Panitumumab
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Also known as AbenixABX-EGFE7.6.3L01xc08Vectibix
Summary
Panitumumab (CHEMBL1201827) is an approved antibody (ATC L01FE02) targeting EGFR; indicated across 38 conditions including colorectal adenocarcinoma and neoplasm; with CIViC clinical evidence for 96 variant-indication associations (e.g. KRAS G12C in colorectal cancer).
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Antibody
- ATC class: L01FE02
- Targets: 1 (EGFR)
- Indications: 38 conditions
- Clinical trials: 217
- Precision-oncology evidence (CIViC): 96 variant–indication associations
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1201827 |
| Name | Panitumumab |
| Type | Antibody |
| Max phase | 4 |
| ATC | L01FE02 |
Also known as: Abenix, ABX-EGF, E7.6.3, L01xc08, Panitumumab, Vectibix, PANITUMUMAB
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 |
|---|---|---|---|---|---|
| EGFR | epidermal growth factor receptor | Antagonist | 10.3 | 17.5% | P00533 |
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
Aggregated over 1 target gene(s): EGFR.
Top Reactome pathways
37 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| Signaling by ERBB2 | 1 | EGFR |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 1 | EGFR |
| Signaling by ERBB4 | 1 | EGFR |
| SHC1 events in ERBB2 signaling | 1 | EGFR |
| PLCG1 events in ERBB2 signaling | 1 | EGFR |
| PIP3 activates AKT signaling | 1 | EGFR |
| Signaling by EGFR | 1 | EGFR |
| GRB2 events in EGFR signaling | 1 | EGFR |
| GAB1 signalosome | 1 | EGFR |
| SHC1 events in EGFR signaling | 1 | EGFR |
| EGFR downregulation | 1 | EGFR |
| GRB2 events in ERBB2 signaling | 1 | EGFR |
| PI3K events in ERBB2 signaling | 1 | EGFR |
| EGFR interacts with phospholipase C-gamma | 1 | EGFR |
| EGFR Transactivation by Gastrin | 1 | EGFR |
| Constitutive Signaling by Aberrant PI3K in Cancer | 1 | EGFR |
| Signal transduction by L1 | 1 | EGFR |
| Constitutive Signaling by EGFRvIII | 1 | EGFR |
| Inhibition of Signaling by Overexpressed EGFR | 1 | EGFR |
| RAF/MAP kinase cascade | 1 | EGFR |
| ERBB2 Regulates Cell Motility | 1 | EGFR |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 1 | EGFR |
| ERBB2 Activates PTK6 Signaling | 1 | EGFR |
| Cargo recognition for clathrin-mediated endocytosis | 1 | EGFR |
| Clathrin-mediated endocytosis | 1 | EGFR |
| PTK6 promotes HIF1A stabilization | 1 | EGFR |
| Downregulation of ERBB2 signaling | 1 | EGFR |
| TFAP2 (AP-2) family regulates transcription of growth factors and their receptors | 1 | EGFR |
| Extra-nuclear estrogen signaling | 1 | EGFR |
| NOTCH3 Activation and Transmission of Signal to the Nucleus | 1 | EGFR |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| cell morphogenesis | 1 |
| ossification | 1 |
| embryonic placenta development | 1 |
| positive regulation of protein phosphorylation | 1 |
| hair follicle development | 1 |
| ubiquitin-dependent protein catabolic process | 1 |
| signal transduction | 1 |
| cell surface receptor signaling pathway | 1 |
| epidermal growth factor receptor signaling pathway | 1 |
| salivary gland morphogenesis | 1 |
| learning or memory | 1 |
| positive regulation of cell population proliferation | 1 |
| gene expression | 1 |
| protein ubiquitination | 1 |
