Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This intervention is a research nutritional supplement consisting of a combination of two long-chain polyunsaturated fatty acids (LCPUFAs): docosahexaenoic acid (DHA), an omega-3 fatty acid, and arachidonic acid (AA), an omega-6 fatty acid. Studied primarily in the Omega Tots trial (NCT01576783) led by Dr. Sarah Keim, the intervention involves a daily oral dose of 200 mg DHA and 200 mg AA in a microencapsulated form. These fatty acids are essential structural components of neuronal and retinal cell membranes and are critical for normal brain development and neurological function. The supplementation was investigated for its potential to improve cognitive development, language, executive function, and behavioral outcomes in children born preterm (less than 35 weeks gestation). While the original trial did not show improvement in primary cognitive outcomes, follow-up studies have continued to evaluate the long-term developmental effects of toddlerhood supplementation into middle childhood.
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 docosahexaenoic acid + arachidonic acid.