Trial Profile

A Randomized, Double-masked, Placebo-controlled Safety, Tolerability, and Efficacy Study of Veligrotug (VRDN-001), a Humanized Monoclonal Antibody Directed Against the IGF-1 Receptor, in Participants With Chronic Thyroid Eye Disease (TED)

Status: Active, no longer recruiting

Phase of Trial: Phase III

Latest Information Update: 30 Apr 2025

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At a glance

24 Apr 2025 Planned End Date changed from 1 Sep 2025 to 1 Aug 2025.
27 Feb 2025 According to a Viridian Therapeutics media release, MAA submission to the European Medicines Agency expected in the first half of 2026.
08 Jan 2025 According to a Viridian Therapeutics media release, company plans to submit a BLA for veligrotug for the treatment of patients with active and chronic TED in the second half of 2025. and anticipated commercial launch.

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