TED Program Details
Viridian’s lead product candidate, veligrotug (VRDN-001), is a potential best-in-class, IV monoclonal antibody targeting IGF-1R. Veligrotug (VRDN-001) acts as a full antagonist of IGF-1R, and based on clinical data to date, has demonstrated robust clinical activity and was generally well-tolerated.
The company conducted two positive global Phase 3 trials, THRIVE (NCT05176639) and THRIVE-2 (NCT06021054), for people living with active and chronic TED, respectively. A Biologics License Application (BLA) for veligrotug was accepted by the U.S. FDA in December 2025 and is currently under Priority Review.

Elegrobart is a subcutaneously delivered, half‑life‑extended monoclonal antibody targeting the insulin‑like growth factor‑1 receptor (IGF‑1R). Elegrobart has the same binding domain as veligrotug and was engineered to have a longer half-life. Elegrobart is designed to be a low volume, infrequently dosed subcutaneous IGF-1R for TED, which we believe has the potential to preserve the efficacy of anti-IGF-1Rs in TED, improve safety, and maximize convenience for patients with subcutaneous delivery.
We reported positive topline results for elegrobart from two pivotal phase 3 clinical trials, REVEAL-1 and REVEAL-2, for people living with active and chronic TED, respectively.
Viridian’s preclinical TSHR inhibitor program includes a potential best-in-class, half-life extended, monoclonal antibody that inhibits TSHR, designed for subcutaneous delivery in an autoinjector with the potential to support extended dosing intervals designed for patient convenience.
