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CING Stock Research Snapshot: Pipeline, Catalysts, and Cash Runway

Cingulate Inc | Needs refresh | Last updated: 2026-06-01T17:55:29Z

TickerCING
Market Cap48.7M
Cash RunwayRunway 6-12 months
Next Catalystn/a

Public Research Snapshot

Cingulate Inc is a publicly tracked healthcare company. This research snapshot summarizes public information on pipeline assets, clinical trials, upcoming catalysts, SEC filings, and cash runway estimates for [18F] Flutemetamol in Healthy (Phase 3).

Pipeline

AssetIndicationModalityStagePublic Note
[18F] FlutemetamolHealthyn/aPhase 3Public pipeline row
Functional Magnetic Resonance Imaging (fMRI)Attention Deficit Hyperactivity Disorder (ADHD) | Impulsive Aggressionn/aPhase 2Public pipeline row
GantenerumabAlzheimer Diseasen/aPhase 3Public pipeline row
MagteinDementia | Alzheimer's Diseasen/aNaPublic pipeline row
Aerobic ExerciseObesityn/aNaPublic pipeline row

Catalyst Preview

No public catalyst rows matched this view yet.

Cash Runway Preview

Estimated cash runway: Runway 6-12 months.

This is an automated estimate and may differ from company guidance.

Recent SEC Filings

  • No public filing rows are loaded yet.

Clinical Trial Activity

NCT IDPhaseStatusEnrollmentPrimary Completion
NCT01265394Phase 3COMPLETED2182011-03
NCT02162524NaWITHDRAWNn/a2015-07
NCT02210286NaCOMPLETED172016-04
NCT03638466Phase 2TERMINATED72019-11-07
NCT03444870Phase 3TERMINATED10532022-12-28

Scientific Context

  • conditions | Attention Deficit Hyperactivity Disorder (ADHD) | Impulsive Aggression
  • conditions | Patients With Severe Mental Illness
  • conditions | Excessive Sleepiness
  • eligibility_criteria | Inclusion Criteria: * Otherwise healthy male or female subjects, aged 8-12 years, inclusive, at the time of screening with primary diagnosis of ADHD and currently receiving monotherapy treatment with an optimized US Food and Drug Administration (FDA)-approved ADHD medication. * Impulsive aggression (IA) confirmed at screening using the R-MOAS and the Vitiello Aggression Scale. Exclusion Criteria: * Current or lifetime diagnosis of epilepsy, major depressive disorder, bipolar disorder, schizophrenia or related disorder, personality disorder, Tourette's disorder, fetal alcohol syndrome, or psychosis not otherwise specified. * Currently meeting DSM criteria for autism spectrum disorder, pervasive developmental disorder, obsessive-compulsive disorder, post-traumatic stress disorder. * Known or suspected IQ \<70, pregnancy, substance or alcohol abuse. * Known history of implanted brain stimulator, vagal nerve stimulator, ventriculoperitoneal shunt, cardiac pacemaker, orthodontic braces, or implanted medication port. Visual and hearing (≥25 dB) impairment. * Pre-existing medical or psychological conditions that preclude being in the MRI scanner (e.g., claustrophobia, morbid obesity, or marked anxiety about the procedure).
  • eligibility_criteria | Inclusion Criteria: * Healthy male or female, 18 - 45 years * Fluent and literate in English and able to provide written informed consent * BMI between 18.5 and 38.0 kg/m2 and minimum body weight of 50 kg Exclusion Criteria: * Recent exposure to any investigational product * Previous exposure to relevant fMRI task(s) * Considered medically unsuitable for participation * Has any contraindication for BOLD fMRI

This page is for informational and educational purposes only and does not constitute investment advice, a recommendation, or an offer to buy or sell securities. Data may be incomplete or delayed. Cash runway and catalyst timing estimates are derived from public sources and may differ from company guidance.