Cingulate Inc. Reports Fourth Quarter and Full Year 2021 Results and Provides Clinical and Business Update Completed Initial Public Offering, Raising Gross Proceeds of $25.0 Million Expedited Clinical Program for CTx-130

Inc. Reports Fourth Quarter and Full Year 2021 Results

Provides Clinical and Business Update

Initial Public Offering, Raising Gross Proceeds of $25.0 Million

Clinical Program for CTx-1301 Expected to Reduce Capital Requirements and Time to Approval

CITY, Kan., March 10, 2022 - Cingulate Inc. (NASDAQ: CING), a

clinical-stage 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

three and 12 months ended December 31, 2021, and provided a clinical and business update.

recent initial public offering was a significant milestone for Cingulate in advancing our mission to help Attention Deficit/Hyperactivity

Disorder (ADHD) patients overcome their significant unmet needs in using currently available treatment options," said Shane J.

Schaffer, PharmD, Chairman and Chief Executive Officer of Cingulate. "We look forward to initiating our pivotal Phase 3 study for

CTx-1301 in the second quarter of 2022 and beginning to dose patients as we progress toward our goal of filing a New Drug Application

(NDA) with the U.S. Food and Drug Administration (FDA) in the second half of 2023."

Brams, M.D., Chief Medical Officer, added, "As a practicing psychiatrist for over 30 years, I'm proud to be a part of the

Cingulate team in realizing our vision to provide patients and providers with a true once-daily medication to overcome the long-standing

unmet needs in ADHD. Our clinical plan will further demonstrate our products' ability to achieve a fast onset of action and provide

entire active-day efficacy without the need for booster or recovery doses."

Cingulate has updated its clinical program for CTx-1301 (dexmethylphenidate), its lead investigational asset for the treatment of

ADHD, based on FDA feedback regarding the Company's CTx-1301 initial Pediatric Study Plan (iPSP), and longstanding guidance on

the accelerated approval pathway under Section 505(b)(2) of the Federal Food, Drug, and Cosmetic Act.

plans to commence two CTx-1301 Phase 3 clinical studies in 2022: (1) a fixed-dose pediatric and adolescent safety and efficacy study,

which will enroll its first patient in the second quarter of 2022; and (2) a pediatric safety and efficacy dose-optimization study to

assess the onset and duration of efficacy, which is targeted to begin in the second half of 2022. Cingulate's clinical plan will

also investigate several exploratory elements critical to ADHD patients, providers, payers, and the larger medical community, such as

the use of booster/recovery doses, the abuse and diversion associated with short-acting medications, and the crash/rebound effects of

early medication wear off. Results from the fixed dose study are expected in late 2022. The entire Phase 3 clinical program is expected

to include approximately 350 patients. Assuming Cingulate receives positive clinical results from its Phase 3 trials, the Company plans

to submit an NDA for CTx-1301 in the second half of 2023 under the Section 505(b)(2) pathway.

believes the updated clinical program for CTx-1301 accelerates the study timeline by condensing the number and design of studies, therefore

potentially reducing the time and expense to submission of the NDA for CTx-1301 to the FDA for potential approval.

order to achieve an expected second half 2023 NDA submission for potential FDA approval, the Company believes it will need approximately

$15 million of additional capital and is evaluating alternatives to raise additional capital, including equity and debt financing and

non-dilutive strategic collaborations in the U.S. and abroad. A commercial collaboration or strategic relationship with an established

pharmaceutical company, which is a key Company initiative, would provide more immediate access to marketing, sales, market access and

distribution infrastructure.

Cingulate plans to initiate a Phase 1/2 bioavailability study in ADHD patients for CTx-1302 (dextroamphetamine), its second investigational

asset for the treatment of ADHD, in 2023 and, if the results from this study are successful, the Company plans to initiate pivotal Phase

3 clinical trials in all patient segments for CTx-1302 in late 2023 with results expected in late 2024.

Cingulate has embarked on a program to develop CTx-2103 (buspirone), which would expand the PTR platform within the anxiety therapeutic

category. The Company plans to initiate a clinical trial for CTx-2103 in the first half of 2022.

Quarter and Full Year Results

Position: As of December 31, 2021, Cingulate had $16.5 million in cash and cash equivalents, as compared to $1.2 million in cash

and cash equivalents as of December 31, 2020. Cash and cash equivalents as of December 31, 2021 reflect the net proceeds of our IPO of

approximately $20.4 million, which closed on December 10, 2021. Based on the Company's current operating plan, Cingulate expects

its cash and cash equivalents as of December 31, 2021 will enable the Company to fund its research and development and general and administrative

expenditures through late 2022.

Expenses: Research and development expenses were $1.3 million for the three months ended December 31, 2021, compared to $0.6 million

for the same period in 2020. Research and development expenses were $8.4 million for the year ended December 31, 2021, compared to $5.1

million for the year ended December 31, 2020. The increase in the three-month period was primarily related to costs incurred in late

2021 in preparation of the manufacturing of Phase 3 clinical supply of CTx-1301. The increase from 2020 to 2021 was related to the recognition

of $4.6 million of R&D expense for a one-time, noncash compensation charge in the third quarter of 2021 due to the exchange of Profits

Interest Units (PIUs) in Cingulate Therapeutics LLC for common stock of Cingulate Inc. prior to the IPO, which was based on the fair

value of the common stock at the time of the exchange, partially offset by a decrease in clinical operations expense of $1.2 million

due to a decrease in clinical activity. In early 2020, the Company incurred significant clinical costs relating to the completion of

the Phase 1/2 comparative bioavailability study for CTx-1301. During 2021, clinical activity primarily consisted of study startup costs

for the fixed dose Phase 3 study for CTx-1301.

Expenses: General and administrative expenses were $1.4 million for the three months ended December 31, 2021, compared to $0.5 million

for the same period in 2020. General and administrative expenses were $12.3 million for the year ended December 31, 2021, compared to

$2.0 million for the year ended December 31, 2020. The increase in the three-month period was primarily due to an increase in personnel

costs relating to annual compensation increases and the addition of personnel in late 2021, as well as an increase in directors'

and officers' insurance costs and professional fees related to legal and investor relations, as the Company was preparing

to operate as a public company. The increase from 2020 to 2021 was primarily related to the recognition of $8.1 million of G&A

personnel expenses for a one-time, noncash compensation charge in the third quarter of 2021 due to the exchange of Profits Interest Units

(PIUs) in Cingulate Therapeutics LLC for common stock of Cingulate Inc. described above. In addition, the increase was due to an increase

in personnel costs relating to annual compensation increases and the addition of personnel in late 2021, as well as an increase in directors'

and officers' insurance costs and professional fees related to legal, consulting, audit and investor relations, as the Company

was preparing to operate as a public company.

Loss: Net loss was $2.7 million for the three months ended December 31, 2021, compared to $1.2 million for the same period in 2020.

Net loss was $20.7 million for the year ended December 31, 2021, compared to $7.2 million for the year ended December 31, 2020.

The increase in the net loss from 2020 to 2021 primarily relates to a one-time, noncash compensation charge of $12.7 million in the third

quarter of 2021 due to the exchange of PIUs in Cingulate Therapeutics LLC for common stock of Cingulate Inc. described above.

Inc. is a clinical-stage 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. 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.

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 prospectus filed with the SEC on December 9, 2021. 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 by law.

Statements of Operations

of Investor & Public Relations, Cingulate

Brimmer / Amy Feng / Tim Ragones

Frank, Wilkinson Brimmer Katcher