Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Mito-MGN (mitochondria-targeted magnolol) is a small molecule derivative of the natural polyphenol magnolol, specifically engineered to accumulate within the mitochondria of cancer cells. By leveraging the elevated mitochondrial membrane potential characteristic of malignant cells, Mito-MGN selectively disrupts mitochondrial bioenergetics. Its primary mechanism of action involves the inhibition of mitochondrial complex I (NADH:ubiquinone oxidoreductase), which suppresses oxidative phosphorylation (OXPHOS) and mitochondrial respiration. This disruption leads to an increase in reactive oxygen species (ROS) production, oxidation of mitochondrial peroxiredoxin, and the induction of mitophagy. Mito-MGN has shown significant potency in inhibiting the proliferation and invasion of melanoma cells, particularly those that have developed resistance to BRAF inhibitors through metabolic reprogramming toward an OXPHOS-dependent state.
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 Mito-MGN.