
Novartis’ Sandoz Receives CRL for Biosimilar to Roche’s Rituximab
The company received a complete response letter from FDA in response to the biologics license application for a proposed rituximab biosimilar.
On May 2, 2018, Novartis’s Sandoz announced that it received a complete response letter (CRL) from FDA in response to the biologics license application (BLA) for the company’s proposed rituximab biosimilar, which references Roche’s Rituxan/MabThera (rituximab). Rituximab made CHF 7.3 billion (US$7.8 billion) globally in
“Sandoz stands behind the robust body of evidence included in the regulatory submission and is currently evaluating the content of the letter,” the company said in a press statement. “While disappointed, Sandoz remains committed to further discussions with FDA in order to bring this important medicine to US patients as soon as possible.”
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Celltrion’s CRLs stem from a
In addition to Sandoz and Celltrion, Pfizer also received a CRL in
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