[Asia Economy Reporter Ji Yeon-jin] Prestige BioPharma announced on the 24th that it has finally confirmed the equivalence in efficacy, safety, and pharmacokinetics between its Herceptin biosimilar (HD201, Tuznue, Tuznue®) and the original drug Herceptin in the Phase 3 clinical trial results.



The company stated, "With the equivalence proven, we expect to provide more economical treatment opportunities to patients suffering from breast cancer through market entry in Europe and worldwide after product approval."


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