Related Experiment Video
Updated: Feb 16, 2026

Implementation of In Vitro Drug Resistance Assays: Maximizing the Potential for Uncovering Clinically Relevant Resistance Mechanisms
Published on: December 9, 2015
Discovery of IDO1 Inhibitors: From Bench to Bedside
George C Prendergast1, William P Malachowski2, James B DuHadaway3
1Lankenau Institute for Medical Research (LIMR), Wynnewood, Pennsylvania. prendergast@limr.org.
Abstract:
Small-molecule inhibitors of indoleamine 2,3-dioxygenase-1 (IDO1) are emerging at the vanguard of experimental agents in oncology. Here, pioneers of this new drug class provide a bench-to-bedside review on preclinical validation of IDO1 as a cancer therapeutic target and on the discovery and development of a set of mechanistically distinct compounds, indoximod, epacadostat, and navoximod, that were first to be evaluated as IDO inhibitors in clinical trials. As immunometabolic adjuvants to widen therapeutic windows, IDO inhibitors may leverage not only immuno-oncology modalities but also chemotherapy and radiotherapy as standards of care in the oncology clinic. Cancer Res; 77(24); 6795-811. ©2017 AACR.
Insights
Small-molecule inhibitors targeting indoleamine 2,3-dioxygenase-1 (IDO1) show promise in oncology. These IDO1 inhibitors, including indoximod, epacadostat, and navoximod, are being explored to enhance cancer immunotherapies.
Area of Science:
- Oncology
- Immunology
- Pharmacology
Background:
- Indoleamine 2,3-dioxygenase-1 (IDO1) is an enzyme implicated in cancer immune evasion.
- Targeting IDO1 is a novel strategy in cancer treatment.
- Small-molecule IDO1 inhibitors represent a new class of experimental cancer agents.
Related Concept Videos
Drug Discovery: Overview
Inhibition of Cdk Activity
Pharmacogenomics: Identification of New Drug Targets
Dipeptidyl Peptidase 4 Inhibitors

