A phase IIa randomized clinical study testing GNbAC1, a humanized monoclonal antibody against the envelope protein of multiple sclerosis associated endogenous retrovirus in multiple sclerosis patients - A twelve month follow-up

被引:33
作者
Derfuss, Tobias [1 ]
Curtin, Francois [2 ]
Guebelin, Claudia [1 ]
Bridel, Claire [3 ]
Rasenack, Maria [1 ]
Matthey, Alain [4 ,5 ]
Du Pasquier, Renaud [6 ]
Schluep, Myriam [6 ]
Desmeules, Jules [4 ,5 ]
Lang, Alois B. [2 ]
Perron, Herve [2 ]
Faucard, Raphael [2 ]
Porchet, Herve [2 ,7 ]
Hartung, Hans-Peter [8 ]
Kappos, Ludwig [1 ]
Lalive, Patrice H. [3 ,9 ,10 ]
机构
[1] Univ Basel Hosp, Dept Neurol, CH-4031 Basel, Switzerland
[2] GeNeuro SA, CH-1228 Geneva, Switzerland
[3] Univ Hosp Geneva, Unit Neuroimmunol & Multiple Sclerosis, Div Neurol, Dept Clin Neurosci, CH-1211 Geneva, Switzerland
[4] Univ Hosp Geneva, Div Pharmacol & Toxicol, CH-1214 Geneva, Switzerland
[5] Univ Hosp Geneva, Clin Trial Unit, CH-1214 Geneva, Switzerland
[6] Univ Lausanne Hosp, Dept Neurol, CH-1011 Lausanne, Switzerland
[7] Univ Pretoria, Dept Pharmacol, ZA-0002 Pretoria, South Africa
[8] Univ Dusseldorf, Dept Neurol, D-40225 Dusseldorf, Germany
[9] Univ Hosp Geneva, Div Lab Med, Dept Genet & Lab Med, CH-1211 Geneva, Switzerland
[10] Univ Geneva, Dept Pathol & Immunol, Fac Med, CH-1211 Geneva, Switzerland
关键词
Multiple sclerosis; Human endogenous retrovirus; Monoclonal antibody; Clinical trial; Safety; BLOOD; CELLS;
D O I
10.1016/j.jneuroim.2015.05.019
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
GNbAC1 is a humanized monoclonal antibody targeting MSRV-Env, an endogenous retroviral protein, which is expressed in multiple sclerosis (MS) lesions, is pro-inflammatory and inhibits oligodendrocyte precursor cell differentiation. This paper describes the open-label extension up to 12 months of a trial testing GNbAC1 in 10 MS patients at 2 and 6 mg/kg. The primary objective was to assess GNbAC1 safety, and other objectives were pharmacokinetic and pharmacodynamic assessments. During the extended study, no safety issues occurred in the 8 remaining patients. No anti-GNbAC1 antibodies were detected. GNbAC1 appears well tolerated. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:68 / 70
页数:3
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