FDA recently approved Provention Bio’s teplizumab, branded as Tzield, to delay the onset of Stage 3 T1DM in adult and pediatric patients aged 8 years and older with Stage 2 T1DM (previous FENIX insight). Additionally, Provention hosted an investor call on Friday, November 18, 2022, to discuss the approved Tzield label, pricing, and commercialization plans (webcast). Below FENIX has conducted a Tzield label and website analysis, including highlights and insights from the investor call (label; previous FENIX insight).
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About The Author
Matthew Maryniak
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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Purchase Blast$599.00
You can read the article’s full content online after purchase.