Cingulate Inc.

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Cingulate® is a biopharmaceutical company utilizing its innovative Precision Timed Release™ (PTR) drug delivery platform technology to build and advance a pipeline of next-generation pharmaceutical products. We aim 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), we believe there are multiple therapeutic areas where our PTR technology may be employed to develop additional product candidates, notably anxiety disorders.

Company Details

Employees
20
Founded
-
Address
1901 W. 47th Place, Suite 310,united States
Industry
Pharmaceutical Manufacturing
NAICS
Pharmaceutical and Medicine Manufacturing
Medicinal and Botanical Manufacturing
Pharmaceutical Preparation Manufacturing
In-Vitro Diagnostic Substance Manufacturing
Biological Product (except Diagnostic) Manufacturing
HQ
Kansas City, Kansas
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News

Cingulate Presents Positive Phase 3 Results for CTx-1301 - GlobeNewswire

Cingulate Presents Positive Phase 3 Results for CTx-1301 GlobeNewswire

Cingulate’s Lead ADHD Candidate CTx-1301 Selected for Podium Presentation at AACAP Annual Meeting - GlobeNewswire

Cingulate’s Lead ADHD Candidate CTx-1301 Selected for Podium Presentation at AACAP Annual Meeting GlobeNewswire

Cingulate Receives $4.3 Million PDUFA Fee Waiver for ADHD Treatment, CTx-1301 - Psychiatric Times

Cingulate Receives $4.3 Million PDUFA Fee Waiver for ADHD Treatment, CTx-1301 Psychiatric Times

FDA Accepts Cingulate’s New Drug Application for CTx-1301 - GlobeNewswire

FDA Accepts Cingulate’s New Drug Application for CTx-1301 GlobeNewswire

Cingulate Provides Management Team Update - GlobeNewswire

Cingulate Provides Management Team Update GlobeNewswire

Cingulate Secures Exclusive Manufacturing Partnership with - GlobeNewswire

Cingulate Secures Exclusive Manufacturing Partnership with GlobeNewswire

Cingulate Submits New Drug Application to FDA for Lead ADHD Asset CTx-1301 - GlobeNewswire

Cingulate Submits New Drug Application to FDA for Lead ADHD Asset CTx-1301 GlobeNewswire

Cingulate Receives $4.3M Waiver from FDA Ahead of Imminent - GlobeNewswire

Cingulate Receives $4.3M Waiver from FDA Ahead of Imminent GlobeNewswire

Cingulate Appoints Nilay Patel as Chief Legal Officer to Support Growth ahead of New Drug Application - GlobeNewswire

Cingulate Appoints Nilay Patel as Chief Legal Officer to Support Growth ahead of New Drug Application GlobeNewswire

Efficacy Results Announced from Cingulate’s Phase 3 Pediatric Study of CTx-1301 (dexmethylphenidate) for ADHD - GlobeNewswire

Efficacy Results Announced from Cingulate’s Phase 3 Pediatric Study of CTx-1301 (dexmethylphenidate) for ADHD GlobeNewswire

Cingulate Inc. Reports Full Year 2024, Fourth Quarter - GlobeNewswire

Cingulate Inc. Reports Full Year 2024, Fourth Quarter GlobeNewswire

Cingulate Receives $3 Million Grant from Private Foundation - GlobeNewswire

Cingulate Receives $3 Million Grant from Private Foundation GlobeNewswire

Cingulate Inc. Reports First Quarter 2025 Financial Results - GlobeNewswire

Cingulate Inc. Reports First Quarter 2025 Financial Results GlobeNewswire

Cingulate reports phase 3 safety data for CTx-1301 to treat ADHD in children, adolescents - Contemporary Pediatrics

Cingulate reports phase 3 safety data for CTx-1301 to treat ADHD in children, adolescents Contemporary Pediatrics

Leadership Change: Cingulate Appoints CFO Jennifer Callahan as Interim CEO Amid ADHD Drug FDA Review - Stock Titan

Leadership Change: Cingulate Appoints CFO Jennifer Callahan as Interim CEO Amid ADHD Drug FDA Review Stock Titan

Cingulate’s Shane Schaffer Joins Cast of Nationally Syndicated Big Biz Show - Yahoo Finance

Cingulate’s Shane Schaffer Joins Cast of Nationally Syndicated Big Biz Show Yahoo Finance

