Kineret®
(anakinra)
Kineret® (anakinra) is a recombinant, nonglycosylated form of the human interleukin-1 receptor antagonist (IL-1Ra). Kineret® differs from native human IL-1Ra in that it has the addition of a single methionine residue at its amino terminus. Kineret® consists of 153 amino acids and has a molecular weight of 17.3 kilodaltons. It is produced by recombinant DNA technology using an E colibacterial expression system.
Kineret® is supplied in single use prefilled glass syringes with 27 gauge needles as a sterile, clear, colorless-to-white, preservative-free solution for daily subcutaneous (SC) administration. Each prefilled glass syringe contains: 0.67 mL (100 mg) of anakinra in a solution (pH 6.5) containing sodium citrate (1.29 mg), sodium chloride (5.48 mg), disodium EDTA (0.12 mg), and polysorbate 80 (0.70 mg) in Water for Injection, USP.
Last updated on RxList: 10/8/2008
Kineret® is indicated for the reduction in signs and symptoms and slowing the progression of structural damage in moderately to severely active rheumatoid arthritis, in patients 18 years of age or older who have failed 1 or more disease modifying antirheumatic drugs (DMARDs). Kineret® can be used alone or in combination with DMARDs other than Tumor Necrosis Factor (TNF) blocking agents (see WARNINGS).
The recommended dose of Kineret® for the treatment of patients with rheumatoid arthritis is 100 mg/day administered daily by subcutaneous injection. Higher doses did not result in a higher response. The dose should be administered at approximately the same time every day.
Physicians should consider a dose of 100 mg of Kineret® administered every other day for RA patients who have severe renal insufficiency or end stage renal disease (defined as creatinine clearance < 30 mL/min, as estimated from serum creatinine levels). See CLINICAL PHARMACOLOGY, Pharmacokinetics: Patients with Renal Impairment.
Instructions on appropriate use should be given by the healthcare provider to the patient or caregiver. Patients or caregivers should not be allowed to administer Kineret® until the patient or caregiver has demonstrated a thorough understanding of procedures and an ability to inject the product. After administration of Kineret®, it is essential to follow the proper procedure for disposal of syringes and needles. See the "Information for Patients" insert for detailed instructions on the handling and injection of Kineret®.
Do not use Kineret® beyond the expiration date shown on the carton. Visually inspect the solution for particulate matter and discoloration before administration. If particulates or discoloration are observed, the prefilled syringe should not be used.
Administer only one dose (the entire contents of one prefilled glass syringe) per day. Discard any unused portions.
Kineret® is supplied in single-use preservative free, prefilled glass syringes with 27 gauge needles. Each prefilled glass syringe contains 0.67 mL (100 mg) of anakinra. Kineret® is dispensed in a 4 x 7 syringe dispensing pack containing 28 syringes (NDC 55513-177-28).
Kineret® should be stored in the refrigerator at 2° to 8° C (36° to 46° F). DO NOT FREEZE OR SHAKE. Protect from light.
This product, its production, and/or its use may be covered by one or more U.S. Patents, including U.S. Patent Nos. 6,599,873 and 5,075,222 as well as other patents or patents pending.
Manufactured by: Amgen Manufacturing Limited, a subsidiary of Amgen Inc, One Amgen Center Drive, Thousand Oaks, CA 91320-1799. Issue Date: 12/15/2006. FDA Rev date: 4/23/2004
Last updated on RxList: 10/8/2008
The most serious adverse reactions were:
The most common adverse reaction with Kineret® is injection-site reactions. These reactions were the most common reason for withdrawing from studies. Because clinical trials are conducted under widely varying and controlled conditions, adverse reaction rates observed in clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not predict the rates observed in a broader patient population in clinical practice.
The data described herein reflect exposure to Kineret® in 3025 patients, including 2124 exposed for at least 6 months and 884 exposed for at least one year. Studies 1 and 4 used the recommended dose of 100 mg per day. The patients studied were representative of the general population of patients with rheumatoid arthritis.
The most common and consistently reported treatment-related adverse event associated with Kineret® is injection-site reaction (ISR). The majority of ISRs were reported as mild. These typically lasted for 14 to 28 days and were characterized by 1 or more of the following: erythema, ecchymosis, inflammation, and pain. In studies 1 and 4, 71% of patients developed an ISR, which was typically reported within the first 4 weeks of therapy. The development of ISRs in patients who had not previously experienced ISRs was uncommon after the first month of therapy.
In studies 1 and 4 combined, the incidence of infection was 39% in the Kineret®-treated patients and 37% in placebo-treated patients during the first 6 months of blinded treatment. The incidence of serious infections in studies 1 and 4 was 2% in Kineret®-treated patients and 1% in patients receiving placebo over 6 months. The incidence of serious infection over 1 year was 3% in Kineret®-treated patients and 2% in patients receiving placebo. These infections consisted primarily of bacterial events such as cellulitis, pneumonia, and bone and joint infections, rather than unusual, opportunistic, fungal, or viral infections. Patients with asthma appeared to be at higher risk of developing serious infections when treated with Kineret® (8 of 177 patients, 4.5%) compared to placebo (0 of 50 patients, 0%). Most patients continued on study drug after the infection resolved.
