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Financial Snapshot

Revenue
TTM
$20.34M
Gross Margin
Last 4 Quarters
N/A
Net Income
TTM
-$24.52M
Current Assets
2026 Q1
Current Liabilities
2026 Q1
Current Ratio
2026 Q1
394.28%
Total Assets
2026 Q1
Total Liabilities
2026 Q1
Book Value
2026 Q1
41.31M
Cash
2026 Q1
P/E
Last 4 Quarters
N/A
Free Cash Flow
Last 4 Quarters
N/A

Stock Price

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Market Cap: $50.645 Million

About SCYNEXIS Inc

SCYNEXIS Inc (NASDAQ: SCYX) is a biopharmaceutical company focused on developing antifungal drug candidates. Revenue is generated through license agreements, as evidenced by license agreement receivables and contract assets on the December 31, 2025 balance sheet, alongside deferred revenue. The company carries product liability insurance coverage for clinical trials and for SCY-247, with an annual limit of $25.0 million per occurrence and $25.0 million aggregate (as disclosed in the 10-K filed 2026-03-04). SCYX operates as a smaller reporting company, not a large accelerated or accelerated filer, and is subject to FDA cGMP manufacturing regulations, labeling requirements, and data privacy obligations across U.S. states and international jurisdictions. The balance sheet as of December 31, 2025 shows convertible debt among liabilities, indicating a debt-carrying capital structure. Guy Macdonald serves on the board and Ivor Macleod serves as Chief Financial Officer, as signed on the 2026-03-04 filing.

Revenue model
License agreements are the identified revenue source, with license agreement receivables, contract assets, and deferred revenue appearing on the December 31, 2025 and 2024 balance sheets. Specific dollar amounts were not legible in the filing excerpts provided.
Products and services
The filing references SCY-247 as a named product candidate with dedicated product liability coverage. Clinical trials are conducted domestically and in selected foreign countries.
Customers and end markets
End markets are in antifungal therapeutics. The filing does not specify named customers or customer concentration data.
Value-chain role
Drug developer and licensor. Manufacturing is conducted through third-party contract manufacturers subject to FDA cGMP compliance requirements. The company is the regulatory sponsor responsible for IND and NDA filings.
Geographic exposure
United States is the primary operating jurisdiction. Clinical trials are also conducted in selected foreign countries. Data privacy obligations span the EEA, UK, and multiple U.S. states including California, Virginia, Colorado, Connecticut, and Utah.

Source: SEC 10-K, filed 2026-03-04

Industry: Pharmaceutical Preparations Peers: Q/C Technologies Inc TherapeuticsMD Inc Anebulo Pharmaceuticals Inc Dare Bioscience Inc Clearside Biomedical, Inc Hyperion DeFi Inc Johnson & Johnson

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