Dr. Reddy’s Laboratories Ltd., an international enterprise specializing in pharmaceuticals, has officially declared the introduction of its drug Versavo® (bevacizumab) to the UK market. The product, Versavo®, is a biosimilar to Avastin®, formulated for the management of various cancer forms, such as metastatic colorectal cancer, progressive non-squamous non-small cell lung cancer, recurring glioblastoma, metastatic renal cell carcinoma, advanced cervical cancer, ovarian cancer, and metastatic breast cancer.
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Dr. Reddy's has successfully obtained approval for and introduced their initial biosimilar, Versavo®, in the United Kingdom. This product is accessible in 100mg and 400mg concentrations, each contained in single-use vials for administration.
The pharmaceutical company first unveiled Versavo® on the Indian market in 2019 before rolling it out to several other regions, including Thailand, Ukraine, Nepal, and Jamaica, maintaining the Versavo® branding. However, in Colombia, the biosimilar is marketed under the name Persivia®.
Global Head of Biologics at Dr. Reddy's, Dr. Jayanth Sridhar, articulated the significance of the launch: "Introducing Versavo® in a stringently regulated market is a testament to our proficiency in the global clinical development of biosimilars of superior quality. As a versatile therapeutic choice for diverse cancer types, Versavo® is pivotal. This move amplifies our dedication to enhancing patient access to vital biosimilars and underscores our deepening engagement with oncology treatment solutions."
Versavo® is a bevacizumab biosimilar developed by Dr. Reddy’s Laboratories. Bevacizumab marks a pioneering advancement in the fight against cancer with its ability to inhibit the proliferation of metastatic conditions. With its design as a humanized monoclonal antibody, it specifically engages with the human vascular endothelial growth factor (VEGF), effectively curbing new blood vessel formation and consequently, tumor expansion.
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According to the data provided by the Synapse Database, As of March 21 2024, there are 182 investigational drugs for the VEGF-A target, including 294 indications, 282 R&D institutions involved, with related clinical trials reaching 4759, and as many as 7127 patents.
Bevacizumab biosimilar is a monoclonal antibody drug that targets VEGF-A. It has been approved for the treatment of various cancers and other diseases. The drug offers a biosimilar alternative to the originator drug, potentially providing cost-effective treatment options for patients.