vTv Therapeutics Reports Third Quarter 2025 Financial Results and Provides Corporate Update
Topline Phase 3 CATT1 data for cadisegliatin in type 1 diabetes expected second half 2026
Announced issuance of new
“The third quarter saw a series of meaningful achievements,” said
Recent Company Highlights
- Strengthened Balance Sheet with
$80 Million Private Placement. InSeptember 2025 , vTv announced the successful closing of an$80 million private placement with new and existing healthcare investors as well as theT1D Fund . The proceeds are expected to fund the ongoing CATT1 Phase 3 trial and continued development of the cadisegliatin program for the treatment of T1D. - First Study Participant Randomized in Cadisegliatin Phase 3 Trial. In
August 2025 ,vTv Therapeutics announced that the first study participant was randomized in the Company’s CATT1 Phase 3 trial evaluating cadisegliatin as an adjunctive therapy to insulin for the treatment of T1D. Topline data from the study is expected in the second half of 2026. - Patent Allowance for Crystalline Salt Form of Cadisegliatin. In
August 2025 , the United States Patent and Trademark Office allowed claims for a patent application directed to compositions of matter of crystalline forms of salts and co-crystals of cadisegliatin. The patent term runs through 2041.
Third Quarter 2025 Financial Results
- Cash Position: The Company’s cash position as of
September 30, 2025 , was$98.5 million compared to$36.7 million as ofDecember 31, 2024 . - Research & Development (R&D) Expenses: R&D expenses were
$7.0 million and$3.2 million in each of the three months endedSeptember 30, 2025 , and 2024, respectively. The increase reflects higher spending on cadisegliatin, and other projects and higher indirect costs primarily related to theNovo Nordisk license milestone accrual and increases in payroll and share-based expenses. - General & Administrative (G&A) Expenses: G&A expenses were
$3.7 million and$3.3 million for each of the three months endedSeptember 30, 2025 , and 2024, respectively. The increase was primarily due to increases in payroll and legal expenses. - Other (Expense)/Income, Net: Other expense for the three months ended
September 30, 2025 , was immaterial. Other income of$0.2 million for the three months endedSeptember 30, 2024 , was driven by gains related to the change in the fair value of the outstanding warrants to purchase shares of our own stock. - Net Loss: Net loss attributable to vTv shareholders for the three months ended
September 30, 2025 , was$8.7 million or$1.08 per basic share. Net loss attributable to vTv shareholders for the comparable period a year ago was$4.8 million or$0.88 per basic share.
Condensed Consolidated Balance Sheets (in thousands) |
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2025 |
2024 |
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| (Unaudited) | |||||||
| Assets | |||||||
| Current assets: | |||||||
| Cash and cash equivalents | $ | 98,504 | $ | 36,746 | |||
| Prepaid expenses | 840 | 1,192 | |||||
| Other current assets | 112 | 175 | |||||
| Total current assets | 99,456 | 38,113 | |||||
| Property and equipment, net | 14 | 28 | |||||
| Operating lease right-of-use assets | 24 | 125 | |||||
| Total assets | $ | 99,494 | $ | 38,266 | |||
| Liabilities and Stockholders’ Equity | |||||||
| Current liabilities: | |||||||
| Accounts payable and accrued expenses | $ | 9,803 | $ | 5,027 | |||
| Current portion of operating lease liabilities | 32 | 169 | |||||
| Current portion of notes payable | 328 | — | |||||
| Total current liabilities | 10,163 | 5,196 | |||||
| Contract liabilities, net of current portion | 18,669 | 18,669 | |||||
| Warrant liability, related party | 37 | 57 | |||||
| Warrant liability | 82 | 43 | |||||
| Total liabilities | 28,951 | 23,965 | |||||
| Commitments and contingencies | |||||||
| Stockholders’ equity: | |||||||
| Class A Common Stock | 39 | 26 | |||||
| Class B Common Stock | — | 6 | |||||
| Additional paid-in capital | 390,058 | 311,885 | |||||
| Accumulated deficit | (319,554 | ) | (299,718 | ) | |||
| Total stockholders’ equity attributable to |
70,543 | 12,199 | |||||
| Noncontrolling interest | — | 2,102 | |||||
| Total stockholders’ equity | 70,543 | 14,301 | |||||
| Total liabilities and stockholders’ equity | $ | 99,494 | $ | 38,266 | |||
Condensed Consolidated Statements of Operations (in thousands, except per share data) |
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| Three Months Ended |
Nine Months Ended |
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| 2025 | 2024 | 2025 | 2024 | ||||||||||||
| (Unaudited) | (Unaudited) | ||||||||||||||
| Revenue | $ | — | $ | — | $ | — | $ | 1,000 | |||||||
| Operating expenses: | |||||||||||||||
| Research and development | 7,020 | 3,224 | 13,953 | 9,312 | |||||||||||
| General and administrative | 3,679 | 3,282 | 10,970 | 10,976 | |||||||||||
| Total operating expenses | 10,699 | 6,506 | 24,923 | 20,288 | |||||||||||
| Operating loss | (10,699 | ) | (6,506 | ) | (24,923 | ) | (19,288 | ) | |||||||
| Interest income | 399 | 504 | 1,005 | 1,136 | |||||||||||
| Interest expense | (5 | ) | — | (5 | ) | — | |||||||||
| Other (expense)/income, net | (40 | ) | 162 | (19 | ) | (16 | ) | ||||||||
| Loss before income taxes and noncontrolling interest | (10,345 | ) | (5,840 | ) | (23,942 | ) | (18,168 | ) | |||||||
| Income tax provision | — | — | — | 100 | |||||||||||
| Net loss before noncontrolling interest | (10,345 | ) | (5,840 | ) | (23,942 | ) | (18,268 | ) | |||||||
| Less: net loss attributable to noncontrolling interest | (1,647 | ) | (1,057 | ) | (4,106 | ) | (3,440 | ) | |||||||
| Net loss attributable to |
$ | (8,698 | ) | $ | (4,783 | ) | $ | (19,836 | ) | $ | (14,828 | ) | |||
| Net loss attributable to |
$ | (8,698 | ) | $ | (4,783 | ) | $ | (19,836 | ) | $ | (14,828 | ) | |||
| Net loss per share of |
$ | (1.08 | ) | $ | (0.88 | ) | $ | (2.80 | ) | $ | (2.70 | ) | |||
| Weighted average number of |
8,055,940 | 5,456,307 | 7,080,681 | 5,498,479 | |||||||||||
About Cadisegliatin
Cadisegliatin (TTP399) is a novel, oral small molecule, liver-selective glucokinase activator being investigated as a potential first-in-class oral adjunctive treatment for type 1 diabetes (T1D). In non-clinical studies, cadisegliatin, acting selectively on the liver, increased the activity of glucokinase independently from insulin which supports clinical investigation of improvement in glycemic control through hepatic glucose uptake and glycogen storage. Cadisegliatin has been granted Breakthrough Therapy designation by the
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.
About
Forward-Looking Statement
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, 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 and our other filings with the
Investor Contact
917-355-2395
jfraunces@lifesciadvisors.com
Media Contact
TellMed Strategies
201-396-8551
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Source: vTv Therapeutics Inc.