| cerebral cortex cell migration | 1 |
Indications & clinical
Indications
38 indications (6 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 |
|---|---|---|---|
| colorectal adenocarcinoma | 4 | MONDO:0005008 | EFO:0000365 |
| neoplasm | 4 | MONDO:0005070 | EFO:0000616 |
| colorectal neoplasm | 4 | MONDO:0005335 | EFO:0004142 |
| colorectal carcinoma | 4 | MONDO:0024331 | EFO:1001951 |
| head and neck squamous cell carcinoma | 3 | MONDO:0010150 | EFO:0000181 |
| squamous cell carcinoma | 3 | MONDO:0005096 | EFO:0000707 |
| head and neck cancer | 3 | MONDO:0005627 | EFO:0006859 |
| colonic neoplasm | 3 | MONDO:0005401 | MONDO:0021063 |
| exocrine pancreatic carcinoma | 2 | MONDO:0005192 | EFO:0002618 |
| carcinoid syndrome | 2 | MONDO:0100347 | EFO:1000852 |
| non-small cell lung carcinoma | 2 | MONDO:0005233 | EFO:0003060 |
| rectal cancer | 2 | MONDO:0006519 | EFO:1000657 |
| carcinoma | 2 | MONDO:0004993 | EFO:0000313 |
| gastric adenocarcinoma | 2 | MONDO:0005036 | EFO:0000503 |
| renal cell carcinoma | 2 | MONDO:0005086 | EFO:0000681 |
| carcinoma of esophagus | 2 | MONDO:0019086 | EFO:0002916 |
| cholangiocarcinoma | 2 | MONDO:0019087 | EFO:0005221 |
| esophageal squamous cell carcinoma | 2 | MONDO:0005580 | EFO:0005922 |
| fallopian tube neoplasm | 2 | MONDO:0021092 | MONDO:0002158 |
| breast neoplasm | 2 | MONDO:0021100 | MONDO:0007254 |
| ovarian cancer | 2 | MONDO:0008170 | MONDO:0008170 |
| lung neoplasm | 2 | MONDO:0021117 | MONDO:0008903 |
| ovarian carcinoma | 2 | MONDO:0005140 | EFO:0001075 |
| triple-negative breast carcinoma | 2 | MONDO:0005494 | EFO:0005537 |
| breast carcinoma | 2 | MONDO:0004989 | EFO:0000305 |
| biliary tract neoplasm | 2 | MONDO:0005304 | EFO:0003891 |
| malignant pancreatic neoplasm | 2 | MONDO:0009831 | EFO:1000359 |
| gallbladder neoplasm | 2 | MONDO:0021253 | MONDO:0005411 |
| kidney cancer | 1 | MONDO:0002367 | MONDO:0002367 |
| brain neoplasm | 1 | MONDO:0021211 | EFO:0003833 |
| brain cancer | 1 | MONDO:0001657 | MONDO:0001657 |
| glioma | 1 | MONDO:0021042 | MONDO:0100342 |
6 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 217.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE2 | 144 |
| PHASE3 | 24 |
| PHASE1 | 21 |
| PHASE1/PHASE2 | 20 |
| Not specified | 5 |
| PHASE4 | 1 |
| PHASE2/PHASE3 | 1 |
| EARLY_PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT02301962 | PHASE4 | UNKNOWN | Phase IV Panitumumab Study in Indian Subjects With Metastatic Colorectal Cancer |
| NCT02885753 | PHASE3 | RECRUITING | Systemic Oxaliplatin or Intra-arterial Chemotherapy Combined With LV5FU2 +/- Irinotecan and an Target Therapy in First Line Treatment of Metastatic Colorectal Cancer Restricted to the Liver |
| NCT03635021 | PHASE3 | ACTIVE_NOT_RECRUITING | Study to Evaluate the Efficacy of FOLFOX + Panitumumab Followed by FOLFIRI + Bevacizumab (Sequence 1) Versus FOLFOX + Bevacizumab Followed by FOLFIRI + Panitumumab (Sequence 2) in Untreated Patients With Wild-type RAS Metastatic, Primary Left-sided, Unresectable Colorectal Cancer |
| NCT05863195 | PHASE3 | RECRUITING | Testing Pump Chemotherapy in Addition to Standard of Care Chemotherapy Versus Standard of Care Chemotherapy Alone for Patients With Unresectable Colorectal Liver Metastases: The PUMP Trial |
