Ocuphire Pharma Results Presentation Deck slide image

Ocuphire Pharma Results Presentation Deck

25 APX3330 Product Candidate Profile for Multiple Retinal Indications Oral, First-In-Class Ref-1 Inhibitor with Favorable Human Safety Data from 12 Completed Trials APX3330: Well-tolerated Oral Dose up to 600 mg/day | Twice Daily Dosing Favorable Safety Profile Over 350 Subjects (Healthy, Liver, Cancer, Diabetic) Treated Notably, Several Subjects Dosed ~1 Yr and Others 24-Wks MOA and Efficacy Signals in DR Novel MOA for Treating Retina ā†“ Inflammation ā†“ Abnormal Angiogenesis Daily vs. episodic exposure Good Patient Compliance in ZETA-1 with Convenient Oral Dosing APX3330 Demonstrated Slowing of Progression of Diabetic Retinopathy Few Systemic AEs Across All Doses (120mg-720mg) < 5% Mild Skin Rash (reversible) < 5% Mild Diarrhea No Treatment-Related Organ Toxicity (Liver, Cardiovascular {BP, HR}, Kidney, Neurologic, Pulmonary) Minimal Ocular Side Effects* Source: ZETA-1 Clinical Trial; *1 subject had vision blur thought to be related by investigator in ZETA-1 Ocuphire
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