EHT0202 in Alzheimer's Disease: A 3-Month, Randomized, Placebo-Controlled, Double-Blind Study

被引:105
作者
Vellas, B. [2 ,3 ]
Sol, O. [1 ]
Snyder, P. J. [4 ,5 ]
Ousset, P. -J. [2 ,3 ]
Haddad, R. [1 ]
Maurin, M. [6 ]
Lemarie, J. -C. [7 ]
Desire, L. [1 ]
Pando, M. P. [1 ]
机构
[1] ExonHit Therapeut SA, F-75013 Paris, France
[2] Fac Med Toulouse, INSERM, U558, F-31073 Toulouse, France
[3] CHU La Grave Casselardit, Toulouse, France
[4] Brown Univ, Alpert Med Sch, Dept Neurol, Providence, RI 02912 USA
[5] Yale Univ, Sch Med, Ctr Child Study, New Haven, CT 06510 USA
[6] GECEM, Paris, France
[7] Effi Stat, Paris, France
关键词
ADAS-COG; alpha-secretase; Alzheimer's disease; ApoE; clinical trials randomized controlled; EHT0202; memory; patient safety; AMYLOID PRECURSOR PROTEIN; CLINICAL-TRIALS; DEMENTIA; ETAZOLATE; INVENTORY; TASK;
D O I
10.2174/156720511795256053
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: EHT0202 (etazolate hydrochloride) is a new compound exhibiting both potential disease-modifying and symptomatic treatment properties in Alzheimer's Disease increasing alpha-secretase activity and sAPP alpha secretion, as well as acting as a GABA-A receptor modulator and as a PDE-4 inhibitor. Methods: This pilot, randomized, double-blind, placebo-controlled, parallel group, multicentre, Phase IIA study was conducted in 159 randomized patients suffering from mild to moderate Alzheimer's Disease. EHT0202 (40 or 80mg bid) or placebo was administered as adjunctive therapy to one acetylcholinesterase inhibitor over a 3-month period. This study was designed to assess the clinical safety and tolerability of EHT0202 as a primary objective, with secondary endpoints (cognitive function, daily living activities, behaviour, caregiver burden and global functioning) included to explore clinical efficacy of EHT0202 versus placebo. Results: EHT0202 was shown to be safe and generally well tolerated. Dose-dependent numbers of early withdrawal and central nervous system related adverse events were observed. As expected, since the study was not powered and not designed to show drug efficacy, and except for ratings on the ADCS-ADL scale, no significant differences were seen between treatment groups. Conclusions: These first encouraging safety results do support further development of EHT0202 in order to assess its clinical efficacy and to confirm its tolerability in a larger cohort of Alzheimer patients and for a longer period.
引用
收藏
页码:203 / 212
页数:10
相关论文
共 19 条
[1]  
[Anonymous], 1976, NATL I MENTAL HLTH P
[2]  
Barger SW, 1997, J NEUROCHEM, V69, P60
[3]   THE NEUROPSYCHIATRIC INVENTORY - COMPREHENSIVE ASSESSMENT OF PSYCHOPATHOLOGY IN DEMENTIA [J].
CUMMINGS, JL ;
MEGA, M ;
GRAY, K ;
ROSENBERGTHOMPSON, S ;
CARUSI, DA ;
GORNBEIN, J .
NEUROLOGY, 1994, 44 (12) :2308-2314
[4]  
Dastidar SG, 2007, CURR OPIN INVEST DR, V8, P364
[5]   Etazolate improves performance in a foraging and homing task in aged rats [J].
Drott, Jason ;
Desire, L. ;
Drouin, D. ;
Pando, M. ;
Haun, Forrest .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2010, 634 (1-3) :95-100
[6]   MINI-MENTAL STATE - PRACTICAL METHOD FOR GRADING COGNITIVE STATE OF PATIENTS FOR CLINICIAN [J].
FOLSTEIN, MF ;
FOLSTEIN, SE ;
MCHUGH, PR .
JOURNAL OF PSYCHIATRIC RESEARCH, 1975, 12 (03) :189-198
[7]  
Galasko D, 1997, ALZ DIS ASSOC DIS, V11, pS33
[8]   Clinical effects of Aβ immunization (AN1792) in patients with AD in an interrupted trial [J].
Gilman, S ;
Koller, M ;
Black, RS ;
Jenkins, L ;
Griffith, SG ;
Fox, NC ;
Eisner, L ;
Kirby, L ;
Rovira, MB ;
Forette, F ;
Orgogozo, JM .
NEUROLOGY, 2005, 64 (09) :1553-1562
[9]   A neuropsychological test battery for use in Alzheimer disease clinical trials [J].
Harrison, John ;
Psychol, C. ;
Minassian, Sonia L. ;
Jenkins, Lisa ;
Black, Ronald S. ;
Koller, Martin ;
Grundman, Michael .
ARCHIVES OF NEUROLOGY, 2007, 64 (09) :1323-1329
[10]   Muscarinic acetylcholine receptor inhibition in transgenic Alzheimer-like Tg2576 mice by scopolamine favours the amyloidogenic route of processing of amyloid precursor protein [J].
Liskowsky, W ;
Schliebs, R .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2006, 24 (2-3) :149-156