In open-label extension studies, the overall rate of serious infections was stable over time and comparable to that observed in controlled trials. In clinical studies and postmarketing experience, rare cases of opportunistic infections have been observed and included fungal, mycobacterial and bacterial pathogens. Infections have been noted in all organ systems and have been reported in patients receiving Kineret® alone or in combination with immunosuppressive agents.
In patients who received both Kineret® and etanercept for up to 24 weeks, the incidence of serious infections was 7%. The most common infections consisted of bacterial pneumonia (4 cases) and cellulitis (4 cases). One patient with pulmonary fibrosis and pneumonia died due to respiratory failure.
Among 5300 RA patients treated with Kineret® in clinical trials for a mean of 15 months (approximately 6400 patient years of treatment),8 lymphomas were observed for a rate of 0.12 cases/100 patient years. This is 3.6 fold higher than the rate of lymphomas expected in the general population, based on the National Cancer Institute's Surveillance, Epidemiology and End Results (SEER) database.9 An increased rate of lymphoma, up to several fold, has been reported in the RA population, and may be further increased in patients with more severe disease activity. Thirty-seven malignancies other than lymphoma were observed. Of these, the most common were breast, respiratory system, and digestive system. There were 3 melanomas observed in study 4 and its long-term open-label extension, greater than the 1 expected case. The significance of this finding is not known. While patients with RA, particularly those with highly active disease, may be at a higher risk (up to several fold) for the development of lymphoma, the role of IL-1 blockers in the development of malignancy is not known.
In placebo-controlled studies with Kineret®, treatment was associated with small reductions in the mean values for total white blood count, platelets, and absolute neutrophil count (ANC), and a small increase in the mean eosinophil differential percentage.
In all placebo-controlled studies, 8% of patients receiving Kineret® had decreases in ANC of at least 1 WHO toxicity grade, compared with 2% of placebo patients. Nine Kineret®-treated patients (0.4%) developed neutropenia (ANC < 1 x 109/L). Two percent of patients treated concurrently with Kineret® and etanercept developed neutropenia (ANC < 1 x 109/L). While neutropenic, one patient developed cellulitis which recovered with antibiotic therapy.
In studies 1 and 4, from which data is available for up to 36 months, 49% of patients tested positively at one or more timepoints for anti-anakinra antibodies in a highly sensitive, anakinra-binding biosensor assay. Of the 1615 patients with available data at Week 12 or later, 30 (2%) were seropositive in a cell-based bioassay for antibodies capable of neutralizing the biologic effects of Kineret®. Of the 13 patients with available follow-up data, 5 patients remained positive for neutralizing antibodies at the end of the studies. No correlation between antibody development and adverse events was observed.
Antibody assay results are highly dependent on the sensitivity and specificity of the assays. Additionally, the observed incidence of antibody positivity in an assay may be influenced by several factors, including sample handling, concomitant medications, and underlying disease. For these reasons, comparison of the incidence of antibodies to Kineret® with the incidence of antibodies to other products may be misleading.
Table 4 reflects adverse events in studies 1 and 4, that occurred with a frequency of ≥ 5% in Kineret®-treated patients over a 6-month period.
Table 4: Percent of RA Patients Reporting Adverse Events
(Studies 1 and 4)
| Preferred term | Placebo (n = 733) |
Kineret® 100 mg/day (n = 1565) |
| Injection Site Reaction | 29% | 71% |
| Worsening of RA | 29% | 19% |
| URI | 17% | 14% |
| Headache | 9% | 12% |
| Nausea | 7% | 8% |
| Diarrhea | 5% | 7% |
| Sinusitis | 7% | 7% |
| Arthralgia | 6% | 6% |
| Flu Like Symptoms | 6% | 6% |
| Abdominal Pain | 5% | 5% |
No drug-drug interaction studies in human subjects have been conducted. Toxicologic and toxicokinetic studies in rats did not demonstrate any alterations in the clearance or toxicologic profile of either methotrexate or Kineret® when the two agents were administered together.
TNF Blocking Agents: A higher rate of serious infections has been observed in patients treated with concurrent Kineret® and etanercept therapy than in patients treated with etanercept alone (see also WARNINGS: Use with TNF Blocking Agents). Two percent of patients treated concurrently with Kineret® and etanercept developed neutropenia (ANC < 1 x 109/L). Use of Kineret® in combination with TNF blocking agents is not recommended.
