QS-21

drug
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Also known as Purified quillaja saponinQs 21Qs-21 adjuvantQs-21 component of alfq qs21Qs-21 component of as01Qs-21 component of as01eQS21Quillaja saponin (qs-21)SAPONIN QA-21V1Stimulon

Summary

Qs-21 (CHEMBL4297817) is a phase-3 clinical-stage unknown; indicated across 15 conditions including cutaneous melanoma and leukemia.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Unknown
  • Indications: 15 conditions
  • Clinical trials: 30

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4297817
NameQS-21
TypeUnknown
Max phase3

Also known as: Purified quillaja saponin, Qs 21, Qs-21, Qs-21 adjuvant, Qs-21 component of alfq qs21, Qs-21 component of as01, Qs-21 component of as01e, QS21, Quillaja saponin (qs-21), SAPONIN QA-21V1, Stimulon, QS-21

Targets

Targets

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

15 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
cutaneous melanoma3MONDO:0005012EFO:0000389
leukemia2MONDO:0005059EFO:0000565
prostate carcinoma2MONDO:0005159EFO:0001663
lung neoplasm2MONDO:0021117MONDO:0008903
herpes simplex infectious disease2MONDO:0004609EFO:1002022
Alzheimer disease2MONDO:0004975MONDO:0004975
exocrine pancreatic carcinoma2MONDO:0005192EFO:0002618
HIV infectious disease1MONDO:0005109EFO:0000764
peritoneal neoplasm1MONDO:0006901MONDO:0002087
fallopian tube neoplasm1MONDO:0021092MONDO:0002158
breast neoplasm1MONDO:0021100MONDO:0007254
ovarian cancer1MONDO:0008170MONDO:0008170
follicular lymphoma1MONDO:0018906MONDO:0018906
neoplasm1MONDO:0005070EFO:0000616

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 30.

Phase distribution

PhaseTrials
PHASE115
PHASE212
Not specified2
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00005052PHASE3UNKNOWNVaccine Therapy in Treating Patients With Primary Stage II Melanoma
NCT05638698PHASE2ACTIVE_NOT_RECRUITINGTg01 Vaccine / Qs-21 Stimulon™ With Or Without Balstilimab As Maintenance Therapy Following Adjuvant Chemotherapy In Patients With Resected Pancreatic Cancer
NCT00003362PHASE2COMPLETEDVaccine Therapy Plus Immune Adjuvants in Treating Patients With Advanced Melanoma
NCT00004052PHASE2COMPLETEDVaccine Therapy in Treating Patients With Chronic Myelogenous Leukemia
NCT00004249PHASE2COMPLETEDVaccine Therapy Plus QS21 in Treating Patients With Small Cell Lung Cancer That Has Responded to Initial Therapy
NCT00479557PHASE2COMPLETEDStudy Evaluating Safety, Tolerability, And Immunogenicity Of ACC-001 In Subjects With Mild To Moderate Alzheimer’s Disease
NCT00498602PHASE2COMPLETEDStudy Evaluating ACC-001 In Subjects With Mild To Moderate Alzheimer’s Disease
NCT00579423PHASE2COMPLETEDMultivalent Conjugate Vaccine Trial for Patients With Biochem. Relapsed Prostate Cancer
NCT00752232PHASE2COMPLETEDStudy Evaluating ACC-001 in Japanese Patients With Mild To Moderate Alzheimer’s Disease
NCT00955409PHASE2COMPLETEDLong Term Extension Study Evaluating Safety, Tolerability and Immunogenicity Of ACC-001 In Subjects With Mild To Moderate Alzheimer’s Disease
NCT00959192PHASE2COMPLETEDSafety, Tolerability, And Immunogenicity Study Of ACC-001 In Japanese Subjects With Mild To Moderate Alzheimer’s Disease
NCT00960531PHASE2TERMINATEDA Long Term Extension Study Evaluating ACC-001 With QS-21 in Subjects With Mild to Moderate Alzheimer’s Disease
NCT01687595PHASE2COMPLETEDBiological Efficacy Study of HerpV Vaccine With QS-21 to Treat Participants With Recurrent Genital Herpes
NCT00000809PHASE1WITHDRAWNSafety and Effectiveness of Two Different Formulations of an HIV Vaccine in Infants Born to HIV-Infected Women
NCT00001044PHASE1COMPLETEDA Phase I, Multicenter, Randomized, Double-Blind, Placebo-Controlled HIV-1 Vaccine Trial to Evaluate the Safety and Immunogenicity of rgp120/HIV-1MN (Genentech) in Combination With QS21 Adjuvant and/or Alum in Healthy Adults.
NCT00001052PHASE1COMPLETEDA Phase I, Multicenter, Randomized, Double-Blind, Placebo-Controlled HIV-1 Vaccine Trial to Evaluate the Safety and Immunogenicity of MN Recombinant Soluble gp120/HIV-1 (rsgp120/HIV-1) (Genentech) in Combination With QS21 Adjuvant and/or Alum in Healthy Adults
NCT00001096PHASE1COMPLETEDA Phase I, Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Safety and Immunogenicity of HIV-1 MN rsgp120 and Bivalent AIDSVAX B/E (HIV-1 MN rgp120/A244 rgp120) in Combination With QS-21 With or Without Alum in Healthy HIV-1 Uninfected Adults
NCT00001572PHASE1COMPLETEDVaccination of Follicular Lymphomas With Tumor-Derived Immunoglobulin Idiotype
NCT00003224PHASE1COMPLETEDVaccine Therapy in Treating Patients With Metastatic Melanoma
NCT00003357PHASE1COMPLETEDVaccine Therapy Plus QS21 in Treating Women With Breast Cancer Who Have No Evidence of Disease
NCT00003819PHASE1COMPLETEDVaccine Therapy Plus QS21 in Treating Patients With Progressive Prostate Cancer
NCT00004156PHASE1COMPLETEDVaccine Therapy in Treating Patients With Breast Cancer
NCT00004929PHASE1COMPLETEDVaccine Therapy Plus QS21 in Treating Patients With Progressive Prostate Cancer
NCT00005632PHASE1COMPLETEDVaccine Therapy Plus QS21 in Treating Patients With Prostate Cancer
NCT00006041PHASE1COMPLETEDVaccine Therapy in Treating Patients With Ovarian, Fallopian Tube, or Peritoneal Cancer
NCT00006387PHASE1COMPLETEDVaccine Therapy Plus QS21 in Treating Patients With Advanced Pancreatic or Colorectal Cancer
NCT00036933PHASE1COMPLETEDVaccine Therapy Plus QS21 in Treating Patients With Prostate Cancer
NCT06741072PHASE1SUSPENDEDBZLF1 Peptide Vaccine (OSU-2131) With QS-21 for the Prevention of Epstein-Barr Virus Related Cancer in Patients Awaiting Solid Organ Transplants
NCT00030823Not specifiedCOMPLETEDVaccine Therapy in Treating Patients at High Risk for Breast Cancer Recurrence
NCT00470574Not specifiedCOMPLETEDVaccine Therapy and QS21 in Treating Patients With Metastatic Breast Cancer

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).