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Reversion From Chronic Migraine to Episodic Migraine in Patients Treated With Fremanezumab: Post Hoc Analysis From HALO CM Study.
Lipton, Richard B; Cohen, Joshua M; Bibeau, Kristen; Galic, Maja; Seminerio, Michael J; Ramirez Campos, Verena; Halker Singh, Rashmi B; Ailani, Jessica.
Affiliation
  • Lipton RB; Albert Einstein College of Medicine, Bronx, NY, USA.
  • Cohen JM; Montefiore Headache Center, Bronx, NY, USA.
  • Bibeau K; Teva Pharmaceutical Industries Ltd., Frazer, PA, USA.
  • Galic M; Teva Pharmaceutical Industries Ltd., Frazer, PA, USA.
  • Seminerio MJ; Teva Pharmaceutical Industries Ltd., Amsterdam, The Netherlands.
  • Ramirez Campos V; Teva Pharmaceutical Industries Ltd., Frazer, PA, USA.
  • Halker Singh RB; Teva Pharmaceutical Industries Ltd., Frazer, PA, USA.
  • Ailani J; Mayo Clinic, Phoenix, AZ, USA.
Headache ; 60(10): 2444-2453, 2020 Nov.
Article in En | MEDLINE | ID: mdl-33179323
ABSTRACT

BACKGROUND:

Migraine preventive medications are used to reduce headache frequency, severity, and duration. In patients with chronic migraine (CM), reversion to episodic migraine (EM) is an important treatment goal.

OBJECTIVE:

To evaluate the effect of fremanezumab on the rate of reversion from CM to EM.

METHODS:

This phase 3, randomized, double-blind, placebo-controlled, parallel-group trial included a 28-day pretreatment period and a 3-month treatment period. Patients with CM received subcutaneous fremanezumab quarterly (675 mg at baseline) or monthly (675 mg at baseline; 225 mg at Weeks 4 and 8), or placebo. Post hoc analyses evaluated the proportion of patients who reverted from CM to EM, defined as either a reduction to an average of <15 headache days per month during the 3-month treatment period or a reduction to <15 headache days per month in all 3 months of the treatment period.

RESULTS:

This analysis included data from 1088 CM patients (quarterly, n = 366; monthly, n = 365; placebo, n = 357). More fremanezumab-treated patients with CM reverted to EM using either the monthly average number of headache days criteria for reversion (quarterly 50.5% [185/366], P = .108; monthly 53.7% [196/365], P = .012; vs placebo 44.5% [159/357]) or the monthly headache day count at Months 1, 2, and 3 criteria for reversion (quarterly 31.2% [114/366], P = .008; monthly 33.7% [123/365], P = .001; vs placebo 22.4% [80/357]). Patients with CM who reported previous topiramate or onabotulinumtoxinA use, concomitant preventive medication use, or medication overuse were less likely to revert to EM.

CONCLUSIONS:

Fremanezumab may offer the benefit of reversion from CM to EM, based on a reduction in the number of headache days over 3 months of treatment.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Outcome Assessment, Health Care / Migraine Disorders / Antibodies, Monoclonal Type of study: Clinical_trials Limits: Adult / Female / Humans / Male Language: En Journal: Headache Year: 2020 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Outcome Assessment, Health Care / Migraine Disorders / Antibodies, Monoclonal Type of study: Clinical_trials Limits: Adult / Female / Humans / Male Language: En Journal: Headache Year: 2020 Type: Article Affiliation country: United States