Clesrovimab

drug
On this page

Also known as Mk-1654

Summary

Clesrovimab (CHEMBL4297783) is a phase-3 clinical-stage antibody; indicated across 1 condition including respiratory syncytial virus infectious disease.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Antibody
  • Indications: 1 condition
  • Clinical trials: 4

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4297783
NameClesrovimab
TypeAntibody
Max phase3

Also known as: Clesrovimab, Mk-1654, MK-1654, CLESROVIMAB

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

1 disease 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
respiratory syncytial virus infectious disease3MONDO:0001577EFO:1001413

Clinical trials

Total trials: 4.

Phase distribution

PhaseTrials
PHASE2/PHASE31
PHASE31
PHASE1/PHASE21
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04767373PHASE2/PHASE3COMPLETEDEfficacy and Safety of Clesrovimab (MK-1654) in Infants (MK-1654-004)
NCT04938830PHASE3COMPLETEDClesrovimab (MK-1654) in Infants and Children at Increased Risk for Severe Respiratory Syncytial Virus (RSV) Disease (MK-1654-007)
NCT03524118PHASE1/PHASE2COMPLETEDSafety, Tolerability, and Pharmacokinetics of Clesrovimab (MK-1654) in Infants (MK-1654-002)
NCT04086472PHASE2COMPLETEDPhase 2a Respiratory Syncytial Virus (RSV) Human Challenge Study of Clesrovimab (MK-1654) in Healthy Participants (MK-1654-005)

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).