Lipocine Announces The Publication And Discussion Of A Manuscript "Oral LPCN 1148 Improves Sarcopenia And Hepatic Encephalopathy In Male Patients With Cirrhosis: A Randomized, Placebo-controlled Phase 2 Trial" In The Journal Hepatology And Discussion...
Lipocine Announces The Publication And Discussion Of A Manuscript "Oral LPCN 1148 Improves Sarcopenia And Hepatic Encephalopathy In Male Patients With Cirrhosis: A Randomized, Placebo-controlled Phase 2 Trial" In The Journal Hepatology And Discussion...
Lipocine Announces The Publication And Discussion Of A Manuscript "Oral LPCN 1148 Improves Sarcopenia And Hepatic Encephalopathy In Male Patients With Cirrhosis: A Randomized, Placebo-controlled Phase 2 Trial" In The Journal Hepatology And Discussion At The Liver Meeting 2024 Editor's Cut
Lipocine宣佈在肝病學雜誌上發表並討論了一份手稿"口服LPCN 1148改善男性肝硬化患者的肌少症和肝性腦病:一項隨機、安慰劑對照的2期試驗",並在2024年肝臟會議上進行了討論。
Lipocine Inc. (NASDAQ:LPCN), a biopharmaceutical company leveraging its proprietary technology platform to augment therapeutics through effective oral delivery, today announced the publication and discussion of a manuscript "Oral LPCN 1148 Improves Sarcopenia and Hepatic Encephalopathy in Male Patients with Cirrhosis: a randomized, placebo-controlled Phase 2 trial" in the journal Hepatology and discussion at The Liver Meeting (AASLD) 2024 Editor's Cut: Clinical Study Session held on November 16, 2024. LPCN 1148 is targeted to be a "First in Class" product candidate with a novel mechanism of action for overt hepatic encephalopathy and sarcopenia indications. A copy of the publication can be accessed here.
Lipocine公司(納斯達克:LPCN)是一家生物製藥公司,利用其專有技術平台通過有效的口服途徑增強治療效果,今天宣佈了一份手稿"口服LPCN 1148改善男性肝硬化患者的肌少症和肝性腦病:一項隨機、安慰劑對照的2期試驗"在肝病學雜誌上發表並進行討論,以及在2024年肝臟會議(AASLD)上的討論。2024年11月16日舉行了臨床研究會話。LPCN 1148旨在成爲一種具有新型作用機制的「首創性」產品候選藥物,用於治療明顯肝性腦病和肌少症症狀。可在此處獲取該項研究成果的副本。
The publication features the results from a Phase 2 proof-of-concept clinical trial (LPCN 1148-21-001) that evaluated LPCN 1148 in men with cirrhosis and sarcopenia awaiting liver transplantation. The trial was conducted in two stages. Stage 1 was double blind, placebo-controlled with participants randomized 1:1, to receive either oral LPCN 1148 or placebo. This was followed by Stage 2, a 28-week single-arm open label extension. The publication reports the analyses from the Stage 1 readout.
該出版物展示了一項II期概念驗證臨床試驗(LPCN 1148-21-001)的結果,該試驗評估了LPCN 1148在等待肝臟移植的肝硬化和肌肉減少症男性中的效果。試驗分爲兩個階段進行。第一階段爲雙盲、安慰劑對照,參與者按1:1隨機分配,接受口服LPCN 1148或安慰劑。隨後進入第二階段,進行爲期28周的單臂開放標籤擴展。該出版物報告了第一階段的分析結果。
The results at 24 weeks showed that LPCN 1148 therapy resulted in a significant improvement in sarcopenia when compared with placebo. Furthermore, despite most participants already on background therapies for HE, participants receiving LPCN 1148 also experienced significantly fewer episodes of overt hepatic encephalopathy (OHE) compared to those on placebo. Additional beneficial effects of LPCN 1148, including improved muscle quality, hemoglobin, and patient reported symptom improvement are also covered in the manuscript.
24周的結果顯示,與安慰劑相比,LPCN 1148治療在肌肉減少症方面顯著改善。此外,儘管大多數參與者已在進行肝性腦病的基礎治療,接受LPCN 1148的參與者經歷了明顯較少的明顯肝性腦病(OHE)事件,相比之下,安慰劑組的參與者則更多。手稿中還涉及了LPCN 1148的其他有益效果,包括改善肌肉質量、血紅蛋白和患者自報的症狀改善。
The publication was discussed at The Liver Meeting during 'The Editors Cut: Clinical Studies' session. This session critically discusses the most notable, influential, cutting edge, game changing clinical research papers published during the past year.
該出版物在肝病會議的「編輯選擇:臨床研究」會議上進行討論。該會議對過去一年發表的最重要、最有影響力、最尖端和具有變革性的臨床研究論文進行了嚴格討論。