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Budesonide oral suspension - Takeda

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Drug Profile

Budesonide oral suspension - Takeda

Alternative Names: Eohilia; Oral viscous budesonide; SHP-621; TAK-721

Latest Information Update: 20 Jan 2025

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At a glance

  • Originator Verus Pharmaceuticals
  • Developer Takeda
  • Class Alcohols; Anti-inflammatories; Antiallergics; Antiasthmatics; Antivirals; Dioxoles; Glucocorticoids; Pregnenediones; Small molecules
  • Mechanism of Action Glucocorticoid receptor agonists
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    Yes - Eosinophilic oesophagitis
  • New Molecular Entity No

Highest Development Phases

  • Marketed Eosinophilic oesophagitis

Most Recent Events

  • 08 Sep 2024 Adverse events and pharmacokinetics data from a phase I trial in healthy volunteers presented at the American College of Clinical Pharmacology Annual Meeting (ACCP -2024)
  • 28 Aug 2024 Launched for Eosinophilic oesophagitis (In adolescents, In children, In the elderly, In adults) in USA (PO), prior to August 2024
  • 15 Feb 2024 Takeda plans to launch budesonide oral suspension for Eosinophilic esophagitis, by end of February 2024

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