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    Eagle Announces Licensing Agreement with AOP Orphan for Landiolol

    Details:

    The Company will support the submission of a new drug application to the U.S. FDA seeking approval for Landiolol for the short-term reduction of ventricular rate in patients with supraventricular tachycardia, including atrial fibrillation and atrial flutter.


    Lead Product(s): Landiolol Hydrochloride

    Therapeutic Area: Cardiology/Vascular Diseases Product Name: LDLL600

    Highest Development Status: Phase IIIProduct Type: Small molecule

    Partner/Sponsor/Collaborator: Eagle Pharmaceuticals

    Deal Size: Undisclosed Upfront Cash: $5.0 million

    Deal Type: Licensing Agreement August 09, 2021

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