Allegro Ophthalmics LLC Receives FDA IND Approval for Phase 2 Clinical Studies With First in Class Integrin Peptide Therapy ALG-1001

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SAN JUAN CAPISTRANO, Calif.--(BUSINESS WIRE)--Allegro Ophthalmics, LLC, a company dedicated to establishing Integrin Peptide Therapy as the next-generation pharmaceutical category for the treatment of vascular eye diseases, today announced that the U.S. Food and Drug Administration (FDA) has approved the company’s Investigational New Drug (IND) application to begin two Phase II clinical studies of ALG-1001. These Phase II clinical trials will be conducted in patients with wet age-related macular degeneration (wet AMD) and in patients with symptomatic vitreomacular traction (VMT).

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