• Mashup Score: 1

    On June 28, 2022, it was announced that the European Commission (EC) has granted approval to axicabtagene ciloleucel (axi-cel), a CD19-directed chimeric antigen receptor T-cell product, for the treatment of relapsed or refractory follicular lymphoma in adult patients who have already received ≥3 lines of systemic therapy. The approval is based on key data obtained from the pivotal phase II ZUMA-5…

    Tweet Tweets with this article
    • 🚨 N E W S 🚨 Axicabtagene ciloleucel receives @EU_Commission approval as a fourth-line treatment of relapsed/refractory follicular lymphoma 👉 https://t.co/Zf5M95sDrI 👈 #mednews #lymsm #FL https://t.co/oKjCkj5WKu

  • Mashup Score: 0

    On June 28, 2022, it was announced that the European Commission (EC) has granted approval to axicabtagene ciloleucel (axi-cel), a CD19-directed chimeric antigen receptor T-cell product, for the treatment of relapsed or refractory follicular lymphoma in adult patients who have already received ≥3 lines of systemic therapy. The approval is based on key data obtained from the pivotal phase II ZUMA-5…

    Tweet Tweets with this article
    • 🚨 N E W S 🚨 Axicabtagene ciloleucel receives @EU_Commission approval as a third-line treatment of relapsed/refractory follicular lymphoma 👉 https://t.co/Zf5M95sDrI 👈 #mednews #lymsm #FL https://t.co/zVgufnlRua