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: 04 May 2026

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At a glance

28 Apr 2026 Actual primary completion date changed from 31 Dec 2022 to 7 Aug 2022.
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.

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