AstraZeneca ((AZN)), Parexel International ((PRXL)), AstraZeneca plc ((GB:AZN)), AstraZeneca ((DE:ZEGA)), AstraZeneca plc US ((AZNCF)) announced an update on their ongoing clinical study.
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AstraZeneca, in collaboration with Parexel International, is conducting a Phase III clinical trial to evaluate the safety and efficacy of AZD9291 compared to standard epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) like gefitinib and erlotinib. The study targets patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) who are positive for EGFR mutations. This trial is significant as it aims to improve first-line treatment options for this patient group.
The intervention being tested is AZD9291, an oral medication administered daily. It is designed to inhibit the EGFR pathway, which is often mutated in NSCLC, thereby potentially improving patient outcomes compared to existing treatments.
The study employs a randomized, parallel assignment model with triple masking (participant, investigator, outcomes assessor) to ensure unbiased results. The primary purpose of the study is treatment-focused, aiming to establish AZD9291 as a viable first-line therapy.
The study began on December 3, 2014, with primary completion in June 2018. The estimated completion date is set for August 2025, with the latest update submitted in August 2025. These timelines are crucial for tracking the study’s progress and anticipating market entry.
This study update could influence AstraZeneca’s stock performance positively, as successful results may lead to increased adoption of AZD9291, enhancing the company’s market position against competitors in the oncology sector. Investors should monitor further developments closely, as they could impact investor sentiment and market dynamics.
The study is ongoing, with further details available on the ClinicalTrials portal.
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