Overview
Atossa Therapeutics Q3 net loss widens to $8.7 mln, operating expenses rise to $9.3 mln
Company advances $(Z)$-endoxifen program with regulatory strategies and clinical trials
Appointed key leadership roles to drive (Z)-endoxifen development and commercialization and streamline development programs
Outlook
Atossa targets IND submission for (Z)-endoxifen in Q4 2025
Company plans to update shareholders on FDA meeting outcome by year-end 2025
Atossa focuses on NDA-enabling activities for (Z)-endoxifen in 2026
Result Drivers
R&D EXPENSES - Increased R&D expenses due to higher spending on (Z)-endoxifen trials and drug development costs
REGULATORY STRATEGY - Co requested a Type C meeting with FDA to accelerate (Z)-endoxifen development for breast cancer risk reduction
TRIAL STREAMLINING - Streamlined EVANGELINE breast cancer trial to focus on NDA-enabling activities and reduce costs
Key Details
Metric | Beat/Miss | Actual | Consensus Estimate |
Q3 EPS | -$0.07 | ||
Q3 Net Income | -$8.69 mln | ||
Q3 Operating Expenses | $9.25 mln | ||
Q3 Operating Income | -$9.25 mln | ||
Q3 Pretax Profit | -$8.69 mln |
Analyst Coverage
The current average analyst rating on the shares is "buy" and the breakdown of recommendations is 4 "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 Atossa Therapeutics Inc is $5.50, about 85% above its November 11 closing price of $0.83
Press Release: ID:nPnBF91Za
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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.)
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