Viridian posts first Lumvoa revenue but net loss widens
Overview
U.S. biotech firm reported first net product revenue from Lumvoa after TED launch in Q3
Q3 net loss widened to $101.2 mln from $34.6 mln a year earlier
R&D expenses fell, while SG&A costs rose to support Lumvoa commercial activities
Outlook
Company plans BLA submission for elegrobart in TED in Q1 2027
VRDN-292 phase 1 trial in Graves’ disease expected to begin in Q4 2026
Company expects VRDN-008 phase 1 data and FcRn portfolio update in Q4 2026
Result Drivers
LUMVOA LAUNCH - Co reported $24.7 mln in net product revenue from Lumvoa in its first quarter of launch, with over 100 patients on therapy and progress in market access
HIGHER SG&A COSTS - SG&A expenses rose due to increased personnel and professional services to support Lumvoa commercial activities and organizational growth
LOWER R&D EXPENSES - R&D expenses declined, mainly due to reduced costs for veligrotug and elegrobart clinical studies, partly offset by higher investment in TSHR and FcRn programs and increased headcount
Company press release:
Key Details
Metric | Beat/Miss | Actual | Consensus Estimate |
Q3 Net Loss | $101.21 mln |
Analyst Coverage
The current average analyst rating on the shares is "buy" and the breakdown of recommendations is 17 "strong buy" or "buy", no "hold" and no "sell" or "strong sell"
The average consensus recommendation for the biotechnology & medical research peer group is "buy"
Wall Street's median 12-month price target for Viridian Therapeutics, Inc. is $35.00, about 39.2% above its November 3 closing price of $25.15
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(This story was created using Reuters automation and AI based on LSEG and company data. It was checked and edited by a Reuters journalist prior to publication.)