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Lifescan/Sanvita Complete CGM Pilot Study; Lupin’s Generic Synjardy XR Receives Tentative FDA Approval

Two diabetes-related news items have been observed: the CT.gov record for Lifescan/Sanvita Medical’s CGM pilot study has been updated to reflect an October 2020 completion; and Lupin Limited announced it received tentative FDA approval for 5mg/1000mg, 10mg/1000mg, 12.5mg/1000mg, and 25mg/1000mg empagliflozin + metformin XR tablets. Below, FENIX provides highlights and insights for the respective news items.

About The Author

Matthew Maryniak

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President of Fenix Group International

Matthew has been a thought leader in the high-growth therapeutic areas of diabetes and cardiovascular medicine since 2006, making regular attendance at large and small CV/met scientific meetings and an architect of novel methods for assessing market opportunities. He has over a decade of experience in leading CV/met consulting engagements, is a published author in PM360 and Diabetes Technology & Therapeutics, and has been quoted in The Pink Sheet on anti-thrombotics.

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