The trial will test the safety and efficacy of the company's lead therapeutic candidate Latiglutenase for the protection of intestinal health and the reduction of symptoms in the presence of a six week gluten challenge treatment period.
Key endpoints include intestinal health measured by villous height to crypt depth ratio (Vh: Cd) from a biopsy at the beginning and end of the treatment period, symptom response utilising a daily diary measuring the severity of 6 gluten-induced symptoms, and intestinal health as measured by the diagnostic method CypCel, which uses simvastatin as a biomarker for villous degradation.
Urine samples will also be collected periodically to measure gluten content for the placebo vs. latiglutenase arms during the gluten challenge period.
This work builds off of positive results reported for Latiglutenase (Syage et al. Dig. Dis. and Sci. 2017) and for CypCel (Moron, Am J Gastroenterol 2013).
The Co-Principle Investigators on the project are Joseph A. Murray MD of the Mayo Clinic and Jack A. Syage PhD of ImmunogenX.
These investigators have worked together on a previous trial that focused on the CypCel diagnostic for disease management.
ImmunogenX (a subsidiary of Immunogenics LLC) is a clinical-stage biotherapeutics company founded in 2013 and is supported by a team of world-renowned clinicians, scientists and advisors in celiac disease research.
The company is developing Latiglutenase for celiac disease therapy.
ImmunogenX is also developing a minimally-invasive diagnostic tool for celiac disease management (CypCel) based on a clinically relevant metabolic marker compound that can assess the state of recovery of a celiac patient adhering to a gluten-free diet or other treatment.
For food safety, ImmunogenX is pioneering advanced mass spectrometry methods to identify and measure physiologically relevant gluten peptide sequences found in wheat, barley, and rye.
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