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NVCT US Equity

Nuvectis Pharma, Inc.Health Care · Pharmaceutical Preparations · CIK 1875558 · FY ends Dec 31
$20.91
+1.83 (+9.59%)
USD · as of 2026-08-18 · marketstack
3 registered studies · 2 active

Studies where NVCT 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.

3 interventional

Held by 5 tracked-famous managers (SUSQUEHANNA INTERNATIONAL GROUP, LLP, CITADEL ADVISORS LLC, AQR CAPITAL MANAGEMENT LLC, JANE STREET GROUP, LLC, Schonfeld Strategic Advisors LLC) · FINRA short interest 7.4 days to cover (settled 2026-07-31) · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionReadout inUpdated
A Phase 1 Clinical Study of NXP900 in Subjects With Advanced CancersNCT05873686Number of patients with treatment related adverse events and/or clinical laboratory abnormalitiesNon-randomized · Open-label · TreatmentPhase 1RecruitingDrug: NXP900Advanced Solid Tumor, NSCLC (Non-small Cell Lung Cancer), Renal Cancer, Mesothelioma, Non-Small Cell Squamous Lung Cancer, Non-small Cell Lung Adenocarcinoma140Mar 2027≤ 224 d2026-07-09
Study of NXP900 With Osimertinib in Subjects With Advanced, EGFR-Mutated Non-Small Cell Lung CancerNCT07315113Number of patients with treatment related adverse events and/or clinical laboratory abnormalitiesOpen-label · TreatmentPhase 1RecruitingDrug: NXP900, OsimertinibEGFR Mutation Positive Non-small Cell Lung Cancer, EGFR Mutated Non-small Cell Lung Cancer Patients18Dec 2026≤ 134 d2026-07-09
A Phase 1 Clinical Study of NXP800 in Subjects With Advanced Cancers and Expansion in Subjects With Ovarian CancerNCT05226507Part A: Number of patients with treatment related adverse events, clinical laboratory abnormalities, dose limiting toxicitiesNon-randomized · Open-label · TreatmentPhase 1Terminatedsponsor's stated reason: Study terminated due to various reasons impacting the feasibility of future clinical developmentDrug: NXP800Advanced Solid Tumor, Ovarian Cancer, Ovarian Clear Cell Carcinoma, Ovarian Clear Cell Tumor, Ovarian Clear Cell Adenocarcinoma, Ovarian Endometrioid Adenocarcinoma, Ovarian Endometrioid Tumor, ARID1A Gene Mutation452025-01-01actual2026-08-06

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