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Clinical Trial Summary

The purpose of this study is to assess the effects of Cetyl Tranexamate Mesylate on acne-related hyperpigmentation through a specific delivery form known as TeraCeutic TXVector.


Clinical Trial Description

Hyperpigmentation is characterized as an increase in pigment on the skin and is a common skin condition in individuals with skin types III to VI on the Fitzpatrick skin classification scale. Hyperpigmentation can be localized to an area in the form of post-inflammatory hyperpigmentation or diffused in the form of melasma. One of the treatments that are used to treat hyperpigmentation is tranexamic acid (TXA) which is a third-generation bioactive and is formally known to work as a plasmin inhibitor. Since TXA is hydrophilic in nature and has a strong hydrogen-bonding capacity, it has an insufficient skin permeability. Similar to TXA esters, Cetyl Tranexamate Mesylate (CTM) is hypothedized to have greater permeability and this study will evaluate the effects of CTM on the appearance of post-inflammatory hyperpigmentation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06080035
Study type Interventional
Source Integrative Skin Science and Research
Contact Nhi P Nguyen, BS
Phone 9167502463
Email nhi@integrativeskinresearch.com
Status Not yet recruiting
Phase N/A
Start date November 1, 2023
Completion date April 30, 2024

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