Vtv Therapeutics Reports First Quarter 2026 Financial Results And Provides Corporate Update
| vTv Therapeutics Inc. Condensed Consolidated Balance Sheets (in thousands) | |||||||
| March 31, 2026 | December 31, 2025 | ||||||
| (Unaudited) | |||||||
| Assets | |||||||
| Current assets: | |||||||
| Cash and cash equivalents | $ | 98,086 | $ | 88,932 | |||
| Prepaid expenses | 521 | 743 | |||||
| Other current assets | 201 | 218 | |||||
| Total current assets | 98,808 | 89,893 | |||||
| Other assets | 5 | 6 | |||||
| Total assets | $ | 98,813 | $ | 89,899 | |||
| Liabilities and Stockholders' Equity | |||||||
| Current liabilities: | |||||||
| Accounts payable and accrued expenses | $ | 6,821 | $ | 6,557 | |||
| Warrant liability, related party | 60 | 84 | |||||
| Total current liabilities | 6,881 | 6,641 | |||||
| Contract liabilities | 1,830 | 18,669 | |||||
| Warrant liability | 143 | 152 | |||||
| Total liabilities | 8,854 | 25,462 | |||||
| Commitments and contingencies | |||||||
| Stockholders' equity: | |||||||
| Class A Common Stock | 39 | 39 | |||||
| Class B Common Stock | - | - | |||||
| Additional paid-in capital | 392,478 | 391,090 | |||||
| Accumulated deficit | (302,558 | ) | (326,692 | ) | |||
| Total stockholders' equity | 89,959 | 64,437 | |||||
| Total liabilities and stockholders' equity | $ | 98,813 | $ | 89,899 | |||
| vTv Therapeutics Inc. Condensed Consolidated Statements of Operations (in thousands, except per share data) | |||||||
| Three Months Ended March 31, | |||||||
| 2026 | 2025 | ||||||
| (Unaudited) | |||||||
| Revenue | $ | 36,839 | $ | - | |||
| Operating expenses: | |||||||
| Research and development | 8,978 | 2,830 | |||||
| General and administrative | 4,598 | 3,673 | |||||
| Total operating expenses | 13,576 | 6,503 | |||||
| Operating income/(loss) | 23,263 | (6,503 | ) | ||||
| Interest income | 838 | 331 | |||||
| Other income (expense), net | 33 | (45 | ) | ||||
| Net income (loss) before income taxes and noncontrolling interest | 24,134 | (6,217 | ) | ||||
| Income tax provision | - | - | |||||
| Net income (loss) before noncontrolling interest | 24,134 | (6,217 | ) | ||||
| Less: net loss attributable to noncontrolling interest | - | (1,125 | ) | ||||
| Net income (loss) attributable to vTv Therapeutics Inc. | $ | 24,134 | $ | (5,092 | ) | ||
| Net income (loss) attributable to vTv Therapeutics Inc. common shareholders | $ | 24,134 | $ | (5,092 | ) | ||
| Basic net income (loss) per share of vTv Therapeutics Inc. Class A common stock | $ | 1.94 | $ | (0.77 | ) | ||
| Basic weighted average number of vTv Therapeutics Inc. Class A common stock | 12,409,278 | 6,582,844 | |||||
| Diluted net income (loss) per share of vTv Therapeutics Inc. Class A common stock | $ | 1.65 | $ | (0.77 | ) | ||
| Diluted weighted average number of vTv Therapeutics Inc. Class A common stock | 14,634,420 | 6,582,844 | |||||
About vTv Therapeutics
vTv Therapeutics is a late-stage biopharmaceutical company focused on developing oral, small molecule drug candidates intended to help treat people living with diabetes and other chronic diseases. vTv's clinical pipeline is led by cadisegliatin, currently in a U.S. Phase 3 trial, a potential first-in-class oral glucokinase activator being investigated for the treatment of type 1 diabetes. vTv and its development partners are investigating multiple molecules across different indications for chronic diseases. Learn more at vtvtherapeutics or follow the company on LinkedIn or X.
About Cadisegliatin
Cadisegliatin (TTP399) is a novel, oral small molecule, liver-selective glucokinase activator being investigated in the U.S. as a potential first-in-class oral adjunctive treatment for type 1 diabetes (T1D). In non-clinical studies, cadisegliatin acted selectively on the liver and increased glucokinase activity independently of insulin. These findings support clinical investigation of whether cadisegliatin can improve glycemic control through hepatic glucose uptake and glycogen storage. Cadisegliatin has been granted Breakthrough Therapy designation by the U.S. Food and Drug Administration (FDA).
Cadisegliatin is under investigation, and the safety and efficacy have not been established. There is no guarantee that this product will receive health authority approval or become commercially available for the use being investigated.
Forward-Looking Statements
This release contains forward-looking statements, which involve risks and uncertainties. These forward-looking statements can be identified by the use of forward-looking terminology, including the terms“anticipate,”“believe,”“could,”“estimate,”“expect,”“intend,”“may,”“plan,”“potential,”“predict,”“project,”“should,”“target,”“will,”“would” and, in each case, their negative or other various or comparable terminology. All statements other than statements of historical facts contained in this release, including statements regarding the timing of our clinical trials, the anticipated effect of Phase 3 topline data on the Company, the benefits of cadisegliatin to people living with T1D, our strategy, future operations, future financial position, future revenue, projected costs, prospects, plans, objectives of management and expected market growth are forward-looking statements. These statements involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance, or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. Important factors that could cause our results to vary from expectations include those described under the heading“Risk Factors” in our Annual Report on Form 10-K, subsequent Quarterly Reports on Form 10-Q and our other filings with the SEC. These forward-looking statements reflect our views with respect to future events as of the date of this release and are based on assumptions and subject to risks and uncertainties. Given these uncertainties, you should not place undue reliance on these forward-looking statements. These forward-looking statements represent our estimates and assumptions only as of the date of this release and, except as required by law, we undertake no obligation to update or review publicly any forward-looking statements, whether as a result of new information, future events or otherwise after the date of this release. We anticipate that subsequent events and developments will cause our views to change. Our forward-looking statements do not reflect the potential impact of any future acquisitions, merger, dispositions, joint ventures, or investments we may undertake. We qualify all our forward-looking statements by these cautionary statements.
Investor Contact
John Fraunces
LifeSci Advisors, LLC
917-355-2395
...
Media Contact
Caren Begun
TellMed Strategies
201-396-8551
...
Legal Disclaimer:
MENAFN provides the
information “as is” without warranty of any kind. We do not accept
any responsibility or liability for the accuracy, content, images,
videos, licenses, completeness, legality, or reliability of the information
contained in this article. If you have any complaints or copyright
issues related to this article, kindly contact the provider above.

Comments
No comment