Core Viewpoint - Dr. Reddy's Laboratories has entered into a license and supply agreement with Alvotech for the commercialization of AVT03, a biosimilar candidate to Amgen's Prolia and Xgeva, which are approved for treating various conditions including osteoporosis and prevention of skeletal-related events in advanced malignancies [1][2]. Group 1: Agreement Details - The collaboration aims to utilize Dr. Reddy's global commercial presence alongside Alvotech's expertise in biosimilar development [2]. - Dr. Reddy's will handle the registration and commercialization of AVT03, while Alvotech will focus on development and manufacturing [2]. - The agreement includes an upfront payment to Alvotech, with additional payments tied to regulatory milestones and sales, although specific financial details remain undisclosed [3]. Group 2: Market Position and Product Development - Dr. Reddy's has exclusive commercialization rights for AVT03 in the United States and semi-exclusive rights in the EU and the UK [3]. - Year-to-date, Dr. Reddy's shares have decreased by 0.9%, contrasting with a 10% rise in the industry [4]. - Alvotech recently reported positive results from a pharmacokinetic study of AVT03 compared to Prolia, and is conducting further studies to confirm efficacy and safety [5]. Group 3: Current Portfolio and Future Prospects - Dr. Reddy's has launched Versavo, a biosimilar of Avastin, in the UK, which is indicated for various cancers [6][7]. - The collaboration with Alvotech is expected to enhance Dr. Reddy's biosimilar portfolio and facilitate entry into highly regulated markets, leveraging its commercial infrastructure for competitive advantage [8].
Dr. Reddy's (RDY), Alvotech Unite for Prolia & Xgeva Biosimilar