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Prestige BioPharma Reports EMA's Acceptance of Marketing Authorization Application for its Tuznue (trastuzumab- biosimilar)

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Prestige BioPharma Reports EMA's Acceptance of Marketing Authorization Application for its Tuznue (trastuzumab- biosimilar)

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  • Prestige Biopharma announces that EMA has accepted & validated MAA for its Tuznue- a biosimilar to Herceptin (trastuzumab) on May 23- 2019
  • Prestige’s Tuznue will be in competition with Celltrion’s Herzuma- Amgen’s Kanjinti- Merck Sharp & Dohme’s Ontruzant & Pfizer’s Trazimera in the European market- dominated by Roche’s Herceptin
  • Tuznue (HD201) is currently evaluated in P-I/P-III global studies and has received CHMP’s positive opinion for marketing authorization from the EMA. Additionally- Prestige has 8 biosimilar & biologics in its portfolio which are at different development stages

Ref: Prestige BioPharma | Image: Prestige Biopharma

Click here to­ read the full press release 

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