MedPath

AstraZeneca

AstraZeneca logo
🇬🇧United Kingdom
Ownership
Public
Employees
89.9K
Market Cap
$270.3B
Website
http://www.astrazeneca.co.uk
Introduction

AstraZeneca Plc is a holding company, which engages in the research, development, manufacture, and commercialization of prescription medicines. The company was founded on June 17, 1992 and is headquartered in Cambridge, the United Kingdom.

globenewswire.com
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Brain Tumor Therapeutics Market Forecast 2025-2030: A $5.28

The Brain Tumor Therapeutics Market is projected to grow from USD 3.28 billion in 2024 to USD 5.28 billion by 2030, driven by advances in healthcare technologies and increased investment in oncology research. Key areas explored include market penetration, development, diversification, competitive assessment, and product innovation. Challenges include high R&D costs and regulatory hurdles. Opportunities lie in personalized medicine and novel drug delivery systems.

Fasenra shows benefit in acute asthma and COPD in Phase II trial

A Phase II trial of AstraZeneca’s Fasenra (benralizumab) for eosinophilic asthma and COPD showed a significant improvement over standard care, with 45% of patients experiencing exacerbations compared to 74% in the steroid group. Fasenra was well-tolerated, with no fatal adverse events reported.
drugs.com
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Scientists Develop Whole New Form of Effective Asthma Treatment

Benralizumab, a monoclonal antibody, outperformed steroids in reducing asthma and COPD symptoms, with fewer attacks and improved quality of life, according to a clinical trial published in The Lancet Respiratory Medicine.
stocktitan.net
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Strengthens QIAstat-Dx With New Barcelona Site to Drive Growth in Infectious

QIAGEN plans to relocate QIAstat-Dx operations to a new 8,000-square-meter site in Barcelona by early 2026, supporting syndromic testing for infectious diseases and precision medicine, with R&D, manufacturing, sales, marketing, and regulatory operations, featuring digitalized production lines and LEED Platinum certification, aiming to strengthen diagnostic capabilities and support partnerships with Eli Lilly and AstraZeneca. The system currently has FDA clearance for four panels and CE-marking for two panels under IVDR.
prnewswire.com
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New Indication of Olverembatinib Included into China 2024 National Reimbursement Drug List

Ascentage Pharma's olverembatinib, a third-generation BCR-ABL inhibitor, has its new indication for adult patients with chronic-phase chronic myeloid leukemia (CML-CP) resistant and/or intolerant of first-and second-generation tyrosine kinase inhibitors (TKIs) included in the China 2024 National Reimbursement Drug List (NRDL), effective January 1, 2025.

U.S. Clinical Trials Market Size, Share & Trends Analysis Report 2025-2030

The U.S. clinical trials market is projected to reach $57.79 billion by 2030, driven by chronic disease prevalence and increased demand. Phase III trials dominated in 2024, with oncology holding the largest revenue share. Key players include IQVIA, Fortrea Inc., PAREXEL, and Thermo Fisher Scientific.
theguardian.com
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Doctors hail first breakthrough in asthma and COPD treatment in 50 years

A trial found that a single high-dose injection of benralizumab, targeting eosinophils to reduce lung inflammation, was more effective than steroid tablets in treating severe asthma and COPD attacks, cutting the need for further treatment by 30%.

Clinical Trials Market Size, Share & Trends Analysis Report 2025-2030

The U.S. clinical trials market is projected to reach $57.79 billion by 2030, driven by chronic disease prevalence and increased demand. Phase III trials dominated in 2024, with oncology leading by indication. Key players include IQVIA, Fortrea Inc., and PAREXEL International Corporation.

Truqap Combination Shines in Phase III Trial for Prostate Cancer

AstraZeneca's Phase III CAPItello-281 trial showed Truqap (capivasertib) + abiraterone + ADT improved rPFS in PTEN-deficient metastatic hormone-sensitive prostate cancer. Early OS signs also suggest benefit, with ongoing trial for further assessment. Truqap + Faslodex was approved in the EU for ER-positive, HER2-negative advanced breast cancer with PIK3CA, AKT1, or PTEN alterations.
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