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A Phase II, Multicentre, Double-blind, Randomised, Placebo Controlled, Dose Escalation and Dose Finding Study to Evaluate the Efficacy and Safety of Dysport in Vulvodynia Patients

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Trial Profile

A Phase II, Multicentre, Double-blind, Randomised, Placebo Controlled, Dose Escalation and Dose Finding Study to Evaluate the Efficacy and Safety of Dysport in Vulvodynia Patients

Status: Discontinued
Phase of Trial: Phase II

Latest Information Update: 06 May 2025

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At a glance

  • Drugs Botulinum-Toxin-A (Primary)
  • Indications Vulvodynia
  • Focus Adverse reactions; Therapeutic Use
  • Acronyms DYVINIA
  • Sponsors Ipsen

Most Recent Events

  • 15 Apr 2025 Results(n=60) evaluating optimal doses of Dysport and evaluate its efficacy and safety compared with placebo published in the Journal of Sexual Medicine.
  • 29 Jan 2021 Status changed from active, no longer recruiting to discontinued.
  • 25 Nov 2020 Planned End Date changed from 31 Dec 2022 to 31 Jan 2021.

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