Press release
Arcturus Therapeutics Announces Initiation of Dosing ARCT-810 in Patients with Ornithine Transcarbamylase (OTC) Deficiency
SAN DIEGO--(BUSINESS WIRE)-- Arcturus Therapeutics Holdings Inc. (the “Company”, “Arcturus”, Nasdaq: ARCT), a leading clinical-stage messenger RNA medicines
About this update from Arcturus Therapeutics Holdings Inc.
[{"type":"text","content":" SAN DIEGO--(BUSINESS WIRE)--\nArcturus Therapeutics Holdings Inc. (the “Company”, “Arcturus”, Nasdaq: ARCT), a leading clinical-stage messenger RNA medicines company focused on the development of infectious disease vaccines and significant opportunities within liver and respiratory rare diseases, today announced that it has initiated dosing in its Phase 1b study of ARCT-810 in patients with Ornithine Transcarbamylase (OTC) deficiency, a serious disease with limited treatment options, at a clinical site in the United States. ARCT-810 is Arcturus’ flagship rare disease asset utilizing the Company’s novel systemically administered mRNA therapeutic platform.\n\nThe ongoing Phase 1b study will evaluate approximately twelve patients with OTC deficiency. ARCT-810 will be administered at doses between 0.2 mg/kg and 0.4 mg/kg, and all dose levels are expected to be within the therapeutic range, based on preclinical study data. The Phase 1b study will assess safety, tolerability and pharmacokinetics, as well as various exploratory biomarkers of drug activity.\n\nArcturus previously announced that it had completed the ARCT-810 Phase 1, dose escalation study in healthy subjects, at doses up to 0.4 mg/kg. In that study, ARCT-810 was found to be generally safe and well tolerated; no severe adverse events were observed, and no steroid pretreatment was required. The pharmacokinetic profile of ARCT-810 was favorable, and preliminary data shows that no ARCT-810 lipid was detectable in the plasma beyond 48 hours following drug administration.\n\n“We are so encouraged by the progress of the ARCT-810 study in OTC deficiency and the promise this novel mRNA therapeutic approach holds for saving and improving the lives of patients affected with this devastating disorder,” said Cynthia Le Mons, Executive Director of National Urea Cycle Disorders Foundation.\n\n“The initiation of dosing in the ARCT-810 Phase 1b clinical trial in patients with OTC deficiency builds upon the favorable prior Phase 1 study results, as well as encouraging preclinical data which showed that ARCT-810 resulted in robust OTC protein expression, improvements in ureagenesis and plasma ammonia, and increased survival,” said Steve Hughes, M.D., Chief Development Officer of Arcturus. “We are pleased to have now initiated dosing of ARCT-810 in patients with OTC deficiency. We look for...