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PSTV US Equity

Plus Therapeutics, Inc.Health Care · Surgical & Medical Instruments & Apparatus · CIK 1095981 · FY ends Dec 31
$3.84
+0.07 (+1.80%)
USD · as of 2026-08-07 · marketstack
stale — last close 2026-08-07, not a live quote
5 registered studies · 5 active

Studies where PSTV 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.

5 interventional

Held by 1 tracked-famous manager (CITADEL ADVISORS LLC) · FINRA short interest 7.8 days to cover (settled 2026-07-31) · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionReadout inUpdated
Safety & Efficacy/Tolerability of Rhenium-186 NanoLiposomes (186RNL) for Patients Who Received a Prior 186RNL TreatmentNCT05460507Assessment of safety and tolerability of a second dose of 186RNL by CED as part of standard of care >30 days following first dose.Open-label · TreatmentPhase 1RecruitingDrug: Retreatment Rhenium LiposomeGlioma402028-03-01in 560 d2025-03-30
Determine Maximum Tolerated Dose, Safety, and Tolerability of Rhenium (186Re) in Pediatric Recurrent, Refractory or Progressive Ependymoma and High-Grade GliomaNCT07061626Maximum Tolerated Dose (MTD)Non-randomized · Open-label · TreatmentPhase 1Not yet recruitingDrug: Rhenium-186 NanoliposomeEpendymoma, High Grade Gliomas56Mar 2027≤ 224 d2025-07-11
Multiple Dose Intraventricular Administration of Rhenium-186 NanoLiposome for Leptomeningeal MetastasesNCT07098806Maximum Tolerated DoseOpen-label · TreatmentPhase 1RecruitingDrug: 186RNLLeptomeningeal Metastasis242026-10-02in 44 d2025-08-01
Maximum Tolerated Dose, Safety, and Efficacy of Rhenium Nanoliposomes in Recurrent Glioma (ReSPECT)NCT01906385Phase 1: Maximum Tolerated DoseOpen-label · TreatmentPhase 1/2RecruitingDrug: Rhenium Liposome TreatmentGlioma55Dec 20252025-03-26
Intraventricular Administration of Rhenium-186 NanoLiposome for Leptomeningeal MetastasesNCT05034497Incidence and severity of adverse events (AE) and serious adverse events (SAE)Open-label · TreatmentPhase 1Active, not recruitingDrug: 186RNLLeptomeningeal Metastasis182025-12-212025-03-26

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