drugset / Trial / NCT05282004

Study of the Safety of Use of Intravitreal SOK583A1 Provided in a Vial Kit

NCT05282004

Phase 3 Completed 36 enrolled Sandoz
NaSingle-groupOpen-labelTreatment

Summary

This is a single-arm, open-label study where all patients will receive a single injection of SOK583A1 (40 mg/mL) provided in a vial kit at Baseline. The total study duration for the individual participant is approximately 31 days.

Timeline

Start
2022-05-16
Primary completion
2022-09-07
Completion
2022-09-07

Drugs

EvaluationDrugModalityDoseRoute
Subject SOK583A1 Protein / enzyme biologic 2 mg Intravitreal