Telomir Pharmaceuticals (NASDAQ: TELO) announced favorable results from a comprehensive series of IND-enabling Good Laboratory Practice toxicology and safety pharmacology studies for its lead therapeutic candidate Telomir-1 (Zn-Telomir), reporting no treatment-related adverse or dose-limiting toxicities across cardiovascular, respiratory, phototoxicity, and repeat-dose evaluations in both rodent and non-rodent models. The preclinical-stage biotechnology company said Telomir-1 was well tolerated with no concerning cardiac or respiratory safety signals, no phototoxic potential, and only limited, reversible, and non-adverse findings in repeated-dose studies, while demonstrating consistent systemic exposure and predictable pharmacokinetics following oral administration, supporting continued advancement toward first-in-human clinical development pending completion of final quality assurance review and applicable regulatory pathways.
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About Telomir Pharmaceuticals
Telomir Pharmaceuticals (NASDAQ:TELO) is a preclinical biotechnology company developing small-molecule therapeutics designed to target the root epigenetic mechanisms underlying cancer, aging, and degenerative disease. The Company’s lead candidate, Telomir-1, has demonstrated activity in preclinical studies involving modulation of DNA and histone methylation, restoration of redox balance, and normalization of cellular function.
NOTE TO INVESTORS: The latest news and updates relating to TELO are available in the company’s newsroom at https://ibn.fm/TELO
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