Favezelimab

drug
On 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

FieldValue
ChEMBL IDCHEMBL4297784
NameFavezelimab
TypeAntibody
Max phase3

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).

IndicationTrial phaseMONDOEFO
Hodgkins lymphoma3MONDO:0004952EFO:0000183
colorectal neoplasm3MONDO:0005335MONDO:0005575
non-small cell lung carcinoma2MONDO:0005233EFO:0003060
urothelial carcinoma2MONDO:0040679EFO:0008528
neoplasm1MONDO:0005070EFO:0000616
non-Hodgkin lymphoma1MONDO:0018908EFO:0005952
renal cell carcinoma1MONDO:0005086EFO:0000681
small cell lung carcinoma1MONDO:0008433EFO:0000702
melanoma1MONDO:0005105EFO:0000756
esophageal squamous cell carcinoma1MONDO:0005580EFO:0005922
lymphoma1MONDO:0005062EFO: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

PhaseTrials
PHASE1/PHASE26
PHASE25
PHASE33
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03486873PHASE3RECRUITINGLong-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)
NCT05064059PHASE3COMPLETEDA 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)
NCT05600309PHASE3COMPLETEDA 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
NCT04626479PHASE1/PHASE2ACTIVE_NOT_RECRUITINGSubstudy 03A: A Study of Immune and Targeted Combination Therapies in Participants With First Line (1L) Renal Cell Carcinoma (MK-3475-03A)
NCT04626518PHASE1/PHASE2ACTIVE_NOT_RECRUITINGSubstudy 03B: A Study of Immune and Targeted Combination Therapies in Participants With Second Line Plus (2L+) Renal Cell Carcinoma (MK-3475-03B/KEYMAKER-U03)
NCT04895722PHASE2ACTIVE_NOT_RECRUITINGEvaluation 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)
NCT02625961PHASE2COMPLETEDStudy 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)
NCT03516981PHASE2COMPLETEDA Study of Biomarker-Directed, Pembrolizumab (MK-3475) Based Combination Therapy for Advanced Non-Small Cell Lung Cancer (MK-3475-495/KEYNOTE-495)
NCT03598608PHASE1/PHASE2COMPLETEDStudy 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)
NCT04303169PHASE1/PHASE2COMPLETEDSubstudy 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)
NCT04305054PHASE1/PHASE2COMPLETEDSubstudy 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)
NCT05508867PHASE2COMPLETEDA 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)
NCT06036836PHASE2COMPLETEDStudy of Favezelimab Coformulated With Pembrolizumab (MK-4280A) in Participants With Selected Solid Tumors (MK-4280A-010)
NCT06395090PHASE1/PHASE2WITHDRAWNA 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)
NCT02720068PHASE1COMPLETEDStudy 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.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).