Sandoz decides not to pursue US biosimilar rituximab; will focus on robust biosimilar portfolio for unmet access and sustainability needs

  • Decision follows FDA request for additional information to complement submission for biosimilar rituximab
  • Sandoz stands behind safety, efficacy and quality of our biosimilar rituximab, which is already approved in EU, Switzerland, Japan and Australia
  • With seven biosimilars already approved globally, Sandoz will focus on progressing robust pipeline to enable early and expanded patient access and healthcare savings  

 

Holzkirchen, Germany, November 2, 2018 — Sandoz, a Novartis division and the pioneer and global …

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