FDA Accepts NDA for CTx-1301 for Treatment of ADHD - Psychiatric Times

FDA Accepts NDA for CTx-1301 for Treatment of ADHD Psychiatric Times

Positive Phase 3 Results: CTx-1301 for the Treatment of Pediatric ADHD - Psychiatric Times

Positive Phase 3 Results: CTx-1301 for the Treatment of Pediatric ADHD Psychiatric Times

Next-Gen ADHD Treatment: Cingulate Locks Exclusive Manufacturing Deal Through 2028 for CTx-1301 - Stock Titan

Next-Gen ADHD Treatment: Cingulate Locks Exclusive Manufacturing Deal Through 2028 for CTx-1301 Stock Titan

Cingulate Saves $4.3M on ADHD Drug Application as FDA Waiver Boosts Commercialization Plans - Stock Titan

Cingulate Saves $4.3M on ADHD Drug Application as FDA Waiver Boosts Commercialization Plans Stock Titan

Cingulate (NASDAQ: CING) to present CTx-1301 Phase 3 pediatric ADHD data at AACAP - Stock Titan

Cingulate (NASDAQ: CING) to present CTx-1301 Phase 3 pediatric ADHD data at AACAP Stock Titan

FDA Clears Cingulate to File NDA for CTx-1301 in the Treatment of ADHD - Psychiatric Times

FDA Clears Cingulate to File NDA for CTx-1301 in the Treatment of ADHD Psychiatric Times

FDA and Cingulate Aligned with Filing Requirements for New Drug Application for Lead ADHD Asset CTx-1301 - Stock Titan

FDA and Cingulate Aligned with Filing Requirements for New Drug Application for Lead ADHD Asset CTx-1301 Stock Titan

PDUFA May 31, 2026: Cingulate NDA Accepted for once-daily CTx-1301 in ADHD under 505(b)(2) - Stock Titan

PDUFA May 31, 2026: Cingulate NDA Accepted for once-daily CTx-1301 in ADHD under 505(b)(2) Stock Titan

Cingulate Bolsters Executive Team With Key Legal Hire as ADHD Drug Heads to FDA Review - Stock Titan

Cingulate Bolsters Executive Team With Key Legal Hire as ADHD Drug Heads to FDA Review Stock Titan

Cingulate (NASDAQ: CING) CTx-1301 delivers 12‑hour symptom control in pediatric ADHD - Stock Titan

Cingulate (NASDAQ: CING) CTx-1301 delivers 12‑hour symptom control in pediatric ADHD Stock Titan

ROTH to Host 4th Annual Healthcare Opportunities Conference on October 9 in New York City - GlobeNewswire

ROTH to Host 4th Annual Healthcare Opportunities Conference on October 9 in New York City GlobeNewswire

Cingulate completes Phase III trial of ADHD therapy in adults - Clinical Trials Arena

Cingulate completes Phase III trial of ADHD therapy in adults Clinical Trials Arena

Cingulate Reports Second Quarter 2024 Financial Results and Provides Development Update on Major Milestones Achieved - Stock Titan

Cingulate Reports Second Quarter 2024 Financial Results and Provides Development Update on Major Milestones Achieved Stock Titan

Cingulate Announces Exercise of Warrants for $1.86 Million Gross Proceeds - Stock Titan

Cingulate Announces Exercise of Warrants for $1.86 Million Gross Proceeds Stock Titan

Positive Top-Line Results Reported for Fed/Fast Study of Novel ADHD Treatment - Psychiatric Times

Positive Top-Line Results Reported for Fed/Fast Study of Novel ADHD Treatment Psychiatric Times

Cingulate Presents Data for Its Triple-Release Buspirone Product Candidate: CTx-2103 - GlobeNewswire

Cingulate Presents Data for Its Triple-Release Buspirone Product Candidate: CTx-2103 GlobeNewswire

Cingulate Inc. Announces Pricing of $25.0 Million Initial Public Offering - Stock Titan

Cingulate Inc. Announces Pricing of $25.0 Million Initial Public Offering Stock Titan

Cingulate (CING) Stock Price, News & Analysis - MarketBeat

Cingulate (CING) Stock Price, News & Analysis MarketBeat

CING Stock Price and Chart — NASDAQ:CING - TradingView

CING Stock Price and Chart — NASDAQ:CING TradingView

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