Inclacumab

drug
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Also known as RG1512RO-4905417RO4905417

Summary

Inclacumab (CHEMBL2109488) is a phase-3 clinical-stage antibody targeting SELP; indicated across 3 conditions including coronary artery disorder and myocardial infarction.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Antibody
  • Targets: 1 (SELP)
  • Indications: 3 conditions
  • Clinical trials: 7

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2109488
NameInclacumab
TypeAntibody
Max phase3

Also known as: Inclacumab, RG1512, RO-4905417, RO4905417, INCLACUMAB

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
SELPselectin P (CD62)BindingP16109

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

Aggregated over 1 target gene(s): SELP.

Top Reactome pathways

5 total, by targets touching each:

PathwayTargetsGenes
Hemostasis1SELP
Platelet degranulation1SELP
Cell surface interactions at the vascular wall1SELP
Platelet activation, signaling and aggregation1SELP
Response to elevated platelet cytosolic Ca2+1SELP

Dominant GO biological processes

GO termTargets
positive regulation of leukocyte migration1
inflammatory response1
cell adhesion1
heterophilic cell-cell adhesion1
leukocyte cell-cell adhesion1
positive regulation of platelet activation1
calcium-dependent cell-cell adhesion1
response to lipopolysaccharide1
regulation of integrin activation1
response to cytokine1
defense response to Gram-negative bacterium1
leukocyte tethering or rolling1
positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction1
cell-cell adhesion1
positive regulation of leukocyte tethering or rolling1

Indications & clinical

Indications

3 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
coronary artery disorder2MONDO:0005010EFO:0001645
myocardial infarction2MONDO:0005068EFO:0000612
peripheral arterial disease1MONDO:0005386EFO:0004265

Clinical trials

Total trials: 7.

Phase distribution

PhaseTrials
PHASE33
PHASE22
PHASE12

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04927247PHASE3TERMINATEDA Study of a Single Dose of Inclacumab to Reduce Re-admission in Participants With Sickle Cell Disease and Recurrent Vaso-occlusive Crises
NCT04935879PHASE3COMPLETEDA Study to Assess the Safety and Efficacy of Inclacumab in Participants With Sickle Cell Disease Experiencing Vaso-occlusive Crises
NCT05348915PHASE3TERMINATEDA Study to Evaluate the Long-term Safety of Inclacumab Administered to Participants With Sickle Cell Disease
NCT01245634PHASE2COMPLETEDA Study of RO4905417 in Patients Undergoing Coronary Artery Bypass Graft (CABG) Surgery
NCT01327183PHASE2COMPLETEDA Study of RO4905417 in Patients With Non ST-Elevation Myocardial Infarction (Non-STEMI) Undergoing Percutaneous Coronary Intervention
NCT00760565PHASE1COMPLETEDA Multiple Ascending Dose Study of RO4905417 in Healthy Volunteers and Patients With Peripheral Arterial Disease (PAD).
NCT01815827PHASE1COMPLETEDA Study of Single Dose Inclacumab in Japanese Healthy Volunteers Compared to Caucasian Healthy Volunteers

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.

2 molecules share ≥1 primary target. Top 2 by shared-target count:

MoleculeSourceStatusShared targets
GALLIC ACIDChEMBL + PubChemPhase 2 (approved)SELP
BIMOSIAMOSEChEMBLPhase 2SELP