Pipeline development and regulatory risk
Drug candidates must clear preclinical, IND, and clinical hurdles before commercialization.
- Scope
- SPC-15, SP-26, SPC-14, SPU-16
- Materiality
- high
Silo Pharma, Inc. is a U.S.-based developmental-stage biopharmaceutical company focused on licensing, developing, and advancing drug candidates for central nervous system and stress-related disorders. Its pipeline includes intranasal, implantable, and peptide-based programs, and the company also holds digital assets as part of a treasury strategy.
38,6 %
−5 863,5 %
11.36
11.36
| % | |
|---|---|
| Lead therapeutic programs | 70% Development-stage drug candidates targeting PTSD, anxiety, fibromyalgia, and CNS disorders. |
| Drug delivery technology | 15% Intranasal and other delivery mechanisms used to improve targeting and onset of action. |
| Licensed intellectual property | 10% Exclusive and option-based rights to external inventions and patents supporting the pipeline. |
| Digital asset treasury | 5% Cryptocurrency holdings and related treasury activities outside the core therapeutics business. |
Silo Pharma does not sell commercial medicines at scale; its economic counterparties are primarily licensors, research...
Provide patents, compounds, or delivery technologies that Silo licenses to build its pipeline.
Support preclinical, toxicology, and regulatory-enabling studies for candidate advancement.
Patients with PTSD, stress-induced anxiety, fibromyalgia, Alzheimer’s disease, or neuroinflammatory conditions who would use approved products.
Psychiatrists, neurologists, pain specialists, and other clinicians who would prescribe or administer therapies.
Silo Pharma is headquartered in the United States and conducts its business through U.S...
Silo Pharma’s strategy is to license or acquire external intellectual property, fund development, and advance a small...
SPC-15 is the lead program and the clearest path to a clinical-stage asset.
Multiple programs reduce dependence on a single asset and expand optionality.
The company relies on external inventions to source differentiated candidates.
The treasury strategy creates a separate investment framework and capital use case.
Silo Pharma faces the typical risks of a development-stage biotech company: clinical, regulatory, and intellectual...
Drug candidates must clear preclinical, IND, and clinical hurdles before commercialization.
The business depends on rights from third parties and may face renewal, scope, or royalty constraints.
Digital assets can be volatile and operational mistakes in custody or trading can create losses.
Maintaining exchange listing supports liquidity and access to capital for a pre-revenue biotech.
Other developers are pursuing similar indications, delivery methods, and assets.
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: 29.4.2026