16 Mar 2022 , 12:40 PM
This trial shall be carried on at NIAID’s Phase I clinical trial units in the USA. The investigational new drug (IND) application for drug study will also be sponsored by NIAID. Wockhardt’s product also received a qualified infectious disease product (QIDP) designation to WCK 6777, which signifies its ability to meet the unmet medical need and facilitates a faster approval process.
Dr. Habil Khorakiwala, Founder and Executive Chairman of the Wockhardt group commented, ”We are grateful that NIH, USA is supporting our phase 1 clinical trial of WCK 6777, which is expected to offer a much needed out-patient-parenteral antimicrobial therapy for MDR infections in ambulatory settings.”
WCK 6777 combines zidebactam and ertapenem and, zidebactam has also been combined with cefepime, the combination designated as WCK 5222. Once-a-day therapeutic profile of WCK 6777 is expected to cut hospital admissions, facilitate early patient discharge, and thus aims to introduce patient-centered care for MDR infections.
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