General Information of Drug (ID: DMMQ6VT)

Drug Name
Leronlimab
Synonyms PRO 140
Indication
Disease Entry ICD 11 Status REF
Coronavirus Disease 2019 (COVID-19) 1D6Y Phase 2 [1]
Therapeutic Class
Antiviral Agents
Drug Type
Monoclonal antibody
ADMET Property
Absorption AUC
The area under the plot of plasma concentration (AUC) of drug is 24.4 mgday/L [2]
Absorption Cmax
The maximum plasma concentration (Cmax) of drug is 6.1 mg/L [2]
Absorption Tmax
The time to maximum plasma concentration (Tmax) is 32 h [2]
Half-life
The concentration or amount of drug in body reduced by one-half in 3.4 days [2]
Metabolism
The drug is metabolized via proteolytic enzymes []
Cross-matching ID
DrugBank ID
DB05941
TTD ID
D0HN8P

Molecular Interaction Atlas of This Drug


Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
HUMAN C-C chemokine receptor 5 (CCR5) TTH91NV CCR5_HUMAN Inhibitor [3]
Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This Drug

References

1 ClinicalTrials.gov (NCT04343651) Study to Evaluate the Efficacy and Safety of Leronlimab for Mild to Moderate COVID-19
2 Anti-HIV-1 activity of weekly or biweekly treatment with subcutaneous PRO 140, a CCR5 monoclonal antibody. J Infect Dis. 2010 May 15;201(10):1481-7. doi: 10.1086/652190.
3 Disruption of the CCL5/RANTES-CCR5 Pathway Restores Immune Homeostasis and Reduces Plasma Viral Load in Critical COVID-19