Biopharmaceutical company AstraZeneca PLC (LSE: AZN) (STO: AZN) (Nasdaq: AZN) announced on Monday that it has received a positive recommendation from the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) for the approval of Imfinzi (durvalumab) as part of a perioperative treatment regimen for adults with resectable non-small cell lung cancer (NSCLC). This approval recommendation is based on the promising results from the AEGEAN Phase III trial, which demonstrated that Imfinzi in combination with chemotherapy reduced the risk of recurrence, progression, or death by 32% compared to chemotherapy alone.
The AEGEAN trial, which published its findings in The New England Journal of Medicine, showed a statistically significant reduction in event-free survival (EFS) for patients receiving the Imfinzi-based regimen, with an EFS hazard ratio of 0.68 (95% CI 0.53-0.88; p=0.003902). In addition, patients treated with Imfinzi showed a 13% higher pathologic complete response (pCR) rate compared to chemotherapy alone (17.2% vs. 4.3%).
While interim overall survival (OS) results showed a favorable trend, final OS data will be further assessed as a key secondary endpoint in the trial. Imfinzi was well tolerated and did not introduce new safety concerns. The combination therapy did not compromise patients' ability to undergo surgery, a critical consideration for resectable NSCLC treatment.
Lung cancer, the leading cause of cancer-related deaths in Europe, presents a significant unmet need, particularly for patients with resectable disease who often face recurrence. AstraZeneca's treatment, if approved, offers a potential breakthrough for these high-risk patients.
Imfinzi is already approved in several countries, including the US, for similar indications, and regulatory applications are ongoing in other regions, including China and Japan. This recommendation is part of AstraZeneca's broader commitment to improving outcomes for lung cancer patients, aligning with the company's strategy to pioneer advancements in oncology.
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Frontage expands early phase clinical research capabilities across US and China
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
InSysBio agrees new collaborative project with BeOne Medicines
Physiomics secures new modelling contract with Numab Therapeutics
Mabwell reports first patient dosed with 7MW4911 in US trial
Atossa Therapeutics' founder and CEO named one of The Top 50 Healthcare Technology CEOs of 2025
Avacta secures FDA clearance for second pre|CISION oncology programme
Guardant Health and Merck enter multi-year oncology diagnostics collaboration
Akeso secures NMPA review acceptance for gumokimab in ankylosing spondylitis