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SCYNEXIS Reports Full Year 2025 Financial Results and Provides Corporate Update

Key Takeaway: SCYNEXIS, Inc. reported its financial results for 2025, highlighting a significant increase in revenue primarily from a license agreement with GSK. The company is advancing its second-generation antifungal drug, SCY-247, and has secured a cash runway of over two years. Despite a decrease in total other income and cash balance, SCYNEXIS remains optimistic about future developments.
Price reaction · baseline $6.2 (2026-03-04 close) · hit pre-market · clean, no other SCYX news in the window
day 0 close
+2.3%

Market Sentiment Analysis

POSITIVE FACTORS

  • SCYNEXIS received $24.8 million from GSK, extending cash runway.
  • Advancements in SCY-247 indicate potential for future growth.
  • Revenue significantly increased due to GSK license agreement.

CONCERNS & RISKS

  • Total other income decreased from $16.0 million to $7.5 million.
  • Cash balance decreased from $75.1 million to $56.3 million.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+56%
120-day peak, hindsight
Typical move
12.1%
average across 3 past catalysts
Cash runway
~11 mo
Medium dilution risk
Lead asset
Ibrexafungerp
Phase 3 · Vulvovaginal Candidiasis

Full Press Release Details

JERSEY CITY, N.J., March 04, 2026 (GLOBE NEWSWIRE) -- SCYNEXIS, Inc. (NASDAQ:SCYX), a biotechnology company pioneering innovative medicines to overcome and prevent difficult-to-treat and drug-resistant infections, today reported financial results for the year ended December 31, 2025.
“In the fourth quarter, we continued to advance our second generation fungerp, SCY-247, and also strengthened our balance sheet with the receipt of $24.8 million from GSK, extending our cash runway for more than two years,” said David Angulo, M.D., President and Chief Executive Officer. “Looking ahead, SCYNEXIS remains well positioned to explore a number of opportunities to enhance shareholder value, including releasing Phase 1 data from our SCY-247 intravenous (IV) formulation study later this year.”

Ibrexafungerp / GSK Update

SCY-247 Development Program Update

Additional Fungerps

Full Year 2025 Financial Results

For the years ended December 31, 2025 and 2024, revenue consists of $20.6 million and $3.7 million in revenue primarily associated with the GSK license agreement. For the year ended December 31, 2025, SCYNEXIS recognized a cumulative catchup of $17.2 million in license agreement revenue associated with the Binding 2025 MOU with GSK. For the year ended December 31, 2025, SCYNEXIS also recognized $1.4 million in product revenue, net for a change in estimate related to prior period revenue associated with the product recall of BREXAFEMME.
Research and development expenses for the year ended December 31, 2025, decreased to $22.3 million from $26.4 million for the year ended December 31, 2024. The decrease of $4.1 million, or 15.6%, was primarily driven by a decrease of $3.8 million in CMC expense, a decrease of $1.0 million in salary expense, a $0.5 million decrease in stock-based compensation and a net decrease in other research and development expense of $0.5 million, offset in part by an increase of $1.2 million in preclinical expense and a $0.5 million increase in clinical expense.
SG&A expenses for the year ended December 31, 2025, decreased to $14.4 million from $14.5 million for the year ended December 31, 2024. The decrease of $0.1 million, or 0.4%, was primarily driven by a decrease of $0.6 million in professional fees, offset in part by an increase of $0.5 million in business development expense.
Total other income was $7.5 million for the full year ended December 31, 2025, versus total other income of $16.0 million for the same period in 2024. The variance is mainly due to the fair value adjustment related to the warrant liabilities. For the years ended December 31, 2025 and 2024, SCYNEXIS recognized gains of $5.8 million and $13.8 million, respectively, for the fair value adjustment for warrant liabilities primarily due to the decrease in SCYNEXIS’ stock price during the periods, respectively.

Cash Balance

Cash, cash equivalents and investments totaled $56.3 million on December 31, 2025, compared to $75.1 million on December 31, 2024. SCYNEXIS received one-time non-refundable payments of $24.8 million from GSK in Q4 of 2025, resulting in a cash runway of more than two years.
About SCYNEXISSCYNEXIS, Inc. (NASDAQ: SCYX) is dedicated to advancing innovative solutions for severe rare diseases, with our lead program in the treatment and prevention of difficult-to-treat and drug-resistant fungal infections. SCYNEXIS is developing the company’s proprietary antifungal platform “fungerps.” Ibrexafungerp, the first representative of this novel class, has been licensed to GSK. The U.S. Food and Drug Administration (FDA) has approved BREXAFEMME®(ibrexafungerp tablets) for the treatment of vulvovaginal candidiasis (VVC) and for reduction in the incidence of recurrent VVC. The second generation fungerp SCY-247 is currently in clinical stages of development and has received QIDP and Fast Track designation from the FDA. Additional antifungal assets from this novel class are currently in pre-clinical and discovery phases. For more information, visitwww.scynexis.com.
Forward-Looking StatementsStatements contained in this press release regarding expected future events or results are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including but not limited to statements regarding: Plans to initiate an expanded access program for SCY-247 in the first half of 2026; having a cash runway of more than two years; releasing data from our Phase 1 IV formulation study in the second half of 2026; a clinical proof-of-concept Phase 2 study of SCY-247 in invasive candidiasis planned for 2026; and receipt of future payments from GSK on sales of BREXAFEMME. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to, risks inherent in regulatory and other costs in developing products. These and other risks are described more fully in SCYNEXIS' filings with the Securities and Exchange Commission, including without limitation, its most recent Annual Report on Form 10-K filed on March 4, 2026, including under the caption "Risk Factors." All forward-looking statements contained in this press release speak only as of the date on which they were made. SCYNEXIS undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.

