| Literature DB >> 12662184 |
Abstract
A global, double-blind, randomized, placebo-controlled, dose-finding, parallel-group trial was conducted to compare three oral doses of RPR100893 (1, 5, 20 mg), a substance-P antagonist, and placebo in 139 patients with migraine attacks with moderate or severe headache intensity. Headache intensity and improvement of headache after 2 h were not different in the four treatment groups. Therefore, it is concluded that this oral substance-P antagonist in the doses used here is not effective.Entities:
Mesh:
Substances:
Year: 2003 PMID: 12662184 DOI: 10.1046/j.1468-2982.2003.00496.x
Source DB: PubMed Journal: Cephalalgia ISSN: 0333-1024 Impact factor: 6.292