Cingulate Inc. Reports First Quarter 2026 Financial Results and Provides an Update of Commercial Readiness Efforts On Track for lead ADHD Asset CTx-1301 Cash Position Grows to $25.9 Million

Inc. Reports First Quarter 2026 Financial Results and Provides an Update of Commercial Readiness Efforts On Track for lead ADHD Asset

Position Grows to $25.9 Million

CITY, Kan., May 14, 2026 (GLOBE NEWSWIRE) -- Cingulate

Inc. (NASDAQ: CING), a biopharmaceutical company utilizing its proprietary Precision Timed Release (PTR ) drug delivery

platform to develop a pipeline of next-generation products, today reported financial results for the quarter ended March 31, 2026, and

provided a corporate update.

remains focused on disciplined execution in 2026 and we believe we are well positioned to bring our lead ADHD asset, CTx-1301, to market,"

said Cingulate CEO Shane J. Schaffer. "We continue to engage constructively with the FDA on our new drug application while advancing

commercial readiness and manufacturing capabilities, and believe our current resources provide an extended cash runway into 2027."

enters the second quarter of 2026 with a meaningfully stronger financial position, having grown its cash and cash equivalents to $25.9

million as of March 31, 2026 - a $14.9 million increase from December 31, 2025 - driven by the successful close of a $12.0

million at-the-market private placement in February 2026 alongside opportunistic usage of the Company's at-the-market and stock

purchase agreements. Working capital increased to $17.0 million from $1.7 million at year-end, reflecting the Company's significantly

improved liquidity. Management believes this capital base is sufficient to fund operations into 2027, supporting key value-creating milestones

including the pursuit of regulatory approval and launch readiness for CTx-1301.

is actively collaborating with the FDA to provide responses to information requests related to the manufacturing and CMC elements of

its CTx-1301 NDA. The Company remains committed to working efficiently with the Agency and will provide updates as the review process

continues to advance its commercialization preparations, with dedicated teams established across all key functional areas. The Company's

launch strategy leverages a commercialization strategy augmented by AI-driven tools designed to optimize targeting, decision-making,

and performance measurement - positioning Cingulate for a rapid commercial launch contingent upon FDA approval. Key areas of focus

and Working Capital: As of March 31, 2026, Cingulate had approximately $25.9 million in cash and cash equivalents, a $14.9 million

increase from December 31, 2025. The increase in cash was primarily driven by capital raised in the first quarter, including the close

of a $12.0 million private placement. As of March 31, 2026, Cingulate had approximately $17.0 million in working capital, an increase

of $15.3 million as compared to $1.7 million as of December 31, 2025.

Expenses: R&D expenses were $2.2 million for the three months ended March 31, 2026, a decrease of 1.8% from the three months

ended March 31, 2025. The decrease is the result of lower clinical operations costs as clinical study activities concluded in early 2025,

offset by an increase in regulatory and manufacturing activities in the first quarter of 2026 relating to the NDA review of CTx-1301.

Expenses: General and administrative expenses were $5.7 million for the three months ended March 31, 2026 compared to $1.5 million

for the same period in 2025. This increase is primarily the result of costs incurred relating to the build-out of the commercial infrastructure

for the launch of CTx-1301, pending FDA approval, including increased headcount.

Loss: Net loss was $9.3 million for the three months ended March 31, 2026, compared to $3.9 million for the three months ended March

31, 2025. The increase in the net loss primarily relates to increased G&A expenses as described above as well as the change in fair

value of derivative and interest on our notes payable.

Consolidated Balance Sheet Data

Consolidated Statements of Operations

Attention Deficit/Hyperactivity Disorder (ADHD)

is a chronic neurobiological and developmental disorder that affects millions of children and often continues into adulthood. The estimated

market size of the US ADHD market is approximately 100 million annual prescriptions. The condition is marked by an ongoing pattern of

inattention and/or hyperactivity-impulsivity that interferes with functioning or development. In the U.S., over 20 million patients have

been diagnosed with ADHD. Among this group, 12 million are adults and over 8 million are under the age of 17. According to the

CDC, just 53.6 percent of all children and teens with ADHD reported they were actively treating their symptoms with medication

in 2022, with 65-90 percent demonstrating clinical ADHD symptoms that persist into adulthood. Current market trends demonstrate that

adult ADHD prevalence is larger and growing faster than the child and adolescent segments combined.

CTx-1301 (dexmethylphenidate HCI) is a once-daily, multi-core tablet utilizing Cingulate's proprietary Precision Timed

Release (PTR ) platform to deliver three precisely timed releases of active medication across the day. This design aims

to provide rapid onset of effect and entire active-day duration. CTx-1301 is being evaluated for the treatment of ADHD under the FDA's

505(b)(2) pathway. In October 2025, Cingulate announced that the U.S. Food and Drug Administration (FDA) had accepted for review the

New Drug Application (NDA) for CTx-1301 and had assigned a Prescription Drug User Fee Act (PDUFA) target action date of May 31, 2026.

NDA acceptance signifies that the FDA has determined the submission is sufficiently complete to permit substantive review. NDA acceptance

does not imply approval, nor does it guarantee any specific outcome or timing.

Precision Timed Release (PTR ) Platform Technology

is developing ADHD and anxiety disorder product candidates capable of achieving true once-daily dosing using Cingulate's innovative

PTR drug delivery platform technology. It incorporates a proprietary Erosion Barrier Layer (EBL) providing control of drug release at

precise, pre-defined times with no release of drug prior to the intended release. The EBL technology is enrobed around a drug-containing

core to give a tablet-in-tablet dose form. It is designed to erode at a controlled rate until eventually the drug is released from the

core tablet. The EBL formulation, Oralogik , is licensed from BDD Pharma. Cingulate intends to utilize its PTR technology to expand

and augment its clinical-stage pipeline by identifying and developing additional product candidates in other therapeutic areas in addition

to Anxiety and ADHD where one or more active pharmaceutical ingredients need to be delivered several times a day at specific, predefined

time intervals and released in a manner that would offer significant improvement over existing therapies. To see Cingulate's PTR

Platform, click here.

Inc. (NASDAQ: CING), is a biopharmaceutical company utilizing its proprietary 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 ADHD, Cingulate is identifying and evaluating additional therapeutic areas where PTR technology may be employed to develop future

product candidates, including to treat anxiety disorders. Cingulate is headquartered in Kansas City. For more information, visit Cingulate.com.

This 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. Specifically, these statements include,

but are not limited to, the timing and process for regulatory approval of CTx-1301 and the potential timing of commercialization of CTx-1301,

if approved, our progress with commercial readiness and manufacturing scale-up activities, statements regarding our expected cash runway,

and anticipated capital needs and financing plans. 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 18, 2026 and our other filings with the SEC. 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.

Vice President, Corporate and Government Relations, Cingulate