HUMALOG PEN (insulin lispro) by Eli Lilly and Company. Approved for insulin analog [epc]. First approved in 1996.
Drug data last refreshed 22h ago · AI intelligence enriched 1w ago
HUMALOG PEN is a rapid-acting insulin analog (insulin lispro) administered via subcutaneous injection, developed by Eli Lilly and approved in 1996. It is used to treat type 1 and type 2 diabetes by mimicking the body's natural rapid insulin response to meals. The drug works by binding to insulin receptors to facilitate glucose uptake into cells.
As a mature product approaching loss of exclusivity, HUMALOG PEN team focus is transitioning from growth initiatives to market defense and transition planning, with team stability dependent on generic/biosimilar strategy.
Insulin Analog
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Phase 2b Trial Comparing HDV-Insulin Lispro to Insulin Lispro in Adults With Type 1 Diabetes Receiving Insulin Degludec
A Study of LY900014 (Lyumjev) Versus Insulin Lispro (Humalog) in Participants With Type 1 Diabetes
A Study of Tirzepatide (LY3298176) Versus Insulin Lispro (U100) in Participants With Type 2 Diabetes Inadequately Controlled on Insulin Glargine (U100) With or Without Metformin
A Trial to Compare BioChaperone Insulin Lispro Formulations With US Approved Humalog® and With EU Approved Humalog® in Patients With Type 1 Diabetes Mellitus
A Study of LY900014 Versus Insulin Lispro (Humalog) on High Blood Sugar in Participants With Type 1 Diabetes Who Use Insulin Pumps
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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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Working on HUMALOG PEN offers exposure to a foundational diabetes franchise with deep clinical expertise and established physician relationships, but career growth is constrained by LOE-approaching status and intense biosimilar competition. Roles emphasize defensive commercial strategy, managed care negotiations, and patient retention rather than market expansion.