REFERENCES
8. Sharp JT, Young DY, Bluhm GB, et al. How many joints in the hands and wrists should be included in a score of radiologic abnormalities used to assess rheumatoid arthritis? Arthritis Rheum. 1985; 28:1326-1335.
9. National Cancer Institute. Surveillance, Epidemiology, and End Results Database (SEER) Program. SEER Incidence Crude Rates, 11 Registries, 1992-1999.
Last updated on RxList: 10/8/2008
Kineret® HAS BEEN ASSOCIATED WITH AN INCREASED INCIDENCE OF SERIOUS INFECTIONS (2%) VS. PLACEBO ( < 1%). ADMINISTRATION OF Kineret® SHOULD BE DISCONTINUED IF A PATIENT DEVELOPS A SERIOUS INFECTION. TREATMENT WITH Kineret® SHOULD NOT BE INITIATED IN PATIENTS WITH ACTIVE INFECTIONS. THE SAFETY AND EFFICACY OF Kineret® IN IMMUNOSUPPRESSED PATIENTS OR IN PATIENTS WITH CHRONIC INFECTIONS HAVE NOT BEEN EVALUATED.
IN A 24-WEEK STUDY OF CONCURRENT Kineret® AND ETANERCEPT THERAPY, THE RATE OF SERIOUS INFECTIONS IN THE COMBINATION ARM (7%) WAS HIGHER THAN WITH ETANERCEPT ALONE (0%). THE COMBINATION OF Kineret® AND ETANERCEPT DID NOT RESULT IN HIGHER ACR RESPONSE RATES COMPARED TO ETANERCEPT ALONE (see Clinical Studies). USE OF Kineret® IN COMBINATION WITH TNF BLOCKING AGENTS IS NOT RECOMMENDED.
Hypersensitivity reactions associated with Kineret® administration are rare. If a severe hypersensitivity reaction occurs, administration of Kineret® should be discontinued and appropriate therapy initiated. The needle cover of the prefilled syringe contains dry natural rubber (a derivative of latex), which may cause allergic reactions in individuals sensitive to latex.
The impact of treatment with Kineret® on active and/or chronic infections and the development of malignancies is not known (see WARNINGS and ADVERSE REACTIONS: Infections and Malignancies).
In a placebo-controlled clinical trial (n = 126), no difference was detected in anti-tetanus antibody response between the Kineret® and placebo treatment groups when the tetanus/diphtheria toxoids vaccine was administered concurrently with Kineret®. No data are available on the effects of vaccination with other inactivated antigens in patients receiving Kineret®. No data are available on either the effects of live vaccination or the secondary transmission of infection by live vaccines in patients receiving Kineret® (see PRECAUTIONS: Immunosuppression). Therefore, live vaccines should not be given concurrently with Kineret®.
If a physician has determined that a patient can safely and effectively receive Kineret® at home, patients and their caregivers should be instructed on the proper dosage and administration of Kineret®. All patients should be provided with the "Information for Patients" insert. While this "Information for Patients" insert provides information about the product and its use, it is not intended to take the place of regular discussions between the patient and healthcare provider.
Patients should be informed of the signs and symptoms of allergic and other adverse drug reactions and advised of appropriate actions. The patient should be informed that the needle cover on the prefilled syringe contains dry natural rubber (a derivative of latex), which should not be handled by persons sensitive to latex. Patients and their caregivers should be thoroughly instructed in the importance of proper disposal and cautioned against the reuse of needles, syringes, and drug product. A puncture-resistant container for the disposal of used syringes should be available to the patient. The full container should be disposed of according to the directions provided by the healthcare provider.
Patients receiving Kineret® may experience a decrease in neutrophil counts. In the placebo-controlled studies, 8% of patients receiving Kineret® had decreases in neutrophil counts of at least 1 World Health Organization (WHO) toxicity grade compared with 2% in the placebo control group. Nine Kineret®-treated patients (0.4%) experienced neutropenia (ANC < 1 x 109/L). This is discussed in more detail in the ADVERSE REACTIONS: Hematologic Events section. Neutrophil counts should be assessed prior to initiating Kineret® treatment, and while receiving Kineret®, monthly for 3 months, and thereafter quarterly for a period up to 1 year .
Kineret® has not been evaluated for its carcinogenic potential in animals. Using a standard in vivo and in vitro battery of mutagenesis assays, Kineret® did not induce gene mutations in either bacteria or mammalian cells. In rats and rabbits, Kineret® at doses of up to 100-fold greater than the human dose had no adverse effects on male or female fertility.
Reproductive studies have been conducted with Kineret® on rats and rabbits at doses up to 100 times the human dose and have revealed no evidence of impaired fertility or harm to the fetus. There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, Kineret® should be used during pregnancy only if clearly needed.
It is not known whether Kineret® is secreted in human milk. Because many drugs are secreted in human milk, caution should be exercised if Kineret® is administered to nursing women.
