DATROWAY Shows Significant Survival Improvement for TNBC Patients
Written by Emily J. Thompson, Senior Investment Analyst
Updated: 1h ago
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Should l Buy AZN?
Source: Newsfilter
- Clinical Trial Results: In the TROPION-Breast02 trial, DATROWAY demonstrated a 5-month improvement in median overall survival (OS) compared to chemotherapy, with a 43% reduction in the risk of disease progression, indicating its potential in treating unresectable or metastatic triple-negative breast cancer (TNBC).
- Priority Review Approval: The supplemental Biologics License Application (sBLA) for DATROWAY has been accepted for Priority Review by the FDA, and if approved, it will set a new standard of care in this setting, addressing the urgent need for effective treatments.
- Global Collaborative Development: The partnership between Daiichi Sankyo and AstraZeneca facilitates the global development of DATROWAY, which is expected to accelerate regulatory submissions for breast and lung cancer, further expanding market reach.
- Safety Profile Analysis: The safety profile of DATROWAY aligns with previous trials, with 33% of patients experiencing grade 3 or higher adverse events; however, its treatment response rate of 62.5% indicates good tolerability and efficacy.
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Analyst Views on AZN
Wall Street analysts forecast AZN stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for AZN is 102.75 USD with a low forecast of 95.00 USD and a high forecast of 108.00 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.
5 Analyst Rating
5 Buy
0 Hold
0 Sell
Strong Buy
Current: 92.770
Low
95.00
Averages
102.75
High
108.00
Current: 92.770
Low
95.00
Averages
102.75
High
108.00
About AZN
AstraZeneca PLC is a United Kingdom-based science-led biopharmaceutical company. The Company focuses on the discovery, development, and commercialization of prescription medicines. The Company operates across therapy areas, including Oncology; Cardiovascular, Renal and Metabolism (CVRM); Respiratory and Immunology (R&I); Vaccines and Immune Therapies (V&I), and Rare Disease. In the Oncology area, its key products include Tagrisso, Imfinzi, Calquence, Lynparza, and Enhertu. The key products of CVRM area include Farxiga/Forxiga, Brilinta/Brilique, Crestor, and Lokelma. In the R&I area, the key products are Symbicort, Fasenra, Breztri/Trixeo, and Tezspire. In the V&I Therapies area, the products are Beyfortus and FluMist. The products in the Rare Disease area are Ultomiris, Soliris, Strensiq, and Koselugo. It has about 191 projects in its development pipeline, including 19 new molecular entities (NMEs) in the late-stage pipeline. The Company distributes its products in over 125 countries.
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.
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- Market Potential: If approved, aPREMIUM as a next-generation therapeutic option could provide AstraZeneca with significant revenue growth opportunities, especially against the backdrop of increasing demand for innovative therapies in the current market.
- R&D Investment: This priority review reflects AstraZeneca's ongoing commitment to research and development, aiming to meet unmet medical needs through innovative products, thereby enhancing the company's long-term growth potential.
- Investor Confidence Boost: The FDA's priority review decision is likely to bolster investor confidence in AstraZeneca's future performance, potentially having a positive impact on the company's stock price and further solidifying its position in the global pharmaceutical industry.
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- Clinical Trial Results: In the TROPION-Breast02 trial, DATROWAY demonstrated a 5-month improvement in median overall survival (OS) compared to chemotherapy, with a 43% reduction in the risk of disease progression, indicating its potential in treating unresectable or metastatic triple-negative breast cancer (TNBC).
- Priority Review Approval: The supplemental Biologics License Application (sBLA) for DATROWAY has been accepted for Priority Review by the FDA, and if approved, it will set a new standard of care in this setting, addressing the urgent need for effective treatments.
- Global Collaborative Development: The partnership between Daiichi Sankyo and AstraZeneca facilitates the global development of DATROWAY, which is expected to accelerate regulatory submissions for breast and lung cancer, further expanding market reach.
- Safety Profile Analysis: The safety profile of DATROWAY aligns with previous trials, with 33% of patients experiencing grade 3 or higher adverse events; however, its treatment response rate of 62.5% indicates good tolerability and efficacy.
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