Condition: Hospital-acquired Bacterial Pneumonia and Ventilator-associated Bacterial Pneumonia · Sponsor: Qilu Pharmaceutical Co., Ltd.
This study is to evaluate the efficacy and safety of Meropenem and Pralurbactam for Injection in Subjects with HABP/VABP. The primary objective is to demonstrate non-inferiority of Meropenem and Pralurbactam to Ceftazidime and Avibactam Sodium for Injection. This study is a randomized, double-blind, active-controlled study. The total duration of the study will be approximately 32 days including screening and follow-up.
This description comes directly from the study's public registry record.
Bin Cao, PhD · 010 8420 6266 · caobin_ben@163.com
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| Hunan University Of Medicine General Hospital | Huaihua, Hunan, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07327619