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来凯医药-B:LAE103的I期单剂量递增研究完成首例受试者给药
Zhi Tong Cai Jing· 2025-12-31 00:42
Core Viewpoint - The company has initiated a Phase I single ascending dose (SAD) study for LAE103, a self-developed ActRIIB monoclonal antibody, in Australia, with the first subject having completed dosing [1] Group 1: Study Details - The SAD study is a randomized, double-blind, placebo-controlled trial aimed at evaluating the safety, tolerability, pharmacokinetics, and pharmacodynamics of LAE103 administered subcutaneously in healthy overweight or obese subjects [1] - The company aims to release the top-line data from this SAD study in the third quarter of 2026 [1] Group 2: Therapeutic Focus - The company is committed to introducing this precision therapy into areas of significant unmet medical needs in cardiovascular and metabolic diseases, such as obesity, sarcopenia, and heart failure [1]
来凯医药-B(02105.HK):LAE103的I期单剂量递增研究完成首例受试者给药
Ge Long Hui· 2025-12-31 00:16
Group 1 - The company, Lai Kai Pharmaceutical-B (02105.HK), has initiated the enrollment of subjects for the Phase I single ascending dose (SAD) study of LAE103, a self-developed ActRIIB monoclonal antibody, in Australia [1] - The SAD study is a randomized, double-blind, placebo-controlled trial aimed at evaluating the safety, tolerability, pharmacokinetics, and pharmacodynamics of LAE103 (subcutaneous injection) in healthy overweight or obese subjects [1] - The company aims to announce the top-line data from this SAD study in the third quarter of 2026, focusing on introducing this precision therapy into areas with significant unmet medical needs in cardiovascular and metabolic diseases, such as obesity, sarcopenia, and heart failure [1]
来凯医药(02105) - 自愿公告LAE103的I期单剂量递增研究完成首例受试者给药
2025-12-31 00:10
香 港 交 易 及 結 算 所 有 限 公 司 及 香 港 聯 合 交 易 所 有 限 公 司 對 本 公 告 的 內 容 概 不 負 責,對其準確性或完整性亦不發表任何聲明,並明確表示,概不對因本公告全部 或任何部份內容而產生或因倚賴該等內容而引致的任何損失承擔任何責任。 (於開曼群島註冊成立之有限公司) (股份代號:2105) 來凱醫藥有限公司 Laekna, Inc. 自願公告 本 公 告 由 來 凱 醫 藥 有 限 公 司(「 本 公 司 」, 連 同 其 附 屬 公 司 統 稱「 本 集 團 」)自 願 作 出,以告知本公司股東及潛在投資者本集團最新業務進展。 – 1 – 本 公 司 董 事(「董 事」)會(「 董 事 會」)欣 然 宣 佈 , 本 集 團 已 在 澳 大 利 亞 啟 動 LAE103 ( 一種自研的Act RIIB單克隆抗體 )的I期單劑量遞增研究(「SAD研究」)的受試者入 組工作。截至本公告日,首位受試者已完成給藥。 該SAD研究為一項隨機、雙盲、安慰劑對照研究,旨在評估LAE103( 皮下注射 )在 健康的超重或肥胖症受試者中的安全性、耐受性、藥代動力學及藥效學特性。本 集團 ...