A Phase III open-label trial to evaluate efficacy and safety of CPI-613 plus modified FOLFIRINOX (mFFX) versus FOLFIRINOX (FFX) in patients with metastatic adenocarcinoma of the pancreas

Author:

Philip Philip A1,Buyse Marc E2,Alistar Angela T3,Lima Caio MSPR4,Luther Sanjeev5,Pardee Timothy S45,Cutsem Eric Van6

Affiliation:

1. Karmanos Cancer Institute, Wayne State University, Department of Oncology, Detroit, MI 48331, USA

2. International Drug Development Institute, Louvain-La-Neuve, Belgium

3. Morristown Medical Center of Atlantic Health System, Morristown, NJ 07152, USA

4. Wake Forest Baptist Comprehensive Cancer Center of Wake Forest University, Department of Oncology, Winston Salem, NC 27157, USA

5. Rafael Pharmaceuticals, Cranbury, NJ 08512, USA

6. University Hospitals & KU Leuven, Department of Digestive Oncology, Leuven, Belgium

Abstract

Devimistat (CPI-613®) is a novel lipoate analog that inhibits the tricarboxcylic acid cycle at two key carbon entry points. Through its inhibition of pyruvate dehydrogenase and a-ketoglutarate dehydrogenase complexes, devimistat inhibits the entry of glucose and glutamine derived carbons, respectively. Pancreatic cancer is dependent on mitochondrial function for enhanced survival and aggressiveness. In a Phase I study of modified FOLFIRINOX, in combination with devimistat for metastatic pancreatic cancer patients, there was a 61% objective response rate including a 17% complete response rate. This report outlines the rationale and design of the AVENGER 500 study, a Phase III clinical trial of devimistat in combination with modified FOLFIRINOX compared with FOLFIRINOX alone for patients with previously untreated metastatic adenocarcinoma of the pancreas. Clinical trial registration: NCT03504423

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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