Kineret® was studied in a single randomized, blinded multi-center trial in 86 patients with polyarticular course Juvenile Rheumatoid Arthritis (JRA; ages 2-17 years) receiving a dose of 1 mg/kg subcutaneously daily, up to a maximum dose of 100 mg. The 50 patients who achieved a clinical response after a 12-week open-label run-in were randomized to Kineret® (25 patients) or placebo (25 patients), administered daily for an additional 16 weeks. A subset of these patients continued open label treatment with Kineret® for up to 1 year in a companion extension study. An adverse event profile similar to that seen in adult RA patients was observed in these studies. Pediatric use of Kineret® is not recommended because the prefilled syringes do not permit accurate dosing lower than 100 mg and efficacy could not be demonstrated due to low trial enrollment.
A total of 752 patients ≥ 65 years of age, including 163 patients ≥ 75 years of age, were studied in clinical trials. No differences in safety or effectiveness were observed between these patients and younger patients, but greater sensitivity of some older individuals cannot be ruled out. Because there is a higher incidence of infections in the elderly population in general, caution should be used in treating the elderly. This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function.
Last updated on RxList: 10/8/2008
There have been no cases of overdose reported with Kineret® in clinical trials of RA. In sepsis trials no serious toxicities attributed to Kineret® were seen when administered at mean calculated doses of up to 35 times those given patients with RA over a 72-hour treatment period.
Kineret® is contraindicated in patients with known hypersensitivity to E coli-derived proteins, Kineret®, or any components of the product.
Last updated on RxList: 10/8/2008
Kineret® blocks the biologic activity of IL-1 by competitively inhibiting IL-1 binding to the interleukin-1 type I receptor (IL-1RI), which is expressed in a wide variety of tissues and organs.1
IL-1 production is induced in response to inflammatory stimuli and mediates various physiologic responses including inflammatory and immunological responses. IL-1 has a broad range of activities including cartilage degradation by its induction of the rapid loss of proteoglycans, as well as stimulation of bone resorption.2 The levels of the naturally occurring IL-1Ra in synovium and synovial fluid from rheumatoid arthritis (RA) patients are not sufficient to compete with the elevated amount of locally produced IL-1.3,4,5
The absolute bioavailability of Kineret® after a 70 mg SC bolus injection in healthy subjects (n = 11) is 95%. In subjects with RA, maximum plasma concentrations of Kineret® occurred 3 to 7 hours after SC administration of Kineret® at clinically relevant doses (1 to 2 mg/kg; n = 18); the terminal half-life ranged from 4 to 6 hours. In RA patients, no unexpected accumulation of Kineret® was observed after daily SC doses for up to 24 weeks.
The influence of demographic covariates on the pharmacokinetics of Kineret® was studied using population pharmacokinetic analysis encompassing 341 patients receiving daily SC injection of Kineret® at doses of 30, 75, and 150 mg for up to 24 weeks. The estimated Kineret® clearance increased with increasing creatinine clearance and body weight. After adjusting for creatinine clearance and body weight, gender and age were not significant factors for mean plasma clearance.
Patients With Renal Impairment: The mean plasma clearance of Kineret® in subjects with mild (creatinine clearance 50-80 mL/min) and moderate (creatinine clearance 30-49 mL/min) renal insufficiency was reduced by 16% and 50%, respectively. In severe renal insufficiency and end stage renal disease (creatinine clearance < 30 mL/min6), mean plasma clearance declined by 70% and 75%, respectively. Less than 2.5% of the administered dose of Kineret® was removed by hemodialysis or continuous ambulatory peritoneal dialysis. Based on these observations, a dose schedule change should be considered for subjects with severe renal insufficiency or end stage renal disease (see DOSAGE AND ADMINISTRATION).
Patients With Hepatic Dysfunction: No formal studies have been conducted examining the pharmacokinetics of Kineret® administered subcutaneously in rheumatoid arthritis patients with hepatic impairment.
The safety and efficacy of Kineret® have been evaluated in three randomized, double-blind, placebo-controlled trials of 1790 patients ≥ 18 years of age with active rheumatoid arthritis (RA). An additional fourth study was conducted to assess safety. In the efficacy trials, Kineret® was studied in combination with other disease-modifying antirheumatic drugs (DMARDs) other than Tumor Necrosis Factor (TNF) blocking agents (studies 1 and 2) or as a monotherapy (study 3).
Study 1 involved 899 patients with active RA who had been on a stable dose of methotrexate (MTX) (10 to 25 mg/week) for at least 8 weeks.All patients had at least 6 swollen/painful and 9 tender joints and either a C-reactive protein (CRP) of ≥ 1.5 mg/dL or an erythrocyte sedimentation rate (ESR) of ≥ 28 mm/hr. Patients were randomized to Kineret® or placebo in addition to their stable doses of MTX. The first 501 patients were evaluated for signs and symptoms of active RA. The total 899 patients were evaluated for progression of structural damage.
