Recombinant Human C1-Esterase Inhibitor to Treat Acute Hereditary Angioedema Attacks in Adolescents

被引:8
|
作者
Baker, James W. [1 ]
Reshef, Avner [2 ]
Moldovan, Dumitru [3 ]
Harper, Joseph R. [4 ]
Relan, Anurag [5 ]
Riedl, Marc A. [6 ]
机构
[1] Baker Allergy Asthma Dermatol Res Ctr LLC, 9495 SW Locust St,Ste A, Portland, OR 97223 USA
[2] Tel Aviv Univ, Sheba Med Ctr, Allergy & Immunol Unit, Tel Aviv, Israel
[3] Univ Med & Pharm, Mures Cty Hosp, Dept Allergol & Immunol, Targu Mures, Romania
[4] Salix Pharmaceut, Raleigh, NC USA
[5] Pharming Technol BV, Leiden, Netherlands
[6] Univ Calif San Diego, Dept Med, Div Rheumatol Allergy & Immunol, San Diego, CA 92103 USA
关键词
C1-esterase; Hereditary angioedema; Adolescent; Safety; Efficacy; Ruconest; Pharmacokinetics; PLACEBO-CONTROLLED TRIAL; C1; INHIBITOR; RECEPTOR ANTAGONIST; HUMAN C1-INHIBITOR; DEFICIENCY; ICATIBANT; SYMPTOMS;
D O I
10.1016/j.jaip.2016.11.005
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
BACKGROUND: Recombinant human C1-esterase inhibitor (rhC1-INH) is efficacious and well tolerated for managing hereditary angioedema (HAE) attacks in adults. However, there are insufficient data on its efficacy and safety in adolescents. OBJECTIVE: To evaluate the efficacy and safety profiles of rhC1-INH for acute HAE attacks in adolescents. METHODS: Adolescents (aged 12-18 y) with HAE enrolled in 2 randomized controlled trials and 2 open-label extension trials were included and received intravenous rhC1-INH for acute attacks. Times to the beginning of sustained symptom relief (visual analog scale change from baseline >= 20 mm) and minimal symptoms (visual analog scale score of <20 mm across locations) were assessed. Safety parameters included hypersensitivity reactions, anti-rhC1-INH antibodies, and host-related impurities. RESULTS: Sixteen adolescents (50 attacks, aged 14-18 y) received rhC1-INH. Attacks were managed with single-dose rhC1-INH 50U/kg (46.0%) and single-dose rhC1-INH 2100 U (16%), and 32.0% were treated with additional doses after receiving an initial rhC1-INH 2100 U dose (total dose, 4200-6300 U). Most attacks (88.0%) occurred at a single location; 59.1% (26 of 44) were abdominal. Across the first 5 attacks, median times to the beginning of symptom relief ranged from 19.0 to 78.5 minutes; median times to minimal symptoms ranged from 120 to 190 minutes. Pharmacokinetics showed that rhC1-INH restored functional plasma C1-esterase inhibitor levels to the normal (>70%) range for almost all evaluable patients. No severe or drug-related adverse events or hypersensitivity reactions occurred. No treatment-emergent antibodies to rhC1-INH or host-related impurities were observed. CONCLUSIONS: rhC1-INH is efficacious and well tolerated among adolescents with HAE. (C) 2017 The Authors. Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology.
引用
收藏
页码:1091 / 1097
页数:7
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