Highlights
- Veligrotug, an anti-IGF-1R antibody, has shown significant efficacy in reducing proptosis and diplopia in both active and chronic thyroid eye disease (TED) in phase 3 clinical trials (THRIVE, THRIVE-2).
- The regimen offers a shortened infusion protocol—five infusions at three-week intervals, each lasting 30 minutes—compared to teprotumumab, potentially improving patient convenience and adherence.
- Safety profile is manageable, with mild adverse events predominating and rates of hearing impairment similar to other IGF-1R inhibitors.
- Veligrotug has received Breakthrough Therapy designation from the FDA, expediting its review as an alternative to teprotumumab.
Clinical Background and Disease Burden
Specialty calculators
For clinical reference; use professional judgment.
