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A Proof of Concept Study to Evaluate the Efficacy, Safety and Tolerability of Secukinumab 300 mg Over 32 Weeks in Adult Patients With Biopsy-proven Forms of Lichen Planus Not Adequately Controlled With Topical Therapies - PRELUDE

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Trial Profile

A Proof of Concept Study to Evaluate the Efficacy, Safety and Tolerability of Secukinumab 300 mg Over 32 Weeks in Adult Patients With Biopsy-proven Forms of Lichen Planus Not Adequately Controlled With Topical Therapies - PRELUDE

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 24 Aug 2023

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At a glance

  • Drugs Secukinumab (Primary)
  • Indications Lichen planus
  • Focus Proof of concept; Therapeutic Use
  • Acronyms PRELUDE
  • Sponsors Novartis; Novartis Pharmaceuticals

Most Recent Events

  • 14 Jul 2022 Status changed from active, no longer recruiting to completed.
  • 19 May 2022 This trial has been completed in Germany, according to European Clinical Trials Database record.
  • 14 May 2022 This trial has been completed in France, according to European Clinical Trials Database record.

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