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AstraZeneca's Imfinzi fails to meet main goal in lung cancer study

EditorAhmed Abdulazez Abdulkadir
Published 2024-06-25, 08:46 a/m
AZN
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AstraZeneca PLC (LSE/STO/NASDAQ: LON:AZN) announced Tuesday that its drug Imfinzi did not meet the primary endpoint of disease-free survival (DFS) in the ADJUVANT BR.31 Phase III trial for early-stage non-small cell lung cancer (NSCLC). The study, sponsored by the Canadian Cancer Trials Group (CCTG), evaluated Imfinzi in patients with Stage IB-IIIA NSCLC who had undergone complete tumor resection and whose tumors expressed PD-L1 on 25% or more tumor cells.

Susan Galbraith, Executive Vice President of Oncology R&D at AstraZeneca (NASDAQ:AZN), expressed disappointment in the results but reaffirmed the company's commitment to addressing unmet needs in lung cancer through their broad development program. Despite the setback, Imfinzi maintains its status as the global standard of care in the curative-intent setting of unresectable, Stage III NSCLC after chemoradiotherapy, based on the PACIFIC Phase III trial.

The safety profile for Imfinzi in the ADJUVANT BR.31 trial was consistent with its known safety profile, with no new safety concerns reported. The results will be presented at an upcoming medical meeting.

Imfinzi continues to be investigated in several other early-stage lung cancer settings, including medically inoperable or unresected Stage I-II NSCLC and unresectable, Stage III NSCLC.

Lung cancer remains the leading cause of cancer death worldwide, with NSCLC accounting for the majority of cases. The high recurrence rate after complete tumor resection and adjuvant chemotherapy underscores the need for effective treatments in early-stage lung cancer.

The ADJUVANT BR.31 trial involved 1,415 patients randomized 2:1 to receive either Imfinzi or a placebo every four weeks for up to 48 weeks. The primary endpoint was DFS in patients with PD-L1 expression on 25% or more tumor cells without common EGFR mutations or ALK rearrangements.

AstraZeneca's oncology portfolio includes other lung cancer medicines and innovations, with a focus on early-stage detection and treatment, as well as improving outcomes in advanced stages of the disease. The company remains a key player in the field of immuno-oncology, pursuing a broad clinical strategy to bring immune-based therapies to a wide range of cancer types.

This announcement is based on information from a SEC filing.

In other recent news, AstraZeneca's drug Imfinzi has shown significant survival benefits in a Phase III bladder cancer trial. The drug, combined with chemotherapy, improved event-free survival and overall survival rates in patients with muscle-invasive bladder cancer. These findings are poised to transform the standard of care for bladder cancer patients.

In the realm of endometrial cancer treatment, the FDA has approved AstraZeneca's Imfinzi for treating adults with advanced or recurrent endometrial cancer that is mismatch repair deficient. This approval follows the successful outcomes of the DUO-E Phase III clinical trial.

On the executive front, AstraZeneca's CEO, Pascal Soriot, transferred a significant number of shares to family members, a move typically seen as a personal estate or financial planning activity. In the meantime, financial analysts from firms such as Citi, BMO (TSX:BMO) Capital, and Deutsche Bank (ETR:DBKGn) have maintained positive ratings on AstraZeneca's shares, due to recent drug approvals and strategic acquisitions.

Moreover, AstraZeneca's supplemental New Drug Application for TAGRISSO, aimed at treating adult patients with unresectable, Stage III epidermal growth factor receptor-mutated non-small cell lung cancer, has received Priority Review status from the FDA. This follows successful outcomes from the LAURA Phase III trial. These are the latest developments in AstraZeneca's journey.

InvestingPro Insights

As AstraZeneca faces the challenge of its Imfinzi drug not meeting the primary endpoint in the ADJUVANT BR.31 Phase III trial, investors and stakeholders are closely monitoring the company's financial health and market position. According to real-time data from InvestingPro, AstraZeneca boasts a robust market capitalization of $246.28 billion USD, reflecting investor confidence in its extensive oncology portfolio and broader pharmaceutical offerings. Despite the recent trial results, the company's revenue growth remains strong, with an 8.6% increase over the last twelve months as of Q1 2024, and a significant quarterly revenue growth of 16.55% in Q1 2024.

Investors should note that AstraZeneca's P/E ratio stands at 38.88, which might suggest a high valuation relative to near-term earnings growth. However, this is mitigated by the company's gross profit margin of 82.5% in the same period, indicating efficient operations and strong pricing power. Moreover, AstraZeneca has been able to maintain dividend payments for 32 consecutive years, with a current dividend yield of 2.43%, a testament to its financial stability and commitment to shareholder returns.

For those considering AstraZeneca as an investment opportunity, two key InvestingPro Tips highlight the company's prospects: net income is expected to grow this year, and two analysts have revised their earnings upwards for the upcoming period. This suggests a positive outlook for the company's financial performance, despite the clinical setback. Additionally, with 17 more InvestingPro Tips available, investors can gain deeper insights into AstraZeneca's market dynamics and future potential by exploring the full range of expert analysis.

To access these valuable InvestingPro Tips and make informed investment decisions, use the exclusive coupon code PRONEWS24 to get an additional 10% off a yearly or biyearly Pro and Pro+ subscription. With AstraZeneca's continued role as a prominent player in the Pharmaceuticals industry and its commitment to innovation in cancer treatment, staying informed with InvestingPro could be crucial for those looking to invest in the healthcare sector.

This article was generated with the support of AI and reviewed by an editor. For more information see our T&C.

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