Viridian Therapeutics wins FDA approval for Lumvoa for thyroid eye disease
The FDA approved Viridian Therapeutics' Lumvoa (veligrotug-vvze) for thyroid eye disease regardless of disease activity or duration, and the company plans to launch it immediately. The approval is Viridian's first FDA-approved product and first commercial product, a milestone that moves the company from development toward sales.
- FDA approval announced June 26, 2026; Lumvoa is the first TED treatment with labeling covering both active and chronic TED
- Launch planned immediately; physicians can prescribe Lumvoa tomorrow, per the press release
- Lumvoa is given as five intravenous infusions over 12 weeks; infusion reactions reported in about 9% of patients
- Conference call and webcast scheduled Monday, June 29, 2026 at 8:00 a.m. ET