| NCT06252649 | PHASE3 | RECRUITING | Study of Sotorasib, Panitumumab and FOLFIRI Versus FOLFIRI With or Without Bevacizumab-awwb in Treatment-naïve Participants With Metastatic Colorectal Cancer With KRAS p.G12C Mutation |
| NCT06490536 | PHASE3 | RECRUITING | The Sagittarius Trial |
| NCT06509126 | PHASE3 | RECRUITING | Intermittent or Continuous Panitumumab Plus FOLFIRI for Left Sided RAS/B-RAF Wild-type Metastatic Colorectal Cancer |
| NCT06998940 | PHASE3 | RECRUITING | Studying Chemotherapy With or Without Panitumumab for Unresectable, Locally Advanced, or Metastatic Pancreatic Cancer Without KRAS Mutations |
| NCT00113763 | PHASE3 | COMPLETED | Evaluating Panitumumab (ABX-EGF) Plus Best Supportive Care Versus Best Supportive Care in Patients With Metastatic Colorectal Cancer |
| NCT00115765 | PHASE3 | COMPLETED | PACCE: Panitumumab Advanced Colorectal Cancer Evaluation Study |
| NCT00339183 | PHASE3 | COMPLETED | Comparison of Treatment Effect of Chemotherapy With Panitumumab to Chemotherapy Alone |
| NCT00364013 | PHASE3 | COMPLETED | PRIME: Panitumumab Randomized Trial In Combination With Chemotherapy for Metastatic Colorectal Cancer to Determine Efficacy |
| NCT00389870 | PHASE3 | COMPLETED | Irinotecan With or Without Panitumumab or Cyclosporine in Treating Patients With Advanced or Metastatic Colorectal Cancer That Did Not Respond to Fluorouracil |
| NCT00647530 | PHASE2/PHASE3 | UNKNOWN | Fluorouracil and Oxaliplatin With or Without Panitumumab In Treating Patients With High-Risk Colon Cancer That Can Be Removed by Surgery |
| NCT00820248 | PHASE3 | COMPLETED | Radiation + Cisplatin or Panitumumab in Locally Advanced Stage III or Stage IV Head and Neck Cancer |
| NCT00824785 | PHASE3 | TERMINATED | REAL3 Trial of Efficacy of EOX With/Without Panitumumab in Previously Untreated Adv OG Cancer |
| NCT01001377 | PHASE3 | COMPLETED | ASPECCT: A Study of Panitumumab Efficacy and Safety Compared to Cetuximab in Patients With KRAS Wild-Type Metastatic Colorectal Cancer |
| NCT01142414 | PHASE3 | WITHDRAWN | Chemotherapy and Radiation Therapy With or Without Panitumumab in Treating Patients Who Have Undergone Surgery for Advanced Hypopharyngeal Cancer, Oropharyngeal Cancer, Laryngeal Cancer, or Oral Cavity Cancer at High Risk of Recurrence |
| NCT01412957 | PHASE3 | COMPLETED | Comparison of Survival Benefit of Panitumumab With Supportive Care to Best Supportive Care Alone in Patients With Metastatic Colorectal Cancer |
| NCT01627379 | PHASE3 | TERMINATED | Cisplatin and 5-FU +/- Panitumumab for Patients With Nonresectable,Advanced or Metastatic Esophageal Squamous Cell Cancer |
| NCT02394795 | PHASE3 | COMPLETED | Panitumumab and RAS, Diagnostically-useful Gene Mutation for mCRC |
| NCT02818725 | PHASE3 | COMPLETED | I-MVAC +/- Panitumumab as First-line Treatment of Advanced Urothelial Carcinoma Without H-Ras Nor K-Ras Mutations |
| NCT03231722 | PHASE3 | COMPLETED | First Line mFOLFOXIRI + PANITUMUMAB vs mFOLFOX + PANITUMUMAB IN RAS AND BRAF WT METASTATIC COLORECTAL CANCER PATIENTS |
| NCT03300609 | PHASE3 | TERMINATED | 5-FU Based Maintenance Therapy in RAS Wild Type Metastatic Colorectal Cancer After Induction With FOLFOX Plus Panitumumab |
| NCT04342676 | PHASE3 | COMPLETED | Lymph Node Ratio and Kras Mutation in R Colon Cancer |
