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SLS US Equity

SELLAS Life Sciences Group, Inc.Health Care · Pharmaceutical Preparations · CIK 1390478 · FY ends Dec 31
$13.10
+0.10 (+0.77%)
USD · as of 2026-08-18 · marketstack
7 registered studies · 2 active

Studies where SLS 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.

6 interventional · 1 expanded access · 4 with posted results

Held by 5 tracked-famous managers (SUSQUEHANNA INTERNATIONAL GROUP, LLP, JANE STREET GROUP, LLC, RENAISSANCE TECHNOLOGIES LLC, AQR CAPITAL MANAGEMENT LLC, Squarepoint Ops LLC) · FINRA short interest 7.9 days to cover (settled 2026-07-31) · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionReadout inUpdated
Study of SLS009 (Formerly GFH009) a Potent Highly Selective CDK9 Inhibitor in Patients With Hematologic Malignancies and High-Risk Newly Diagnosed AMLNCT04588922Safety and Tolerability: Dose Limiting Toxicities (DLTs)Randomized · Open-label · TreatmentPhase 1/2RecruitingDrug: SLS009, venetoclax, azacitidineHematologic Malignancies1602026-12-30in 133 d2026-07-29
Galinpepimut-S Versus Investigator's Choice of Best Available Therapy for Maintenance in AML CR2/CRp2NCT04229979OSRandomized · Open-label · TreatmentPhase 3Active, not recruitingBiological: Galinpepimut-S, GM-CSF · Drug: Azacitidine, Venetoclax, Decitabine, Cytarabine · Other: Observation, MontanideAcute Myeloid Leukemia127Dec 20252025-10-01
Galinpepimut-S in Combination With Pembrolizumab in Patients With Selected Advanced CancersNCT03761914results2024-11-19Overall Response Rate (ORR) - Best Overall ResponseNon-randomized · Open-label · TreatmentStudy Protocol and Statistical Analysis PlanPhase 1/2CompletedBiological: galinpepimut-S, pembrolizumab, GM-CSF · Other: MontanideAcute Myelogenous Leukemia, Ovarian Cancer, Colorectal Cancer, Triple-negative Breast Cancer, Small-cell Lung Cancer262022-07-05actual2024-11-19
WT1 Vaccine Treatment of Patients With Multiple Myeloma After Autologous Stem Cell TransplantationNCT01827137results2024-09-19WT1 T-cell Immune Response (IR) 12-14 Weeks After First GPS Administration (6 x Administrations)Open-label · TreatmentPhase 1/2CompletedBiological: Galinpepimut-S, GM-CSF · Other: Montanide · Drug: lenalidomide, bortezomibMultiple Myeloma202016-12-07actual2024-09-19
Galinpepimut-S (WT-1 Analog Peptide) Vaccine in Malignant Pleural Mesothelioma After Combined Modality TherapyNCT01265433results2024-10-091-year Progression-free SurvivalRandomized · Double-masked · TreatmentStudy Protocol, Statistical Analysis Plan, and Informed Consent FormPhase 2CompletedBiological: Galinpepimut-S + Montanide + GM-CSF, Montanide + GM-CSFMalignant Pleural Mesothelioma412016-11-30actual2024-10-09
WT1 Vaccine Treatment of Patients in Remission From Acute Myeloid Leukemia (AML) or Acute Lymphoblastic Leukemia (ALL)NCT01266083results2024-11-19Overall SurvivalOpen-label · TreatmentPhase 2CompletedBiological: Galinpepimut-S, GM-CSF · Other: MontanideAcute Myeloid Leukemia, Acute Lymphoblastic Leukemia222016-09-30actual2024-11-19
Expanded Access Program (EAP) for Galinpepimut-S (GPS) in Patients Diagnosed With AML or MDSNCT05593185expanded accessAvailableBiological: Galinpepimut-SAcute Myeloid Leukemia, Myelodysplastic Syndromes2026-04-24

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