allowed.
12.Receipt of a vaccine within 4 weeks prior to enrolment visit.
13.History of severe allergic or anaphylactic reactions to latex
14.History of primary or secondary immunodeficiency.
15.Evidence of significant uncontrolled concomitant diseases such as cardiovascular disease, nervous system, renal, hepatic, endocrine, gastrointestinal, or pulmonary disease, including any pulmonary or other condition that would preclude subject participation.
16.Known active bacterial, viral, fungal, mycobacterial, or other infection (including tuberculosis or atypical mycobacterial disease, but excluding fungal infections of nail beds).
17.History of travel to areas endemic for mycoses, such as histoplasmosis, coccidioidomycosis or blastomycosis.
18.History of recurrent significant infection or any significant episode of infection requiring hospitalization or treatment with IV antibiotics within 4 weeks of screening or oral antibiotics within 2 weeks prior to screening.
19.History of cancer, including solid tumors and hematologic malignancies (except basal cell and squamous cell carcinoma of the skin that have been excised and cured).
20.Lack of peripheral venous access.
21.History of chronic daily use of narcotic analgesics.
22.History of alcohol, drug, or chemical abuse within 6 months prior to screening.
23.Positive Hepatitis B surface antigen or antibodies to Hepatitis C.
24.History of significant cytopenias or other bone marrow disorders.
25.Laboratory Exclusion Criteria: Patients may not participate in this study until any of the following that are present have resolved.
a.Serum creatinine > 1.4 mg/dL for women or 1.6 mg/dL for men.
b.AST or ALT > 2.5 times upper limit of normal (UNL).
c.Platelet count < 100,000/µL.
d.Hemoglobin < 8.0 g/dL.
e.Neutrophil < 1.5 � 103/µL.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method