Study 2 evaluated 419 patients with active RA who had received MTX for at least 6 months including a stable dose (15 to 25 mg/week) for at least 3 consecutive months prior to enrollment. Patients were randomized to receive placebo or one of five doses of Kineret® SC daily for 12 to 24 weeks in addition to their stable doses of MTX.
Study 3 evaluated 472 patients with active RA and had similar inclusion criteria to study 1 except that these patients had received no DMARD for the previous 6 weeks or during the study.7 Patients were randomized to receive either Kineret® or placebo. Patients were DMARD-naïve or had failed no more than 3 DMARDs.
Study 4 was a placebo-controlled, randomized trial designed to assess the safety of Kineret® in 1414 patients receiving a variety of concurrent medications for their RA including some DMARD therapies, as well as patients who were DMARD-free. The TNF blocking agents etanercept and infliximab were specifically excluded. Concurrent DMARDs included MTX, sulfasalazine, hydroxychloroquine, gold, penicillamine, leflunomide, and azathioprine. Unlike studies 1, 2 and 3, patients predisposed to infection due to a history of underlying disease such as pneumonia, asthma, controlled diabetes, and chronic obstructive pulmonary disease (COPD) were also enrolled (see ADVERSE REACTIONS: Infections).
In studies 1, 2 and 3, the improvement in signs and symptoms of RA was assessed using the American College of Rheumatology (ACR) response criteria (ACR20, ACR50, ACR70). In these studies, patients treated with Kineret® were more likely to achieve an ACR20 or higher magnitude of response (ACR50 and ACR70) than patients treated with placebo (Table 1). The treatment response rates did not differ based on gender or ethnic group. The results of the ACR component scores in study 1 are shown in Table 2.
Most clinical responses, both in patients receiving placebo and patients receiving Kineret®, occurred within 12 weeks of enrollment.
Table 1: Percent of Patients with ACR Responses in Studies
1 and 3
| Study 1 (Patients on MTX) | Study3 (No DMARDs) | ||||
| Response | Placebo (n = 251) |
Kineret® 100 mg/day (n = 250) |
Placebo (n = 119) |
Kineret® | |
| 75 mg/day (n = 115) |
150 mg/day (n = 115) |
||||
| ACR20 | |||||
| Month 3 | 24% | 34%a | 23% | 33% | 33% |
| Month 6 | 22% | 38%c | 27% | 34% | 43%a |
| ACR50 | |||||
| Month 3 | 6% | 13%b | 5% | 10% | 8% |
| Month 6 | 8% | 17%b | 8% | 11% | 19%a |
| ACR70 | |||||
| Month 3 | 0% | 3%a | 0% | 0% | 0% |
| Month 6 | 2% | 6%a | 1% | 1% | 1% |
| a p < 0.05,Kineret® versus placebo b p < 0.01,Kineret® versus placebo c p < 0.001,Kineret® versus placebo |
|||||
Table 2: Median ACR Component Scores in Study 1
| Placebo/MTX (n =251) |
Kineret®/MTX 100mg/day (n =250) |
|||
| Parameter (median) | Baseline | Month 6 | Baseline | Month 6 |
| Patient Reported Outcomes | ||||
| Disability indexa | 1.38 | 1.13 | 1.38 | 1.00 |
| Patient global assessmentb | 51.0 | 41.0 | 51.0 | 29.0 |
| Painb | 56.0 | 44.0 | 63.0 | 34.0 |
| Objective Measures | ||||
| ESR (mm/hr) | 35.0 | 32.0 | 36.0 | 19.0 |
| CRP (mg/dL) | 2.2 | 1.6 | 2.2 | 0.5 |
| Physician's Assessments | ||||
| Tender/painful jointsc | 20.0 | 11.0 | 23.0 | 9.0 |
| Physician global assessmentb | 59.0 | 31.0 | 59.0 | 26.0 |
| Swollen jointsd | 18.0 | 10.5 | 17.0 | 9.0 |
| a Health Assessment Questionnaire; 0 = best, 3
= worst; includes eight categories: dressing and grooming, arising, eating,
walking, hygiene, reach, grip, and activities. b Visual analog scale; 0 = best, 100 = worst c Scale 0 to 68 d Scale 0 to 66 |
||||
A 24-week study was conducted in 242 patients with active RA on background methotrexate who were randomized to receive either etanercept alone or the combination of Kineret® and etanercept. The ACR50 response rate was 31% for patients treated with the combination of Kineret® and etanercept and 41% for patients treated with etanercept alone, indicating no added clinical benefit of the combination over etanercept alone. Serious infections were increased with the combination compared to etanercept alone (see WARNINGS).
