Pexelizumab
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Also known as H-5G1.1 SCFVH5G1.1 SCFVH5G1.1 SCFV (CDR)
Summary
Pexelizumab (CHEMBL2107979) is a phase-3 clinical-stage antibody; indicated across 2 conditions including coronary artery disorder and acute myocardial infarction.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Antibody
- Indications: 2 conditions
- Clinical trials: 2
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL2107979 |
| Name | Pexelizumab |
| Type | Antibody |
| Max phase | 3 |
Also known as: H-5G1.1 SCFV, H5G1.1 SCFV, H5G1.1 SCFV (CDR), Pexelizumab, PEXELIZUMAB
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
2 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).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| coronary artery disorder | 3 | MONDO:0005010 | EFO:0001645 |
| acute myocardial infarction | 3 | MONDO:0004781 | EFO:0008583 |
Clinical trials
Total trials: 2.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE3 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00048308 | PHASE3 | COMPLETED | Effect of Pexelizumab on All-Cause Mortality and Myocardial Infarction in Patients Undergoing Coronary Artery Bypass Graft Surgery With Cardio-Pulmonary Bypass |
| NCT00091637 | PHASE3 | COMPLETED | Pexelizumab in Conjunction With Angioplasty in Acute Myocardial Infarction (APEX-AMI) |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).