Drug Search Results
More Filters [+]

MK-4830

Alternative Names: mk-4830, mk 4830, mk4830, mk-4830a, mk 4830a, mk4830a
Latest Update: 2024-12-17
Latest Update Note: Clinical Trial Update

Product Description

A human monoclonal antibody directed against the inhibitory immune checkpoint receptor immunoglobulin-like transcript 4 (ILT4; leukocyte immunoglobulin-like receptor subfamily B member 2; LILRB2; lymphocyte immunoglobulin-like receptor 2; LIR2; monocyte/macrophage immunoglobulin-like receptor 10; MIR-10; CD85d), with potential immunomodulating and antineoplastic activities. Upon administration, anti-ILT4 monoclonal antibody MK-4830 targets and binds to ILT4. This prevents the binding of ILT4 ligands to their receptor and prevents ILT4-mediated signaling. This abrogates the immunosuppressive activities of ILT4 in the tumor microenvironment (TME), activates the expression of pro-inflammatory cytokines, including GM-CSF and tumor necrosis factor alpha (TNFalpha), and enhances a cytotoxic T-lymphocyte (CTL)-mediated anti-tumor immune response. ILT4, plays a key role in tumor immune evasion. ILT4, a transmembrane protein and inhibitory member of the immunoglobulin-like transcript (ILT) family of proteins, is expressed primarily by myeloid cells, including monocytes, macrophages, dendritic cells (DCs) and granulocytes, and certain tumor cells. (Sourced from: https://www.cancer.gov/publications/dictionaries/cancer-drug/def/anti-ilt4-monoclonal-antibody-mk-4830)

Mechanisms of Action: ILT4 Inhibitor

Novel Mechanism: Yes

Modality: Antibody

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Merck
Company Location: KENILWORTH NJ 07033
Company CEO: Robert M. Davis
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for MK-4830

Countries in Clinic: Australia, Belgium, Canada, Chile, China, France, Greece, Israel, Italy, Japan, Korea, Poland, Singapore, South Africa, South Korea, Spain, Taiwan, United States, Unknown Location

Active Clinical Trial Count: 5

Highest Development Phases

Phase 2: Ovarian Cancer

Phase 1: Oncology Solid Tumor Unspecified

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

MK-4830-001

P1

Active, not recruiting

Oncology Solid Tumor Unspecified

2025-09-28

Genomic and immune markers of response in ILT4- and pembrolizumab-treated ovarian cancer

P2

Active, not recruiting

Ovarian Cancer

2024-08-21

MK-4830-002

P2

Completed

Ovarian Cancer

2023-12-20

jRCT2031210025

P1

Completed

Oncology Solid Tumor Unspecified

2022-08-04

Recent News Events