Celiac disease (CeD) is an immune-mediated disorder triggered by the ingestion of gluten. Despite adhering to a gluten-free diet (the only management option available to patients with CeD), many patients continue to experience symptoms and intestinal injury. Degradation of immunogenic fractions of gluten peptides in the stomach has been proposed as an approach to reduce toxicity of ingested gluten; however, no enzymes evaluated to date have demonstrated sufficient gluten degradation in complex meals. TAK-062 is a novel, computationally designed endopeptidase under development for the treatment of patients with CeD.Pharmacokinetics, safety, and tolerability of TAK-062 100-900 mg were evaluated in a phase 1 dose escalation study in healthy participants and patients with CeD. Gluten degradation by TAK-062 was evaluated under simulated gastric conditions in vitro and in healthy participants in the phase 1 study, with and without pretreatment with a proton pump inhibitor. Residual gluten (collected via gastric aspiration in the phase 1 study) was quantified using R5 and G12 monoclonal antibody enzyme-linked immunosorbent assays.In vitro, TAK-062 degraded more than 99% gluten (3 g and 9 g) within 10 minutes. In the phase 1 study, administration of TAK-062 was well tolerated and resulted in a median gluten degradation ranging from 97% to more than 99%, in complex meals containing 1-6 g gluten, at 20-65 minutes post dose.TAK-062 is well tolerated, and rapidly and effectively degrades large amounts of gluten, supporting the development of this novel enzyme as an oral therapeutic for patients with CeD.
Ingrid Swanson Pultz, Malcolm Hill, Joanne M Vitanza, Clancey Wolf, Lasse Saaby, Tina Liu, Peter Winkle, Daniel A Leffler