Full Press Release Details
Inc. Reports Fourth Quarter and Full Year 2023 Financial Results and Provides Clinical and Business Update
Million Raised Since Beginning of 2023
Million of Debt Converted to Equity at a Premium
3 ADHD Data Continues to Impress
CITY, Kan., April 1, 2024 - Cingulate Inc. (NASDAQ: CING), a biopharmaceutical company utilizing its proprietary Precision Timed
Release (PTR ) drug delivery platform technology to build and advance a pipeline of next-generation pharmaceutical products,
today announced its financial results for the twelve months ended December 31, 2023, and provided a clinical and business update. Highlights
include capital raised from multiple sources and the addition of three independent board members.
am pleased to report that Cingulate is stronger today than the end of last year," said Shane J. Schaffer, Chairman and CEO of Cingulate
Inc. "With the addition of three independent directors, each of whom possess deep experience in the pharmaceutical industry,
small-cap publicly traded companies, and hold executive leadership roles within pharma, the Cingulate board is equipped to overcome the
lead asset CTx-1301 continues to impress clinical investigators and key opinion leaders as we share our Phase 3 results. In addition,
pharmaceutical companies in the U.S., Europe, and other territories have engaged in licensing discussions regarding their interest to
commercialize our product. These tailwinds put Cingulate in a position to obtain non-dilutive capital and expand our pipeline
are encouraged to see the capital markets improving as evidenced by our ability to raise more than $17 million over the past year. Looking
ahead, Cingulate has several financial instruments in place to raise additional capital while fighting to preserve shareholders'
I am very pleased with the progress made by our
team in 2023 and into 2024. Our focus remains on executing our strategic plan and submitting CTx-1301 to the FDA."
Data Exhibits Strong Effect Size
January 20, 2024, Cingulate presented results from the Phase 3 adult efficacy and safety study of its lead candidate, CTx-1301 (dexmethylphenidate),
for the treatment of Attention Deficit / Hyperactivity Disorder (ADHD), at the 2024 American Professional Society of ADHD and Related
Disorders (APSARD) conference in Orlando, FL.
results were previously presented at the 36th Annual Psych Congress in September 2023, where the data was selected as a finalist
for the Psych Congress's First Annual Poster Awards.
Cingulate poster presented at APSARD provided additional insight regarding CTx-1301's impressive effect size. Effect size conveys
clinical significance rather than statistical significance, is not reliant on sample size, and allows for comparison across trials. The
poster presented may be viewed here. The study was not intended nor did it achieve statistical significance on the primary endpoint
but demonstrated a trend towards significance despite its modest sample size in improving ADHD symptoms with a rapid onset of action
and entire active-day duration.
Receives Guidance from FDA on Path Forward for Anxiety Asset CTx-2103 (buspirone)
December 2023, Cingulate received input from the FDA regarding the regulatory pathway for CTx-2103, and the design of clinical studies
for filing of an IND. Based on this FDA feedback, we believe that we can seek and win approval of CTx-2103 under the 505(b)(2) pathway,
which typically requires less time and resources than the 505(b)(1) full NDA pathway.
Million of Capital Raised and $3.3 Million of Debt Converted to Equity in 2024
January 1, 2024, the Company sold shares of common stock under its At the Market Offering Agreement with H.C. Wainwright & Co., LLC
for gross proceeds of $3.2 million. In February 2024, the Company closed a $7.5 million public offering of its common stock (or pre-funded
warrants in lieu thereof) and Series A and Series B warrants to purchase shares of common stock, at a public offering price of $2.00
per share (or common stock equivalent in lieu thereof) and accompanying warrants. Additionally, in January 2024, Werth Family Investment
Associates, LLC (WFIA), the manager of which is Peter J. Werth, a member of the Cingulate board of directors, converted at a 10 percent
premium to market the remaining $3.3 million of outstanding debt plus accrued interest into pre-funded warrants to purchase shares
Million of Capital Raised and $5.8 Million of Debt Converted to Equity in 2023
September 2023, Cingulate closed a $4.0 million public offering of shares of common stock (or common stock equivalents in lieu thereof)
and Series A and Series B warrants to purchase shares of common stock, at public offering price of $11.55 per share (or common stock
equivalent in lieu thereof) and accompanying warrants.
addition, during 2023, Cingulate sold shares of common stock through its ATM Agreement and its Purchase Agreement with Lincoln Park Capital
Fund, LLC for aggregate gross proceeds of $2.1 million. Finally, in August 2023, WFIA purchased shares of common stock for $1.0 million
through a private placement priced at the market, and in September 2023, WFIA converted at a 47% premium to market $5.8 million
of outstanding debt and accrued interest into pre-funded warrants to purchase shares of common stock.
Callahan Promoted to CFO
January 2024, Cingulate promoted longtime Controller Jennifer Callahan to Chief Financial Officer, succeeding Lou Van Horn, who retired
from the company in December 2023.
Independent Directors Appointed to Cingulate Board
February 2024, Cingulate appointed three independent directors to its board: Jay Roberts, Bryan Lawrence, and Jeff Ervin. Please visit
Cingulate.com for more information about the new directors.
