CuraTeQ Biologics receives approval for biosimilar Dazublys from UK's MHRA
Earlier in July 2025, Dazublys has received the marketing authorisation in the European Union from the European Commission
Earlier in July 2025, Dazublys has received the marketing authorisation in the European Union from the European Commission
The companies will now begin detailed contract negotiations and proceed with necessary consultations and approval processes
She was Group Chief Marketing Officer at CKA Birla Group in her last role
Vevzuo is authorized for the prevention of skeletal related events in adults with advanced malignancies involving bone
Over 100 million cartridges of rh-insulin supplied to Malaysian health ministry; 345,000+ patients served
The approval is based on a comprehensive package of analytical, nonclinical, and clinical data
The program will start with providing bTrastuzumab to cancer patients facing treatment delays due to budget constraints
The decision to withdraw the BLA is based on topline overall survival (OS) results from the confirmatory HERTHENA-Lung02 Phase 3 trial where OS did not meet statistical significance
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