Drug data last refreshed 5h ago · AI intelligence enriched 1w ago
SEMGLEE is a biosimilar insulin glargine approved by the FDA in June 2020 for the treatment of diabetes mellitus. It is administered via subcutaneous injection and provides long-acting basal insulin coverage for patients requiring insulin therapy. The drug works by binding to insulin receptors to facilitate glucose uptake and utilization in target tissues.
As a recently approved biosimilar in peak lifecycle stage, SEMGLEE is actively building market share in a competitive insulin market, requiring robust commercial and field teams to drive adoption.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
A Research Study to See How a Weekly Insulin, Insulin Icodec, Helps in Reducing the Blood Sugar Compared to Daily Insulin Glargine, Both in Combination With Insulin Aspart, in Adults With Type 1 Diabetes
A Research Study to See How Switching From a Daily Basal Insulin to a New Weekly Insulin, Insulin Icodec, Helps in Reducing the Blood Sugar Compared to Daily Insulin Glargine in Adults With Type 2 Diabetes
A Research Study to See How Well New Weekly Medicine IcoSema, Which is a Combination of Insulin Icodec and Semaglutide, Controls Blood Sugar Levels in People With Type 2 Diabetes (T2D), Compared to Daily Insulin Glargine (COMBINE 4)
A Study of Orforglipron (LY3502970) in Participants With Type 2 Diabetes and Inadequate Glycemic Control With Insulin Glargine, With or Without Metformin and/or SGLT-2 Inhibitor
A Study of Daily Oral Orforglipron (LY3502970) Compared With Insulin Glargine in Participants With Type 2 Diabetes and Obesity or Overweight at Increased Cardiovascular Risk
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Upgrade to Pro — $25/moSEMGLEE represents a mid-career opportunity in biosimilar commercialization, requiring expertise in competitive insulin market dynamics, payer negotiations, and field execution. Roles focus on capturing market share from reference products and competing biosimilars through formulary placement and provider education.