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Telomir Pharmaceuticals, Inc. (Nasdaq: TELO) and Argenta to conduct a study on the efficacy of Telomir-1 in treating osteoarthritis in canines. The study aims to evaluate the potential of Telomir-1 to mitigate the clinical signs of osteoarthritis and other age-related diseases, with the possibility of extending its use to humans. Telomir-1 could offer a disease-modifying therapy for canines, enhancing their quality of life and mobility.
Positive
- Telomir Pharmaceuticals, Inc. partners with Argenta to study Telomir-1’s efficacy in treating osteoarthritis in canines.
- Telomir-1 may potentially address age-related conditions in canines and humans through telomere regeneration.
- The study aims to evaluate Telomir-1’s impact on symptomatic, radiographic, and histopathologic evaluations of osteoarthritis in canines.
- Telomir-1 could provide a disease-modifying therapy for canines with osteoarthritis, offering a potential treatment where current options only manage symptoms.
The partnership between Telomir Pharmaceuticals and Argenta to study Telomir-1’s impact on canine osteoarthritis is a significant step in veterinary medicine. The focus on telomere lengthening as a potential treatment is a novel approach. Telomeres, which are protective caps at the end of chromosomes, tend to shorten as organisms age, leading to cellular aging and associated diseases. If Telomir-1 can effectively lengthen telomeres, it may not only slow down the progression of osteoarthritis but also improve overall cellular health in canines.
Considering the large number of dogs affected by osteoarthritis and the limitations of current treatments, which are mainly symptomatic, a successful outcome from this study could disrupt the market for canine osteoarthritis treatments. It’s important to note that while the study’s success could pave the way for human trials, translating results from animal models to humans is complex and not always straightforward.
From an industry perspective, Telomir Pharmaceuticals’ strategic collaboration with Argenta could be a smart move to leverage Argenta’s expertise in animal health research. This could expedite the study and potentially enhance the credibility of the results. The focus on a disease-modifying therapy is particularly interesting as it addresses the root cause rather than just managing symptoms. This could set a new standard in the treatment of age-related diseases.
The stock market often reacts positively to announcements of innovative treatments entering the study phase, especially when they target conditions with high prevalence and unmet medical needs. However, investors should be aware that this is still a pre-clinical study and there are several regulatory hurdles and a long road ahead before potential commercialization. The mention of an Investigational New Drug (IND) application indicates a forward-looking strategy but does not guarantee FDA approval or market success.
The regulatory pathway for a novel drug like Telomir-1 is complex and requires rigorous evaluation of both efficacy and safety. The fact that Telomir Pharmaceuticals is already considering an IND application to the FDA suggests confidence in their pre-clinical data. However, the transition from animal studies to human trials is a critical juncture, with many compounds failing to demonstrate the same level of efficacy or safety in humans.
For stakeholders, the potential benefits are substantial if Telomir-1 proves to be safe and effective in humans. However, the risks associated with investing in pre-clinical stage companies should not be underestimated. The drug development process is fraught with challenges and many candidates never make it to market. The long-term implications for Telomir Pharmaceuticals will depend on successful clinical trials and the ability to navigate the regulatory environment effectively.
Study to determine the efficacy of Telomir-1 on mitigating the clinical signs of osteoarthritis and other age-related diseases
This study is believed to be the first and only known study focused on reversing aging in canines
BALTIMORE, March 29, 2024 (GLOBE NEWSWIRE) — Telomir Pharmaceuticals, Inc. (Nasdaq:TELO) (“Telomir” or the “Company”), a pre-clinical-stage pharmaceutical company focused on the development and commercialization of Telomir-1 as the first novel small molecule to lengthen the DNA’s protective telomere caps in order to potentially address age-related conditions, today announced that Telomir and global animal health contract research, development and manufacturing organisation Argenta have agreed to begin a three to six-months study on the efficacy of Telomir-1 as a treatment for osteoarthritis and other diseases of aging in canines.
The study will evaluate the efficacy of Telomir-1 for mitigating the progression of osteoarthritis based on symptomatic, radiographic, gross pathologic and histopathologic evaluations. In addition, Telomir believes that this study could be used as part of its pre-clinicial program for eventually evaluating Telomir-1 in humans.
It is estimated that nearly 18 million canines in the United States are affected by osteoarthritis. Of those, only one third of the afflicted canines have a confirmed diagnosis and are being treated for the disease. Current treatments only address the symptoms of osteoarthritis, using behavioral therapies like weight management and pain medications such as NSAIDs and injectables.
