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A Phase 3, Multicenter, Randomized, Double-Blinded and Placebo-Controlled Study Evaluating the Efficacy and Safety of 0.25% HBM9036 (HL036) Ophthalmic Solution Compared to Placebo in Chinese Subjects With Moderate and Severe Dry Eye

Trial Profile

A Phase 3, Multicenter, Randomized, Double-Blinded and Placebo-Controlled Study Evaluating the Efficacy and Safety of 0.25% HBM9036 (HL036) Ophthalmic Solution Compared to Placebo in Chinese Subjects With Moderate and Severe Dry Eye

Status: Discontinued
Phase of Trial: Phase III

Latest Information Update: 07 Jun 2024

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At a glance

  • Drugs Tanfanercept (Primary)
  • Indications Dry eyes
  • Focus Registrational; Therapeutic Use
  • Sponsors Harbour BioMed

Most Recent Events

  • 28 Apr 2023 According to an HanAll Biopharma media release, Harbour BioMed, a licensed partner of HanAll in China, closed its Phase 3 China study in DED, based on the Independent Data Monitoring Committee's (IDMC) evaluation of the efficacy data from the second interim analysis.
  • 28 Apr 2023 Status changed to discontinued, according to an HanAll Biopharma media release.
  • 23 Feb 2023 Planned End Date changed from 7 Jan 2023 to 7 Apr 2023.

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