Tenaya Therapeutics Q3 net loss narrows
Overview
US heart disease therapy developer's Q3 net loss narrowed, beating analyst expectations
Q3 operating loss was lower than analyst expectations
Company expects cash to fund operations into Q4 2027
Outlook
Company expects to report longer-term follow-up data from the MyPEAK-1 trial data by year end
Company to provide additional interim RIDGE-1 clinical trial data by year end
Tenaya plans to start at least one Phase 2 TN-301 trial in H2 2027
Result Drivers
REGULATORY DESIGNATION - FDA granted RMAT designation to TN-401, supported by positive interim data from RIDGE-1 trial
CASH - As of September 30, 2026, cash and cash equivalents were $66.8 million
LOWER R&D EXPENSES - R&D expenses declined year-over-year, partly due to lower stock-based compensation
Company press release:
Key Details
Metric | Beat/Miss | Actual | Consensus Estimate |
Q3 Net Loss | $18.94 mln | ||
Q3 Operating Income | Beat | -$19.57 mln | -$22.67 mln (3 Analysts) |
Q3 Pretax Loss | Beat | $18.94 mln | $21.73 mln (4 Analysts) |
Q3 Loss Per Basic Share | $0.08 | ||
Q3 Operating Expenses | $21.27 mln |
Analyst Coverage
The current average analyst rating on the shares is "buy" and the breakdown of recommendations is 6 "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 Tenaya Therapeutics, Inc. is $3.50, about 871.4% above its November 3 closing price of $0.36
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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.)