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MicuRx Announces the Successful Completion of Phase 1 Clinical Trial of MRX-5 in Australia

MicuRx Announces the Successful Completion of Phase 1 Clinical Trial of MRX-5 in Australia

MicuRx宣佈MRX-5在澳洲完成了第1階段臨床試驗。
PR Newswire ·  10/25 19:29

SHANGHAI, Oct. 25, 2024 /PRNewswire/ -- Recently, Shanghai MicuRx Pharmaceutical Co., Ltd. ("MicuRx", 688373.SH) announced the successful completion of Phase I clinical trial of MRX-5 in Australia, a self-developed oral antibacterial agent in development for the treatment of nontuberculous mycobacterial (NTM) infections.

2024年10月25日上海 / 全球貨幣新聞社報道:最近,上海米諾藥業股份有限公司("米諾",688373.SH)宣佈了在澳大利亞完成了MRX-5口服抗菌藥物的I期臨床試驗。該藥物是自主研發的口服抗菌藥,旨在治療非結核分枝桿菌(NTM)感染。

Details and Results of the Phase I Clinical Trial in Australia

澳大利亞I期臨床試驗的詳細信息和結果

This trial represents the first time MRX-5 was administered to humans in a Phase I clinical trial, conducted at the Nucleus Network Research Center in Australia. This trial evaluated the safety, tolerability, PK and food effect of orally administered MRX-5 at single and multiple oral doses.

這次試驗是MRX-5首次在人體進行I期臨床試驗,由澳大利亞Nucleus Network研究中心進行。此次試驗評估了單次和多次口服MRX-5的安全性、耐受性、藥代動力學和飲食影響。

The results of the phase 1 study indicate that MRX-5 was generally well tolerated among the healthy adult subjects participating in this study. There were no serious adverse events reported and all participants completed the trial, and there were no drug-related adverse events rated CTCAE Grade 3 or higher. The majority of TEAEs were CTCAE Grade 1(mild), and resolved without intervention.

第1期研究結果表明,MRX-5在參與該研究的健康成年受試者中普遍耐受良好。未報告任何嚴重不良事件,所有參與者完成了試驗,也未報告與藥物有關的CTCAE 3級或更高級別的不良事件。大部分TEAEs爲CTCAE 1級(輕度),並且無需干預即可解決。

Pharmacokinetic analysis showed that MRX-6038, the active metabolite of MRX-5, exhibited linear and predictable pharmacokinetic profile after single oral doses ranging from 50mg~1200mg. Food intake did not significantly affect its absorption.

藥代動力學分析顯示,MRX-5的活性代謝物MRX-6038在單劑50mg~1200mg口服後表現出線性和可預測的藥代動力學特徵。飲食攝入對其吸收沒有顯著影響。

Impact of the Study and Future Plans

研究的影響和未來計劃

The Phase 1 data supports the further development of MRX-5 ,and boosts confidence in the future application of MRX-5 in treating NTM infections.

I期數據支持進一步發展MRX-5,並增強MRX-5在治療NTM感染中的信心。

Currently, NTM infections are increasing globally with relatively few new drug developments targeting this area. MRX-5, specifically developed for treatment of NTM pulmonary disease, has the potential advantages of high specificity, oral bioavailability, low resistance rates, and a favorable safety profile. Moving forward, the company plans to explore an all-oral treatment strategy incorporating MRX-5, with the goal of providing patients with safer and more effective options for treating NTM infections.

目前,全球NTM感染在增加,針對該領域的新藥物研發相對較少。MRX-5專門爲治療NTM肺部疾病而開發,具有高特異性、口服生物利用度高、抗藥率低和良好的安全性等優勢。未來,公司計劃探索以MRX-5爲中心的全口服治療策略,目標是爲患者提供更安全更有效的NTM感染治療選擇。

About MRX-5

關於MRX-5

MRX-5 is a novel benzoxazole antibiotic developed for the treatment of mycobacteria infections, particularly infections caused by non-tuberculous Mycobacteria (NTM).

