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According to GlobalData’s Technology Foresights, which uses over 756,000 patents to analyse innovation intensity for the pharmaceutical industry, there are 110 innovation areas that will shape the future of the industry. Several platinum-based drugs such as cisplatin, carboplatin and oxaliplatin are widely used in cancer therapy.
According to GlobalData’s Technology Foresights, which uses over 756,000 patents to analyse innovation intensity for the pharmaceutical industry, there are 110 innovation areas that will shape the future of the industry. Among its key functions, it interacts with nucleic acids and enzymes during their synthesis and function.
In 2021, the FDA granted Amgen’s (NASDAQ:AMGN) non-small cell lung cancer (NSCLC) drug Lumakras (sotorasib) an expedited approval, making it the first FDA-approved KRAS inhibitor. In 2021, Amgen agreed to conduct a Phase II study (NCT04933695), which is supposed to complete in May 2024, according to Clinicaltrials.gov.
It is therefore an interesting development that sugemalimab was given an Innovation Passport in NICE’s Innovative Licensing and Access Pathway (ILAP) in October 2021. Single Technology Appraisal: Sugemalimab with chemotherapy for untreated metastatic non-small-cell lung cancer ID4001. National Institute for Clinical Excellence.
Antibody drug conjugates (ADCs) are an upcoming class of targeted therapeutic agents that have garnered the attention of pharmaceuticalcompanies, and academic / research institutions across the world. Examples of recently approved ADCs include Enhertu (2021), Blenrep (2020) and Polivy (2020).
The decision – which comes after an earlier rejection by NICE in March 2021 – covers Lynparza’s approval for prostate cancer cases with BRCA1 or BRCA2 mutations that has spread (metastasised) to other parts of the body and has relapsed after prior treatment with the hormonal drugs abiraterone or enzalutamide.
Designated as BG01-2202, this latest trial will be an open-label, randomised, controlled clinical study of UTD1 versus chemotherapy drug docetaxel. A Phase III study to evaluate UTD1 versus docetaxel in patients that have failed chemotherapy with a platinum-containing regimen is also currently underway in China. ORR, 81.0%
Thomas Wozniewski, Global Manufacturing and Supply Officer at Takeda PharmaceuticalCompany Ltd, presented on “Future-proofing a Global TechOps Organization: The Transformation of Global Manufacturing and Supply at Takeda.”. Jörg Zimmermann. Vice President, Vetter Development Service, External Affairs. Next Slide ??. Michael Kopcha.
Shots: Drug patent expiry is when a patent granted to a pharmaceuticalcompany for a particular drug expires, allowing other companies to produce and sell generic versions Like every other utility patent, pharmaceuticals also get market exclusivity of 20 years.
The conclusion is that backlog clearance will extend into 2021. “It Because of the lockdown, it is not surprising, but very worrying, that cancer specialists reported delays in diagnoses, surgeries and chemotherapy during each of the three waves of interviews. Pharmaceuticalcompanies cannot address this challenge alone.
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