drugset / Trial / NCT05301751

A Single Ascending Dose Cohort Study of AG-73305 in DME Patients

NCT05301751 ↗

Non-randomizedSequentialOpen-labelTreatment

Summary

This is a multi-centered, open-labeled, single ascending-dose-cohort study to evaluate the safety and efficacy of 4 dose cohorts of AG-73305 administered by intravitreal injection in patients with diabetic macular edema (DME). The objectives of this study were to evaluate the safety, tolerability, duration of effect, systemic pharmacokinetic and immunogenicity profiles of ascending doses of AG-73305 administered by intravitreal injection to patients with DME. Pharmacodynamic endpoints (e.g., best-corrected visual acuity \[BCVA\], spectral domain optical coherence tomography \[SD-OCT\], and optical coherence tomography angiography \[OCT-A\]) were evaluated over 6 months post-treatment. The maximum tolerated dose or the highest administered dose was evaluated for future studies.

Timeline

Start
2022-05-19
Primary completion
2023-09-28
Completion
2023-12-26

Drugs

EvaluationDrugModalityDoseRoute
Subject AG-73305 Unknown 0.5 mg Intravitreal
Subject AG-73305 Unknown 1 mg Intravitreal
Subject AG-73305 Unknown 2 mg Intravitreal
Subject AG-73305 Unknown 4 mg Intravitreal