In study 1, the effect of Kineret® on the progression of structural damage was assessed by measuring the change from baseline at month 12 in the Total Modified Sharp Score (TSS) and its subcomponents, erosion score, and joint space narrowing (JSN) score.8 Radiographs of hands/wrists and forefeet were obtained at baseline, 6 months and 12 months and scored by readers who were unaware of treatment group. A difference between placebo and Kineret® for change in TSS, erosion score (ES)and JSN score was observed at 6 months and at 12 months (Table 3).
Table 3: Mean Radiographic Changes Over 12 Months in Study
1
| Placebo/MTX (N =450) |
Kineret® 100 mg/day/MTX (N= 449) |
Placebo/MTX vs. Kineret®/MTX | ||||
| Baseline | Change at Month 12 | Baseline | Change at Month 12 | 95% Confidence Interval* | p-value** | |
| TSS | 52 | 2.6 | 50 | 1.7 | 0.9 [0.3, 1.6] | <0.001 |
| Erosion | 28 | 1.6 | 25 | 1.1 | 0.5 [0.1, 1.0] | 0.024 |
| JSN | 24 | 1.1 | 25 | 0.7 | 0.4 [0.1, 0.7] | <0.001 |
| *Differences and 95% confidence intervals for the differences
in change scores between Placebo/MTX and Kineret®/MTX ** Based on Wilcoxon rank-sum test |
||||||
The disability index of the Health Assessment Questionnaire (HAQ)was administered monthly for the first six months and quarterly thereafter during study 1. Health outcomes were assessed by the Short Form-36 (SF-36) questionnaire. The 1-year data on HAQ in study 1 showed more improvement with Kineret® than placebo. The physical component summary (PCS) score of the SF-36 also showed more improvement with Kineret® than placebo but not the mental component summary (MCS).
REFERENCES
1. Hannum CH, Wilcox CJ, Arend WP, et al. Interleukin-1 receptor antagonist activity of a human interleukin-1 inhibitor. Nature. 1990; 343:336-40.
2. Van Lent PLEM, Fons AJ, Van De Loo AEM, et al, Major role for interleukin 1 but not for tumor necrosis factor in early cartilage damage in immune complex in mice. J Rheumatol. 1995; 22:2250–2258.
3. Deleuran BW, Shu CQ, Field M, et al. Localization of interleukin-1 alpha, type 1 interleukin-1 receptor and interleukin-1 receptor antagonist in the synovial membrane and cartilage/pannus junction in rheumatoid arthritis. Br J Rheumatol. 1992; 31:801-809.
4. Chomarat P, Vannier E, Dechanet J, et al. Balance of IL-1 receptor antagonist/IL-1B in rheumatoid synovium and its regulation by IL-4 and IL-10. J Immunol. 1995; 1432-1439.
5.Firestein GS, Boyle DL, Yu C, et al. Synovial interleukin-1 receptor antagonist and interleukin-1 balance in rheumatoid arthritis. Arthritis Rheum. 1994; 37:644-652.
6. Cockcroft DW and Gault HM. Prediction of creatinine clearance from serum creatinine. Nephron1976; 16:31-41.
7. Bresnihan B, Alvaro-Gracia JM, Cobby M, et al. Treatment of rheumatoid arthritis with recombinant human interleukin-1 receptor antagonist. Arthritis Rheum. 1998; 41:2196-2204.
Last updated on RxList: 10/8/2008
Kineret®
(KIN-eh-ret) (anakinra)
Read the patient information that comes with Kineret® before you start taking it and each time you get a refill. There may be new information. This leaflet does not take the place of talking with your healthcare provider about your medical condition or your treatment.
What is the most important information I should know about Kineret®?
Kineret® is a medicine that affects your immune system. Kineret® can lower the ability of your immune system to fight infections. Serious infections have happened in patients taking Kineret®. Taking Kineret® may give you a higher chance for getting an infection or make any infection you have worse.
Before starting Kineret®, tell your healthcare provider if you:
If you take other medicines that affect the immune system, such as ENBRELR (etanercept), HumiraR (adalimumab), or RemicadeR (infliximab) while you are taking Kineret®, you could also have an increased risk for getting a serious infection. It is recommended that you do not take these medications (Tumor Necrosis Factor or TNF blocking agents) while taking Kineret®.
What is Kineret®?
Kineret® is an interleukin-1 receptor antagonist (IL-1ra). Kineret® is used to reduce the signs and symptoms, and slow down damage that happens in patients with moderate to severe active Rhematoid Arthritis (RA), but it can also lead to serious side effects because of the affects on your immune system. See "What is the most important information I should know about Kineret®?" and "What are the possible side effects with Kineret®?"
Kineret® is only for adults who have taken other medicines for their RA that have not worked. Kineret® can be taken alone or along with other RA medicines except for TNF blocking agents.
Who should not take Kineret®?
Do not take Kineret® if you have an allergy to:
What should I tell my healthcare provider before taking Kineret®?
