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HURA US Equity

TuHURA Biosciences, Inc./NVHealth Care · Pharmaceutical Preparations · CIK 1498382 · FY ends Dec 31
$2.16
-0.12 (-5.26%)
USD · as of 2026-08-18 · marketstack
6 registered studies · 2 active

Studies where HURA 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 · 1 expanded access · 2 with posted results

Held by 8 tracked-famous managers (MILLENNIUM MANAGEMENT LLC, AQR CAPITAL MANAGEMENT LLC, CITADEL ADVISORS LLC, JANE STREET GROUP, LLC, Qube Research & Technologies Ltd, +3 more) · FINRA short interest 31.9 days to cover (settled 2026-07-31) · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionReadout inUpdated
Placebo-Controlled Trial of IFx-Hu2.0 Followed By Pembrolizumab In Checkpoint Inhibitor Naïve Participants With Advanced Or Metastatic Merkel Cell CarcinomaNCT06947928Objective response rate (ORR)Randomized · Quadruple-masked · TreatmentPhase 2/3RecruitingDrug: IFx-Hu2.0, Placebo, PembrolizumabAdvanced Or Metastatic Merkel Cell Carcinoma1182027-03-31in 224 d2026-04-17
IFx-Hu2.0 As An Adjunctive Therapy To Pembrolizumab In Advanced Or Metastatic Merkel Cell Carcinoma (MCC)NCT06940440SafetyOpen-label · TreatmentPhase 1RecruitingDrug: IFx-Hu2.0, PembrolizumabAdvanced Or Metastatic Merkel Cell Carcinoma92026-05-312025-10-15
Immunotherapy With IFx-Hu2.0 Vaccine for Advanced Non-melanoma Skin CancersNCT04160065Number of Grade 3-5, Treatment-Related Adverse Events per CTCAE 5.0Open-label · TreatmentPhase 1CompletedBiological: IFx-Hu2.0Merkel Cell Carcinoma, Cutaneous Squamous Cell Carcinoma, Non-Melanoma Skin Cancers232023-10-19actual2024-09-23
IFx-Hu2.0 for the Treatment of Patients With Skin CancerNCT04925713results2024-08-02Rate of Adverse EventsOpen-label · TreatmentStudy Protocol · Statistical Analysis PlanPhase 1CompletedBiological: IFx-Hu2.0Cutaneous Squamous Cell Carcinoma, Basal Cell Carcinoma52021-10-07actual2024-08-02
pDNA Intralesional Cancer Vaccine for Cutaneous MelanomaNCT03655756results2022-08-08Number of Participants With Serious Adverse Events (SAEs) and/or Dose Limiting Toxicities (DLTs)Open-label · TreatmentStudy Protocol and Statistical Analysis Plan · Informed Consent FormEarly Phase 1CompletedBiological: IFx-Hu2.0Cutaneous Melanoma, Stage III, Cutaneous Melanoma, Stage IV72020-07-10actual2022-08-08
IFx-Hu2.0 Expanded Access ProgramNCT04853602expanded accessAvailableBiological: IFx-Hu2.0Cutaneous Melanoma, Stage III, Cutaneous Melanoma, Stage IV, Merkel Cell Carcinoma, Cutaneous Squamous Cell Carcinoma2024-08-12

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