MRX-5是一種新型苯並咪唑類抗生素,專門用於治療分枝桿菌感染,特別是由非結核分枝桿菌(NTM)引起的感染。

There are many species of NTM, and the incidence and prevalence of NTM diseases are increasing. MRX-5 has shown potent antibacterial activity against NTM pathogens in animal studies and this human trial, along with favorable safety and pharmacokinetic profiles. Additionally, MRX -5 features minimal interactions, low resistance potential, and high oral bioavailability, making it suitable for long-term use in treating chronic infections.

NTM及其市場需求 對於NTM病原菌的動物研究以及這項人體試驗顯示,MRX-5對NTM病原體表現出強效的抗菌活性,同時具有良好的安全性和藥代動力學特徵。此外,MRX-5具有很少的相互作用、低抗藥性潛力和高口服生物利用度的特點,使其適合長期用於治療慢性感染。

NTM and Its Market Demand

NTM及其市場需求

NTM refer to a group of mycobacteria other than the Mycobacterium tuberculosis complex and Mycobacterium leprae. To date, over 190 species and 14 subspecies of NTM have been identified. Among them, the most common pathogenic NTM include the Mycobacterium avium complex and Mycobacterium abscessus complex.

NTM指的是除分枝桿菌結核分枝桿菌複合體和麻風分枝桿菌之外的一組分枝桿菌。到目前爲止,已經確認了超過190種NTM物種和14個亞種。其中,最常見的致病性NTM包括分枝桿菌亞目複合體和分枝桿菌膿腫複合體。

In recent years, the incidence of NTM infections has been increasing, posing a significant public health threat.[1] NTM infections in humans can lead to lesions in related tissues and organs, with NTM lung disease being the most common manifestation. Currently, the treatment of NTM infections mainly relies on multidrug combination therapy with antibiotics. However, treatment courses are long, and traditional drugs often face challenges such as drug resistance, poor efficacy, and numerous adverse effects.

近年來,NTM感染的發病率不斷增加,構成了重要的公共衛生威脅。人類的NTM感染可能導致相關組織和器官的損傷,其中NTM肺部疾病是最常見的表現。目前,NTM感染的治療主要依賴於抗生素的多藥聯合療法。然而,治療過程漫長,傳統藥物常常面臨抗藥性、療效不佳以及許多副作用等挑戰。

About Shanghai MicuRx Pharmaceutical Co., Ltd.

關於上海微高藥業有限公司

MicuRx is a biopharmaceutical company focusing on novel therapeutics for infectious diseases. With global independent intellectual property and competitiveness, we are committed to the discovery, development, and commercialization of innovative drugs for unmet medical needs. Since the company was founded in 2007, MicuRx has adhered to the principle of " Better Therapy Through Superior Medicine", focusing on the increasingly serious problem of global antimicrobial resistance.

MicuRx是一家專注於感染症新型治療藥物的生物製藥公司。憑藉全球獨立的知識產權和競爭力,我們致力於發現、開發和商業化滿足醫療需求的創新藥物。自2007年成立以來,MicuRx一直秉持「通過卓越醫學實現更好的治療」原則,專注於全球抗菌耐藥問題日益嚴重的挑戰。

For more information, please visit our website at

欲了解更多信息,請訪問我們的網站:

Reference:

[1] Chinese Medical Association Tuberculosis Branch. Diagnosis and Treatment Guidelines for Non-tuberculous Mycobacterial Diseases (2020 Edition) [J]. Chinese Journal of Tuberculosis and Respiratory Diseases, 2020, 43(11): 918-946. DOI: 10.3760/cma.j.cn112147-20200508-00570.

參考資料:

[1] 中國醫學會結核病學分會。《非結核分枝桿菌病診療指南(2020年版)》[J]。《中華結核和呼吸雜誌》, 2020, 43(11): 918-946。DOI: 10.3760/cma.j.cn112147-20200508-00570。

SOURCE MicuRx Pharmaceuticals

來源MicuRx藥品

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