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 (VRDN-003) is a potential best-in-class subcutaneous monoclonal antibody targeting IGF-1R. Elegrobart has the same binding domain as its parent molecule, veligrotug (VRDN-001), and was engineered to have a longer half-life. Elegrobart is designed to maintain the clinical response of veligrotug (VRDN-001) IV while significantly increasing patient convenience and potentially improving safety.
The company initiated two phase 3 clinical trials of elegrobart in August 2024.
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.
