- Viridian Therapeutics Inc VRDN announced topline clinical data from the third, low-dose cohort in its ongoing Phase 1/2 trial of VRDN-001 for active thyroid eye disease (TED).
- VRDN-001 was evaluated at 3, 10, and 20 mg/kg doses. The company previously announced positive results from the first two dose cohorts, demonstrating a favorable safety profile.
- The third cohort evaluated a VRDN-001 dose of 3 mg/kg with 6-week data.
- Related: Viridian Therapeutics' Lead Product Has An Opportunity To Differentiate, Analyst, Sees 85% Upside.
- Among 3 mg/kg VRDN-001 treated patients, 67% were proptosis (bulging eyes) responders, 56% were overall responders, 67% achieved a Clinical Activity Score (CAS) of 0 or 1, and 20% had complete resolution of their diplopia (double vision).
- Across all 21 VRDN-001 treated patients to date, 71% were proptosis responders, 67% were overall responders, 62% achieved a CAS of 0 or 1, and 54% had complete resolution of their diplopia, with a favorable safety profile seen across all dose levels –
- 3 mg/kg data support planned once-monthly low-volume subcutaneous dosing profile for VRDN-002 and VRDN-003.
- Price Action: VRDN shares are up 11.60% at $30.64 on the last check Monday.
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