Over half of patients with migraine-related cognitive symptoms reported improvements in all domains in the prospective real world INFUSE study of 190 participants who had failed on at least one previous CGRP-targeted preventive therapy. At baseline, 93.7% (178/190) reported brain fog, 78.9% (150/190) reported difficulty making decisions, 82.6% (157/190) reported difficulty reading, and 82.6% (157/190) …
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Results of the Phase 3, open label UNCHAINED study have shown that adding atogepant 60 mg to onabotulinumtoxinA 155-200U in patients with chronic migraine was associated with consistent increases in cardinal and complete migraine symptom-free days over 24 weeks of treatment (NCT05216263). In the modified intention-to-treat population of 72 patients, incremental symptom burden days from …
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Primary care physicians (PCPs) account for only one in five gepant prescriptions despite seeing the majority of patients with migraine, report US headache specialists. In a study examining gepant prescribing at the University of Washington, a tertiary academic medical centre with dedicated headache specialists and multiple primary care clinics, 145 patients were identified who were …
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Exposure to CGRP mAbs during pregnancy is associated with a 50% increased risk of spontaneous abortion before 20 weeks, according to results of a Canadian retrospective cohort study of 11,819 pregnancies in women with pregestational migraine. Of these, 319 (2.7%) were exposed to anti-CGRP mAbs (+/-propranolol), 299 to propranolol (without anti-CGRP mAb), and 11,201 to neither, …
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The PACAP-targeting monoclonal antibody, bocunebart, significantly reduces monthly migraine days (MMDs), according to results of the Phase 2b, dose finding PROCEED trial with patients who had failed at least 1 to 4 different migraine preventive medications in the previous 10 years and had at least 4 migraine days per month for each month in the …
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Encouraging Phase 1 pharmacokinetic data for the investigational TRPM8-targeting agent, elismetrep, have shown more rapid absorption with a novel liquid-filled softgel capsule (LSGC) than with the dry-filled capsule (DFC) formulation used in the Phase 2b study of the agent.1 In the study, median time to maximum concentration [Tmax] was 1 hour with the LSGC formulation …
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