Atossa Therapeutics (ATOS) Receives FDA Orphan Drug Designation, Shares Rise 13%
Written by Emily J. Thompson, Senior Investment Analyst
Updated: 3h ago
0mins
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.
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.





