Rilonacept for Treatment of Familial Mediterranean Fever (FMF)
Mo kle
Abstrè
Deskripsyon
Familial Mediterranean fever (FMF) is an autosomal recessive autoinflammatory genetic disorder resulting in recurrent attacks of fever, serositis, arthritis and rash. Late complications of untreated FMF include the development of renal amyloidosis. FMF is a rare orphan disease in the United States. Treatment with colchicine is effective in reducing the frequency of episodes in most patients and the development of amyloidosis in nearly all patients. However, there are still 5-15% of patients who continue to have acute FMF attacks despite colchicine therapy or are intolerant of colchicine, usually from gastrointestinal adverse effects. Currently there are no effective alternatives to colchicine. Pyrin, the mutated protein in FMF has an important role in the regulation of IL-1 beta production and activity. Mutations in pyrin result in increased IL-1 beta levels in mice and humans. IL-1 beta is an important pro-inflammatory cytokine. Thus, we hypothesize that inhibition of IL-1 will decrease acute attacks in patients with FMF. We propose to use IL-1 Trap (Rilonacept), a fusion protein consisting of human IL-1 cytokine receptor extracellular domains and the FC portion of human IgG1 that binds and neutralizes IL-1.
We will enroll 17 subjects from the age of 4 years, including adults, from multiple centers in the United States with active FMF (at least 1 attack per month) despite receiving at least 1.2-1.5 mg/d of colchicine (dose dependent on age) or are intolerant of colchicine. Subjects will be diagnosed by clinical criteria with at least one heterozygote mutation of the MEFV (pyrin) gene. After screening subjects will be monitored for a month to observe for acute FMF attacks or if they did not develop an attack in that month until they develop two attacks. We will then use a single-subject alternating treatments design with subjects receiving in random order two 3-month courses of Rilonacept at 2.2 mg/kg (max 160 mg) by weekly SC injection and two 3-month courses of comparable volume placebo. Subjects will continue the usual colchicine dose they were on when they started the study. Subjects with 2 acute FMF attacks during a treatment course will be able to crossover to the other treatment arm until the end of that treatment course. There will be 10 study visits: 1. Screening. 2. Treatment baseline after one month or after subjects have developed FMF attacks as described above. After 1 month of each treatment course and at the end of each treatment course (overall 8 visits). At each visit subjects will return completed diary forms, used and unused drug, queried on adverse effects, undergo a physical examination and laboratory tests obtained for inflammation, safety and in some visits for translational studies. Subjects will also fill out quality of life questionnaires and give an overall estimation of the disease activity. Results will be analyzed by traditional frequency statistics (using an intent to treat analysis) and by Bayesian hierarchical modeling. Our primary aim is to assess the efficacy of Rilonacept in decreasing the number of acute FMF attacks while monitoring drug safety.
The significance of the study includes short and long-term benefits. Fewer FMF attacks will result in less functional impairment and a higher quality of life in colchicine resistant or intolerant patients. Once weekly injections have the potential to improve treatment compliance. Fewer acute attacks of arthritis may prevent the development of chronic joint damage. In the long-term, better FMF control may prevent amyloidosis. This study may confirm the importance of IL-1 in the pathogenesis of FMF and provide support for an FDA filing for use of Rilonacept in FMF. The study design may serve as a template for trials of new biologic drugs for rare diseases.
Dat
| Dènye verifye: | 01/31/2013 |
| Premye Soumèt: | 12/18/2007 |
| Enskripsyon Estimasyon Soumèt: | 12/18/2007 |
| Premye afiche: | 12/27/2007 |
| Dènye Mizajou Soumèt: | 02/04/2013 |
| Dènye Mizajou afiche: | 02/10/2013 |
| Dat premye rezilta yo soumèt: | 08/24/2012 |
| Dat premye rezilta QC yo soumèt: | 10/28/2012 |
| Dat premye rezilta ki afiche yo: | 10/30/2012 |
| Dat aktyèl kòmanse etid la: | 07/31/2008 |
| Dat Estimasyon Prensipal Estimasyon an: | 08/31/2011 |
| Dat estime fini etid la: | 08/31/2011 |
Kondisyon oswa maladi
Entèvansyon / tretman
Drug: 1
Drug: 2
Faz
Gwoup bra
| Bra | Entèvansyon / tretman |
|---|---|
| Experimental: 1 Treatment Arm A: Rilonacept (IL-1 Trap) at a dose of 2.2 mg/kg/wk (max 160 mg)given by subcutaneous injection for 3 months plus colchicine at a stable dose for those subjects already taking colchicine, or without colchicine for those intolerant or non-compliant with colchicine. Since the colchicine dose is stable throughout the study for each subject, at the prestudy dose, colchicine was not considered an intervention | Drug: 1 2.2 mg/kg/wk by subcutaneous injection, for 3 months |
| Placebo Comparator: 2 Treatment Arm B: Placebo given by subcutaneous injection weekly with or without colchicine for 3 months. Since the colchicine dose is stable throughout the study for each subject, at the prestudy dose, colchicine was not considered an intervention. | Drug: 2 placebo by subcutaneous injection weekly for 3 months |
Kritè kalifikasyon yo
| Laj ki kalifye pou etid | 4 Years Pou 4 Years |
| Sèks ki kalifye pou etid | All |
| Aksepte Volontè Healthy | Wi |
