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BI 44370 TA, an oral CGRP antagonist for the treatment of acute migraine attacks: Results from a phase II study
被引:182
|作者:
Diener, Hans-Christoph
[1
]
Barbanti, Piero
[2
]
Dahloef, Carl
[3
]
Reuter, Uwe
[4
]
Habeck, Julia
[5
]
Podhorna, Jana
[5
]
机构:
[1] Univ Duisburg Essen, Univ Hosp Essen, Dept Neurol, D-45147 Essen, Germany
[2] Hosp IRCCS San Raffaele, Milan, Italy
[3] Gothenburg Migraine Clin AB, Gothenburg, Sweden
[4] Charite, Berlin, Germany
[5] Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim, Germany
来源:
关键词:
Migraine;
attacks;
acute treatment;
CGRP-antagonist;
phase II study;
GENE-RELATED PEPTIDE;
RECEPTOR ANTAGONIST;
TRIPTANS SEROTONIN;
5-HT1B/1D AGONISTS;
CONTROLLED-TRIAL;
SUMATRIPTAN;
ELETRIPTAN;
METAANALYSIS;
DISEASE;
D O I:
10.1177/0333102410388435
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Methods: Four hundred and sixty-one adult subjects with migraine were randomised to one of five treatments, the oral antagonist at the calcitonin gene-related peptide (CGRP) receptor BI 44370 TA (50 mg, 200 mg, 400 mg), active comparator eletriptan 40 mg or placebo. The analysis included 341 subjects who took study medication. Results: The primary endpoint, pain-free after two hours, was reached by significantly more subjects in the BI 44370 TA 400 mg (20/73=27.4%) and eletriptan 40 mg (24/69=34.8%) groups compared to placebo (6/70=8.6%, p=.0016), but not by subjects in the BI 44370 TA 200 mg group (14/65=21.5%). The effect of 50 mg BI 44370 TA (5/64=7.8%) was similar to that of placebo. Analysis of secondary endpoints supported the conclusion from the primary analysis. The frequency of adverse events was low in all groups. Conclusion: Efficacy of BI 44370 TA was shown in a dose-dependent manner in the treatment of acute migraine attacks.
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页码:573 / 584
页数:12
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