Respiratory Syncytial Virus Pre-Fusion Glycoprotein F

drug
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Also known as AbrysvoArexvy

Summary

Respiratory Syncytial Virus Pre-Fusion Glycoprotein F (CHEMBL6068489) is an approved vaccine component; indicated across 2 conditions including respiratory syncytial virus infectious disease.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Vaccine component
  • Indications: 2 conditions
  • Clinical trials: 13

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL6068489
NameRespiratory Syncytial Virus Pre-Fusion Glycoprotein F
TypeVaccine component
Max phase4

Also known as: Abrysvo, Arexvy

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

2 indications (2 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
respiratory syncytial virus infectious disease4MONDO:0001577EFO:1001413

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

Clinical trials

Total trials: 13.

Phase distribution

PhaseTrials
Not specified5
PHASE13
PHASE42
PHASE32
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05170399PHASE4RECRUITINGVaccine Responses in Patients With B Cell Malignancies
NCT06551506PHASE4COMPLETEDThe Immunology and Safety of Maternal RSV Vaccination (ABRYSVO), Infant Nirsevimab (BEYFORTUS) Immunization, or Both Products
NCT07041190PHASE3NOT_YET_RECRUITINGPregnancy and Infant PrEparedness pLatform IN Europe, RSV-International Adaptive Platform Trial to Evaluate Two Approved Prevention Options to Prevent Respiratory Syncytial Virus in Infants: Maternal Vaccine to Women in Pregnancy and Monoclonal Antibody to the Infants, Given Alone or in Combination.
NCT07232706PHASE3RECRUITINGPrevention of RSV Infection in Infants by Administering Nirsevimab to Infants, With or Without Maternal RSV Vaccination
NCT07050732PHASE2RECRUITINGImmunogenicity of RSVPreF3 Vaccine in Immunocompromised Persons
NCT06556147PHASE1ACTIVE_NOT_RECRUITINGA Study of RSV-HMPV Bivalent Vaccine VXB-241 in Older Adults
NCT06843317PHASE1RECRUITINGSafety and Immunogenicity Study of Revaccination With SCB-1019T in Healthy Adults
NCT06194318PHASE1COMPLETEDFirst-in-human Safety and Immunogenicity Study of SCB-1019 and SCB-1019T in Healthy Adults
NCT06647654Not specifiedACTIVE_NOT_RECRUITINGImpact and Effectiveness of ABRYSVO® Vaccination During Pregnancy
NCT06813872Not specifiedACTIVE_NOT_RECRUITINGEffectiveness of ABRYSVO® Maternal Respiratory Syncytial Virus (RSV) Vaccine Against RSV in Infants in Western Pennsylvania
NCT07122661Not specifiedACTIVE_NOT_RECRUITINGSTudy of Real World vaccinE Effectiveness of maTernal RSVpreF vaccinatiON Against Respiratory Syncytial Virus (RSV) in Hospitalised Infants in Australia (STREETON)
NCT07235397Not specifiedNOT_YET_RECRUITINGEvaluating the Benefits of RSV Maternal Vaccination Using a Scottish National Dataset
NCT07249320Not specifiedACTIVE_NOT_RECRUITINGEvaluating ABRYSVO Maternal Vaccine Effectiveness Among Infants

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).