Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Lusduna Nexvue** is a long-acting, recombinant human insulin analogue (insulin glargine) designed as a follow-on biologic (“biosimilar”) referencing Lantus (insulin glargine) for once-daily subcutaneous injection. It is indicated for the treatment of diabetes mellitus (both type 1 and type 2) in adults, adolescents, and children aged 2 years and older. The mechanism of action involves stimulating peripheral glucose uptake and inhibiting hepatic glucose production, thereby lowering blood glucose. Lusduna Nexvue has a prolonged duration of action due to its unique amino acid modifications, leading to slow absorption and consistent basal insulin levels. Developed by Merck, with funding/support from Samsung Bioepis, it underwent regulatory review in both the EU (approved but withdrawn) and the US (tentative approval, final approval pending patent litigation with Sanofi, the sponsor of Lantus)[1][2][3][4][5][6][7][8][9][10][12].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on lusduna nexvue.