Edding Genor Group Doses First Patient in Phase II Trial of EDP167 for HoFH

Reuters

Feb 09

Edding Genor Group Doses First Patient in Phase II Trial of EDP167 for HoFH

Edding Genor Group Holdings Limited has announced the completion of the first subject dosing in a Phase II clinical trial of its innovative small nucleic acid drug, EDP167. The Phase II trial is a multicenter, dose-finding, and open-label study evaluating the efficacy and safety of EDP167 in adult patients with Homozygous Familial Hypercholesterolemia (HoFH). The primary endpoint is the change in low-density lipoprotein cholesterol (LDL-C) levels relative to baseline after 24 weeks of treatment. Previous Phase I studies in healthy subjects and individuals with mild dyslipidemia indicated that EDP167 demonstrated a favorable safety and tolerability profile. The results of these studies are scheduled to be disclosed at a medical conference in 2026.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Edding Genor Group Holdings Ltd. published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20260209-12018764), on February 09, 2026, and is solely responsible for the information contained therein.

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