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Effects of fremanezumab on the use of acute headache medication and associated symptoms of migraine in patients with episodic migraine.
Brandes, Jan Lewis; Kudrow, David; Yeung, Paul P; Sakai, Fumihiko; Aycardi, Ernesto; Blankenbiller, Tricia; Grozinski-Wolff, Melissa; Yang, Ronghua; Ma, Yuju.
Afiliação
  • Brandes JL; Nashville Neuroscience Group, Vanderbilt Department of Neurology, Nashville, TN, USA.
  • Kudrow D; California Medical Clinic for Headache, Santa Monica, CA, USA.
  • Yeung PP; Teva Pharmaceutical Industries Ltd, Frazer, PA, USA.
  • Sakai F; Saitama International Headache Center, Saitama Neuropsychiatric Institute, Saitama, Japan.
  • Aycardi E; Teva Pharmaceutical Industries Ltd, Frazer, PA, USA.
  • Blankenbiller T; Teva Pharmaceutical Industries Ltd, Frazer, PA, USA.
  • Grozinski-Wolff M; Teva Pharmaceutical Industries Ltd, Frazer, PA, USA.
  • Yang R; Teva Pharmaceutical Industries Ltd, Frazer, PA, USA.
  • Ma Y; Teva Pharmaceutical Industries Ltd, Frazer, PA, USA.
Cephalalgia ; 40(5): 470-477, 2020 04.
Article em En | MEDLINE | ID: mdl-31752521
BACKGROUND: Fremanezumab, a fully humanized monoclonal antibody targeting calcitonin gene-related peptide, has demonstrated efficacy for the preventive treatment of migraine in adults. OBJECTIVE: To evaluate the effect of fremanezumab treatment on acute headache medication use and migraine-associated symptoms in patients with episodic migraine. METHODS: In the Phase 3 HALO trial, patients with episodic migraine were randomized to receive subcutaneous fremanezumab monthly (225 mg at baseline, weeks 4 and 8), fremanezumab quarterly (675 mg at baseline, placebo at weeks 4 and 8), or placebo over a 12-week period. The secondary endpoint was change from baseline in the monthly number of days with use of any acute headache mediation or migraine-specific acute headache medication; exploratory endpoints were change from baseline in the monthly number of days with nausea or vomiting, photophobia, or phonophobia. RESULTS: Of 875 patients randomized, 865 were included in the analysis (monthly, n = 287; quarterly, n = 288; placebo, n = 290). Baseline mean ± standard deviation days with: Any acute headache medication use (monthly: 7.7 ± 3.4; quarterly: 7.8 ± 3.7; placebo: 7.7 ± 3.6), migraine-specific acute headache medication use (6.1 ± 3.1; 6.6 ± 3.1; 7.1 ± 3.0), nausea or vomiting (4.5 ± 3.6; 4.9 ± 3.7; 4.5 ± 3.3) and photophobia and phonophobia (5.5 ± 4.1; 6.3 ± 4.1; 6.0 ± 3.9) were similar among treatment arms. Fremanezumab reduced the number of days of acute headache medication use ([least-squares mean change vs. placebo] monthly: -1.4 [95% confidence interval: -1.84, -0.89], p < 0.001; quarterly: -1.3 [-1.76, -0.82], p < 0.001) and migraine-specific acute headache medication use (monthly: -2.2 [-2.80, -1.56], p < 0.001; quarterly: -2.2 [-2.81, -1.58], p < 0.001) compared with placebo. Fremanezumab also reduced nausea or vomiting, photophobia, and phonophobia compared with placebo. CONCLUSIONS: Fremanezumab reduced the need for acute headache medications, including migraine-specific medications, while treating migraine-associated symptoms in patients with episodic migraine. TRIAL REGISTRATION: Clinicaltrials.gov NCT02629861.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos de Enxaqueca / Anticorpos Monoclonais Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos de Enxaqueca / Anticorpos Monoclonais Idioma: En Ano de publicação: 2020 Tipo de documento: Article