bimatoprost
Phase 2- Indications
- Glaucoma, Ocular hypertension
Company intelligence / Profile preview
The company completed enrollment in Phase I/II trials in November 2024. 18-month data showed 100% of patients remained off all topical IOP-lowering drops, all patients achieved an IOP reduction of more than 20% from baseline, and 96% of patients maintained an IOP ≤18 mmHg. The platform was well-tolerated with no product-related adverse events.[4][5]
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