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A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Meropenem-Vaborbactam in Children With Complicated Urinary Tract Infection, Including Acute Pyelonephritis

Active, not recruiting · Phase 2 · NCT06672978

Conditions: Acute Pyelonephritis, Complicated Urinary Tract Infection

At a glance

Research payments reported, 2025
$40,201
U.S. investigators named
5
Sites paid
1
Planned or actual enrollment
66

About the trial

Sponsor
Rempex (a wholly owned subsidiary of Melinta Therapeutics, LLC) (with Biomedical Advanced Research and Development Authority)
Tested
Meropenem-Vaborbactam (drug), Antibiotics (drug)
Dates
Started 2025-06-03; completion 2027-07
Results posted
Not yet

The primary objective of the study is to assess the safety and tolerability of meropenem-vaborbactam administered by intravenous (IV) infusion in children 3 months and above to less than 12 years with complicated urinary tract infections (cUTI), including acute pyelonephritis (AP).

From ClinicalTrials.gov, last updated 2026-09-10. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Melinta Therapeutics, LLC reported $40,201 in research payments for this study in 2025 (62 payments).

Products named: Vabomere

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.