Telomir Pharmaceuticals reports breakthrough in AMD treatment

Published 29/05/2025, 13:08
Telomir Pharmaceuticals reports breakthrough in AMD treatment

Telomir Pharmaceuticals, Inc., a Florida-based biopharmaceutical company with a market capitalization of $61.6 million, announced today that its investigational drug, Telomir-1, has shown promising results in a preclinical study using an animal model for age-related macular degeneration (AMD (NASDAQ:AMD)). The study, conducted on Sen57wrn-/-ND6-/+ zebrafish, which exhibit characteristics similar to human dry AMD and geographic atrophy, demonstrated that oral administration of Telomir-1 over a two-week period led to significant improvements in vision and retinal structure. According to InvestingPro data, the company currently operates with moderate debt levels while focusing on this promising development.

The key findings from the study include improved central vision response and motion detection, regeneration of critical retinal layers, a reduction in oxidative stress markers, and a survival benefit with no mortality observed in treated groups. These results are particularly noteworthy as the endpoints used in the study align with FDA-recognized surrogate markers for visual function.

The company believes these outcomes represent a significant step forward in the development of Telomir-1 and support its continued progress towards an Investigational New Drug (IND) submission. The ability of Telomir-1 to restore vision-related function, regenerate retinal tissue, and improve survival in a validated model of AMD could potentially translate into a novel oral treatment option for patients with this condition. While the stock has declined nearly 68% over the past year and currently trades at $2.07, near its 52-week low, analysts maintain an optimistic price target of $15.25. InvestingPro analysis suggests the stock may be undervalued at current levels, though investors should note the company’s weak financial health score.

The news follows Telomir Pharmaceuticals’ recent updates on its ongoing efforts to address unmet medical needs in the treatment of AMD, a leading cause of vision loss among older adults. The company is preparing for further development and clinical testing of Telomir-1, as indicated by the information provided in the SEC filing.

Investors and stakeholders in the pharmaceutical industry will be watching closely as Telomir Pharmaceuticals advances its drug candidate through the regulatory process, potentially offering new hope for those affected by age-related macular degeneration. For deeper insights into Telomir’s financial health and growth prospects, including 8 additional ProTips and comprehensive financial metrics, visit InvestingPro. The details of the announcement were based on a press release statement filed with the Securities and Exchange Commission.

In other recent news, Telomir Pharmaceuticals has reported a $3 million equity investment from The Bayshore Trust, its largest shareholder, marking a significant financial development for the company. This investment, made at an 18% premium over the closing share price, is aimed at supporting the regulatory and development activities of Telomir-1, a drug candidate targeting rare diseases. The company also announced the appointment of Alan Weichselbaum as the new Chief Financial Officer, bringing decades of experience in corporate finance to the role. Additionally, Telomir has unveiled Telomir-Ag2, a novel drug candidate designed to combat bacterial infections, including drug-resistant strains. The compound has shown promise in preclinical studies, particularly against methicillin-resistant Staphylococcus aureus. Telomir Pharmaceuticals is also advancing its Telomir-1 platform, which has shown potential in reversing signs of cellular aging in preclinical studies. The company plans to engage with the FDA’s Rare Disease Endpoint Advancement Pilot Program to further develop Telomir-1, especially for conditions like Progeria and Wilson’s disease. These developments underscore Telomir’s ongoing efforts in drug development and regulatory submissions.

This article was generated with the support of AI and reviewed by an editor. For more information see our T&C.

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