June 29, 2026
1 min read
Add topic to email alerts
Receive an email when new articles are posted on
Please provide your email address to receive an email when new articles are posted on .
The FDA approved Lumvoa, a full insulin-like growth factor 1 receptor antagonist, for the treatment of thyroid eye disease, according to a press release from Viridian Therapeutics. The approval was supported by data from the phase 3 THRIVE and THRIVE-2 pivotal clinical trials, which investigated Lumvoa (veligrotug-vvze, 500 mg) for active and chronic thyroid eye disease (TED), respectively. In
June 29, 2026
1 min read
Add topic to email alerts
Receive an email when new articles are posted on
Please provide your email address to receive an email when new articles are posted on .

Viridian Therapeutics Announces U.S. FDA Approval and Launch of Lumvoa™ (veligrotug-vvze) for the Treatment of Thyroid Eye Disease

FDA approves Viridian eye drug, stoking competition with Amgen's Tepezza

Viridian Secures First FDA Approval, Sets Up Challenge To Amgen's Tepezza For Thyroid Eye Disease - Virid

New Drug Approved for Thyroid Eye Disease

Viridian may have edge over Amgen in eye drug showdown, analysts argue

Look out, Amgen. Here comes Viridian with FDA nod for TED med Lumvoa

FDA Grants Priority Review To Genentech’s Application for Enspryng, the First and Only At-Home Subcutaneous Treatment Option for Thyroid Eye Disease (TED)

Otsuka reports long-term kidney data key to Voyxact's bid for full approval