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Viridian Therapeutics/$VRDN

1D1W1M3M6MYTD1Y5YMAX

About Viridian Therapeutics

Viridian Therapeutics Inc is a clinical-stage biopharmaceutical company that engages in developing multiple product candidates to treat patients who suffer from thyroid eye disease. The company is developing two anti-IGF-1R product candidates, veligrotug for intravenous (IV) administration and elegrobart (formerly VRDN-003) for subcutaneous (SC) administration, to treat patients with TED. Our most advance program, veligrotug, is a differentiated humanized monoclonal antibody targeting IGF-1R intravenously administered for the treatment of TED.
Ticker
$VRDN
Sector
Health
Primary listing
NASDAQ
Employees
252

VRDN Metrics

BasicAdvanced
$2.9B
-
-$3.46
0.96
-

What the Analysts think about VRDN

Analyst ratings (Buy, Hold, Sell) for Viridian Therapeutics stock.
Analyst projections of the future price of Viridian Therapeutics stock.

Bulls say / Bears say

Lumvoa is now FDA-approved on the strength of trials in active and chronic TED, with a shorter five-infusion course than Tepezza’s eight. In the active-disease trial, 70% of patients had a proptosis response versus 5% on placebo, and the approval gives Viridian a commercial product rather than a development-stage story alone. (Reuters, American Academy of Ophthalmology)
Early launch indicators point to meaningful physician interest: Viridian had engaged 95% of its 2,000 core prescribers by the end of July, and said initial patient forms showed broad demand. Payer coverage efforts were also reported to be progressing. (Viridian Therapeutics)
Elegrobart has positive phase 3 results in both active and chronic TED, and the active-disease trial met its primary endpoint with both monthly and every-eight-week dosing. If approved, its self-administered subcutaneous format could offer a lower-burden option; Viridian was targeting a BLA filing in Q1 2027. (Ophthalmology Management, Viridian Therapeutics)
Lumvoa must win share from Amgen’s established Tepezza franchise, and Amgen is developing a subcutaneous Tepezza that could narrow any convenience gap. That may limit Viridian’s ability to turn its shorter infusion regimen into lasting differentiation. (BioSpace)
Commercial uptake may take time to translate into sales: Viridian’s September update described slow prior-authorisation processes and a market that remains only partly developed. Strong physician engagement is encouraging, but it does not yet show that patients are progressing quickly through payer approval and treatment. (Investing.com)
Hearing impairment is a material safety concern for Lumvoa: in its clinical trials, it was reported in 17% of treated participants versus 6% on placebo, and the label calls for hearing checks before, during and after treatment. This could deter some patients or prescribers, even though hearing risks are also associated with the drug class. (MedCity News)
Data summarised monthly by Lightyear AI. Last updated on 20 Oct 2026.

VRDN Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

VRDN Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
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