FDA rejects Janssen's canagliflozin/metformin combo in type 2 diabetes
This article was originally published in Scrip
Executive Summary
Johnson & Johnson unit Janssen Research & Development will need to provide additional information before the US FDA will approve the firm's new drug application (NDA) for a fixed-dose combination (FDC) of canagliflozin and immediate-release metformin to treat adults with type 2 diabetes, the company said, revealing it had received a complete response letter (CRL).
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