Gan & Lee Pharmaceuticals Announced Positive Phase 1 Results for Its Oral GLP-1 Receptor Agonist GZR18 Tablet in Healthy Participants, Demonstrating 4.16% Weight Reduction in Two Weeks
Gan & Lee Pharmaceuticals Announced Positive Phase 1 Results for Its Oral GLP-1 Receptor Agonist GZR18 Tablet in Healthy Participants, Demonstrating 4.16% Weight Reduction in Two Weeks
- After two weeks of treatment, GZR18 tablets resulted in an average weight reduction of up to 4.16%, with continued weight loss observed even after discontinuation.
- The pharmacokinetic profile supports a once-daily oral dosing regimen for GZR18 tablets.
- The safety and tolerability of GZR18 tablets align with the known safety characteristics of GLP-1 receptor agonists, with no unexpected safety signals during the study.
- 經過兩週的治療,GZR18片劑導致體重平均減輕高達4.16%,甚至在停藥後仍持續觀察到體重減輕。
- 藥代動力學特徵支持GZR18片劑的一天一次口服給藥方案。
- GZR18片劑的安全性和耐受性與GLP-1受體激動劑已知的安全特性一致,在研究過程中未觀察到任何意外的安全信號。
BEIJING, Nov. 12, 2024 /PRNewswire/ -- Gan & Lee Pharmaceuticals (Gan & Lee, Shanghai Stock Exchange: 603087) announced the positive topline results of a Phase 1 clinical trial its oral glucagon-like peptide-1 receptor agonist (GLP-1 RA) GZR18 tablets in healthy participants in China.
2024年11月12日,北京 / PRNewswire / -- 甘研製藥(甘研製藥,上海證券交易所:603087)宣佈了其口服胰高血糖素樣肽-1受體激動劑(GLP-1 RA)GZR18片劑在中國健康受試者中進行的一項Phase 1臨床試驗的積極頭等結果。
Statement:
聲明:
- GZR18 tablet is an ivestigational drug and has not yet been approved in China.
- Gan & Lee Pharmaceuticals does not recommend the use of any unapproved drugs/indications.
- GZR18片劑是一種正在研究的藥物,尚未在中國獲得批准。
- 甘研製藥不建議使用任何未經批准的藥物/適應症。
The Phase 1 clinical trial (CTR20240663) was a randomized, open-label, first-in-human study involving 92 participants, designed to assess the bioavailability, pharmacokinetics (PK), pharmacodynamics (PD), safety, and tolerability of GZR18 tablets in healthy adult participants. The study also evaluated the effect of meal timing on the drug's PK, PD, safety, and tolerability.
第1期臨床試驗(CTR20240663)是一項隨機、開放、首次在人體內的研究,共涉及92名受試者,旨在評估成人健康受試者中GZR18片劑的生物利用度、藥代動力學(PK)、藥效學(PD)、安全性和耐受性。該研究還評估了進餐時間對藥物的PK、PD、安全性和耐受性的影響。
In this study, GZR18 tablets were safe and well-tolerated, with the most common adverse events being gastrointestinal reactions, consistent with the established safety profile of GLP-1 based therapies. PK data indicated favorable absorption, supporting a once-daily oral regimen. Both single and multiple doses showed a dose-response relationship in terms of PK and PD parameters. Participants treated with the target dose of 60 mg daily for two weeks exhibited an average weight reduction of 4.16% from baseline. Furthermore, a week after stopping treatment, subjects continued to lose weight 0.51%, reaching an average total reduction of 4.67% compared to baseline. At 21 days after discontinuation, neither the participants' body weight nor BMI had returned to baseline values.
在這項研究中,GZR18片劑安全耐受性良好,最常見的不良事件是胃腸反應,與基於GLP-1的治療的已建立的安全性概況一致。藥代數據表明有利的吸收,支持一天一次口服方案。單一和多次劑量均顯示藥代和藥效參數存在劑量-反應關係。接受每天60毫克目標劑量治療兩週的參與者,體重平均從基線減少4.16%。此外,停止治療一週後,受試者體重持續減輕0.51%,與基線相比,平均減少4.67%。在停藥後21天,參與者的體重和BMI均未恢復到基線水平。
About GZR18 Tablets
關於GZR18片劑
GZR18 tablet is an investigational, once-daily oral GLP-1 receptor agonist developed by Gan & Lee Pharmaceuticals. It utilizes a small molecule absorption enhancer, SNAC (N-[8-(2-hydroxybenzoyl)amino] caprylate), to facilitate drug absorption in the stomach by resisting pepsin degradation, thus prolonging the drug's half-life and enhancing its bioavailability. GZR18 tablets are currently in global Phase 1 clinical development.
