Favezelimab
drugOn this page
Also known as MavezelimabMk-4280MK4280
Summary
Favezelimab (CHEMBL4297784) is a phase-3 clinical-stage antibody; indicated across 13 conditions including hodgkins lymphoma and colorectal neoplasm.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Antibody
- Indications: 13 conditions
- Clinical trials: 15
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL4297784 |
| Name | Favezelimab |
| Type | Antibody |
| Max phase | 3 |
Also known as: Favezelimab, Mavezelimab, Mk-4280, MK-4280, MK4280, FAVEZELIMAB
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
13 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 |
|---|---|---|---|
| Hodgkins lymphoma | 3 | MONDO:0004952 | EFO:0000183 |
| colorectal neoplasm | 3 | MONDO:0005335 | MONDO:0005575 |
| non-small cell lung carcinoma | 2 | MONDO:0005233 | EFO:0003060 |
| urothelial carcinoma | 2 | MONDO:0040679 | EFO:0008528 |
| neoplasm | 1 | MONDO:0005070 | EFO:0000616 |
| non-Hodgkin lymphoma | 1 | MONDO:0018908 | EFO:0005952 |
| renal cell carcinoma | 1 | MONDO:0005086 | EFO:0000681 |
| small cell lung carcinoma | 1 | MONDO:0008433 | EFO:0000702 |
| melanoma | 1 | MONDO:0005105 | EFO:0000756 |
| esophageal squamous cell carcinoma | 1 | MONDO:0005580 | EFO:0005922 |
| lymphoma | 1 | MONDO:0005062 | EFO:0000574 |
2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 15.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE1/PHASE2 | 6 |
| PHASE2 | 5 |
| PHASE3 | 3 |
| PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT03486873 | PHASE3 | RECRUITING | Long-term Safety and Efficacy Extension Study for Participants With Advanced Tumors Who Are Currently on Treatment or in Follow-up in a Pembrolizumab (MK-3475) Study (MK-3475-587/KEYNOTE-587) |
| NCT05064059 | PHASE3 | COMPLETED | A Study of Coformulated Favezelimab/Pembrolizumab (MK-4280A) Versus Standard of Care in Subjects With Previously Treated Metastatic PD-L1 Positive Colorectal Cancer (MK-4280A-007) |
| NCT05600309 | PHASE3 | COMPLETED | A Study of Coformulated Favezelimab/Pembrolizumab (MK-4280A) Versus Standard of Care in Subjects With Previously Treated Metastatic PD-L1 Positive Colorectal Cancer (MK-4280A-007)-China Extension Study |
| NCT04626479 | PHASE1/PHASE2 | ACTIVE_NOT_RECRUITING | Substudy 03A: A Study of Immune and Targeted Combination Therapies in Participants With First Line (1L) Renal Cell Carcinoma (MK-3475-03A) |
| NCT04626518 | PHASE1/PHASE2 | ACTIVE_NOT_RECRUITING | Substudy 03B: A Study of Immune and Targeted Combination Therapies in Participants With Second Line Plus (2L+) Renal Cell Carcinoma (MK-3475-03B/KEYMAKER-U03) |
| NCT04895722 | PHASE2 | ACTIVE_NOT_RECRUITING | Evaluation of Co-formulated Pembrolizumab/Quavonlimab (MK-1308A) Versus Other Treatments in Participants With Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient (dMMR) Stage IV Colorectal Cancer (CRC) (MK-1308A-008/KEYSTEP-008) |
| NCT02625961 | PHASE2 | COMPLETED | Study of Pembrolizumab (MK-3475) and Pembrolizumab With Other Investigational Agents in Participants With High Risk Non-muscle Invasive Bladder Cancer (MK-3475-057/KEYNOTE-057) |
| NCT03516981 | PHASE2 | COMPLETED | A Study of Biomarker-Directed, Pembrolizumab (MK-3475) Based Combination Therapy for Advanced Non-Small Cell Lung Cancer (MK-3475-495/KEYNOTE-495) |
| NCT03598608 | PHASE1/PHASE2 | COMPLETED | Study to Evaluate the Safety and Efficacy of a Combination of Favezelimab (MK-4280) and Pembrolizumab (MK-3475) in Participants With Hematologic Malignancies (MK-4280-003) |
| NCT04303169 | PHASE1/PHASE2 | COMPLETED | Substudy 02C: Safety and Efficacy of Pembrolizumab in Combination With Investigational Agents or Pembrolizumab Alone in Participants With Stage III Melanoma Who Are Candidates for Neoadjuvant Therapy (MK-3475-02C/KEYMAKER-U02) |
| NCT04305054 | PHASE1/PHASE2 | COMPLETED | Substudy 02B: Safety and Efficacy of Pembrolizumab in Combination With Investigational Agents or Pembrolizumab Alone in Participants With First Line (1L) Advanced Melanoma (MK-3475-02B/KEYMAKER-U02) |
| NCT05508867 | PHASE2 | COMPLETED | A Study of Coformulated Favezelimab/Pembrolizumab (MK-4280A) Versus Physician’s Choice Chemotherapy in PD-(L)1-refractory, Relapsed or Refractory Classical Hodgkin Lymphoma (MK-4280A-008) |
| NCT06036836 | PHASE2 | COMPLETED | Study of Favezelimab Coformulated With Pembrolizumab (MK-4280A) in Participants With Selected Solid Tumors (MK-4280A-010) |
| NCT06395090 | PHASE1/PHASE2 | WITHDRAWN | A Study of Pembrolizumab in Combination With Investigational Agents in Pediatric and Young Adult Participants With Hematologic Malignancies or Solid Tumors (MK-9999-01B/LIGHTBEAM-U01) |
| NCT02720068 | PHASE1 | COMPLETED | Study of Favezelimab (MK-4280) as Monotherapy and in Combination With Pembrolizumab (MK-3475) With or Without Chemotherapy or Lenvatinib (MK-7902) AND Favezelimab/Pembrolizumab (MK-4280A) as Monotherapy in Adults With Advanced Solid Tumors (MK-4280-001) |
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).
Related Atlas pages
- Diseases: Hodgkins lymphoma, colorectal neoplasm