Quarter and Full Year Results
Position: As of December 31, 2023, Cingulate had $52,416 in cash and cash equivalents. Additionally, we have raised $10.7 million
from the sale of securities in 2024 to date and we believe that our cash will satisfy our capital needs through late in the second quarter
of 2024 under our current business plan. Management continues to evaluate additional strategies to obtain funding, which may include
additional equity offerings, issuance of debt, or other capital sources, including potential collaborations with other companies or other
strategic transactions.
Expenses: Research and development expenses were $5.0 million for the three months ended December 31, 2023, compared to $1.9 million
for the same period in 2022. Research and development expenses were $15.5 million for the year ended December 31, 2023, compared to $9.0
million for the year ended December 31, 2022. These increases were primarily the result of increased clinical activity in 2023 as compared
to 2022. During the third quarter of 2023, we initiated two Phase 3 studies for CTx-1301, the pediatric dose optimization onset and duration
study and the fixed dose pediatric and adolescent safety and efficacy study. In addition, the Phase 3 adult dose-optimization study for
CTx-1301 was completed in June 2023. Manufacturing for these Phase 3 studies also occurred during 2023.
Expenses: General and administrative expenses were $1.8 million for the three months ended December 31, 2023, compared to $2.5 million
for the same period in 2022. General and administrative expenses were $7.3 million for the year ended December 31, 2023, compared to
$8.5 million for the year ended December 31, 2022. These decreases were primarily the result of a decrease in our directors' and
officers' insurance premium from 2022 to 2023. The decrease in directors' and officers' insurance premium was offset
by increases in certain professional fees primarily the result of the timing of services performed relating to our annual audit.
Loss: Net loss was $6.9 million for the three months ended December 31, 2023, compared to $4.6 million for the same period in 2022.
Net loss was $23.5 million for the year ended December 31, 2023, compared to $17.7 million for the year ended December 31, 2022. The
increase in the net loss from 2022 to 2023 primarily relates to a significant increase in development activity as described above.
| December 31, 2023 | December 31, 2022 | |||||||
| Cash and cash equivalents | $ | 52,416 | $ | 5,356,276 | ||||
| Total assets | $ | 3,491,436 | $ | 11,405,057 | ||||
| Total liabilities | $ | 10,360,865 | $ | 7,523,035 | ||||
| Accumulated deficit | $ | (92,943,443 | ) | $ | (69,408,496 | ) | ||
| Total stockholders' equity | $ | (6,869,429 | ) | $ | 3,882,022 |
Statements of Operations
| Three Months Ended December 31, | Year Ended December 31, | |||||||||||||||
| 2023 | 2022 | 2023 | 2022 | |||||||||||||
| Operating expenses: | ||||||||||||||||
| Research and development | $ | 4,984,909 | $ | 1,931,654 | $ | 15,493,304 | $ | 8,995,280 | ||||||||
| General and administrative | 1,812,242 | 2,543,371 | 7,265,885 | 8,506,438 | ||||||||||||
| Operating loss | (6,797,151 | ) | (4,475,025 | ) | (22,759,189 | ) | (17,501,718 | ) | ||||||||
| Interest and other income (expense), net | (137,546 | ) | (130,002 | ) | (775,758 | ) | (174,514 | ) | ||||||||
| Loss before income taxes | (6,934,697 | ) | (4,605,027 | ) | (23,534,947 | ) | (17,676,232 | ) | ||||||||
| Income tax benefit (expense) | - | - | - | - | ||||||||||||
| Net loss | $ | (6,934,697 | ) | $ | (4,605,027 | ) | $ | (23,534,947 | ) | $ | (17,676,232 | ) |
Inc. is a biopharmaceutical company utilizing its proprietary Precision Timed Release (PTR ) drug delivery platform technology
to build and advance a pipeline of next-generation pharmaceutical products, designed to improve the lives of patients suffering from
frequently diagnosed conditions characterized by burdensome daily dosing regimens and suboptimal treatment outcomes. With an initial
focus on the treatment of Attention Deficit/Hyperactivity Disorder (ADHD), Cingulate is identifying and evaluating additional therapeutic
areas where its PTR technology may be employed to develop future product candidates, such as anxiety disorders.
is headquartered in Kansas City, KS. For more information visit Cingulate.com.
press release contains "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933, as amended,
and Section 21E of the Securities Exchange Act of 1934, as amended. These forward-looking statements include all statements, other than
statements of historical fact, regarding our current views and assumptions with respect to future events regarding our business, including
statements with respect to our plans, assumptions, expectations, beliefs and objectives with respect to product development, clinical
studies, clinical and regulatory timelines, market opportunity, competitive position, business strategies, potential growth opportunities
and other statements that are predictive in nature. These statements are generally identified by the use of such words as "may,"
"could," "should," "would," "believe," "anticipate," "forecast,"
"estimate," "expect," "intend," "plan," "continue," "outlook,"
"will," "potential" and similar statements of a future or forward-looking nature. Readers are cautioned that
any forward-looking information provided by us or on our behalf is not a guarantee of future performance. Actual results may differ materially
from those contained in these forward-looking statements as a result of various factors disclosed in our filings with the Securities
and Exchange Commission (SEC), including the "Risk Factors" section of our Annual Report on Form 10-K filed with the SEC
on March 10, 2023. All forward-looking statements speak only as of the date on which they are made, and we undertake no duty to update
or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except to the extent required
Vice President, Investor & Public Relations, Cingulate