| NCT05198934 | PHASE3 | COMPLETED | Sotorasib and Panitumumab Versus Investigator’s Choice for Participants With Kirsten Rat Sarcoma (KRAS) p.G12C Mutation |
| NCT02876107 | PHASE2 | ACTIVE_NOT_RECRUITING | Carboplatin and Paclitaxel With or Without Panitumumab in Treating Patients With Invasive Triple Negative Breast Cancer |
| NCT02925234 | PHASE2 | RECRUITING | The Drug Rediscovery Protocol (DRUP Trial) |
| NCT02980510 | PHASE2 | ACTIVE_NOT_RECRUITING | Comparison FOLFIRINOX Panitumumab vs mFOLFOX6 Panitumumab in RAS/B-RAF Wild-type Metastatic Colorectal Cancer Patients |
| NCT03087071 | PHASE2 | ACTIVE_NOT_RECRUITING | Panitumumab With or Without Trametinib in Treating Patients With Stage IV Colorectal Cancer |
| NCT03384238 | PHASE1/PHASE2 | RECRUITING | Panitumumab-IRDye800 in Patients With Pancreatic Cancer Undergoing Surgery |
| NCT03510208 | PHASE1/PHASE2 | RECRUITING | Panitumumab-IRDye800 in Diagnosing Participants With Malignant Glioma Undergoing Surgery |
| NCT03983993 | PHASE2 | ACTIVE_NOT_RECRUITING | Niraparib and Panitumumab in Patients With Advanced or Metastatic Colorectal Cancer |
| NCT04034173 | PHASE2 | NOT_YET_RECRUITING | Optimal Anti-EGFR Treatment of mCRC Patients With Low-Frequency RAS Mutation |
| NCT04117945 | PHASE2 | ACTIVE_NOT_RECRUITING | Regorafenib, With Cetuximab or Panitumumab, for the Treatment of Unresectable, Locally Advanced, or Metastatic Colorectal Cancer |
| NCT04587128 | PHASE2 | ACTIVE_NOT_RECRUITING | Early-Line Anti-EGFR Therapy to Facilitate Retreatment for Select Patients With mCRC |
| NCT04787341 | PHASE2 | ACTIVE_NOT_RECRUITING | PAnitumumab REchallenge Followed by REgorafenib Versus the Reverse Sequence |
| NCT05007132 | PHASE2 | RECRUITING | Trifluridine/ Tipiracil Plus Panitumumab Versus Trifluridine/ Tipiracil Plus Bevacizumab as First-line Treatment of Metastatic Colorectal Cancer |
| NCT05121038 | PHASE1/PHASE2 | ACTIVE_NOT_RECRUITING | CEND-1 in Combination with Neoadjuvant FOLFIRINOX with or Without Panitumumab |
| NCT05423197 | PHASE2 | NOT_YET_RECRUITING | 89Zr-Panitumumab for Assessment of Suspected Metastatic Lesions on 18F-FDG-PET/CT in HNSCC |
Clinical evidence (CIViC)
Variant × indication × effect (96 predictive associations from 115 curated evidence items):
| Variant | Indication | Effect | Therapy | Level | CIViC |
|---|---|---|---|---|---|
| KRAS G12C | Colorectal Cancer | Sensitivity/Response | Sotorasib + Panitumumab | CIViC A | EID12264 |
| KRAS Wildtype | Colorectal Cancer | Sensitivity/Response | Chemotherapy + Panitumumab | CIViC A | EID11264 |
| NRAS Wildtype | Colorectal Cancer | Sensitivity/Response | Chemotherapy + Panitumumab | CIViC A | EID11270 |
| KRAS Mutation | Colorectal Cancer | Resistance | Cetuximab + Panitumumab | CIViC A | EID5345 |
| NRAS Mutation | Colorectal Cancer | Resistance | Panitumumab + Cetuximab | CIViC A | EID5344 |
| BRAF V600E | Colorectal Cancer | Sensitivity/Response | Panitumumab + Vemurafenib | CIViC B | EID1413 +1 |
| AREG Expression | Colorectal Cancer | Sensitivity/Response | Panitumumab | CIViC B | EID1020 |
| BRAF Class 2 Mutations | Colorectal Cancer | Sensitivity/Response | Cetuximab + Panitumumab | CIViC B | EID7574 |
