drugset / Trial / NCT05134974

Safety and Efficacy of Nyxol (0.75% Phentolamine Ophthalmic Solution) to Reverse Pharmacologically-Induced Mydriasis (MIRA-3)

NCT05134974

Phase 3 Completed 368 enrolled Ocuphire Pharma, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

The objectives of this study are: * To evaluate the efficacy of Nyxol to expedite the reversal of pharmacologically-induced mydriasis across multiple mydriatic agents with an emphasis on phenylephrine * To evaluate the efficacy of Nyxol to return subjects to baseline accommodation after worsening (with cycloplegic agents tropicamide and Paremyd) * To evaluate the safety of Nyxol * To evaluate any additional benefits of the reversal of pharmacologically-induced mydriasis * To evaluate the systemic exposure of Nyxol on pharmacokinetic (PK) sampling

Timeline

Start
2021-11-18
Primary completion
2022-03-18
Completion
2022-03-29

Drugs

EvaluationDrugModalityDoseRoute
Comparator Phentolamine Small molecule 0.75 % Topical

Indications

No indication recorded.