In the phase 3 study REGAIN, patients with chronic migraine were randomised to placebo (n=558), galcanezumab 120 mg (n=278), or galcanezumab 240 mg (n=277). A 3-month double-blind period was followed by a 9-month open-label extension (OLE) phase with flexible dosing. Changes in mean migraine-specific healthcare resource utilisation across baseline, double-blind, and OLE phases (per 100 patient-years) were calculated for healthcare professional visits, emergency room visits, admissions to hospital, and overnight hospital stays. Mean reductions from baseline across time in number of MHD/month with acute medication use were significant in each of the 3 groups (see Table).
Table: Change in mean migraine headache days per month across different stages of REGAIN [1]

The majority of patients in the REGAIN study shifted from chronic to episodic migraine status [2]. After 3 months, a greater proportion of galcanezumab-treated patients shifted from chronic to episodic status (30.9%) versus placebo-treated patients (19.7%). Across the 12-month period, 65.1% of galcanezumab-treated patients shifted to episodic status for ≥3 consecutive months. The authors concluded that long-term treatment with galcanezumab may lead to substantial reductions in disability and economic burden.
- Joshi S, et al. EAN 2019, EPO2137.
- Detke H, et al. EAN 2019, EPO1134.
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Table of Contents: EAN 2019
Featured articles
Letter from the Editor
Alzheimer’s Disease and other Dementias
A necessary shift of focus to the earlier stages of Alzheimer’s
Antipsychotics increase mortality regardless of comorbidity
Epilepsy
Neuroinflammatory pathways as biomarkers and treatment targets
Long-term effect of recurrent febrile seizures
Migraine
The role of neurogenic inflammation in migraine
Multiple Sclerosis
Treating MS from disease onset
Randomised and observational studies comparing treatments
Autologous haematopoietic stem cell transplantation
Neuromuscular Disorders
Parkinson's Disease and other Movement Disorders
Inflammation may change the course of Parkinson’s disease
Opicapone: follow-up on the BIPARK I and II trials
Epigallocatechin gallate does not modify MSA progression
Stroke
Thrombo-inflammation during ischaemia/reperfusion
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