Drug intelligence / Profile preview

mk-4830

Development stage
Phase 2
Lead developer
Merck
Modality
Recombinant Proteins and Enzymes, Immune Checkpoint Inhibitors → Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

MK-4830 is a fully human monoclonal antibody that targets the inhibitory immune checkpoint receptor immunoglobulin-like transcript 4 (ILT4, also known as LILRB2), which is primarily expressed on myeloid cells such as monocytes, macrophages, dendritic cells, and granulocytes. By binding to ILT4, MK-4830 blocks its interaction with ligands and prevents ILT4-mediated signaling. This action abrogates the immunosuppressive activities of ILT4 in the tumor microenvironment, reprograms tumor-associated macrophages to relieve myelosuppression, enhances T cell activity and cytotoxic T lymphocyte-mediated anti-tumor responses, and stimulates pro-inflammatory cytokine production. The drug is being developed for use in various advanced solid tumors both as monotherapy and in combination with pembrolizumab (KEYTRUDA). It has reached Phase II clinical trials for ovarian cancer and has been studied or discontinued in several other cancers including head and neck cancer, soft tissue sarcoma, colorectal cancer, malignant melanoma, non-small cell lung cancer (NSCLC), esophageal cancer, renal cell carcinoma (RCC), small cell lung cancer (SCLC), solid tumors generally; it is also under investigation for pancreatic adenocarcinoma, glioblastoma multiforme (GBM), gastric/gastroesophageal junction adenocarcinoma, triple-negative breast cancer (TNBC), mesothelioma.

Other names
anti-ILT4 monoclonal antibody MK-4830anti-ILT-4 monoclonal antibody MK-4830anti-ILT 4 monoclonal antibody MK-4830anti-immunoglobulin-like transcript 4 monoclonal antibody
02

Targets

LILRB2 (Leukocyte immunoglobulin-like receptor subfamily B member 2)

Beyond the preview

Go deeper on mk-4830.

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Clinical trials

Full profile access

Follow clinical development from study design and recruitment through results.

  • Trial phase
  • Status
  • Readouts

Indications & development

Full profile access

Explore development by indication, patient population, and geography.

  • Indications
  • Development status
  • Countries

Licensing & deals

Full profile access

Trace asset ownership, licensing agreements, and commercial partnerships.

  • Partners
  • Deal terms
  • Milestones

Patents & exclusivity

Full profile access

Explore the patent landscape and regulatory exclusivity around an asset.

  • Patents
  • Expiration dates
  • Exclusivity

Competitive landscape

Full profile access

Compare development programs by target, modality, and indication.

  • Competing assets
  • Targets
  • Development stage

Research & analysis

Full profile access

Connect source evidence and development news to your research questions.

  • Publications
  • News
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on mk-4830.

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call