Viridian Therapeutics (VRDN) Secures FDA Priority Review for Veligrotug in Thyroid Eye Disease
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Dec 23 2025
0mins
Source: NASDAQ.COM
- FDA Priority Review: Viridian Therapeutics' Biologics License Application for Veligrotug has been accepted for priority review by the FDA, with a decision expected by June 30, 2026, which will expedite its entry into the thyroid eye disease treatment market to meet growing patient needs.
- Clinical Trial Success: Veligrotug met all primary and secondary endpoints in the THRIVE and THRIVE 2 phase 3 clinical trials, demonstrating significant improvement in chronic thyroid eye disease patients' diplopia symptoms, with rapid clinical benefits enhancing its market competitiveness.
- Breakthrough Therapy Designation: In May 2025, the FDA granted Veligrotug breakthrough therapy designation, indicating its potential in treating thyroid eye disease, which further elevates investor and market interest in the drug.
- European Market Plans: Viridian plans to submit a Marketing Authorisation Application to the European Medicines Agency in the first quarter of 2026, reflecting its strategic intent for global expansion and aiming to capture growth opportunities in international markets.
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Analyst Views on VRDN
Wall Street analysts forecast VRDN stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for VRDN is 41.71 USD with a low forecast of 14.20 USD and a high forecast of 61.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.
17 Analyst Rating
17 Buy
0 Hold
0 Sell
Strong Buy
Current: 33.570
Low
14.20
Averages
41.71
High
61.00
Current: 33.570
Low
14.20
Averages
41.71
High
61.00
About VRDN
Viridian Therapeutics, Inc. is a biopharmaceutical company focused on engineering and developing potential medicines for patients with serious and rare diseases. The Company is advancing multiple candidates in the clinic for the treatment of patients with thyroid eye disease (TED). The Company is conducting two global Phase 3 clinical trials (THRIVE and THRIVE-2) to evaluate the safety and efficacy of veligrotug in patients with active and chronic TED. It is also conducting two global Phase 3 clinical trials, REVEAL-1 and REVEAL-2, to evaluate the efficacy and safety of VRDN-003 in patients. Its advanced program, veligrotug, is a differentiated humanized monoclonal antibody targeting IGF-1R intravenously administered for the treatment of TED. In addition to its TED portfolio, the Company is advancing a novel portfolio of neonatal Fc receptor (FcRn) inhibitors, including VRDN-006 and VRDN-008, which has the potential to be developed in multiple autoimmune diseases.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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Viridian Therapeutics (VRDN) Secures FDA Priority Review for Veligrotug in Thyroid Eye Disease
- FDA Priority Review: Viridian Therapeutics' Biologics License Application for Veligrotug has been accepted for priority review by the FDA, with a decision expected by June 30, 2026, which will expedite its entry into the thyroid eye disease treatment market to meet growing patient needs.
- Clinical Trial Success: Veligrotug met all primary and secondary endpoints in the THRIVE and THRIVE 2 phase 3 clinical trials, demonstrating significant improvement in chronic thyroid eye disease patients' diplopia symptoms, with rapid clinical benefits enhancing its market competitiveness.
- Breakthrough Therapy Designation: In May 2025, the FDA granted Veligrotug breakthrough therapy designation, indicating its potential in treating thyroid eye disease, which further elevates investor and market interest in the drug.
- European Market Plans: Viridian plans to submit a Marketing Authorisation Application to the European Medicines Agency in the first quarter of 2026, reflecting its strategic intent for global expansion and aiming to capture growth opportunities in international markets.
Continue Reading