Fomivirsen

被引:187
作者
Perry, CM [1 ]
Balfour, JAB [1 ]
机构
[1] Adis Int Ltd, Auckland 10, New Zealand
关键词
D O I
10.2165/00003495-199957030-00010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Fomivirsen (ISIS 2922) is an antisense oligonucleotide which specifically inhibits replication of human cytomegalovirus. It achieves this by binding to complementary sequences on messenger RNA transcribed from the major immediate-early transcriptional unit of the virus. It Is being developed for the treatment of cytomegalovirus retinitis. Mean maximum retinal concentrations of fomivirsen occurred approximate to 2 days after a single intravitreal injection in monkeys. The elimination half-life of fomivirsen (after a single 115 mu g dose) in monkey retina was 78 hours. Fomivirsen, administered as an intravitreal injection, significantly delayed progression of cytomegalovirus retinitis in patients with AIDS in preliminary clinical trials. In 18 patients with newly diagnosed, unilateral, peripheral cytomegalovirus retinitis treated with fomivirsen 165 mu g once weekly for 3 weeks, then 165 mu g every second week, the median time to disease progression was significantly longer than in 10 patients in whom fomivirsen treatment was deferred until early disease progression (71 vs 14 days). In patients with advanced, refractory, sight-threatening disease, treatment with fomivirsen 330 mu g once weekly for 3 weeks and then 330 mu g every 2 weeks (n = 34) or 330 mu g on days 1 and 15 and then monthly (n = 20) significantly delayed disease progression. The interpolated median time to disease progression was 90 days in both treatment groups. The most common adverse events reported in clinical trials of fomivirsen were increased intraocular pressure and mild to moderate intraocular inflammation These events were generally transient or reversible with topical steroid treatment.
引用
收藏
页码:375 / 380
页数:6
相关论文
共 20 条
[1]   Inhibition of human cytomegalovirus immediate-early gene expression by an antisense oligonucleotide complementary to immediate-early RNA [J].
Anderson, KP ;
Fox, MC ;
BrownDriver, V ;
Martin, MJ ;
Azad, RF .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (09) :2004-2011
[2]   ANTIVIRAL ACTIVITY OF A PHOSPHOROTHIOATE OLIGONUCLEOTIDE COMPLEMENTARY TO RNA OF THE HUMAN CYTOMEGALOVIRUS MAJOR IMMEDIATE-EARLY REGION [J].
AZAD, RF ;
DRIVER, VB ;
TANAKA, K ;
CROOKE, RM ;
ANDERSON, KP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (09) :1945-1954
[3]   ANTIVIRAL ACTIVITY OF A PHOSPHOROTHIOATE OLIGONUCLEOTIDE COMPLEMENTARY TO HUMAN CYTOMEGALOVIRUS RNA WHEN USED IN COMBINATION WITH ANTIVIRAL NUCLEOSIDE ANALOGS [J].
AZAD, RF ;
BROWNDRIVER, V ;
BUCKHEIT, RW ;
ANDERSON, KP .
ANTIVIRAL RESEARCH, 1995, 28 (02) :101-111
[4]   Prospects for antisense therapy are looking brighter [J].
Bonn, D .
LANCET, 1996, 347 (9004) :820-820
[5]  
FRASER GL, 1995, EXPERT OPIN INV DRUG, V4, P637
[6]  
Henahan S., 1998, INPHARMA WKLY, V1138, P11
[7]  
Hudson H. L., 1997, OPHTHAL CLIN N AM, V10, P61
[8]  
HUTCHERSON SL, 1995, 35 INT C ANT AG CHEM, P204
[9]  
*IS, 1998, PINK SHEET 0727, P5
[10]  
*IS PHARM US, 1998, FOM SOD PRESCR INF