“Osteoarthritis is the most common ailment in canines yet there are currently no treatments that combat the disease. As with human osteoarthritis, medical professionals are limited to treatments that only help manage the symptoms,” stated Chris Chapman, MD, Co-founder, Chairman, Chief Executive Officer and President of Telomir Pharmaceuticals. “Working with Argenta, a leading worldwide animal health research company, this study has the potential to demonstrate both the efficacy of Telomir-1 as well as a benign safety profile. We believe that Telomir-1 will offer an attractive treatment for this indication. Just as important, we believe that the results of this trial could be used to enable our submission of an Investigation New Drug Application to the FDA to study the potential effect of Telomir-1 on osteoarthritis in humans.”
“Based on our initial research, we believe that Telomir-1 can offer an effective disease-modifying therapy that enhances the quality of life and mobility for canines with osteoarthritis,” commented Dr. Michael Roizen, Special Advisor on Age Reversal to Telomir Pharmaceuticals. “As with human indications, we believe that Telomir-1 may have the potential to treat age-related conditions in canines through telomere regeneration as we believe it may enable the production of more stem cells which essentially may allow the body, in effect, to repair itself.”
To be added to the Telomir Pharmaceuticals email distribution list, please email telomir@kcsa.com with TELO in the subject line.
About Telomir Pharmaceuticals, Inc.
Telomir Pharmaceuticals, Inc. (Nasdaq:TELO) is a pre-clinical-stage pharmaceutical company focused on the development and commercialization of Telomir-1 as the first novel small molecule to lengthen the DNA’s protective telomere caps in order to potentially reverse age-related conditions. Telomeres are the protective end caps of a chromosome made up of DNA sequences and proteins. As humans age, telomeres shorten, with metal reactivity accelerating the process, which presents us with an increased chance of contracting a number of degenerative and age-related diseases. Telomir’s goal is to develop and commercialize Telomir-1 (which is proposed to be dosed orally) for hemochromatosis (iron overload) and ultimately post-chemotherapy recovery and a broader range of other age-related inflammatory conditions such as osteoarthritis.
The Nobel Assembly at Karolinska Institute (Sweden) awarded the Nobel Prize in Physiology or Medicine in 2009 for the discovery of how chromosomes are protected by telomeres and the enzyme telomerase.
Cautionary Note Regarding Forward-Looking Statements
This press release and the statements of the Company’s management related thereto contains “forward-looking statements,” which are statements other than historical facts made pursuant to the safe harbor provisions of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These statements may be identified by words such as “aims,” “anticipates,” “believes,” “could,” “estimates,” “expects,” “forecasts,” “goal,” “intends,” “may,” “plans,” “possible,” “potential,” “seeks,” “will,” and variations of these words or similar expressions that are intended to identify forward-looking statements. Any such statements in this press release that are not statements of historical fact may be deemed to be forward-looking statements. These forward-looking statements include, without limitation, statements regarding Telomir’s technologies potential in reversing age-related decline and TELOMIR-1’s ability to result in an individual’s ability to repair oneself by using TELOMIR-1. Any forward-looking statements in this press release are based on Telomir’s current expectations, estimates and projections only as of the date of this release and are subject to a number of risks and uncertainties (many of which are beyond the Company’s control) that could cause actual results (including the results of the proposed canine osteoarthritis study referenced herein) to differ materially and adversely from those set forth in or implied by such forward-looking statements. These and other risks concerning Telomir’s programs and operations are described in additional detail in its registration statement on Form S-1 and other SEC filings, which are on file with the SEC at www.sec.gov and the Company’s website at https://ir.telomirpharma.com. Telomir explicitly disclaims any obligation to update any forward-looking statements except to the extent required by law.
For further information, please contact:
KCSA Strategic Communications
Phil Carlson
telomir@kcsa.com
Telomir Pharmaceuticals
info@Telomirpharma.com
(813) 864-2558
The study aims to determine the efficacy of Telomir-1 in treating osteoarthritis and other age-related diseases in canines.
The study is expected to last between three to six months.
It is estimated that nearly 18 million canines in the United States are affected by osteoarthritis.
Current treatments for osteoarthritis in canines focus on managing symptoms using weight management and pain medications like NSAIDs and injectables.
Chris Chapman holds the positions of Co-founder, Chairman, CEO, and President of Telomir Pharmaceuticals.
