Safety, Tolerability and Pharmacokinetics of Single Rising Intravitreal Doses and Multiple Intravitreal Dosing of BI 754132 in Patients With Geographic Atrophy Secondary to Age-related Macular Degeneration (Open Label, Non-randomized, Uncontrolled)

Status: Discontinued

Phase of Trial: Phase I

Latest Information Update: 19 Sep 2023

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At a glance

Drugs BI 754132 (Primary)
Indications Age-related macular degeneration
Focus Adverse reactions; First in man
Sponsors Boehringer Ingelheim

Most Recent Events

23 Aug 2022 Status changed from suspended to discontinued.
26 Jul 2022 Planned End Date changed from 15 Aug 2022 to 9 Aug 2022.
26 Jul 2022 Planned primary completion date changed from 15 Aug 2022 to 9 Aug 2022.

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