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A Double Blind, Prospective, Randomized, Placebo Controlled, Multi-center Phase 3 Study to Evaluate Efficacy and Safety of Cevira in Patients With Cervical Histologic High-grade Squamous Intraepithelial Lesions (HSIL)

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Trial Profile

A Double Blind, Prospective, Randomized, Placebo Controlled, Multi-center Phase 3 Study to Evaluate Efficacy and Safety of Cevira in Patients With Cervical Histologic High-grade Squamous Intraepithelial Lesions (HSIL)

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 28 Apr 2025

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At a glance

  • Drugs Hexyl aminolevulinate (Primary) ; Hexyl aminolevulinate (Primary)
  • Indications Cervical intraepithelial neoplasia; Human papillomavirus infections; Squamous cell cancer
  • Focus Registrational; Therapeutic Use
  • Acronyms APRICITY
  • Sponsors Asieris Pharmaceuticals

Most Recent Events

  • 18 Apr 2025 According to an Asieris Pharmaceuticals media release, In May 2024 marketing application was officially accepted by the National Medical Products Administration (NMPA). As of the report release, the Center for Drug Evaluation (CDE), NMPA had completed the first round of technical reviews, covering toxicology, clinical data, biostatistics, clinical pharmacology, and pharmaceutical quality.
  • 17 Sep 2024 According to an Asieris Pharmaceuticals media release, company announces that its partner Asieris Pharmaceuticals have been accepted for oral presentation of this study by the International Photodynamic Therapy & Photodiagnosis Update Conference in Germany on September 17, 2024. focusing on the efficacy data related to the regression of the histological grade of cervical precancerous lesions.
  • 17 Sep 2024 Results presented in the Asieris Pharmaceuticals Media Release.

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