Regdanvimab

drug
On this page

Also known as Ct-p59CTP-59CTP59Regkirona

Summary

Regdanvimab (CHEMBL4650462) is an approved antibody (ATC J06BD06); indicated across 1 condition including covid-19.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Antibody
  • ATC class: J06BD06
  • Indications: 1 condition
  • Clinical trials: 4

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4650462
NameRegdanvimab
TypeAntibody
Max phase4
ATCJ06BD06

Also known as: Ct-p59, CT-P59, CTP-59, CTP59, Regdanvimab, Regkirona, REGDANVIMAB

Targets

Targets

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
CoV Spike glycoproteinBinding10.57

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 indication (1 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
COVID-194MONDO:0100096MONDO:0100096

Clinical trials

Total trials: 4.

Phase distribution

PhaseTrials
PHASE12
PHASE41
PHASE2/PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05982704PHASE4UNKNOWNStudy of Tixagevimab/Cilgavimab and Regdanvimab Efficacy for Treatment of COVID-19
NCT04602000PHASE2/PHASE3COMPLETEDA Phase 2/3 Study to Evaluate the Efficacy and Safety of CT-P59 in Patients With Mild to Moderate SARS-CoV-2 Infection
NCT04525079PHASE1COMPLETEDTo Evaluate the Safety, Tolerability and Pharmacokinetics of CT-P59 in Healthy Subjects
NCT04593641PHASE1COMPLETEDThis is a Phase 1 Study to Evaluate the Safety,Tolerability and Virology of CT P59 in Patients With Mild Symptoms of Symptoms of Coronavirus Disease (COVID-19)

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).