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An Open-Label, Phase 1 Clinical Study to Evaluate the Safety and Tolerability of Subcutaneous Elamipretide in Subjects With Intermediate Age-Related Macular Degeneration

2016-07-29 04:08:21 | BioPortfolio

Summary

This is an open-label, Phase 1 single-center study in approximately 40 subjects who have 1 eye with intermediate AMD, including a high-risk drusen without geographic atrophy (GA) subgroup and a noncentral GA subgroup. Eligible subjects will receive 40 mg of elamipretide administered as a once daily 1.0 mL subcutaneous injection for 12 weeks.

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Conditions

Age-Related Macular Degeneration

Intervention

Elamipretide

Location

Duke University School of Medicine / Dept. of Ophthalmology (Duke Eye Center)
Durham
North Carolina
United States
27710

Status

Not yet recruiting

Source

Stealth BioTherapeutics Inc.

Results (where available)

View Results

Links

Published on BioPortfolio: 2016-07-29T04:08:21-0400

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