10-K · February 26, 2026
Viridian positions itself as a clinical‑stage biopharma focused on best‑in‑class antibody therapeutics for thyroid eye disease (TED) and autoimmune disorders, advancing veligrotug (IV) and elegrobart (SC) as lead IGF‑1R…
Earnings analysis · 10-Q
Filed May 5, 2026 · Our reading of the company's report
The latest report
Viridian Therapeutics reported substantial financial losses in Q1 2026, with a revenue of only $6, a stark decline from prior periods, resulting in an EPS of -$0.90. The company highlighted the launch readiness for its…
Viridian Therapeutics reported substantial financial losses in Q1 2026, with a revenue of only $6, a stark decline from prior periods, resulting in an EPS of -$0.90. The company highlighted the launch readiness for its therapy veligrotug, pending PDUFA approval scheduled for June 30, 2026. Management also noted a significant increase in SG&A expenses related to commercialization preparation.
How much of each revenue dollar the business keeps.
One point per quarterly or annual filing. Both margins are shares of that report's revenue.
Our analysis across the last few reports.
Our model's reading of each filing, not the share price or the market's reaction. Annual and quarterly reports each occupy one position.
The company recorded revenues of $6, sharply down compared to $72 million in Q1 2025.
Viridian incurred a net loss of $104.9 million in Q1 2026, increased from a net loss of $86.9 million in Q1 2025.
Total cash, cash equivalents and marketable securities stood at $762.2 million as of March 31, 2026.
R&D expenses totaled $77.6 million, slightly higher than $76.8 million in Q1 2025.
SG&A expenses escalated to $38.7 million from $17.1 million year-over-year.
Other income, net was reported at $11.3 million, an increase from $7.0 million in Q1 2025.
The company reported an accumulated deficit of $1.444 billion as of March 31, 2026.
Operating cash flow was $(119.7) million in Q1 2026, worse than $(92.7) million for the same period last year.
PDUFA for veligrotug is set for June 30, 2026, with uncertain outcomes affecting future sales.
The company did not provide specific numeric guidance in the filing, focusing on upcoming regulatory timelines.
Viridian positions itself as a clinical‑stage biopharma focused on best‑in‑class antibody therapeutics for thyroid eye disease (TED) and autoimmune disorders, advancing veligrotug (IV) and elegrobart (SC) as lead IGF‑1R…
Viridian reported collaboration revenue of $72 for Q1 2025 and a net loss of $86,912, driven by a $76,835 R&D spend. The company holds approximately $636.6 million of cash, cash equivalents and short-term investments…
Viridian’s 10-K emphasizes a clinical-stage, fast-follower biologics strategy focused on thyroid eye disease (TED) and engineered FcRn inhibitors, with pivotal phase 3 successes for veligrotug (THRIVE and THRIVE-2) and…
Viridian reported collaboration revenue of $86,000 for Q3 2024 and a GAAP net loss of $76,689,000 (EPS $(1.15)) for the three months ended September 30, 2024. Revenue rose modestly versus the prior-year quarter…
This is our reading of a public filing, not the filing itself. Analysis can contain errors; check the source document for full context.