Overview
Biotechnology firm's Q4 revenue missed analyst expectations
Net loss for Q4 widened compared to last year
Company maintains strong cash position, expects to fund plans through profitability
Outlook
Viridian expects veligrotug's U.S. commercial launch in mid-2026, pending FDA approval
Company anticipates elegrobart topline data in Q1 and Q2 2026
Viridian plans to fund business plans through profitability with cash and potential revenues
Result Drivers
R&D EXPENSES - Increase driven by ongoing clinical trials and manufacturing activities for TED portfolio, and advancing FcRn inhibitor portfolio and TSHR program
SG&A EXPENSES - Rise due to preparatory commercial activities for veligrotug, including increased personnel costs
CASH POSITION - Strong cash reserves expected to fund business plans through profitability
Company press release: ID:nBw7mLxhNa
Key Details
Metric | Beat/Miss | Actual | Consensus Estimate |
Q4 Revenue | Miss | $132,000 | $12.73 mln (13 Analysts) |
Q4 Net Income | -$120.36 mln |
Analyst Coverage
The current average analyst rating on the shares is "buy" and the breakdown of recommendations is 17 "strong buy" or "buy", 2 "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 $42.00, about 45.1% above its February 25 closing price of $28.94
For questions concerning the data in this report, contact Estimates.Support@lseg.com. For any other questions or feedback, contact reuters.support@thomsonreuters.com.
(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.)
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