| BRAF Class 3 Mutations | Colorectal Cancer | Sensitivity/Response | Cetuximab + Panitumumab | CIViC B | EID7575 |
| BRAF Mutation | Colorectal Cancer | Sensitivity/Response | Panitumumab + Cetuximab | CIViC B | EID1404 |
| BRAF V600E | Colorectal Cancer | Sensitivity/Response | Panitumumab + Dabrafenib + Trametinib | CIViC B | EID6123 |
| BRAF V600E | Colorectal Adenocarcinoma | Sensitivity/Response | Trametinib + Panitumumab | CIViC B | EID6124 |
| CDKN2A p16 Expression | Head And Neck Squamous Cell Carcinoma | Sensitivity/Response | Panitumumab | CIViC B | EID753 |
| EGFR Amplification | Colorectal Cancer | Sensitivity/Response | Cetuximab + Panitumumab | CIViC B | EID854 |
| EGFR Expression | Colorectal Cancer | Sensitivity/Response | Panitumumab | CIViC B | EID1708 |
| EREG EXPRESSION | Colorectal Cancer | Sensitivity/Response | Panitumumab | CIViC B | EID1021 |
| EGFR G465R | Colorectal Cancer | Resistance | Panitumumab + Cetuximab | CIViC B | EID7083 +1 |
| PIK3CA H1047R | Colorectal Cancer | Resistance | Cetuximab + Panitumumab | CIViC B | EID258 +1 |
| BRAF V600 | Colorectal Cancer | Resistance | Panitumumab | CIViC B | EID88 |
| BRAF V600E | Colorectal Cancer | Resistance | Panitumumab + Cetuximab | CIViC B | EID2115 |
| BRAF V600E | Colorectal Cancer | Resistance | Cetuximab + Panitumumab | CIViC B | EID816 |
| CDKN2A p16 Expression | Head And Neck Squamous Cell Carcinoma | Resistance | Panitumumab | CIViC B | EID696 |
| EGFR F404I | Colorectal Cancer | Resistance | Panitumumab + Cetuximab | CIViC B | EID7099 |
| EGFR F404V | Colorectal Cancer | Resistance | Cetuximab + Panitumumab | CIViC B | EID7100 |
| EGFR G465E | Colorectal Cancer | Resistance | Cetuximab + Panitumumab | CIViC B | EID7084 |
| EGFR G465V | Colorectal Cancer | Resistance | Panitumumab + Cetuximab | CIViC B | EID7085 |
| EGFR I462K | Colorectal Cancer | Resistance | Panitumumab + Cetuximab | CIViC B | EID7079 |
| EGFR I462R | Colorectal Cancer | Resistance | Cetuximab + Panitumumab | CIViC B | EID7080 |
| EGFR I491K | Colorectal Cancer | Resistance | Cetuximab + Panitumumab | CIViC B | EID7090 |
| EGFR I491R | Colorectal Cancer | Resistance | Panitumumab + Cetuximab | CIViC B | EID7091 |
+66 more predictive associations (showing top 30 by level).
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.
158 molecules share ≥1 primary target. Top 60 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| AFATINIB | ChEMBL + PubChem | Phase 4 (approved) | EGFR |
| SELUMETINIB | ChEMBL + PubChem | Phase 4 (approved) | EGFR |
| ABEMACICLIB | ChEMBL | Phase 4 (approved) | EGFR |
| ACALABRUTINIB | ChEMBL | Phase 4 (approved) | EGFR |
| AFATINIB DIMALEATE | ChEMBL | Phase 4 (approved) | EGFR |
| ALECTINIB | ChEMBL | Phase 4 (approved) | EGFR |
| ASTEMIZOLE | ChEMBL | Phase 4 (approved) | EGFR |
| AXITINIB | ChEMBL | Phase 4 (approved) | EGFR |
| BACITRACIN | ChEMBL | Phase 4 (approved) | EGFR |
| BITHIONOL | ChEMBL | Phase 4 (approved) | EGFR |
| BOSUTINIB | ChEMBL | Phase 4 (approved) | EGFR |
| BRIGATINIB | ChEMBL | Phase 4 (approved) | EGFR |
| CABOZANTINIB | ChEMBL | Phase 4 (approved) | EGFR |
| CERITINIB | ChEMBL | Phase 4 (approved) | EGFR |
| CHLORPROMAZINE | ChEMBL | Phase 4 (approved) | EGFR |
| CHROMIC CHLORIDE | ChEMBL | Phase 4 (approved) | EGFR |