GZR18片劑是由迦南利製藥開發的一種調查中的一天一次口服GLP-1受體激動劑。它利用小分子吸收增強劑SNAC(N-[8-(2-羥基苯甲酰)氨基]癸酸酯)在胃中促進藥物吸收,抵抗胃蛋白酶降解,從而延長藥物的半衰期,提高生物利用度。目前GZR18片劑正處於全球I期臨床開發階段。
Forward-looking statements
前瞻性聲明 本新聞稿中包括的關於未來表現和結果、預期、規劃、策略、重點、承諾和其他聲明(包括與我們社會、環境和其他可持續性目標有關的聲明)的非歷史事實的前瞻性聲明,是根據美國聯邦證券法的定義而作出的前瞻性聲明。本新聞稿中關於我們環境和其他可持續性計劃和目標的前瞻性聲明以及其他聲明並不意味着這些聲明對於投資者、我們的業務、運營結果、財務狀況、前景或策略、對我們在可持續發展事項上的影響或其他當事方來說均是重要的,或者必須披露在我們向證券交易委員會(「SEC」)或其他監管機構的備案中。此外,歷史、現有及未來涉及社會、環境和可持續性的相關聲明可能是基於仍在發展的衡量進展的標準、不斷演變的內部控制和流程以及假設,在將來可能會發生變化。前瞻性聲明基於當前的信仰、期望和假設,並受到可能導致實際結果與前瞻性聲明有實質性差異的重大風險、不確定性和情況變化的影響。
Forward-looking statements are based on our expectations and assumptions as of the date of the statements. Actual results may differ materially from those expressed in these forward-looking statements due to a variety of factors, and we can give no assurance that such results will be achieved in the future. We undertake no obligation to update or revise any forward-looking statements, whether as a result of new information, future events, or otherwise.
前瞻性聲明基於我們對聲明日期的期望和假設。由於各種因素,實際結果可能與這些前瞻性聲明中表達的不同,我們不能保證未來會實現這樣的結果。我們不承諾更新或修訂任何前瞻性聲明,無論是基於新信息、未來事件還是其他原因。
About Gan & Lee
關於贊利
Gan & Lee Pharmaceuticals developed the first Chinese domestic insulin analog. Currently, Gan & Lee has six core insulin products, including five insulin analog varieties: long-acting glargine injection (Basalin), fast-acting lispro injection (Prandilin), fast-acting aspart injection (Rapilin), mixed protamine zinc lispro injection (25R) (Prandilin25), aspart 30 injection (Rapilin30), and one human insulin injection - mixed protamine human insulin injection (30R) (Similin30). The company has two approved medical devices in China, namely reusable insulin injection pen (GanleePen), and disposable pen needle (GanleeFine).
贊利製藥研發了中國首個國產胰島素類似物。目前,贊利擁有六種核心胰島素產品,包括五種胰島素類似物品種:長效格列汀注射液(巴斯林)、快速作用林普先注射液(普蘭肽林)、快速作用阿斯巴特注射液(拉皮林)、混合蛋白鋅林普先注射液(25R)(普蘭肽林25)、阿斯巴特30注射液(拉皮林30),以及一種人用胰島素注射液-混合蛋白人胰島素注射液(30R)(盛美林30)。該公司在中國獲得了兩款批准的醫療設備,分別是可重複使用的胰島素注射筆(贊利筆)和一次性針筆頭(贊利Fine)。
In China's 2024 National Insulin-Specific Centralized Procurement, Gan & Lee Pharmaceuticals ranked first among all selected companies in terms of procurement demand for insulin analogs. The company is also making strides in international markets, with the disposable pen needle (GanleeFine) approved by the US Food and Drug Administration (FDA) in 2020 and received GMP inspection approval from the European Medicines Agency (EMA) in 2024. These achievements significantly boost Gan & Lee's competitiveness in both international and domestic markets.
2024年中國國家胰島素集中採購中,賽諾菲製藥公司在所有選定公司中的胰島素類似物採購需求中排名第一。該公司還在國際市場取得進展,其一次性針頭(賽諾菲)於2020年獲得美國食品和藥品管理局(FDA)批准,並在2024年獲得了歐洲藥品管理局(EMA)的GMP檢查批准。這些成就顯著提升了賽諾菲在國際和國內市場的競爭力。
In the future, Gan & Lee will strive for comprehensive coverage in diabetes treatment. Moving forward with its mission to become a world-class pharmaceutical company, Gan & Lee will also actively develop new chemical entities and biological drugs, focusing on treatments for metabolic diseases, cardiovascular diseases, and other therapeutic areas.
未來,贊利將致力於全面覆蓋糖尿病治療。秉承成爲世界一流製藥公司的使命,贊利還將積極開發新的化學品和生物藥物,着重治療代謝性疾病、心血管疾病和其他治療領域。
SOURCE Gan & Lee Pharmaceuticals
SOURCE 甘利製藥
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