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INKT US Equity

MiNK Therapeutics, Inc.Health Care · Biological Products, (No Diagnostic Substances) · CIK 1840229 · FY ends Dec 31
$11.13
-0.87 (-7.25%)
USD · as of 2026-08-19 · marketstack
4 registered studies · 1 active

Studies where INKT 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

Held by 1 tracked-famous manager (CITADEL ADVISORS LLC) · FINRA short interest 9.4 days to cover (settled 2026-07-31) · insider 90d: 0 buys / 2 sells · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionReadout inUpdated
A Clinical Trial to Evaluate agenT-797 Plus Standard of Care in Participants With Severe Pneumonia With Moderate to Severe Acute Hypoxemic Respiratory FailureNCT07615010Number of Deaths (All-cause Mortality)Randomized · Quadruple-masked · TreatmentPhase 2RecruitingDrug: agenT-797, Placebo, Standard of Care (SOC)Pneumonia90Jun 2027≤ 314 d2026-06-26
A Study Investigating agenT-797 in Participants With Relapsed/Refractory Solid TumorsNCT05108623Number Of Participants With Treatment-emergent Adverse Events (TEAEs)Non-randomized · Open-label · TreatmentPhase 1CompletedDrug: agenT-797, Approved ICIsTumor, Solid342024-01-02actual2024-04-24
A Clinical Trial to Evaluate the Safety of agenT-797 in COVID-19 Participants With ARDSNCT04582201Number of Participants with Treatment-emergent Adverse EventsOpen-label · TreatmentPhase 1CompletedDrug: agenT-797Respiratory Distress Syndrome, Adult202023-04-23actual2025-12-30
agenT-797 in Participants With Relapsed/Refractory Multiple MyelomaNCT04754100Number Of Participants With Treatment-related Adverse EventsOpen-label · TreatmentPhase 1CompletedDrug: agenT-797Relapsed/Refractory Multiple Myeloma132023-01-13actual2023-06-06

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