ASTR

NSE:ASTRAZEN

AstraZeneca India

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  • Stock

8,393.00

−3.32%

−288.00

INR last updated 11/08 02:03:55

Last Close

8,681.00

02/05 08:51

Market Cap

171.96B

Beta: 0.39

Volume Today

17.94K

Avg: 4.82K

PE Ratio

108.89

PFCF: 7,021.31

Dividend Yield

0.24%

Payout:0%

The gastric cancer treatment market is expected to grow from 2020 to 2034, driven by advancements in targeted and immunotherapies. The United States holds the largest market share, followed by EU-4 (Germany, France, Italy, Spain), the UK, and Japan. The total number of incident gastric cancer cases (including GEJ) in the 7MM was approximately 211,000 in 2024 and is projected to increase. Key therapies such as Bemarituzumab, ZIIHERA (zanidatamab), ENHERTU, and KEYTRUDA are advancing through clinical trials and gaining regulatory approval. HER2-targeted treatments and combinations with immune checkpoint inhibitors are improving efficacy and patient outcomes. Despite promising developments, challenges such as high R&D costs, resistance to therapies, unaffordable pricing, market access issues, and low screening rates may hinder market growth. The report covers epidemiology, treatment guidelines, clinical trial updates, and competitive dynamics among major pharmaceutical companies.

globenewswire.com

AstraZeneca, in collaboration with Parexel International, is conducting a Phase III clinical trial to evaluate the safety and efficacy of AZD9291, an oral medication targeting EGFR-mutated non-small cell lung cancer (NSCLC), compared to standard EGFR-TKIs like gefitinib and erlotinib. The trial involves patients with locally advanced or metastatic NSCLC and is designed to establish AZD9291 as a viable first-line treatment. The study uses a randomized, parallel assignment model with triple masking and began on December 3, 2014, with primary completion in June 2018 and an estimated completion date of August 2025. The latest update was submitted in August 2025, and successful results could positively impact AstraZeneca’s stock performance and market position in oncology.

tipranks.com

The global cell regeneration medicine market is projected to reach US$90.1 billion by 2031, growing at a compound annual growth rate (CAGR) of 12.8% from 2024 to 2031, driven by advances in cell therapies, gene editing, tissue engineering, and increased investments and regulatory support. Key developments in 2025 include AstraZeneca's acquisition of Belgium-based EsoBiotec for up to $1 billion, and Bristol Myers Squibb's acquisition of 2seventy bio for $286 million. Technological advancements such as stem cell-based therapies, CRISPR gene editing, 3D bioprinting, and biomaterials are fueling innovation. The U.S. market leads with a 2024 value of $10.4 billion and is expected to reach $43.3 billion by 2033 at a 15.6% CAGR, supported by strong R&D, clinical trials, and regulatory incentives. Japan shows rapid growth at 18.2% CAGR, driven by government investment, aging population, and supportive regulatory frameworks. Major players include AstraZeneca, Bristol Myers Squibb, Novartis, Amgen, Bayer, Merck, Fate Therapeutics, Japan Tissue Engineering, Takeda Pharmaceutical, Astellas Pharma, Fujifilm Cellular Dynamics, and Delta-Fly Pharma.

openpr.com

Boehringer Ingelheim has received FDA accelerated approval for Hernexeos (zongertinib), an oral, targeted therapy for previously treated patients with HER2-mutant advanced non-small cell lung cancer (NSCLC). The approval is based on data from the Beamion LUNG-1 study, showing a 71% objective response rate and a duration of response of 14.1 months. The therapy offers a durable effect with a manageable safety profile, positioning it as a significant advancement in treatment for a patient population with limited options. Boehringer's move comes after the discontinuation of its MDM2-p53 antagonist brigimadlin due to poor clinical results. The company is now expanding its oncology efforts to include other HER2-altered cancers such as breast and gastrointestinal tumors, as well as non-HER2 lung cancer. Competitors include Bayer's sevabertinib and AstraZeneca and Daiichi Sankyo's Enhertu, which was approved in 2022 for the same indication.

pharmaphorum.com

Tempus AI, Inc. has published its latest Form 10-Q report, reporting a 90% year-over-year increase in total net revenue to $314.6 million, driven by higher test volumes in the Genomics segment and increased data deliveries in the Data and Services line. The company highlights improved operational efficiency, with a significant reduction in loss from operations from $(533.5) million to $(61.8) million and a net loss decrease from $(552.2) million to $(42.8) million. Key growth drivers include the acquisition of Ambry Genetics, increased sales of 212,000 Genomics tests (up from 66,500), and new product developments such as Intelligent Diagnostics using AI. Strategic collaborations with AstraZeneca and Pathos are underway to co-develop a multimodal oncology model using de-identified datasets. The company is also investing in technology and data infrastructure to enhance data flow between healthcare providers and life science companies.

tradingview.com

    Description

    AstraZeneca Pharma India Limited, a biopharmaceutical company, manufactures, distributes, and markets pharmaceutical products in India and internationally. It manufactures and sells cardiovascular disease and diabetes medicines under the Brilinta, Betaloc, Crestor, Forxiga, Imdur, Kombiglyze XR, Onglyza, Seloken XL, Xigduo XR, and QTERN brands; Respiratory medicines under the S...Show More

    Earnings

    Earnings per Share (Estimate*)

    -551015202018-12-312020-12-312023-02-102024-02-092024-08-08

    Revenue (Estimate*)

    1B2B3B4B2018-12-312020-12-312023-02-102024-02-092024-08-08

    *Estimate based on analyst consensus