FDA Grants Orphan Drug Designation to MicuRx's MRX-5 for NTM Infections
Shanghai MicuRx Pharmaceutical Co., Ltd. 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.
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 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.
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.
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.
Optimize Your trial insights with Clival Database.
Are you exhausted from the uncertainty of trial insights pricing? Clival Database ensures the clarity in the midst of the global scenario for clinical trials to you.Clival Database is one of the best databases that offers an outstanding number of clinical trial data in terms of 50,000+ molecules and from primary regulatory markets as well as new entrants like Indian and Chinese markets.
With Clival, you get accurate positioning of historical sales data, patent database, company profiling, safety & efficacy, and prediction of launch of new innovative molecules helping you to align your research and driving down the cost.
To add value, we further break down our analytics for you so that improving your operational effectiveness; optimizing your clinical trials; and offering you accurate and high-quality data at lowest possible prices becomes possible.
Elevate your trial success rate with the cutting-edge insights from Clival database.
Check it out today and make more informed sourcing decisions! Learn More!