Silo Pharma Provides Update on Progress in PTSD Drug Development and Launches New Digital Assets Treasury Initiative
Biopharmaceutical Developments: Silo Pharma is preparing to submit an investigational new drug (IND) application for its lead candidate SPC-15, an intranasal treatment for PTSD, following positive safety study results and completion of necessary toxicology studies.
Digital Assets Strategy: The company has launched a digital assets treasury strategy, making initial cryptocurrency purchases and appointing a lead crypto strategy advisor to manage its portfolio and enhance compliance.
Future Catalysts: Key upcoming milestones include data from the IND-enabling study expected in 2026, FDA discussions to finalize IND submission requirements, and plans to expand therapeutic indications for SPC-15.
Company Overview: Silo Pharma focuses on developing treatments for underserved conditions, including PTSD and chronic pain, while also engaging in cryptocurrency investments to strengthen its capital resources.
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- Share Repurchase Program: Silo Pharma's board has authorized a share repurchase program of up to $1 million, which is expected to enhance investor confidence and potentially boost stock prices, thereby improving the company's market performance in the biopharmaceutical sector.
- Stock Price Surge: Following the announcement, SILO shares rose 32.75% to $0.37 in premarket trading, indicating positive market sentiment regarding the company's future, particularly in its drug development efforts.
- R&D Progress: The company plans to submit an IND application for SPC-15 to the FDA this year as a treatment for PTSD and stress-induced anxiety disorders, which, if approved, will initiate the first-in-human trial and further advance the commercialization of its product pipeline.
- Financial Performance: For the quarter ended September 30, 2025, Silo Pharma reported a wider net loss of $1.20 million, or $0.19 per share, while license revenue remained flat, highlighting the need for cost control measures to achieve sustainable growth.
- Strong Earnings Performance: Keysight Technologies reported earnings per share of $2.17, exceeding Wall Street's expectation of $2, demonstrating robust profitability that boosts investor confidence.
- Significant Revenue Growth: The quarterly revenue reached $1.6 billion, surpassing the analyst consensus of $1.54 billion, indicating successful business expansion and strong market demand, further solidifying its market position.
- Stock Price Surge: Keysight's shares jumped 16.8% to $286.03 in pre-market trading, reflecting a positive investor reaction to the company's financial performance, which may attract more investor interest.
- Market Dynamics Impact: Keysight's strong results could influence the performance of other related stocks, particularly in the technology and electronics sectors, signaling an overall improvement in market sentiment.
- Buyback Program Initiated: Silo Pharma has approved a share repurchase program to buy back up to $1 million of its common stock, aiming to enhance earnings per share and boost investor confidence by reducing the number of shares outstanding.
- Strong Stock Performance: As of November 13, 2025, the company had 13.32 million shares of common stock outstanding, and the implementation of the buyback program is expected to further elevate the stock price, attracting more investor interest.
- Positive Market Reaction: Following the announcement of the buyback program, SILO shares surged 45.8% in after-hours trading, indicating a bullish market sentiment towards the company's future prospects, which may draw in more institutional investors.
- Clear Strategic Positioning: As a developmental-stage biotech firm, Silo Pharma focuses on integrating traditional therapeutics with psychedelic research, and the buyback program will provide financial support for its future R&D and market expansion efforts.

- Company Announcement: Silo Pharma has received a notice of allowance in Japan for its SP-15 product.
- Global Expansion: This development is part of Silo Pharma's strategy to expand its global intellectual property portfolio.
- Clinical Research Collaboration: Silo Pharma has signed a Letter of Intent with global CRO Allucent to conduct two Phase 1 studies for its SPC-15 nasal spray, marking a significant advancement in the treatment of psychiatric disorders.
- Study Design Details: The studies will include an Open-Label Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) design, aimed at efficiently generating safety and pharmacokinetic data to expedite SPC-15's clinical development.
- Strategic Importance: CEO Eric Weisblum stated that this collaboration will enhance the rigor and speed of the research, further advancing SPC-15's development to provide new therapies for PTSD and anxiety patients.
- Product Background: SPC-15 is an investigational intranasal 5-HT4 receptor agonist designed for rapid brain action using a special soft mist delivery system, with plans to leverage biomarkers for an accelerated FDA approval pathway.
- Clinical Research Collaboration: Silo Pharma has signed a Letter of Intent with global CRO Allucent to conduct two Phase 1 studies for its SPC-15 nasal spray, marking a significant advancement in the treatment of PTSD and anxiety.
- Agreement Details: The LOI outlines comprehensive support for clinical operations, pharmacovigilance, and data management, which is expected to accelerate the clinical development of SPC-15, enhancing the company's competitiveness in the biopharmaceutical sector.
- Drug Development Context: SPC-15 is an investigational intranasal 5-HT4 receptor agonist targeting stress-induced psychiatric conditions, aiming for rapid brain action to alleviate PTSD and anxiety symptoms, indicating its potential market value.
- Long-term Value Creation: The CEO of Silo Pharma stated that this collaboration will facilitate the efficient generation of safety and pharmacokinetic data, further driving innovation and long-term growth in the mental health space.






