Orencia (abatacept) is a soluble fusion protein, which links the extracellular domain of human cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) to the modified Fc (hinge, CH2, and CH3 domains) portion of human immunoglobulin G1 (IgG1). It is produced through recombinant DNA technology in mammalian cells. The drug has activity as a selective costimulation modulator with inhibitory activity on T lymphocytes.
Orencia is specifically indicated for the second line reduction of the signs and symptoms of moderate-to-severe active rheumatoid arthritis, inducing inducing major clinical response, slowing the progression of structural damage, and improving physical function in adult patients who have had an inadequate response to one or more disease-modifying anti-rheumatic drugs (DMARDs), such as methotrexate or TNF antagonists. It is indicated both as a monotherapy and for use in combination with a continued regimen of DMARDs (not including TNF antagonists).
Orencia is supplied as a lyophilized powder for intravenous infusion in an individually packaged, single-use vial with a silicone-free disposable syringe. Recommended dosage is depended on body weight:
Treatment was to be administered via 30-minute infusion. The second dose should be administered 2 to 4 weeks after the first, then every 4 weeks thereafter.
Approval of Orencia was supported by five randomized, double-blind, placebo-controlled clinical trials. In all five studies, subjects received treatments with Orencia or placebo at weeks 0, 2, and 4, then every 4 weeks thereafter.
The first trial enrolled 122 patients with active rheumatoid arthritis who had failed at least one regimen of etanercept or a non-biologic DMARD. Subjects received one of three doses of Orencia monotherapy (0.5 mg/kg, 2 mg/kg, or 10 mg/kg) or placebo for 8 weeks. Trial data increased the portion of subjects achieving 20%, 50% and 70% reductions in American College of Rheumatology (ACR) symptom severity scores in the 10 mg/kg dosing group (n=32 subjects) at 3 months, compared to the placebo group (n=32 subjects):
This trial enrolled patients who had demonstrated an inadequate response to methotrexate monotherapy (MTX). Subjects received one of two doses of Orencia (2 mg/kg or 10 mg/kg) or placebo in additioned to maintained treatment with MTX for 12 months. Results indicated that the addition of Orencia to MTX produced a significant improvement from baseline on the Health Assessment Questionaire Disability Index (HAQ-DI) at 1 year, compared to MTX plus placebo (plus 0.40 points for Orencia, vs. 0.15 points for placebo; p<0.001). Further, Orencia improved quality of life scores on the Physical Component Summary (PCS) diagnostic scale, Mental Compnent Summary (MCS) diagnostic scale, and all 8 domains of the SF-36 diagnostic questionnaire at 6 and 12 months.
This trial, like Study II, enrolled patients who had failed MTX therapy. 638 patients received Orencia or placebo (dose based on body weight; see General Information, above) for 12 months, in additioned to maintained treatment with MTX. Trial data yielded significant improvements (p<0.001 for all values) in ACR 20, ACR 50, and ACR 70 rates at 3, 6 and 12 months, and in rates of Major Clinical Response (ACR 70 maintained continuously for 6 months):
Orencia also significantly improved a number of secondary measures at 6 months, including number of tender joints, number of swollen joints, pain, HAQ-DI, patient global assessment, physician global assessment, C-reactive protein levels (p<0.001 for all endpoints) and radiographic structural joint health scores (p<0.03 for three radiographic endpoints).
This trial enrolled patients who had failed to respond well on a treatment regimen with a TNF antagonist. 489 patients received Orencia or placebo (dose based on body weight; see General Information, above) for 6 months; TNF-antagonist treatment was discontinued prior to treatment with Orencia, but continued treatment with other DMARDs was allowed to continue. Trial data yielded significant improvements in ACR 20, ACR 50, and ACR 70 rates at 3 and 6 months:
Orencia also significantly improved a number of secondary measures at 6 months, including number of tender joints, number of swollen joints, HAQ-DI, patient global assessment, physician global assessment, C-reactive protein levels (p<0.001 for all endpoints) and pain (p<0.01).
Study V was designed to investigate the safety of Orencia therapy in a number of clinically relevant circumstances, including treatment in combination with other approved DMARDs and in patients with comorbid contditions. Patients received Orencia or placebo (dose based on body weight; see General Information, above) for 12 months, in addition to maintained therapy. The drug produced HAQ-DI response similar to that observed in Studies II and III. Exacerbations of respiratory symptoms was noted in patients with comorbid COPD (see Side Effects section below).
Ongoing Study Commitments
Adverse events associated with the use of Orencia may include, but are not limited to, the following:
Administration of Orencia in patients with chronic obstructive pulmonary disorder (COPD) has associated with exacerbation and increased incidence of COPD symptoms. Patients suffering from both rheumatoid arthritis and COPD who elect to pursue Orencia therapy should monitor symptoms carefully, and in collaboration with their physicians.
In addition, Orencia has demonstrated or is predicted to demonstrate negative interactions with other classes of drugs. First, clinical data indicate that concomitant use of TNF antagonists does yield a significant enhancement of efficacy compared to either drug alone, and is associated with increased rates of infection (68%) and serious infection (4.4%), compared to TNF antagonists alone (43% and 0.8%, respectively). As such, concomitant use of Orencia and TNF antagonists is not recommended, and patients should be monitored for signs of infection when transitioning from one drug to the other. Further, based on Orencia's mechanism of action, it is predicted that the efficacy of vaccinations may be reduced while receiving the drug. Data are not available reagarding secondary transmission of infection in patients receiving live vaccines while on Orencia therapy. It is recommended that patients not receive live vaccines while on Orencia therapy or within 3 months of its discontinuation.
Orencia is a selective costimulation modulator, shown to inhibit Tcell (T lymphocyte) activation by binding to CD80 and CD86, thereby blocking interaction with CD28. Blockade of this interaction has been shown to inhibit the autoimmune T-Cell activation that has been implcated in the pathogenesis of rheumatoid arthritis.
For additional information regarding Orencia or rheumatoid arthritis, please visit the Orencia web page.
The Orencia (abatacept) drug information shown above is licensed from Thomson CenterWatch. The information provided here is for general educational purposes only and does not constitute medical or pharmaceutical advice which should be sought from qualified medical and pharmaceutical advisers.