US FDA ने ठोस ट्यूमर के इलाज के लिए दाइची, एस्ट्राजेनेका दवा को मंजूरी दी

US FDA ने ठोस ट्यूमर के इलाज के लिए दाइची, एस्ट्राजेनेका दवा को मंजूरी दी

US FDA Approves Daiichi, AstraZeneca Drug for Treatment of Solid Tumors

FA approves Daiichi, AstraZeneca drug for treating solid tumors, expanding treatment options for cancer patients in the United

  • Global News
  • 416
  • 06, Apr, 2024
Jivika Chawla
Jivika Chawla
  • @JivikaChawla

US FDA Approves Daiichi, AstraZeneca Drug for Treatment of Solid Tumors

The U.S. FDA has granted accelerated approval to Enhertu, a drug developed by Daiichi Sankyo and AstraZeneca, for the treatment of solid tumours. Initially sanctioned for HER-2-positive breast cancer, it has now received authorization for various HER2-expressing solid tumours. HER2 is a protein that spurs cancer cell proliferation and is prevalent in diverse solid tumours such as those in the biliary tract, bladder, cervical, endometrial, ovarian, and pancreatic areas.

Clinical trials showcased notable survival advantages among previously treated patients. AstraZeneca acquired partial rights to Enhertu through a $6.9 billion agreement with Daiichi Sankyo in 2019. Sales of Enhertu amounted to $1.28 billion in 2023, catering to patients with breast, gastric, and lung cancers.

Enhertu operates as an antibody-drug conjugate, merging trastuzumab (Herceptin) with a chemotherapy drug. This combination targets cancer cells effectively, delivering a powerful blow to the disease.

The FDA's accelerated approval underscores the drug's potential in addressing a broad spectrum of solid tumours, offering hope to patients facing various forms of cancer. The expanded indication for Enhertu represents a significant milestone in cancer treatment, widening the therapeutic options available for those afflicted with HER2-expressing tumours.

AstraZeneca's investment in Enhertu reflects the pharmaceutical industry's commitment to innovation and collaboration in the fight against cancer. The substantial sales figures indicate the drug's acceptance and adoption within the medical community, highlighting its efficacy and clinical utility.

As Enhertu continues to make strides in cancer therapy, ongoing research and development efforts will likely explore its potential in additional tumour types and patient populations. Ultimately, the FDA's approval of Enhertu reaffirms the importance of advancing precision medicine approaches to tackle cancer, offering renewed hope and optimism to patients and healthcare providers alike.

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Jivika Chawla

Jivika Chawla

  • @JivikaChawla