MATRIX-M1 ADJUVANT

drug
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Also known as Matrix-m

Summary

Matrix-M1 Adjuvant (CHEMBL4650407) is a phase-3 clinical-stage unknown; indicated across 7 conditions including severe acute respiratory syndrome and malaria.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Unknown
  • Indications: 7 conditions
  • Clinical trials: 11

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4650407
NameMATRIX-M1 ADJUVANT
TypeUnknown
Max phase3

Also known as: Matrix-m, Matrix-m1 adjuvant, MATRIX-M1 ADJUVANT

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

6 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.

Disease (in trials)PhaseMONDOEFO
severe acute respiratory syndrome3MONDO:0005091EFO:0000694
malaria3MONDO:0005136EFO:0001068
respiratory syncytial virus infectious disease2MONDO:0001577EFO:1001413
influenza2MONDO:0005812EFO:0007328
Plasmodium falciparum malaria2MONDO:0005920EFO:0007444
Ebola hemorrhagic fever1MONDO:0005737EFO:0007243

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

Clinical trials

Total trials: 11.

Phase distribution

PhaseTrials
PHASE15
PHASE24
PHASE31
PHASE1/PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04704830PHASE3ACTIVE_NOT_RECRUITINGR21/Matrix-M in African Children Against Clinical Malaria
NCT03026348PHASE2COMPLETEDSafety and Immunogenicity Study to Evaluate Single- or Two-Dose Regimens Of RSV F Vaccine With and Without Aluminum Phosphate or Matrix-M1™ Adjuvants In Clinically-Stable Older Adults
NCT03658629PHASE2TERMINATEDPhase 2 Dose and Formulation Confirmation of Quad-NIV in Older Adults
NCT03947190PHASE2TERMINATEDA Study to Determine if New Types of Malaria Vaccines Are Safe, Effective and Lead to Immunity in Kenyan Adults
NCT04533399PHASE2COMPLETEDA Study Looking at the Effectiveness and Safety of a COVID-19 Vaccine in South African Adults
NCT05683834PHASE1/PHASE2COMPLETEDTrial Evaluating the Immunogenicity and Safety of an Adjuvanted Epstein-Barr Virus (EBV) Glycoprotein 350 Vaccine in EBV-seronegative Persons
NCT02370589PHASE1COMPLETEDStudy to Evaluate the Immunogenicity and Safety of an Ebola Virus (EBOV) Glycoprotein (GP) Vaccine in Healthy Subjects
NCT04271306PHASE1TERMINATEDSafety, Immunogenicity and ex Vivo Efficacy of Pfs25-IMX313/Matrix-M in Healthy Volunteers in Bagamoyo, Tanzania.
NCT04318002PHASE1COMPLETEDSafety and Immunogenicity of RH5.1/Matrix-M in Adults and Infants Living in Tanzania
NCT05913973PHASE1COMPLETEDStudy of the Plasmodium Vivax Transmission-blocking Vaccine Pvs230D1-EPA/Matrix-M to Assess Safety, Immunogenicity, and Transmission-blocking Activity in Healthy Malaria-naive Adults
NCT06507605PHASE1COMPLETEDDose-Escalating Study of Pfs230D1 in Combination With R21 in Matrix-M in African Adults

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).