CONTACT:Investor RelationsIrina KofflerLifeSci AdvisorsTel: 917-734-7387ikoffler@lifesciadvisors.com

SCYNEXIS, INC.CONSOLIDATED BALANCE SHEETS(in thousands, except share and per share data)
December 31, 2025 December 31, 2024
Assets
Current assets:
Cash and cash equivalents $ 21,259 $ 16,051
Short-term investments (See Note 3) 18,772 43,249
Prepaid expenses and other current assets (See Note 4) 263 2,184
License agreement receivable 753
License agreement contract asset 9,509
Restricted cash 80 435
Total current assets 40,374 72,181
Investments (See Note 3) 16,247 15,846
Deferred offering costs 533 417
Restricted cash 109 109
Operating lease right-of-use asset (Note 6) 1,764 2,090
Total assets $ 59,027 $ 90,643
Liabilities and stockholders’ equity
Current liabilities:
Accounts payable $ 2,225 $ 4,569
Accrued expenses (See Note 5) 2,791 3,793
Deferred revenue, current portion 235 1,642
Operating lease liability, current portion (Note 6) 483 407
Convertible debt and derivative liability (Note 6) 13,688
Total current liabilities 5,734 24,099
Deferred revenue 1,294
Warrant liability 2,225 7,998
Operating lease liability (Note 6) 1,692 2,175
Total liabilities 9,651 35,566
Commitments and contingencies
Stockholders’ equity:
Preferred stock, $0.001 par value, authorized 5,000,000 shares as of December 31, 2025 and December 31, 2024; 0 shares issued and outstanding as of December 31, 2025 and December 31, 2024
Common stock, $0.001 par value, 150,000,000 shares authorized as of December 31, 2025 and 2024; 43,541,510 and 37,973,991 shares issued and outstanding as of December 31, 2025, and December 31, 2024, respectively 46 41
Additional paid-in capital 434,474 431,571
Accumulated deficit (385,144 ) (376,535 )
Total stockholders’ equity 49,376 55,077
Total liabilities and stockholders’ equity $ 59,027 $ 90,643
SCYNEXIS, INC.CONSOLIDATED STATEMENTS OF OPERATIONS(in thousands, except share and per share data)
Years Ended December 31,
2025 2024
Revenue:
Product revenue, net $ 1,444 $
License agreement revenue 19,157 3,746
Total revenue 20,601 3,746
Operating expenses:
Research and development 22,280 26,405
Selling, general and administrative 14,395 14,458
Total operating expenses 36,675 40,863
Loss from operations (16,074 ) (37,117 )
Other expense (income):
Amortization of debt issuance costs and discount 312 1,726
Interest income (2,177 ) (4,291 )
Interest expense 173 828
Other income (235 )
Warrant liability fair value adjustment (5,773 ) (13,812 )
Derivative liability fair value adjustment (196 )
Total other income (7,465 ) (15,980 )
Loss before taxes (8,609 ) (21,137 )
Income tax expense (151 )
Net loss $ (8,609 ) $ (21,288 )
Net loss per share – basic and diluted $ (0.17 ) $ (0.44 )
Weighted average common shares outstanding – basic and diluted 49,933,381 48,513,073

Frequently Asked Questions

What were SCYNEXIS's total revenues for 2025?

SCYNEXIS reported total revenues of $20.6 million for the year 2025.

How much cash does SCYNEXIS have as of December 31, 2025?

As of December 31, 2025, SCYNEXIS had $56.3 million in cash, cash equivalents, and investments.

What is SCY-247?

SCY-247 is SCYNEXIS's second-generation antifungal drug currently in clinical development.

What significant payment did SCYNEXIS receive in Q4 2025?

SCYNEXIS received a one-time non-refundable payment of $24.8 million from GSK.

What is the status of BREXAFEMME?

BREXAFEMME has been approved by the FDA for treating vulvovaginal candidiasis.

Last updated: Mar 5, 2026