Olokizumab

drug
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Also known as CDP-6038CDP6038

Summary

Olokizumab (CHEMBL1743050) is a phase-3 clinical-stage antibody (ATC L04AC23); indicated across 5 conditions including rheumatoid arthritis and severe acute respiratory syndrome.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Antibody
  • ATC class: L04AC23
  • Indications: 5 conditions
  • Clinical trials: 15

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1743050
NameOlokizumab
TypeAntibody
Max phase3
ATCL04AC23

Also known as: CDP-6038, CDP6038, Olokizumab, OLOKIZUMAB

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

5 indications (0 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
rheumatoid arthritis3MONDO:0008383EFO:0000685
severe acute respiratory syndrome3MONDO:0005091MONDO:0100096
immune system disorder3MONDO:0005046EFO:0000540
Crohn disease2MONDO:0005011EFO:0000384
osteoarthritis1MONDO:0005178MONDO:0005178

Clinical trials

Total trials: 15.

Phase distribution

PhaseTrials
PHASE25
PHASE33
PHASE13
PHASE2/PHASE32
PHASE1/PHASE21
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02760368PHASE3COMPLETEDEvaluation of the Effectiveness and Safety of Two Dosing Regimens of Olokizumab (OKZ), Compared to Placebo, in Subjects With Rheumatoid Arthritis (RA) Who Are Taking Methotrexate But Have Active Disease
NCT02760433PHASE3COMPLETEDEvaluation of the Efficacy and Safety of Two Dosing Regimens of Olokizumab (OKZ), Compared to Placebo, in Subjects With Rheumatoid Arthritis (RA) Who Were Taking an Existing Medication Called a Tumour Necrosis Factor Alpha Inhibitor But Had Active Disease
NCT04380519PHASE2/PHASE3COMPLETEDStudy of the Efficacy and Safety of a Single Administration of Olokizumab and RPH-104 With Standard Therapy in Patients With Severe Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection (COVID-19)
NCT04452474PHASE2/PHASE3WITHDRAWNStudy of the Efficacy and Safety of a Single Administration of Olokizumab vs. Placebo in Addition to Standard Treatment in Patients With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection (COVID-19).
NCT05187793PHASE3UNKNOWNStudy of Efficacy of Different Treatment Regimens of Olokizumab
NCT01009242PHASE1/PHASE2COMPLETEDTo Evaluate the Blood Levels and Safety of IV and Subcutaneous CDP6038 in Subjects With Rheumatoid Arthritis Using Methotrexate
NCT01242488PHASE2COMPLETEDEfficacy and Safety of CDP6038 in Patients With Rheumatoid Arthritis With an Unsuccessful Response to Anti-Tumor Necrosis Factor (Anti-TNF) Therapy
NCT01296711PHASE2TERMINATEDOpen-label Study to Assess the Safety and Efficacy of CDP6038 (Olokizumab) in Patients Who Completed RA0056
NCT01463059PHASE2COMPLETEDEfficacy and Safety of Olokizumab With Rheumatoid Arthritis With Previously Failed to Anti-tumor Necrosis Factor (Anti-TNF) Therapy
NCT01533714PHASE2TERMINATEDThe Long-term Safety and Efficacy of CDP6038 (Olokizumab) With Active Rheumatoid Arthritis
NCT01635621PHASE2WITHDRAWNA Phase II Study to Assess the Efficacy and Safety of Olokizumab in Patients With Crohn’s Disease
NCT01262794PHASE1COMPLETEDPharmacokinetic (PK)/Pharmacodynamic (PD), Study of Single-dose Subcutaneous CDP6038 in Healthy Japanese Male Subjects
NCT01276119PHASE1COMPLETEDThe First Clinical Study to Test Safety, Blood Levels and Other Effects of CDP6038 in Healthy Males
NCT04246762PHASE1COMPLETEDStudy in Subjects With Rheumatoid Arthritis to Evaluate the Effect of a Single Dose of Olokizumab on the Pharmacokinetics of Substrates for CYP1A2, CYP2C9, CYP2C19 and CYP3A4
NCT05196477Not specifiedCOMPLETEDStudy of the Outcomes of Olokizumab Therapy in Hospitalized Patients With SARS-CoV-2 (COVID-19) Infection

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).