Biocon Biologics secures market enattempt date for Denosumab biosimilars in Europe, Rest of the World
The agreement allows Biocon Biologics to commercialize both its Denosumab biosimilars (Vevzuo and Evfraxy) in Europe starting December 2, 2025
Biocon Biologics Ltd. (BBL), a fully integrated global biosimilars company and subsidiary of Biocon Ltd. announced a settlement agreement with Amgen Inc. that clears the path for the commercialization of its Denosumab biosimilars in Europe and the rest of the world.
The agreement allows Biocon Biologics to commercialize both its Denosumab biosimilars (Vevzuo and Evfraxy) in Europe starting December 2, 2025. The other terms of the settlement remain confidential.
Shreehas Tambe, CEO & Managing Director, Biocon Biologics, stated, “This settlement sets the stage for Biocon Biologics to bring our Denosumab biosimilars, Vevzu and Evfraxy, to patients across Europe and key international markets. This follows our settlement in the U.S. in October and further broadens our reach across the world in the oncology and bone health therapeutic areas, as we work with healthcare systems to expand access to affordable biologics globally.”
The European Commission (EC) had approved Vevzuo and Evfraxy in July 2025.
Biocon Biologics had secured a market enattempt date for its Denosumab biosimilars Bodeclarea (denosumabkyqq) and Aukelso™ (denosumab-kyqq) for the United States previously.
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