Atossa Therapeutics (ATOS) Receives FDA Orphan Drug Designation, Shares Rise 13%
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Jan 16 2026
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Should l Buy ATOS?
Source: seekingalpha
- Orphan Drug Designation: Atossa Therapeutics has received FDA orphan drug designation for its soft tissue sarcoma treatment, which may expedite clinical trial processes and enhance market recognition for this rare cancer therapy.
- Stock Surge: Following this announcement, Atossa Therapeutics' shares rose over 13% to $0.66 in premarket trading, reflecting investor optimism about the company's future prospects and potentially attracting more investor interest.
- Market Advantages: The orphan drug designation not only provides Atossa with market access advantages but may also lead to tax incentives and market exclusivity, thereby strengthening its position in the competitive cancer treatment market.
- R&D Support: This designation will assist Atossa in securing additional funding for its research and development efforts, particularly in the rare cancer sector, further solidifying its strategic position in the biopharmaceutical industry.
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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: 5.330
Low
4.00
Averages
6.33
High
8.00
Current: 5.330
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.
- PRV Program Reauthorization: The U.S. Congress has passed a five-year reauthorization of the Rare Pediatric Disease Priority Review Voucher (PRV) program, enabling Atossa to qualify for a future PRV upon FDA approval, signaling strong support for the drug development industry.
- Potential of (Z)-endoxifen: Atossa's (Z)-endoxifen has received Rare Pediatric Disease (RPD) designation for treating Duchenne Muscular Dystrophy (DMD), providing new opportunities for the company in both cancer and rare diseases, potentially leading to non-dilutive value creation.
- Strong Market Demand: DMD is a fatal childhood disease, and families urgently need treatment options beyond steroids and gene-targeted therapies; the development of (Z)-endoxifen aims to offer a broader treatment approach to meet significant unmet medical needs.
- Positive Preclinical Data: Atossa is optimistic about the emerging preclinical data for (Z)-endoxifen and plans to advance it to clinical trials, aiming to provide more effective treatment options for DMD patients and further solidify the company's market position in the biopharmaceutical sector.
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- 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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- 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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- FDA Orphan Drug Designation: Atossa Therapeutics (ATOS) announced that its (Z)-endoxifen received Orphan Drug Designation from the FDA, leading to a 12.98% stock increase to $0.69, marking a significant milestone in the treatment of Duchenne muscular dystrophy and expected to drive future R&D progress.
- Clinical Trial Progress: ImmunityBio (IBRX) reported that over 85% of the study population has been enrolled in its registrational trial QUILT-2.005 for BCG-naïve non-muscle-invasive bladder cancer, with stock rising 9.43% to $6.04, and full enrollment anticipated by Q2 2026, enhancing market confidence.
- NASDAQ Compliance Extension: Femasys (FEMY) received NASDAQ approval for a 180-day extension to meet the minimum $1.00 bid price requirement, with stock climbing 10.68% to $0.72, providing the company until July 13, 2026, to regain compliance, alleviating investor concerns.
- Successful Financing: Foghorn Therapeutics (FHTX) closed a $50 million registered direct financing at a 30% premium, resulting in a 4.02% stock increase to $6.26, demonstrating market confidence and support for its future development.
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- 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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- Orphan Drug Designation: Atossa Therapeutics' (Z)-Endoxifen has received Orphan Drug Designation from the FDA, marking a significant advancement in the treatment of Duchenne Muscular Dystrophy (DMD) and is expected to accelerate clinical development while enhancing market competitiveness.
- Support for Rare Pediatric Diseases: This designation complements the previously received Rare Pediatric Disease designation, demonstrating Atossa's commitment to addressing the unmet medical needs of DMD patients, which may attract more investment and collaboration opportunities.
- Market Exclusivity Potential: The Orphan Drug Designation provides Atossa with potential eligibility for a period of market exclusivity upon approval, which could help the company secure a favorable position in the competitive biopharmaceutical market and drive revenue growth.
- Advancement of R&D Strategy: Atossa plans to continue engaging with the FDA to advance the development of (Z)-Endoxifen, which is expected to lay the groundwork for future clinical trials and market promotion, thereby enhancing its influence in oncology and rare diseases.
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