Clinical trials
Follow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
MEDICA 16 (3,3,14,14-tetramethylhexadecanedioic acid) is a non-metabolizable long-chain dicarboxylic fatty acid analogue originally developed by researchers at the Hebrew University of Jerusalem as a hypolipidemic, antiobesity, and antidiabetic agent. It acts as a dual inhibitor of ATP-citrate lyase (ACLY) and acetyl-CoA carboxylase (ACC), thereby suppressing de novo lipogenesis and cholesterogenesis. Additionally, MEDICA 16 acts as an agonist of free fatty acid receptor 1 (FFAR1/GPR40) and peroxisome proliferator-activated receptor alpha (PPARα), and functions as a mitochondrial uncoupling agent. Although it demonstrated significant efficacy in improving insulin sensitivity and reducing plasma triglycerides in various rodent models of obesity and insulin resistance, MEDICA 16 did not advance beyond preclinical development.
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 MEDICA 16.