Skip to content
KStart free
AI InfrastructureDefenseQuantumAll studies →

QNTM US Equity

Quantum Biopharma Ltd.Health Care · Pharmaceutical Preparations · CIK 1771885 · FY ends Dec 31
$3.52
+0.18 (+5.39%)
USD · as of 2026-08-19 · marketstack
4 registered studies · 0 active

Studies where QNTM is the lead sponsor, as filed with ClinicalTrials.gov. Completion dates are the sponsor's own projected windows and are revised as a study runs. Active studies first, then completed and stopped — newest readout first within each.

4 interventional · 1 with posted results

Held by 2 tracked-famous managers (JANE STREET GROUP, LLC, CITADEL ADVISORS LLC) · FINRA short interest 3.5 days to cover (settled 2026-07-31) · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionUpdated
Assessing the Safety and Efficacy of FSD-F2R6-A-CP in Volunteers in an Induced State of Alcohol IntoxicationNCT06505239IntoxicationRandomized · Triple-masked · TreatmentNot applicableCompletedDietary supplement: FSD-F2R6-A-CP, PlaceboAcute Alcohol Intoxication262024-11-07actual2025-05-22
Evaluating the Safety, Tolerability, Pharmacokinetics, and Effect of Food of Lucid-21-302 in Healthy VolunteersNCT05821387Single Dose Safety Outcome MeasuresRandomized · Triple-masked · TreatmentPhase 1CompletedDrug: Lucid-21-302, PlaceboHealthy Participants402023-07-29actual2023-08-29
Safety and Efficacy of FSD201 for the Treatment of Chronic Pain Associated With Idiopathic MCAS (MCAD)NCT05652907results2026-04-21Targeted Treatment Effect of 30% Decrease From Baseline to Day 28 in the Average Daily Pain IntensityRandomized · Quadruple-masked · TreatmentStudy Protocol and Statistical Analysis PlanPhase 2Terminatedsponsor's stated reason: For business reasons and not for reasons related to safety or efficacyDrug: FSD201, PlaceboMast Cell Activation Syndrome, Mast Cell Activation Disorder Idiopathic22023-05-24actual2026-04-21
Ultramicronized Palmitoylethanolamide (PEA) Treatment in Hospitalized Participants With COVID-19NCT04619706Percentage of Participants With Disease Progression at Day 28Randomized · Quadruple-masked · TreatmentPhase 2Terminatedsponsor's stated reason: Difficulties recruiting new subjectsDrug: FSD201, Placebo · Other: Standard of Care for Covid-19COVID-19532021-08-24actual2022-12-05

Primary completion is the date the sponsor filed with the registry — their own projection, revised whenever they revise it, unless the row is marked actual.

Source: ClinicalTrials.gov, retrieved 2026-08-19