Viridian Therapeutics/$VRDN

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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
$2.4B
-
-$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

FDA approval of Lumvoa on June 26, 2026 gives Viridian its first commercial product and a differentiated label covering thyroid eye disease regardless of disease activity or duration, including both active and chronic TED. (Viridian Therapeutics)
Elegrobart produced positive Phase 3 results in both active and chronic TED, with statistically significant proptosis responses and generally favorable tolerability; if approved, its low-volume subcutaneous autoinjector could offer a more convenient at-home alternative and expand Viridian’s TED franchise. (Viridian Therapeutics)
Viridian had $981.5 million in cash, cash equivalents and marketable securities at June 30, 2026, supplemented by approximately $334.7 million of net proceeds from its May financing, providing substantial resources for Lumvoa commercialization, elegrobart development and earlier pipeline programs. (Viridian Therapeutics)
Lumvoa’s commercial execution remains unproven: first doses were administered only in July 2026, while payer-coverage work was still ongoing as of July 31; meanwhile, Q2 selling, general and administrative expense rose to $55.0 million and net loss reached $127.1 million. (Viridian Therapeutics)
Lumvoa carries meaningful treatment-burden and safety considerations: it requires five intravenous infusions over 12 weeks, with reported risks including infusion reactions in approximately 9% of patients, hyperglycemia in 12%, and potentially permanent hearing impairment. (Viridian Therapeutics)
Viridian increased financing risk in May 2026 by issuing $225.0 million of convertible notes and 7.35 million common shares; future conversion or further capital needs could dilute shareholders, particularly while the company remains loss-making. (Viridian Therapeutics)
Data summarised monthly by Lightyear AI. Last updated on 8 Sept 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

Funds containing VRDN

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