- EyeGate Pharmaceuticals Inc EYEG has dosed the patient in Phase 2 proof-of-concept study evaluating its lead product candidate, PP-001, in patients with ocular surface inflammation due to ocular surface diseases including dry eyes.
- Topline results are expected by the end of 2021.
- PP-001, an immune-modulating molecule, is an inhibitor of dihydroorotate dehydrogenase (DHODH) and is first-in-class for ophthalmology indications, the company said.
- The randomized, double-masked, placebo-controlled study is designed to evaluate the safety, tolerability, and efficacy of PP-001.
- A total of 21 patients will receive 0.15% of PP-001 or placebo for 12 days.
- The outcome of this study will guide the U.S. clinical development program for dry eye disease following the filing of the IND, which is expected in Q4 2021.
- Price Action: EYEG shares up 7.35% at $4.82 during the premarket session on the last check Monday.
EYEGAB Corporate Bond ETF
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