Mupadolimab
drugOn this page
Also known as Cpi-006CPI006CPX-006
Summary
Mupadolimab (CHEMBL4802200) is a phase-3 clinical-stage antibody targeting NT5E; indicated across 4 conditions including severe acute respiratory syndrome and neoplasm.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Antibody
- Targets: 1 (NT5E)
- Indications: 4 conditions
- Clinical trials: 3
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL4802200 |
| Name | Mupadolimab |
| Type | Antibody |
| Max phase | 3 |
Also known as: Cpi-006, CPI-006, CPI006, CPX-006, Mupadolimab, MUPADOLIMAB
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).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| NT5E | Ecto-5’-Nucleotidase | Inhibition | 8.15 | 0% | P21589 |
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
Aggregated over 1 target gene(s): NT5E.
Top Reactome pathways
14 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| Metabolism | 1 | NT5E |
| Metabolism of nucleotides | 1 | NT5E |
| Disease | 1 | NT5E |
| Nicotinate metabolism | 1 | NT5E |
| Metabolism of water-soluble vitamins and cofactors | 1 | NT5E |
| Metabolism of vitamins and cofactors | 1 | NT5E |
| Infectious disease | 1 | NT5E |
| Pyrimidine catabolism | 1 | NT5E |
| Purine catabolism | 1 | NT5E |
| Nucleotide catabolism | 1 | NT5E |
| Leishmania infection | 1 | NT5E |
| Purinergic signaling in leishmaniasis infection | 1 | NT5E |
| Cell recruitment (pro-inflammatory response) | 1 | NT5E |
| Parasitic Infection Pathways | 1 | NT5E |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| AMP catabolic process | 1 |
| DNA metabolic process | 1 |
| leukocyte cell-cell adhesion | 1 |
| response to ATP | 1 |
| ADP catabolic process | 1 |
| ATP metabolic process | 1 |
| adenosine biosynthetic process | 1 |
| negative regulation of inflammatory response | 1 |
| calcium ion homeostasis | 1 |
| inhibition of non-skeletal tissue mineralization | 1 |
| nucleotide catabolic process | 1 |
Indications & clinical
Indications
4 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 |
|---|---|---|---|
| severe acute respiratory syndrome | 3 | MONDO:0005091 | MONDO:0100096 |
| neoplasm | 1 | MONDO:0005070 | EFO:0000616 |
| infectious disease | 1 | MONDO:0005550 | EFO:0005741 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 3.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE1 | 2 |
| PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04734873 | PHASE3 | TERMINATED | CPI-006 Plus Standard of Care Versus Placebo Plus Standard of Care in Mild to Moderately Symptomatic Hospitalized Covid-19 Patients |
| NCT03454451 | PHASE1 | COMPLETED | CPI-006 Alone and in Combination With Ciforadenant and With Pembrolizumab for Patients With Advanced Cancers |
| NCT04464395 | PHASE1 | COMPLETED | Study of CPI-006 as Immunotherapy for Hospitalized COVID-19 Patients |
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
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.
7 molecules share ≥1 primary target. Top 7 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| FLUDARABINE | ChEMBL + PubChem | Phase 3 (approved) | NT5E |
| QUERCETIN | ChEMBL + PubChem | Phase 3 (approved) | NT5E |
| ELLAGIC ACID | ChEMBL | Phase 2 | NT5E |
| FTIVAZIDE | ChEMBL | Phase 2 | NT5E |
| QUEMLICLUSTAT | ChEMBL | Phase 2 | NT5E |
| adenosine | PubChem | Approved | NT5E |
| Tiamulin | PubChem | Approved | NT5E |
Related Atlas pages
- Genes: NT5E
- Diseases: severe acute respiratory syndrome
- Drugs: Fludarabine, Quercetin, adenosine