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  • FDA Approves Brekiya (dihydroergotamine mesylate) Injection . . .
    BRIDGEWATER, N J , May 15, 2025 -- Amneal Pharmaceuticals, Inc (Nasdaq: AMRX) (“Amneal” or the “Company”) today announced that the U S Food and Drug Administration (FDA) has approved Brekiya (dihydroergotamine mesylate) injection, the first and only dihydroergotamine (DHE) autoinjector for the acute treatment of migraine with or
  • Amneal Receives U. S. FDA Approval for Brekiya® - GlobeNewswire
    DHE can be used at any point during a migraine attack, and may protect patients from headache recurrence 1, 3,4 Approximately 39 million Americans are living with migraine 7, and up to one
  • Brekiya Approved for Acute Treatment of Migraine and Cluster . . .
    The FDA has approved Brekiya (dihydroergotamine mesylate) injection for the acute treatment of migraine with or without aura and the acute treatment of cluster headaches in adults
  • New Treatments for Migraines: What Actually Works in 2025?
    In response, the American Headache Society now recommends CGRP-targeting therapies as first-line options for eligible patients, supporting broader adoption and access This article reviews the most effective migraine treatments available in 2025, focusing on their mechanisms of action, clinical evidence, and their role in modern migraine
  • Best New Migraine Medications and Treatments — Migraine Again
    In April 2025, the FDA approved the first prescription-based digital therapeutic for episodic migraine prevention Click Therapeutics’ CT-132 is a 12-week app-based intervention that integrates multiple evidence–based behavioral techniques, including elements of cognitive behavioral therapy (CBT)





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