Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Biphasic insulin aspart is a premixed suspension consisting of rapid-acting soluble insulin aspart and intermediate-acting insulin aspart protamine crystals. This formulation is designed to mimic the physiological insulin response by providing both a rapid onset of action to control postprandial glucose spikes and a prolonged duration of action to maintain basal insulin levels. It is primarily indicated for the treatment of diabetes mellitus in adults, adolescents, and children. The most common ratio is 30% soluble insulin aspart and 70% insulin aspart protamine (NovoMix 30), though other ratios like 50/50 also exist. Several pharmaceutical companies, including Yichang Dongyangguang Yangtze River Pharmaceutical (HEC Pharm) and Tonghua Dongbao Pharmaceutical, have developed biosimilar versions of this insulin mixture.
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 biphasic insulin aspart.