| Kritè | Inclusion Criteria: - Subject has a definitive diagnosis of FMF as by the Tel-Hashomer clinical criteria (long version of criteria) with at least one mutation on one of the MEFV gene alleles. However, subjects with an isolated heterozygous mutation of exon 2 of the MEFV gene (including E148Q) will not be eligible. - Subject must have an estimated mean of at least one acute FMF attack per month before and during the month of screening. - Subject is at least four years of age (with no upper limit of age). - Subjects must have received an adequate trial of colchicine defined as treatment of at least 1.5 mg/d for at least 3 months if ≥6 years old or 1.2 mg/d if less than 6 years, or an inability to tolerate colchicine due to adverse effects in a dose that controls acute attacks in the frequency of less than one attack per month. - If subject is being treated with anakinra at the time of consent, washout must be done (about 3 days). Subject must experience 2 attacks before randomization visit can occur. - If subject has been treated previously with anti-TNF drugs, appropriate washout must be done. Etanercept must be discontinued for 4 weeks prior to randomization; Adalimumab and Infliximab must be discontinued for 8 weeks prior to randomization. - If subject is a female of childbearing potential, she must agree to use adequate contraception (adequate contraception can include abstinence) for the duration of the trial and 3 months after and must have a negative serum or urine pregnancy test prior to administration of study medication. - If subject is a male and has reached puberty, he must agree to use adequate contraception or abstinence during the study and for 3 months after discontinuation from study. - Subject's parent or legal guardian has provided written informed consent prior to screening for this study or if subject is older than 18 years has provided informed consent him/herself. - Subject, if applicable, has assented to participate prior to screening for this study. - Subject and, if applicable, parent/legal guardian, agree to comply with study requirements and are able to come to the clinic for all required study visits. Exclusion Criteria: - The subject has existing biopsy proven amyloidosis or proteinuria >0.5 gram per day. - The subject has another active inflammatory rheumatic disease. - The subject has an active malignancy of any type, or history of a malignancy. - The subject has active GI disease (e.g., inflammatory bowel disease), a chronic or acute renal or hepatic disorder, or a significant coagulation defect. - The subject has an AST (SGOT), ALT (SGPT) or BUN >2 x ULN or creatinine >1.5 mg/dL or any other laboratory abnormality considered by the examining physician to be clinically significant within 28 days before the Baseline visit. - Current use of an anti-tumor necrosis factor drug. - The subject has, in the investigator's opinion, a chronic condition (e.g., diabetes, epilepsy) that is either not stable or well-controlled and may interfere with the conduct of the study. - The subject has received any investigational medication within 30 days before the first dose of study medication or is scheduled to receive an investigational drug, other than study medications described in this protocol, during the course of the study. - The subject has chronic or active infection or any major episode of infection requiring hospitalization or treatment with i.v. antibiotics within 30 days or oral antibiotics within 14 days prior to the screening evaluation. - The subject has known positive human immunodeficiency virus (HIV) status. - The subject has known past or current hepatitis. - The subject has received a live virus vaccine within 1 month prior to the baseline visit. - The subject has a positive PPD test. - The subject is sexually active and not practicing effective birth control. - The subject is pregnant or breast feeding a child. - Any concurrent medical condition which would, in the investigator's opinion, compromise the subject's ability to tolerate the study drug or would make the subject unable to cooperate with the protocol. - History of/or current psychiatric illness that would interfere with ability to comply with protocol requirements or give informed consent. - Subject has a history of alcohol or drug abuse within the past 6 months that would interfere with ability to comply with protocol requirements. - Inability to comply with the study requirements for any reason. |
Rezilta
Mezi Rezilta Prensipal yo
1. To Assess the Efficacy of Rilonacept in Decreasing the Number of Acute FMF Attacks. [attacks were assessed at the end of each 3 month treatment course (overall up to 6 month of rilonacept and 6 months of placebo, each)]
2. To Determine if There is a Medically Important Difference Between the Safety Profiles of Rilonacept vs. Placebo. [12 months of entire study length]
Mezi Rezilta Segondè
1. To Determine the Difference in the Length of Attacks During Treatment With Rilonacept vs. Placebo. [12 months]
2. Percentage of Treatment Courses Without FMF Attacks in Rilonacept Courses as Compared to Placebo Courses. [Each treatment course of up to 3 months]
3. To Determine the Proportion of Courses in Which Subjects Attained at Least a 50% Decrease in Acute FMF Attacks During Rilonacept Courses as Compared to Placebo Courses. [Up to 3 months for each treatment course]
4. To Determine Differences in the Time to the Development of Attacks Between the Treatment Arms (Rilonacept vs. Placebo). [3 months]
5. To Determine the Differences in the Erythrocyte Sedimentation Rate Between the Treatment Arms (Rilonacept vs. Placebo). [3 months (each treatment course, overall 12 months)]
6. To Determine the Differences in C-Reactive Protein Between the Treatment Arms (Rilonacept vs. Placebo) [3 months (each treatment course, overall 12 months)]
7. To Determine the Differences in the Platelet Count Between the Treatment Arms (Rilonacept vs. Placebo) [3 months (each treatment course, overall 12 months)]
8. To Determine the Differences in the Fibrinogen Levels Between the Treatment Arms (Rilonacept vs. Placebo) [3 months (each treatment course, overall 12 months)]
9. To Determine the Differences in Serum Amyloid A Levels Between the Treatment Arms (Rilonacept vs. Placebo) [3 months (each treatment course, overall 12 months)]
10. To Determine the Differences in the Quality of Life Between the Treatment Arms (Rilonacept vs. Placebo). [12 months]
11. To Determine the Differences in the FMF Severity Score of the Subjects Between the Treatment Arms (Rilonacept vs. Placebo). [overall 12 months]
12. To Determine the Differences in the Proportion of Time Subjects Received Rilonacept vs Placebo [12 months]
