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Post-marketing surveillance of DIACOMIT (Capsule: 250 mg or 500 mg, Powder for Oral Suspension: 250 mg or 500 mg)

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Trial Profile

Post-marketing surveillance of DIACOMIT (Capsule: 250 mg or 500 mg, Powder for Oral Suspension: 250 mg or 500 mg)

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 02 Jan 2023

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At a glance

  • Drugs Stiripentol (Primary)
  • Indications Dravet syndrome
  • Focus Adverse reactions
  • Sponsors Meiji Seika Pharma

    • Most Recent Events

    • 30 Dec 2022 Status changed from recruiting to completed.
    • 23 Dec 2021 New trial record

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