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Assessment of the Initial Efficacy and Safety of BRM424 Ophthalmic Solutions in Patients With Neurotrophic Keratitis

Assessment of the Initial Efficacy and Safety of BRM424 Ophthalmic Solutions in Patients With Neurotrophic Keratitis

Recruiting
18 years and older
All
Phase 2

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Overview

The objective of this study is to obtain initial efficacy of BRM424 in patients with Stage 2 and Stage 3 NK and evaluate safety and tolerability.

Eligibility

Inclusion Criteria:

  • Be at least 18 years of age;
  • Provide written informed consent;
  • Patients with NK Stage 2 (PED) or Stage 3 (corneal ulcer);

Exclusion Criteria:

  • Any active ocular infection (bacterial, viral, fungal or protozoal) or active ocular inflammation not related to NK;
  • Anticipated need to use therapeutic contact lenses or contact lens wear for refractive correction during the 28-days Treatment Period in the eye(s) with NK;
  • Be a woman of childbearing potential who is not using an acceptable means of birth control;

Study details
    Neurotrophic Keratitis

NCT05927428

BRIM Biotechnology Inc.

21 August 2025

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