Atossa Therapeutics (ATOS) Receives FDA Orphan Drug Designation, Stock Rises 12.98%
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Jan 17 2026
0mins
Source: NASDAQ.COM
- Orphan Drug Designation: Atossa Therapeutics' (Z)-endoxifen has received FDA Orphan Drug Designation for treating Duchenne muscular dystrophy (DMD), indicating the drug's significance in rare disease treatment and potentially accelerating its clinical development process.
- Regulatory Incentives: This designation provides Atossa with crucial regulatory incentives to support the development of therapies in the rare disease sector, further underscoring the drug's potential to address unmet medical needs for DMD patients.
- Stock Performance: Atossa closed Friday's regular trading session at $0.6150, up 6.02% from the previous day, reflecting positive market sentiment regarding its new drug development prospects.
- After-Hours Trading Surge: In after-hours trading, Atossa's stock rose further to $0.6948, a gain of 12.98%, indicating investor optimism following the FDA designation announcement.
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Analyst Views on ATOS
Wall Street analysts forecast ATOS stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for ATOS is 6.33 USD with a low forecast of 4.00 USD and a high forecast of 8.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.
4 Analyst Rating
4 Buy
0 Hold
0 Sell
Strong Buy
Current: 0.616
Low
4.00
Averages
6.33
High
8.00
Current: 0.616
Low
4.00
Averages
6.33
High
8.00
About ATOS
Atossa Therapeutics, Inc. is a clinical-stage biopharmaceutical company. It is engaged in developing medicines in areas of unmet medical need in oncology with a focus on women’s breast cancer and other breast conditions. Its lead drug candidate under development is oral (Z)-endoxifen, which it is developing for both the prevention and treatment of breast cancer. (Z)-endoxifen is the potent Selective Estrogen Receptor Modulator for estrogen receptor inhibition and causes estrogen receptor degradation. In addition to its potent anti-estrogen effects, (Z)-endoxifen has been shown to target PKCB1, a known oncogenic protein, at clinically attainable blood concentrations. It is developing a form of (Z)-endoxifen which is administered orally for the potential treatment of breast cancer and reduction of breast density. It has completed four Phase I clinical studies and two Phase II clinical studies with its proprietary (Z)-endoxifen (including oral and topical formulations).
About the author

Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
Atossa Therapeutics CEO Steven Quay Named One of Top 50 Healthcare Technology CEOs of 2025
- Leadership Recognition: Atossa Therapeutics' Founder and CEO Steven Quay has been named one of the Top 50 Healthcare Technology CEOs of 2025, highlighting his exceptional leadership in biotechnology innovation and team building, which enhances the company's reputation in the industry.
- Precision Therapy Advancement: Under Quay's leadership, Atossa's lead product (Z)-endoxifen is being optimized across multiple Phase 2 clinical trials, aiming to provide consistent systemic treatment for breast cancer patients, which is expected to significantly improve patient outcomes.
- Multiple Indication Exploration: The company is exploring the application of (Z)-endoxifen for Duchenne Muscular Dystrophy (DMD), which, if successful, will further expand its market potential and strengthen the company's competitiveness in the rare disease sector.
- Strategic Investment Focus: Atossa emphasizes a disciplined capital allocation strategy in clinical development, concentrating on projects that can support future regulatory submissions and commercialization, ensuring sustainable growth in the biopharmaceutical industry.

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Atossa Therapeutics CEO Steven Quay Recognized as Top 50 Healthcare Technology CEO of 2025
- Leadership Recognition: Atossa Therapeutics' Founder and CEO Steven Quay has been named one of the Top 50 Healthcare Technology CEOs of 2025, highlighting his exceptional leadership in advancing biotechnology innovation and building a high-performing, people-centered organization.
- Precision Therapy Advancement: Under Quay's guidance, Atossa's lead product (Z)-endoxifen is being optimized across multiple Phase 2 clinical trials, aiming to provide a unique selective estrogen receptor modulator/degrader that significantly enhances breast cancer treatment outcomes.
- Exploration of Multiple Indications: Atossa is also investigating the application of (Z)-endoxifen for Duchenne Muscular Dystrophy (DMD), showcasing its potential to address high unmet clinical needs and potentially open new market opportunities for the company.
- Strategic Investment Focus: The company emphasizes disciplined capital allocation in clinical development, concentrating on projects that can support future regulatory submissions and commercialization, ensuring sustained competitiveness and innovation in the biopharmaceutical sector.

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