Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Insulin lispro (Wockhardt) is a biosimilar version of the rapid-acting insulin analogue, insulin lispro, which was originally developed and marketed by Eli Lilly as Humalog. Developed by the Indian pharmaceutical company Wockhardt Ltd, this recombinant protein biologic is designed for subcutaneous administration to manage postprandial blood glucose levels in patients with type 1 diabetes mellitus. The drug functions by binding to and activating the insulin receptor, which stimulates glucose uptake into peripheral tissues such as skeletal muscle and fat, while simultaneously inhibiting hepatic glucose production. Wockhardt intended to market the product under the brand name Listro, including various premixed formulations. However, the clinical development program in the United States was largely discontinued following the withdrawal of a Phase 3 trial and multiple Phase 1 studies in early 2013.
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 insulin lispro (Wockhardt).