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NCT01381549 · ClinicalTrials.gov registry record · Phase 2

GSK2251052 in Complicated Urinary Tract Infection

A Phase 2 study, sponsored by GlaxoSmithKline.

Terminated
Registry status
Phase 2
Development phase
20
Enrollment target

NCT01381549: Clinical Trial Phase 2 study, sponsored by GlaxoSmithKline.

NCT01381549 is a Phase 2 study that was terminated before completion, run by GlaxoSmithKline. The registered enrollment target is 20 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01381549, a Phase 2 study, was terminated before completion, sponsored by GlaxoSmithKline.

TERMINATED
Registry status
Phase 2
Development phase
20 participants
Enrollment target

Study Summary

This study is being conducted to evaluate the safety, efficacy (clinical and microbiological), pharmacokinetics/pharmacodynamics of GSK2251052 and to assess whether it would be a suitable antibiotic for the treatment for febrile lower cUTI and pyelonephritis(complicated and uncomplicated). GSK2251052 will be compared to imipenem-cilastatin, which is an antibiotic commonly used to treat serious cUTI infections. GSK2251052 has a spectrum of microbiological activity that includes pathogens responsible for cUTI.

Primary Outcome

Clinical laboratory parameters included albumin and total protein. Baseline was Day 1. Change from Baseline was calculated by subtracting Baseline values from individual post-Baseline values. Mean change from Baseline up to Late follow-up visit in albumin and total protein are presented.

Interventions

  • OTHER Placebo
  • DRUG GSK2251052
  • DRUG imipenem-cilastatin

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2011-06-28
Est. Completion 2012-03-06
Phase Phase 2
GlaxoSmithKline

1,345 total trials

Why NCT01381549 stopped before completion

NCT01381549 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower).

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT01381549 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01381549 about?

NCT01381549 is a clinical study titled "GSK2251052 in Complicated Urinary Tract Infection". This study is being conducted to evaluate the safety, efficacy (clinical and microbiological), pharmacokinetics/pharmacodynamics of GSK2251052 and to assess whether it would be a suitable antibiotic for the treatment for febrile lower cUTI and pyelonephritis(complicated and uncomplicated). GSK225105...

What is the current status of trial NCT01381549?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2011-06-28. Estimated completion is 2012-03-06.

What interventions are being tested in trial NCT01381549?

The interventions under investigation include: Placebo (OTHER), GSK2251052 (DRUG), imipenem-cilastatin (DRUG).

Who is sponsoring clinical trial NCT01381549?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01381549's enrollment target sits among peer trials

20 1805th of 2000 higher than 107 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01381549, the US trial registry maintained by the National Library of Medicine. NCT01381549 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.