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Tytuł pozycji:

Randomized, double-blind, placebo-controlled, proof-of-concept study of the cortical spreading depression inhibiting agent tonabersat in migraine prophylaxis.

Tytuł:
Randomized, double-blind, placebo-controlled, proof-of-concept study of the cortical spreading depression inhibiting agent tonabersat in migraine prophylaxis.
Autorzy:
Goadsby PJ; Headache Group, Institute of Neurology, London, UK. />Ferrari MD
Csanyi A
Olesen J
Mills JG
Corporate Authors:
Tonabersat TON-01-05 Study Group
Źródło:
Cephalalgia : an international journal of headache [Cephalalgia] 2009 Jul; Vol. 29 (7), pp. 742-50. Date of Electronic Publication: 2009 Feb 13.
Typ publikacji:
Journal Article; Multicenter Study; Randomized Controlled Trial; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Publication: Jan. 2010- : London : Sage
Original Publication: Oslo : Universitetsforlaget.
MeSH Terms:
Benzamides/*therapeutic use
Benzopyrans/*therapeutic use
Migraine Disorders/*prevention & control
Adolescent ; Adult ; Cortical Spreading Depression/drug effects ; Double-Blind Method ; Female ; Humans ; Male ; Middle Aged ; Young Adult
Substance Nomenclature:
0 (Benzamides)
0 (Benzopyrans)
2XD9773ZMN (tonabersat)
Entry Date(s):
Date Created: 20090219 Date Completed: 20090819 Latest Revision: 20121115
Update Code:
20240104
DOI:
10.1111/j.1468-2982.2008.01804.x
PMID:
19222510
Czasopismo naukowe
Tonabersat is a novel putative migraine prophylactic agent with an unique stereospecific binding site in the brain. Tonabersat has been shown, in animal models, to inhibit experimentally induced cortical spreading depression, the likely underlying mechanism for migraine aura, and cerebrovascular responses to trigeminal nerve stimulation. The aim was to study the potential for tonabersat as a migraine preventive. A randomized, double-blind, placebo-controlled, multicentre, parallel group study recruited patients with migraine with and without aura experiencing between two and six migraine attacks per month. After a 1-month baseline they received tonabersat 20 mg daily for 2 weeks and 40 mg daily for a further 10 weeks. The primary end-point was the change in mean number of migraine headache days between the third month and the baseline period in the intention-to-treat population comparing the placebo (n = 65) and tonabersat (n = 58) groups. At the primary end-point there was a 1.0-day (95% confidence interval -0.33, 2.39; P = 0.14) difference in reduction in migraine days between tonabersat and placebo. There were 10 secondary efficacy end-points, of which two were statistically significant. In month 3 of treatment, the responder rate, defined as a 50% reduction in migraine attacks, was 62% for tonabersat and 45% for placebo (P < 0.05), and the rescue medication use was reduced in the tonabersat group compared with placebo by 1.8 days (P = 0.02). Placebo responses were particularly high for all end-points. At least one treatment-emergent adverse event was reported in the tonabersat group in 61% of patients compared with 51% in the placebo group; none was worrisome. Placebo responses were unexpectedly high in this trial, complicating straightforward interpretation of the study results. The good tolerability and promising efficacy results support further exploration of higher doses of tonabersat in larger controlled trials.

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