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Telomir Pharmaceuticals, Inc. has published a peer-reviewed preclinical study in Advances in Redox Research, highlighting the biological activity of its compound Telomir-Zn in Wilson disease, a rare genetic disorder.
The publication marks a significant step in advancing new treatments for Wilson disease, which is characterized by excess copper accumulation in the body. The peer-reviewed results suggest Telomir-Zn could potentially become a new therapeutic candidate for this condition. Further clinical studies are anticipated.
Telomir has previously presented preclinical findings on Telomir-1, a novel iron-targeting epigenetic therapy, at the AACR Annual Meeting. The company later reported that Telomir 1 showed strong safety with no adverse effects in GLP studies. Telomir continues to broaden its research activities in rare disease therapeutics.