FDA Grants Orphan Drug Designation to MicuRx's MRX-5 for NTM Infections
FDA Grants Orphan Drug Designation to MicuRx's MRX-5 for NTM Infections
SHANGHAI, Jan. 1, 2025 /PRNewswire/ -- Shanghai MicuRx Pharmaceutical Co., Ltd. ("MicuRx",688373.SH) announced that MRX-5, its self-developed anti-infection drug, has been granted Orphan Drug Designation (ODD) by the U.S. Food and Drug Administration (FDA) for the treatment of non-tuberculous mycobacteria (NTM) infections. This designation marks a significant milestone for MicuRx in the field of NTM infection treatment.
上海,2025年1月1日 /PRNewswire/ -- 上海米庫瑞藥品有限公司("米庫瑞",688373.SH)宣佈其自主研發的抗感染藥物MRX-5已獲得美國食品和藥物管理局(FDA)授予的孤兒藥資格(ODD),用於治療非結核分枝桿菌(NTM)感染。這一認證標誌着米庫瑞在NTM感染治療領域的重要里程碑。
MRX-5 is a novel benzoxazole antibiotic developed for the treatment of mycobacteria infections, particularly infections caused by non-tuberculous Mycobacteria (NTM). In recent years, NTM diseases have been increasing rapidly and have become one of the major public health threats worldwide[1]. However, current treatment options for NTM infections are limited, and traditional drugs face common challenges such as drug resistance, poor efficacy, and numerous adverse effects[1,2].
MRX-5是一種新型苯並噁唑抗生素,專爲治療分枝桿菌感染而開發,尤其是由非結核分枝桿菌(NTM)引起的感染。近年來,NTM疾病迅速增加,已成爲全球主要公共健康威脅之一[1]。然而,目前針對NTM感染的治療選擇有限,傳統藥物面臨藥物支撐位、療效差和諸多不良反應等普遍挑戰[1,2]。
MRX-5 is a new drug specifically aimed at treating drug-resistant NTM infections, demonstrating good antibacterial activity against common NTM strains. It has also shown potent antibacterial activity against NTM pathogens in both animal studies and human trial, along with favorable safety and pharmacokinetic profiles. Additionally, MRX -5 features minimal interactions, low potential for resistance, and high oral bioavailability, making it suitable for long-term use in treating chronic infections.
MRX-5是一種新藥,專門針對耐藥NTM感染,顯示出對常見NTM菌株良好的抗菌活性。它在動物研究和人類試驗中也表現出對NTM病原體的強大抗菌活性,並具有良好的安全性和藥物代謝動力學特徵。此外,MRX-5具有最小的相互作用、低耐藥潛力和高口服生物利用度,適合長期用於治療慢性感染。
The granting of ODD is not only an important milestone in the development of MRX-5, but also a recognition of research and development capabilities of MicuRx. ODD applies to drugs used to prevent, treat, or diagnose rare diseases that affect fewer than 200,000 people in the U.S., including biologics. According to the Orphan Drug Act, applicants who receive ODD are eligible for various benefits, including tax credits, waivers for certain clinical trial costs, exemption from New Drug Application (NDA)/Biologics License Application (BLA) fees, and seven years of market exclusivity after approval. This designation will help accelerate the clinical development and commercialization process of MRX-5.
獲得ODD不僅是MRX-5開發的重要里程碑,也是對米庫瑞研發能力的認可。ODD適用於用於預防、治療或診斷影響少於200,000人的稀有疾病的藥物,包括生物製品。根據孤兒藥法案,獲得ODD的申請者有資格享受各種好處,包括稅收抵免、某些臨牀試驗費用的豁免、新藥申請(NDA)/生物製品許可申請(BLA)費用的豁免,以及批准後七年的市場獨佔權。該認證將幫助加速MRX-5的臨牀開發和商業化進程。
Moving forward, MicuRx will continue to advance the clinical development and commercialization of MRX-5, actively exploring oral treatment strategies that include MRX-5, with the goal of providing safer and more effective treatment options for patients with NTM infections.
展望未來,MicuRx將繼續推進MRX-5的臨牀開發和商業化,積極探索包括MRX-5在內的口服治療策略,旨在爲NTm感染患者提供更安全有效的治療選擇。
Reference: |
[1] Chinese Thoracic Society, The Diagnosis and Treatment Guidelines for Non-tuberculous Mycobacterial Disease (2020 Edition), Chinese Journal of Tuberculosis and Respiratory Diseases, 2020, 43(11): 918-946. DOI: 10.3760/cma.j.cn112147-20200508-00570. |
[2] Zhiming Ma. Treatment of Non-Tuberculous Mycobacteria: Challenges and Prospects. |
參考: |
[1] 中國胸科學會,《非結核分枝桿菌病診斷與治療指南(2020年版)》,《中國結核與呼吸疾病雜誌》,2020,43(11):918-946。DOI:10.3760/cma.j.cn112147-20200508-00570。 |
[2] 馬志明。《非結核分枝桿菌的治療:挑戰與前景》。 |
SOURCE MicuRx Pharmaceuticals
來源:MicuRx製藥