A Phase 1/2 Multicenter, Multidose, Dose Escalation Study to Evaluate the Safety, Tolerability and Clinical Activity of RXI-109 Administered by Intravitreal Injection to Reduce the Progression of Subretinal Fibrosis in Subjects With Advanced Neovascular Age-related Macular Degeneration

Status: Active, no longer recruiting

Phase of Trial: Phase I/II

Latest Information Update: 06 Nov 2021

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At a glance

Drugs PH 109 (Primary)
Indications Scars; Wet age-related macular degeneration
Focus Adverse reactions; First in man; Pharmacokinetics
Sponsors Phio Pharmaceuticals

Most Recent Events

01 Aug 2018 Results presented in a RXi Pharmaceuticals Media Release.
22 Feb 2018 Planned End Date changed from 1 Sep 2017 to 1 May 2018.
22 Feb 2018 Planned primary completion date changed from 1 Jul 2017 to 1 Apr 2018.

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