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Double-blind, Vehicle-controlled, Phase I Study to Evaluate Safety and Efficacy of a 0.3% and 1% Topical Formulation of KM-001 for Management of Moderate to Severe Pruritus in Adult Patients With Lichen Simplex Chronicus (LSC)

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Trial Profile

Double-blind, Vehicle-controlled, Phase I Study to Evaluate Safety and Efficacy of a 0.3% and 1% Topical Formulation of KM-001 for Management of Moderate to Severe Pruritus in Adult Patients With Lichen Simplex Chronicus (LSC)

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 05 Apr 2024

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At a glance

  • Drugs KM-001 (Primary)
  • Indications Neurodermatitis; Pruritus
  • Focus Adverse reactions; Pharmacokinetics
  • Sponsors Kamari Pharma

Most Recent Events

  • 05 Apr 2024 Last checked against ClinicalTrials.gov record.
  • 31 Mar 2024 Status changed from recruiting to completed.
  • 15 Jun 2023 Planned End Date changed from 31 May 2023 to 1 Jul 2023.

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