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  • ePoster
  • P104

A Phase 2/3 Open-label, Long-term, Safety Trial of Zavegepant 10 mg Nasal Spray for the Acute Treatment of Migraine

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Poster

A Phase 2/3 Open-label, Long-term, Safety Trial of Zavegepant 10 mg Nasal Spray for the Acute Treatment of Migraine

Themen

  • CGRP inhibitors in the clinic
  • Migraine

Mitwirkende

Robert Croop (Nerw Haven, CT/ US), Jennifer Madonia (Nerw Haven, CT/ US), Jennifer Hould (Nerw Haven, CT/ US), Linda Mosher (Nerw Haven, CT/ US), Meghan Lovegren (Nerw Haven, CT/ US), Vladimir Coric (Nerw Haven, CT/ US), Richard B. Lipton (Bronx, NY/ US)

Abstract

Abstract text (incl. figure legends and references)

Objective

Evaluate the safety of zavegepant 10 mg nasal spray, the only small molecule CGRP receptor antagonist (gepant) for intranasal administration in late-stage development for the acute treatment of migraine.

Methods

This was a Phase 2/3, 1-year open-label safety study (NCT04408794) of zavegepant nasal spray for the acute treatment of migraine. Adults aged ≥18 years with a history of 2 to 8 moderate-severe monthly migraine attacks were eligible. Use of another gepant was prohibited. Subjects self-administered 1 dose of zavegepant 10 mg nasal spray per calendar day as needed to treat migraine attacks of any severity, up to 8 times per month, for 52 weeks. Months were defined as 4-week intervals. Safety assessments included adverse events (AEs), vital signs, ECG, nasal inspection, and clinical laboratory tests. Subjects who took ≥1 dose of zavegepant were included in the analysis.

Results

Of 608 subjects who entered the long-term treatment phase, 603 were treated with zavegepant 10 mg nasal spray. At baseline, the mean (SD) number of attacks per month was 5.0 (1.89), and 18.1% of treated subjects used preventive migraine medication. Treatment-emergent AEs reported in ≥ 5% of subjects (Figure) were dysgeusia (39.1%); nasal discomfort (10.3%); COVID-19 (7.5%); nausea (6.1%); nasal congestion and throat irritation (5.5% each); and back pain (5.3%). In total, 6.8% of subjects discontinued due to AEs; 1.5% discontinued due to dysgeusia. The majority of AEs (96.4%) were mild to moderate. Of the 7 serious AEs reported, none was considered related to treatment by the investigators. Aminotransferases >3x the upper limit of normal (ULN) occurred in 2.6% of subjects, none of whom had concurrent elevations in bilirubin >2x ULN. Subjects used a mean (SD) of 3.1 (1.6) zavegepant doses per month.

Conclusion

Favorable safety and tolerability profiles were observed with 1 year of open-label zavegepant 10 mg nasal spray for the acute treatment of migraine.

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