Kineret® may not be right for you. Tell your healthcare provider about all of your medical conditions, including if you:
Tell your healthcare provider if you are pregnant, plan to become pregnant, or breastfeeding. Kineret® has not been studied in pregnant or nursing women. Kineret® should be used during a pregnancy only if needed. It is not known if Kineret® will pass into your breast milk. Discuss treatment options with your doctor if you plan on breastfeeding.
Tell your healthcare provider about all the medicines you take, including prescription and non-prescription medicines, vitamins, and herbal supplements. Tell your healthcare provider if you take other medicines that affect your immune system.
Know the medicines you take. Keep a list of your medicines and show it to your healthcare provider and pharmacist when you get a new prescription.
How should I take Kineret®?
What are the possible side effects of Kineret®?
Kineret® may cause serious side effects, including:
The most common side effect with Kineret® is injection site reaction. These reactions may include redness, swelling, bruising, itching and stinging. Most injection site reactions are mild and last about 2 to 4 weeks.
Side effects that are rare include:
These are not all of the possible side effects of Kineret®. For more information, ask your healthcare provider or pharmacist.
How should I store Kineret®?
Keep Kineret® and all medicines out of the reach of children.
General Information about Kineret®
Medicines are sometimes prescribed for conditions that are not mentioned in the patient leaflet. Do not use Kineret® for a condition for which it was not prescribed. Do not give Kineret® to other people, even if they have the same symptoms that you have. It may harm them.
This patient information leaflet summarizes the most important information about Kineret®. If you would like more information about Kineret® talk with your healthcare provider. You can ask your healthcare provider or pharmacist for information about Kineret® that is written for health professionals. For more information go to www.kineretrx.com or call 1-866-546-3738.
What are the ingredients in Kineret®?
Active ingredients: anakinra
Inactive ingredients:sodium citrate, sodium chloride, disodium EDTA, and polysorbate 80 in Water for Injection, USP
What do I need to know to prepare and give an injection of Kineret®?
Each Kineret® dose comes in a prefilled glass syringe. There are 7 syringes in each box, one for each day of the week. Use a new syringe each day. Use the Kineret® prefilled syringe that matches the day of the week until all 7 are used.
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Use each Kineret® prefilled syringe only once. Be sure to inject all of the solution in the syringe. If you notice some solution remaining in the syringe, do not re-inject. You should discard the syringe with any remaining solution in the puncture-resistant container. (See "Disposal of Syringes and Supplies").
If you drop a syringe, do not use the syringe. This is for your safety in case the glass syringe is broken, or the needle is bent or dirty. Dispose of the syringe and replace it with a new one. Take the new syringe from what would be the last day of the week in your current box. For example, if you start on Wednesday, the last day of the week in your series is Tuesday. After using all the remaining syringes in your current box, start your next box.
Setting up for an Injection
Selecting and preparing the injection site
1. Choose an injection site. Recommended injection sites include:
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Choose a new site each time you use Kineret®. Choosing a new site can help avoid soreness at any one site. Do not inject Kineret® into an area that is tender, red, bruised, or hard. Avoid areas with scars or stretch marks. Do not inject close to a vein that you can see under the surface of your skin.
2. Clean the injection site with an alcohol swab. Let the area dry completely. Injecting through a site that is still moist from an alcohol swab may cause stinging.
Administering the subcutaneous injection
1. Pick up the prefilled syringe from your flat work surface. Hold the syringe in the hand you will use to inject Kineret®. Remove the needle cover. Twisting the needle cover while pulling will help in the removal. Do not touch the needle or allow it to touch any surface. You may notice a small air bubble in the prefilled syringe. You do not have to remove the air bubble. Injecting the solution with the air bubble is harmless.
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2. With your free hand, gently pinch a fold of skin at the cleaned injection site.
3. Hold the syringe (like a pencil) at a 45 to 90 degree angle to the skin. With a quick, dart-like motion insert the needle into the skin.
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4. After the needle is inserted‚ gently let go of the skin. Pull the plunger back slightly. If no blood appears in the syringe, slowly push the plunger all the way down to inject Kineret®.
If blood comes into the syringe, do not inject Kineret®, because the needle has entered a blood vessel. Withdraw the needle. Dispose of the used prefilled syringe in a puncture-resistant container. Prepare a new injection site and use a new prefilled syringe.
5. When the syringe is empty, pull the needle out of the skin, being careful to keep it at the same angle as inserted.
6. Place a cotton ball or gauze over the injection site and press for several seconds. Do not use an alcohol swab as it may cause stinging. If there is a little bleeding, you may cover the injection site with a small bandage.
Disposal of the syringe and supplies
Last updated on RxList: 10/8/2008
IMPORTANT NOTE: This is a summary and does not contain all possible information about this product. For complete information about this product or your specific health needs, ask your health care professional. Always seek the advice of your health care professional if you have any questions about this product or your medical condition. This information is not intended as individual medical advice and does not substitute for the knowledge and judgment of your health care professional. This information does not contain any assurances that this product is safe, effective, or appropriate for you.
