Atossa Therapeutics Receives FDA Orphan Drug Designation for (Z)-Endoxifen in Duchenne Muscular Dystrophy
Written by Emily J. Thompson, Senior Investment Analyst
Updated: 38m ago
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Source: Newsfilter
- 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.
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 6.25 USD with a low forecast of 4.00 USD and a high forecast of 7.75 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: 0.580
Low
4.00
Averages
6.25
High
7.75
Current: 0.580
Low
4.00
Averages
6.25
High
7.75
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.





