Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Aestox is a highly purified (99.5%) formulation of Botulinum Toxin Type A developed by the South Korean company Medytox. It functions as a neuromuscular blocking agent by inhibiting the release of acetylcholine at the neuromuscular junction. Specifically, the toxin enters nerve terminals and cleaves the SNAP-25 protein, which is essential for the fusion of neurotransmitter vesicles with the presynaptic membrane. This action results in temporary muscle paralysis and chemical denervation. Aestox is primarily utilized for aesthetic procedures, including the reduction of dynamic facial wrinkles, masseter muscle reduction (jaw slimming), and body contouring (calf and arm reduction). It is also indicated for the treatment of focal hyperhidrosis, such as excessive armpit sweating. The product is certified by the Korea Food & Drug Administration (KFDA) and typically provides clinical effects lasting up to six months.
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 Aestox.