| CISPLATIN | ChEMBL | Phase 4 (approved) | EGFR |
| CLOTRIMAZOLE | ChEMBL | Phase 4 (approved) | EGFR |
| COLISTIN | ChEMBL | Phase 4 (approved) | EGFR |
| CRIZOTINIB | ChEMBL | Phase 4 (approved) | EGFR |
| DACOMITINIB | ChEMBL | Phase 4 (approved) | EGFR |
| DASATINIB | ChEMBL | Phase 4 (approved) | EGFR |
| DOBUTAMINE | ChEMBL | Phase 4 (approved) | EGFR |
| DOCETAXEL | ChEMBL | Phase 4 (approved) | EGFR |
| EBASTINE | ChEMBL | Phase 4 (approved) | EGFR |
| ECONAZOLE | ChEMBL | Phase 4 (approved) | EGFR |
| ERLOTINIB | ChEMBL | Phase 4 (approved) | EGFR |
| FEDRATINIB | ChEMBL | Phase 4 (approved) | EGFR |
| FLUPHENAZINE | ChEMBL | Phase 4 (approved) | EGFR |
| GEFITINIB | ChEMBL | Phase 4 (approved) | EGFR |
| GENTIAN VIOLET | ChEMBL | Phase 4 (approved) | EGFR |
| GILTERITINIB | ChEMBL | Phase 4 (approved) | EGFR |
| HEXACHLOROPHENE | ChEMBL | Phase 4 (approved) | EGFR |
| IBRUTINIB | ChEMBL | Phase 4 (approved) | EGFR |
| IMATINIB | ChEMBL | Phase 4 (approved) | EGFR |
| LAPATINIB | ChEMBL | Phase 4 (approved) | EGFR |
| LAPATINIB DITOSYLATE | ChEMBL | Phase 4 (approved) | EGFR |
| LAZERTINIB | ChEMBL | Phase 4 (approved) | EGFR |
| LEVODOPA | ChEMBL | Phase 4 (approved) | EGFR |
| LORLATINIB | ChEMBL | Phase 4 (approved) | EGFR |
| METHYLDOPA | ChEMBL | Phase 4 (approved) | EGFR |
| MICONAZOLE | ChEMBL | Phase 4 (approved) | EGFR |
| MIDOSTAURIN | ChEMBL | Phase 4 (approved) | EGFR |
| MITOXANTRONE | ChEMBL | Phase 4 (approved) | EGFR |
| MOBOCERTINIB | ChEMBL | Phase 4 (approved) | EGFR |
| MONTELUKAST | ChEMBL | Phase 4 (approved) | EGFR |
| NELFINAVIR | ChEMBL | Phase 4 (approved) | EGFR |
| NERATINIB | ChEMBL | Phase 4 (approved) | EGFR |
| NICLOSAMIDE | ChEMBL | Phase 4 (approved) | EGFR |
| OLMUTINIB | ChEMBL | Phase 4 (approved) | EGFR |
| OSIMERTINIB | ChEMBL | Phase 4 (approved) | EGFR |
| PERHEXILINE | ChEMBL | Phase 4 (approved) | EGFR |
| PONATINIB | ChEMBL | Phase 4 (approved) | EGFR |
| SORAFENIB | ChEMBL | Phase 4 (approved) | EGFR |
| SULOCTIDIL | ChEMBL | Phase 4 (approved) | EGFR |
| SUNITINIB | ChEMBL | Phase 4 (approved) | EGFR |
| TAMOXIFEN | ChEMBL | Phase 4 (approved) | EGFR |
| TERFENADINE | ChEMBL | Phase 4 (approved) | EGFR |
| THIORIDAZINE | ChEMBL | Phase 4 (approved) | EGFR |
| TRIBROMSALAN | ChEMBL | Phase 4 (approved) | EGFR |
Related Atlas pages
- Genes: EGFR
- Diseases: colorectal adenocarcinoma, neoplasm, colorectal neoplasm, colorectal carcinoma, head and neck squamous cell carcinoma, squamous cell carcinoma, head and neck cancer, colonic neoplasm
- Drugs: Afatinib, Selumetinib, Abemaciclib, Acalabrutinib, Alectinib, Astemizole, Axitinib, Bacitracin, Bithionol, Bosutinib, Brigatinib, Cabozantinib, Ceritinib, Chlorpromazine, Chromic Chloride, Cisplatin, Clotrimazole, Colistin, Crizotinib, Dacomitinib, Dasatinib, Dobutamine, Docetaxel, Ebastine, Econazole, Erlotinib, Fedratinib, Fluphenazine, Gefitinib, Gilteritinib, Hexachlorophene, Ibrutinib, Imatinib, Lapatinib, Lazertinib, Levodopa, Lorlatinib, Methyldopa, Miconazole, Midostaurin, Mitoxantrone, Mobocertinib, Montelukast, Nelfinavir, Neratinib, Niclosamide, Olmutinib, Osimertinib, Perhexiline, Ponatinib, Sorafenib, Suloctidil, Sunitinib, Tamoxifen, Terfenadine, Thioridazine, Tribromsalan
- Biomarker genes: AREG, CDKN2A, EREG