Overview

NCI Definition [1]:
An orally available, small molecule inhibitor of the immunosuppressive ligand, programmed cell death-1 ligand 1 (PD-L1; cluster of differentiation 274; CD274) with potential immune checkpoint inhibitory and antineoplastic activities. Upon administration, PD-L1 inhibitor INCB086550 specifically targets PD-L1 expressed on tumor cells preventing the binding and subsequent activation of its receptor, programmed cell death 1 (PD-1; PDCD1; CD279; programmed death-1). This reverses T-cell inactivation caused by PD-L1/PD-1 signaling, increases T-cell expansion and enhances the cytotoxic T-lymphocyte (CTL)-mediated anti-tumor immune response against PD-L1-expressing tumor cells. PD-L1, a transmembrane protein expressed on activated T-cells, is overexpressed in some cancer types and plays a significant role in immune evasion by tumor cells.

Incb086550 has been investigated in 2 clinical trials, of which 2 are open and 0 are closed. Of the trials investigating incb086550, 2 are phase 1 (2 open).

CDKN2A Overexpression, Deficient DNA Mismatch Repair (dMMR), and HPV Positive are the most frequent biomarker inclusion criteria for incb086550 clinical trials.

Malignant solid tumor is the most common disease being investigated in incb086550 clinical trials [2].

Top Biomarker Inclusion Criteria for Open Clinical Trials Investigating Incb086550
This graph displays the 20 most frequently occurring biomarkers curated on clinical trials investigating incb086550 and the cancer types associated with these biomarkers. These numbers are derived from a set of 5,956 clinical trials for which biomarker status defines treatment.

Drug Details

Synonyms [2]:
incb86550, incb-86550, incb-086550, incb 86550, incb 086550, pd-1 ligand 1 inhibitor incb086550, pd-l1 inhibitor incb086550
Drug Categories [2]:
Immunotherapies
Drug Target(s) [2]:
CD274
NCIT ID [1]:
C158532

References

1. National Cancer Institute. NCI Thesaurus Version 18.11d. https://ncit.nci.nih.gov/ncitbrowser/. [2018-07-30] [2018-08-02].

2. All assertions and clinical trial landscape data are curated from primary sources. You can read more about the curation process here.