Safety and Efficacy Evaluation of PerkinRA in Comparison with Kineret in Systemic Juvenile Idiopathic Arthritis Patients

被引:0
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作者
Mirzaee, Azadeh Zeinab [1 ,2 ]
Sadeghi, Setayesh [3 ]
Shiari, Reza [1 ]
Ziaee, Vahid [4 ]
Karagah, Amirhossein [3 ]
Sinaei, Reza [7 ]
Ghotbabadi, Shabnam Hajiani [8 ]
Tahghighi, Fatemeh [4 ]
Fathi, Mohammad Reza [9 ]
Shirvani, Armin [5 ]
Miremarati, Aye [10 ]
Ghasemi, Leila [11 ]
Rahmani, Khosro [1 ]
Araghi, Shahram [13 ]
Parvaneh, Vadood Javadi [1 ]
Jaffaraghaei, Morteza [12 ]
Mohammadkarim, Alireza [6 ]
机构
[1] Shahid Beheshti Univ Med Sci, Dept Pediat Rheumatol, Fac Med, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Natl Res Inst TB & Lung Dis NRITLD, Pediat Resp Dis Res Ctr PRDRC, Tehran, Iran
[3] Univ Tehran Med Sci, Dept Clin Pharm, Fac Pharm, Tehran, Iran
[4] Univ Tehran Med Sci, Dept Pediat, Tehran, Iran
[5] Shahid Beheshti Univ Med Sci, Res Inst Childrens Hlth, Tehran, Iran
[6] Aja Univ Med Sci, Radiat Sci Res Ctr RSRC, Tehran, Iran
[7] Kerman Univ Med Sci, Sch Med, Dept Pediat, Kerman, Iran
[8] Shiraz Univ Med Sci, Dept Pediat Rheumatol, Shiraz, Iran
[9] Ahwaz Jondishapur Univ Med Sci, Dept Pediat Rheumatol, Ahvaz, Iran
[10] Guilan Univ Med Sci, Pediat Dis Res Ctr, Rasht, Iran
[11] Qazvin Univ Med Sci, Dept Pediat Rheumatol, Qazvin, Iran
[12] Univ Guilan, Fac Basic Sci, Dept Biochem, Guilan, Iran
[13] Islam Azad Univ Iran, Fac Adv Sci & Technol, Dept Microbiol, Tehran Med Sci, Tehran, Iran
来源
关键词
American College of Rheumatology; anakinra; juvenile idiopathic arthritis; systemic juvenile idiopathic arthritis; CHALLENGES; ANAKINRA; CHILDREN;
D O I
10.4103/bbrj.bbrj_155_24
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Systemic juvenile idiopathic arthritis (sJIA) is marked with arthritis and several features of systemic inflammation, including fever, rashes, hepatosplenomegaly, lymphadenopathy, and serositis. Interleukin-1 receptor blockers have been used as one of the most effective biologics for the treatment of resistant types of disease. The main purpose of this study was to evaluate the safety and efficacy of PerkinRA in comparison with Kineret in patients with sJIA. Methods: This was a double-blind, randomized clinical trial conducted on 72 patients with sJIA. The patients were enrolled based on the 2018 International League of Associations for Rheumatology criteria and were treated at the outpatient clinic of Mofid Children's Hospital, Pediatric Medical Center, and four other centers between February 2020 and March 2021. Patients were randomly assigned in a 1:1 ratio to one of two treatment groups: one group received PerkinRA (manufactured by Persis Gene, n = 36), while the other group received Kineret (manufactured by SOBI, n = 36). The primary outcome measure was the proportion of patients achieving an American College of Rheumatology (ACR) 30, ACR 50, and ACR 70 response. Secondary outcomes included changes in vital signs, incidence of adverse events, clinical laboratory assessments, and findings from physical examinations. These parameters were evaluated at 1, 2, 4, 8, 12, 16, 20, and 24 weeks after the first injection, and the two treatment groups were compared. Results: A total of 35 patients in the PerkinRA group and 32 patients in the Kineret group were included in the final analysis. The results showed no clinically significant differences between the two treatment groups. Patients in both the PerkinRA and Kineret groups achieved similar proportions of ACR 30, ACR 50, and ACR 70 responses over the 6-month evaluation period. Conclusion: Based on the findings of this study, the two investigational medications, PerkinRA and Kineret, demonstrated comparable efficacy in the treatment of sJIA. The two treatment groups showed no significant differences in the primary and secondary outcomes assessed. Therefore, it can be concluded that PerkinRA and Kineret are noninferior to each other for the management of sJIA.
引用
收藏
页码:363 / 368
页数:6
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