Prestige Biopharma has marked two more milestones in the journey to bringing its HD201 proposed trastuzumab biosimilar rival to Herceptin to international markets, with positive Phase III data and a European good manufacturing practice certification bringing the Singapore-based firm “one step closer to global launch of Tuznue.”
Announcing positive efficacy and safety results from its “TROIKA” Phase III study for HD201, Prestige said the study met its primary endpoint and showed equivalent efficacy and
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