| Symbol | SILO |
|---|---|
| Name | SILO PHARMA, INC. |
| Sector | CONSUMER DISCRETIONARY |
| Region | North America |
| Industry | Apparel |
| Address | 677 N. WASHINGTON BOULEVARD, SARASOTA, Florida, 34236, United States |
| Telephone | +1 -718 400-9031 |
| Fax | — |
| — | |
| Website | https://www.silopharma.com |
| Incorporation | UNDEFINED |
| Incorporated On | — |
| Employees | — |
| Fiscal Year | — |
| Public Since | — |
| Exchanges | NASDAQ |
| Auditor | — |
| Audit Status | NOT PROVIDED |
| Reporting Status | — |
| CIK | 0001514183 |
| Description | Silo Pharma Inc. (Nasdaq: SILO) is a developmental stage biopharmaceutical company developing novel therapeutics that address underserved conditions including stress-induced psychiatric disorders, chronic pain conditions, and central nervous system (CNS) diseases. Silo focuses on developing traditional therapies and psychedelic treatments in novel formulations and drug delivery systems. The Companys lead program, SPC-15, is an intranasal treatment targeting PTSD and stress-induced anxiety disorders. SP-26 is a time-release ketamine-loaded implant for fibromyalgia and chronic pain relief. Silos two preclinical programs are SPC-14, an intranasal compound for the treatment of Alzheimers disease, and SPU-16, a CNS-homing peptide targeting multiple sclerosis (MS). Silos research and development programs are conducted through collaborations with Columbia University and the University of Maryland, Baltimore. Additional info from NASDAQ: |
Silo Pharma Subsidiary QwikAgents Set to Advance Enterprise AI Agent Platform through NVIDIA Developer Program
Read moreNew Form ARS - Silo Pharma, Inc. <b>Filed:</b> 2026-06-30 <b>AccNo:</b> 0001213900-26-073369 <b>Size:</b> 1 MB
Read moreNew Form DEFA14A - Silo Pharma, Inc. <b>Filed:</b> 2026-06-30 <b>AccNo:</b> 0001213900-26-073368 <b>Size:</b> 1 MB
Read moreNew Form DEF 14A - Silo Pharma, Inc. <b>Filed:</b> 2026-06-30 <b>AccNo:</b> 0001213900-26-073367 <b>Size:</b> 2 MB
Read moreSilo Pharma Advances SPC-15 PTSD Therapeutic with Drug-Device Robustness Study Ahead of Planned FDA Type C Meeting Request
Read more