vTv Therapeutics Announces 2024 First Quarter Financial Results and Provides Corporate Update
May 09 2024 - 3:51PM
vTv Therapeutics Inc. (Nasdaq: VTVT), a clinical stage
biopharmaceutical company focused on the development of an
adjunctive therapy to insulin for the treatment of type 1 diabetes
("T1D"), today reported financial results for the first quarter
ended March 31, 2024, and provided an update on recent corporate
developments.
“The first quarter of 2024 saw us reach several
important milestones, which we believe position vTv well for
continued execution of our corporate and clinical development
strategy,” said Paul Sekhri, Chief Executive Officer of vTv. “The
proceeds of the private placement we announced at the end of
February are expected to fully fund the first Phase 3 study of
cadisegliatin in patients with T1D, for which we expect to report
top line data in the first quarter of 2026. Site activation
activities for this trial are well underway and we continue to
expect enrollment of the first patient during the second quarter.
We believe that the body of evidence generated to-date, including
the data from the Phase 2 SimpliciT-1 study provides a compelling
scientific rationale supporting the potential of cadisegliatin as
an adjunctive therapy to insulin for the treatment of this highly
prevalent disease. In parallel with the upcoming launch of this
Phase 3 study, we are in the planning stages for two international
registrational trials of cadisegliatin in T1D which we expect to
initiate in 2026. We are also continuing our close collaboration
with G42 Investments to support the launch of the planned Phase 2
trial in the Middle East, evaluating cadisegliatin in 450 T2D
patients currently on insulin therapy. That trial remains on-track
to commence in the second half of 2024.”
Recent Company Highlights
- Significantly strengthened the
Company’s balance sheet through a $51 million private placement
with healthcare-focused institutional investors and the JDRF T1D
Fund. The proceeds of the private placement are expected to fund
the continued development of cadisegliatin through top-line data
from the first Phase 3 study, which is anticipated by the first
quarter of 2026.
- On March 4, 2024, the Company
announced the submission to the FDA of the protocol for the first
Phase 3 clinical trial of cadisegliatin in patients with T1D. The
randomized, double-blind, placebo-controlled study is expected to
enroll approximately 150 patients at up to 20 sites in the U.S.,
with the first patient expected to be enrolled in the second
quarter. It will assess two doses of cadisegliatin versus placebo
in patients currently being treated with multiple daily insulin
injections and continuous subcutaneous insulin infusion, who use
continuous glucose monitoring. The primary efficacy endpoint of the
study is the incidence of Level 2 or Level 3 hypoglycemic
events.
First Quarter 2024 Financial
Results
- Cash Position: The
Company’s cash position as of March 31, 2024, was $52.3 million
compared to $9.4 million as of December 31, 2023. The increase is
attributed to receipt of the proceeds from the private placement
financing on February 27, 2024.
- Research & Development
(R&D) Expenses: R&D expenses were $2.6 million and
$3.9 million in each of the three months ended March 31, 2024, and
2023, respectively. The decrease of $1.3 million is primarily
attributable to lower spending on cadisegliatin, due to decreases
in i) toxicity study costs and drug manufacturing related costs,
partially offset by increases in clinical trial start-up costs and
ii) an increase in indirect costs and other projects.
- General &
Administrative (G&A) Expenses: G&A expenses were
$4.0 million and $3.5 million for each of the three months ended
March 31, 2024, and 2023, respectively. The increase of $0.5
million was primarily due to increases in legal expense and higher
payroll costs offset by lower other G&A costs and share-based
expense.
- Other
(Expense)/Income: Other expense for the three months ended
March 31, 2024, was $0.4 million and was driven by losses related
to the change in the fair value of the outstanding warrants to
purchase shares of our stock issued to related parties. Other
income for the three months ended March 31, 2023, was $1.6 million
and was driven by an unrealized gain related to our investment in
Reneo, losses related to the change in the fair value of the
outstanding warrants to purchase shares of our stock issued to
related parties and the loss from the G42 promissory note early
redemption.
- Net Loss: Net loss
attributable to vTv shareholders for the three months ended March
31, 2024, was $4.9 million or $1.17 per basic share. Net loss
attributable to vTv shareholders for the comparable period a year
ago was $4.5 million or $2.16 per basic share.
