Cingulate Inc., a biopharmaceutical company, develops pharmaceutical products using its drug delivery platform technology for the treatment of attention deficit/hyperactivity disorder (ADHD) and anxiety in the United States. The company's lead product candidate is CTx-1301 (dexmethylphenidate), which is in Phase 3 clinical trials for the treatment of ADHD in children, adolescents, and adults. It also develops CTx-2103 (buspirone), which is in a formulation stage for the treatment of anxiety. In addition, the company plans to initiate a clinical plan for CTx-1302 (dextroamphetamine) to treat ADHD. Cingulate Inc. was founded in 2012 and is headquartered in Kansas City, Kansas. Show more

1901 West 47th Place, Kansas City, KS, 66205, United States

Biotechnology

Healthcare

Market Cap

59.48M

52 Wk Range

$3.20 - $11.89

Previous Close

$4.48

Open

$4.38

Volume

229,865

Day Range

$4.33 - $4.51

Enterprise Value

41.41M

Cash

25.89M

Avg Qtr Burn

-6.913M

Insider Ownership

30.97%

Institutional Own.

8.99%

Qtr Updated

03/31/26

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Drug & Indication	Stage & Event	Catalyst Date
CTx-1301 (dexmethylphenidate) Details Attention deficit hyperactivity disorder	PDUFA Approval decision	Some catalyst date You must sign up to see the catalyst details. You must sign up to see the catalyst details. You must sign up to see the catalyst details. You must sign up to see the catalyst details.Sign up now.
CTx-1302 (dextroamphetamine) Details Attention deficit hyperactivity disorder	Phase 1/2 Initiation	Some catalyst date You must sign up to see the catalyst details. You must sign up to see the catalyst details. You must sign up to see the catalyst details. You must sign up to see the catalyst details.Sign up now.
CTx-2103 (buspirone) Details Anxiety Disorders	IND Submission	Some catalyst date You must sign up to see the catalyst details. You must sign up to see the catalyst details. You must sign up to see the catalyst details. You must sign up to see the catalyst details.Sign up now.