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Food and Medication Administration granted Fast Monitor Designation to AR-301, the Company's fully human being anti-Staphylococcal alpha-toxin IgG1 monoclonal antibody . AR-301 happens to be in Phase 2a medical trial for the treatment of hospital-acquired and ventilator-associated pneumonia caused by Staphylococcus aureus, including multi-medication resistant ‘MRSA’ strains. Vu Truong, Ph.D., CEO and Founder of Aridis, stated, ‘This is our second item candidate to receive FDA Fast Monitor designation this year, which provides an accelerated development and regulatory review pathway. Aeruginosa, these innovative mAbs give a significant possibility to improve individual outcomes from potentially life-threatening infections caused by two of the very most common and difficult to take care of pathogens.