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.
Celltrion's STOBOCLO and OSENVELT biosimilars receive US FDA approval
Faron Pharmaceuticals' bexmarilimab receives FDA Orphan Drug Designation for MDS
AstraZeneca's Imfinzi recommended for EU approval in resectable NSCLC treatment
Innovent Biologics doses first patient in registrational study assessing IBI363
Qlucore launches first CE-marked diagnostic test for paediatric leukaemia
AstraZeneca's camizestrant shows significant PFS benefit in HR+ breast cancer
FDA accepts Telix Pharmaceuticals' BLA for Zircaix and grants Priority Review
Summit Therapeutics and Pfizer partner to evaluate ivonescimab with ADCs in solid tumor trials
Bristol Myers Squibb's application for Opdivo-Yervoy combo in colorectal cancer accepted by U.S. FDA
Redx Pharma reports positive Phase 1 results for RXC008 in fibrostenotic Crohn's disease
Sectra and Siemens Healthineers collaborate to enhance radiology diagnostics
ValiRx Plc concludes evaluation project with Imperial College London