ANAKINRA DISPOSABLE SYRINGE SUBCUTANEOUS - INJECTION
(an-a-KIN-ra)
COMMON BRAND NAME(S): Kineret
USES: This medication is used to treat rheumatoid arthritis that has not improved with other drugs (disease-modifying antirheumatic drugs-DMARDs). Anakinra slows the worsening of rheumatoid arthritis by preventing a certain protein (interleukin-1) from causing more damage. This effect may reduce pain, swelling, and tenderness in your joints, allowing you to do your normal activities.
HOW TO USE: Read the Patient Information Leaflet provided by your pharmacist before you start using anakinra and each time you get a refill. Learn how to prepare and inject this medication. If you have any questions, consult your doctor or pharmacist.
This medication is injected under the skin, usually once daily or as directed by your doctor.
Before using, check the single-use pre-filled glass syringe for any particles or color changes. Use the medication only if it is clear and colorless/white. Do not shake the syringe. Let the syringe warm to room temperature for 60 to 90 minutes before injecting the medicine.
Before injecting each dose, clean the injection site with rubbing alcohol. It is important to change the location of the injection site daily to avoid problem areas under the skin. Learn how to use and discard needles and medical supplies safely. Consult your doctor or pharmacist for details.
Dosage is based on your medical condition and response to treatment.
Use this medication regularly to get the most benefit from it. To help you remember, use it at the same time each day.
Tell your doctor if your condition does not improve or if it worsens after 4 weeks.
Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.
Serious infections (e.g., skin infections, pneumonia, bone/joint infections, sinusitis) may occur. Tell your doctor immediately if any of these signs of infection occur: spreading redness/swelling/tenderness of the skin, fever, chills, cough with mucus, bone pain/soreness, persistent sore throat, pain over cheeks or around eyes.
Tell your doctor immediately if any of these rare but very serious side effects occur: swollen glands (lymph nodes), night sweats, unusual weight loss, persistent itching, lump in breast, nipple discharge.
A very serious allergic reaction to this drug is rare. However, seek immediate medical attention if you notice any symptoms of a serious allergic reaction, including: rash, itching, swelling, severe dizziness, trouble breathing.
This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.
Contact your doctor for medical advice about side effects. The following numbers do not provide medical advice, but in the US you may report side effects to the Food and Drug Administration (FDA) at 1-800-FDA-1088. In Canada, you may call Health Canada at 1-866-234-2345.
PRECAUTIONS: Before using anakinra, tell your doctor or pharmacist if you are allergic to it; or to proteins made from a certain bacteria (E. coli); or to latex; or if you have any other allergies.
This medication should not be used if you have certain medical conditions. Before using this medicine, consult your doctor or pharmacist if you have: current/ongoing infection.
Before using this medication, tell your doctor or pharmacist your medical history, especially of: kidney disease, asthma, immune system problems, cancer.
Do not have immunizations/vaccinations without the consent of your doctor, and avoid contact with people who have recently received oral polio vaccine or flu vaccine inhaled through the nose.
Kidney function declines as you grow older. This medication is removed by the kidneys. Therefore, elderly people may be at greater risk for side effects (e.g., infections) while using this drug.
During pregnancy, this medication should be used only when clearly needed. Discuss the risks and benefits with your doctor.
It is not known whether this drug passes into breast milk. Consult your doctor before breast-feeding.
This drug should not be used with the following products because very serious interactions may occur: abatacept, live vaccines (e.g., polio vaccine taken by mouth, flu vaccine inhaled through the nose, measles/mumps/rubella vaccine), TNF blockers (adalimumab, certolizumab, etanercept, infliximab).
If you have recently received any of these products listed above, tell your doctor or pharmacist before starting anakinra.
Before using this medication, tell your doctor or pharmacist of all prescription and nonprescription/herbal products you may use.
This document does not contain all possible interactions. Therefore, before using this product, tell your doctor or pharmacist of all the products you use. Keep a list of all your medications with you, and share the list with your doctor and pharmacist.
OVERDOSE: If overdose is suspected, contact your local poison control center or emergency room immediately. US residents can call the US National Poison Hotline at 1-800-222-1222. Canada residents can call a provincial poison control center.
NOTES: Do not share this medication with others.
Laboratory and/or medical tests (e.g., white blood cell count) should be performed periodically to monitor your progress or check for side effects. Consult your doctor for more details.
MISSED DOSE: If you miss a dose, use it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.
STORAGE: Store in the refrigerator between 36-46 degrees F (2-8 degrees C) away from light. Do not freeze. Keep all medicines away from children and pets.
Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company for more details about how to safely discard your product.
Information last revised July 2008 Copyright(c) 2008 First DataBank, Inc.
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