drugset / Trial / NCT03293485

Efficacy and Safety of Imipenem+Cilastatin/Relebactam (MK-7655A) in Japanese Participants With Complicated Intra-abdominal Infection or Complicated Urinary Tract Infection (MK-7655A-017)

NCT03293485

Phase 3 Completed 83 enrolled Merck Sharp & Dohme LLC
NaSingle-groupOpen-labelTreatment

Summary

The study will evaluate the efficacy and safety of imipenem+cilastatin/relebactam (IMI/REL, MK-7655A) in Japanese participants with complicated intra-abdominal infection (cIAI) or complicated urinary tract infection (cUTI).

Timeline

Start
2017-10-04
Primary completion
2018-09-14
Completion
2018-09-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Cilastatin Small molecule 200 mg Intravenous
Subject Cilastatin Small molecule 500 mg Intravenous
Subject IMIPENEM ANHYDROUS Small molecule 200 mg Intravenous
Subject IMIPENEM ANHYDROUS Small molecule 500 mg Intravenous
Subject Relebactam Small molecule 100 mg Intravenous
Subject Relebactam Small molecule 250 mg Intravenous