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Silo Pharma to discuss ketamine treatments at FDA event

EditorNatashya Angelica
Published 14/05/2024, 18:40
SILO
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SARASOTA, FL - Silo Pharma, Inc. (NASDAQ:SILO), a biopharmaceutical company in the developmental stage, is set to participate in an FDA-sponsored public meeting on June 27, 2024, to discuss the use of ketamine in emerging therapeutic areas. The event, organized in collaboration with the Reagan-Udall Foundation for the FDA, aims to examine the increasing interest in ketamine as a potential treatment for conditions like depression and chronic pain.

The company's CEO, Eric Weisblum, along with a scientific advisor, will join clinicians, researchers, and patient advocates at the hybrid in-person and virtual meeting. Silo Pharma is currently developing several drug candidates that feature ketamine as a primary therapeutic agent.

Among these, its lead program, SPC-15, is an intranasal treatment targeting PTSD and anxiety disorders related to stress. Moreover, SP-26 is being developed as a ketamine-based injectable implant for chronic pain and fibromyalgia treatment, designed to control dosage and release timing.

Silo Pharma has also exercised an exclusive licensing option with Columbia University to develop, manufacture, and commercialize SPC-15 globally. The company's research endeavors extend to preclinical programs such as SPC-14 and SPU-16, which target Alzheimer's disease and multiple sclerosis, respectively, through collaborations with academic institutions including the University of Maryland, Baltimore.

The company's involvement in the upcoming FDA meeting underscores its commitment to exploring novel formulations and delivery systems for drugs that address conditions with limited treatment options. This announcement is based on a press release statement and includes forward-looking statements that involve risks and uncertainties.

Silo Pharma cautions that these statements are subject to changes based on various factors, and there can be no assurance that the company's expectations will prove accurate.

InvestingPro Insights

As Silo Pharma, Inc. (NASDAQ:SILO) gears up for the significant FDA-sponsored public meeting, investors are closely monitoring the company’s financial health and market performance. The company, which is a niche player in the biopharmaceutical industry, has shown a commitment to innovation in drug development, particularly with its focus on ketamine-based therapies.

InvestingPro data reveals that Silo Pharma holds a market capitalization of 5.03 million USD, reflecting its status as a smaller player in the pharmaceutical sector. Despite the challenges often faced by developmental-stage companies, Silo Pharma has demonstrated impressive gross profit margins, at 91.9% for the last twelve months as of Q4 2023.

This margin suggests efficiency in the company's cost management and production processes. Furthermore, the company's management has been actively engaged in share buybacks, a move that can signal confidence in the future of the business and potentially enhance shareholder value.

InvestingPro Tips highlight that Silo Pharma maintains a strong liquidity position, with cash holdings that surpass its debt levels. Moreover, the company’s liquid assets exceed its short-term obligations, providing a cushion for operational needs and investment in research and development.

Still, analysts indicate that the company is not expected to be profitable this year, and it has not been profitable over the last twelve months. It is also worth noting that Silo Pharma does not pay dividends, which may be a consideration for income-focused investors.

For those interested in a deeper dive into Silo Pharma's financials and market performance, InvestingPro offers additional insights and metrics. There are 6 more InvestingPro Tips available for Silo Pharma, which can be accessed at InvestingPro. To enhance your experience with InvestingPro, use coupon code PRONEWS24 to get an additional 10% off a yearly or biyearly Pro and Pro+ subscription.

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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