vTv Therapeutics Inc.Condensed Consolidated
Balance Sheets(in thousands) |
|
March 31,2024 |
|
December 31,2023 |
|
(Unaudited) |
|
|
Assets |
|
|
|
Current assets: |
|
|
|
Cash and cash equivalents |
$ |
52,255 |
|
|
$ |
9,446 |
|
Accounts receivable |
|
981 |
|
|
|
102 |
|
Prepaid expenses and other current assets |
|
571 |
|
|
|
1,044 |
|
Current deposits |
|
65 |
|
|
|
65 |
|
Total current assets |
|
53,872 |
|
|
|
10,657 |
|
Property and equipment,
net |
|
95 |
|
|
|
117 |
|
Operating lease right-of-use
assets |
|
216 |
|
|
|
244 |
|
Total assets |
$ |
54,183 |
|
|
$ |
11,018 |
|
Liabilities,
Redeemable Noncontrolling Interest and Stockholders’ Equity
(Deficit) |
|
|
|
Current liabilities: |
|
|
|
Accounts payable and accrued expenses |
$ |
8,731 |
|
|
$ |
10,242 |
|
Current portion of operating lease liabilities |
|
173 |
|
|
|
169 |
|
Current portion of contract liabilities |
|
17 |
|
|
|
17 |
|
Current portion of notes payable |
|
— |
|
|
|
191 |
|
Total current liabilities |
|
8,921 |
|
|
|
10,619 |
|
Contract liabilities, net of
current portion |
|
18,669 |
|
|
|
18,669 |
|
Operating lease liabilities,
net of current portion |
|
125 |
|
|
|
169 |
|
Warrant liability, related
party |
|
481 |
|
|
|
110 |
|
Total liabilities |
|
28,196 |
|
|
|
29,567 |
|
Commitments and
contingencies |
|
|
|
Redeemable noncontrolling
interest |
|
— |
|
|
|
6,131 |
|
Stockholders’ equity
(deficit): |
|
|
|
Class A Common Stock |
|
24 |
|
|
|
21 |
|
Class B Common Stock |
|
6 |
|
|
|
6 |
|
Additional paid-in capital |
|
306,887 |
|
|
|
256,335 |
|
Accumulated deficit |
|
(286,121 |
) |
|
|
(281,042 |
) |
Total stockholders’ equity
(deficit) attributable to vTv Therapeutics Inc. |
|
20,796 |
|
|
|
(24,680 |
) |
Noncontrolling interest |
|
5,191 |
|
|
|
— |
|
Total stockholders’ equity
(deficit) |
|
25,987 |
|
|
|
(24,680 |
) |
Total liabilities, redeemable
noncontrolling interest and stockholders’ equity (deficit) |
$ |
54,183 |
|
|
$ |
11,018 |
|
vTv Therapeutics Inc.Condensed Consolidated
Statements of Operations(in thousands, except per share
data) |
|
Three Months EndedMarch 31, |
|
|
2024 |
|
|
|
2023 |
|
|
(Unaudited) |
Revenue |
$ |
1,000 |
|
|
$ |
— |
|
Operating expenses: |
|
|
|
Research and development |
|
2,649 |
|
|
|
3,942 |
|
General and administrative |
|
3,978 |
|
|
|
3,485 |
|
Total operating expenses |
|
6,627 |
|
|
|
7,427 |
|
Operating loss |
|
(5,627 |
) |
|
|
(7,427 |
) |
Interest income |
|
79 |
|
|
|
100 |
|
Other (expense) income, net |
|
(371 |
) |
|
|
1,553 |
|
Loss before income taxes and noncontrolling interest |
|
(5,919 |
) |
|
|
(5,774 |
) |
Income tax provision |
|
100 |
|
|
|
— |
|
Net loss before noncontrolling interest |
|
(6,019 |
) |
|
|
(5,774 |
) |
Less: net loss attributable to noncontrolling interest |
|
(1,154 |
) |
|
|
(1,275 |
) |
Net loss attributable to vTv Therapeutics Inc. |
$ |
(4,865 |
) |
|
$ |
(4,499 |
) |
Net loss attributable to vTv
Therapeutics Inc. common shareholders |
$ |
(4,865 |
) |
|
$ |
(4,499 |
) |
Net loss per share of vTv Therapeutics Inc. Class A common stock,
basic and diluted(*) |
$ |
(1.17 |
) |
|
$ |
(2.16 |
) |
Weighted average number of vTv Therapeutics Inc. Class A common
stock, basic and diluted(*) |
|
4,141,492 |
|
|
|
2,084,973 |
|
(*) Adjusted retroactively for
reverse stock split |
|
|
|
About vTv TherapeuticsvTv
Therapeutics Inc. is a clinical stage biopharmaceutical company
focused on developing oral, small molecule drug candidates. vTv has
a pipeline of clinical drug candidates led by cadisegliatin
(TTP399), a potential oral adjunctive therapy to insulin for the
treatment of type 1 diabetes. vTv and its development partners are
pursuing additional indications including type 2 diabetes and other
chronic conditions.
Forward-Looking StatementsThis
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,” "seek,"
“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 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 of
our forward-looking statements by these cautionary statements.
Contacts:
Investors:Lee RothBurns
McClellanlroth@burnsmc.com
Media:Selina Husain / Robert Flamm, Ph.D.Burns
McClellan, Inc.shusain@burnsmc.com / rflamm@burnsmc.com
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