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Neurology
Generic: eptinezumab-jjmr
Vyepti (eptinezumab-jjmr) is a preventive treatment for migraine in adults. It is a monoclonal antibody that targets calcitonin gene-related peptide (CGRP), a molecule that plays a central role in migraine attacks. Vyepti was approved by the FDA in February 2020 and is made by Lundbeck. It was the first anti-CGRP treatment given by intravenous (IV) infusion, and it is taken only once every 3 months.
During a migraine, CGRP is released around nerves in the head, where it widens blood vessels and drives pain signaling and inflammation. Vyepti binds to CGRP and blocks it from acting on its receptor. Over time, this lowers how often migraine attacks happen. Vyepti is a preventive medicine. It is not used to treat a migraine attack that has already started.
Because Vyepti is given by IV, the full dose enters the bloodstream at once, and some patients notice fewer migraine days as early as the day after their first infusion. FDA approval was based on two Phase 3 trials: PROMISE-1 in episodic migraine and PROMISE-2 in chronic migraine. In both trials, patients treated with Vyepti had significantly fewer monthly migraine days than patients given placebo. Quarterly in-office infusions also mean there are no monthly self-injections or daily pills to remember.
Before starting treatment, the care team reviews:
Patients are encouraged to keep a headache diary so the care team can track how well Vyepti is working.
Vyepti is generally well tolerated. The most common side effects in clinical trials were:
Serious but less common risks include:
Patients with a history of serious hypersensitivity to eptinezumab or any of its ingredients should not receive Vyepti. Healthcare providers monitor patients closely and act promptly if any reaction occurs.
Vyepti offers adults living with migraine a targeted preventive option. It blocks CGRP directly, can begin working quickly, and needs only four infusions a year. For many patients, it means fewer migraine days and a better quality of life.
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