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NCT00770978 · ClinicalTrials.gov registry record · Phase 1

Open Label Study of Ceftobiprole to Evaluate Pharmacokinetics in Adults Hospitalized in the ICU

A Phase 1 study, sponsored by Basilea Pharmaceutica.

Completed
Registry status
Phase 1
Development phase
33
Enrollment target

NCT00770978: Completed Phase 1 study, sponsored by Basilea Pharmaceutica.

NCT00770978 is a Phase 1 study that has completed, run by Basilea Pharmaceutica. The registered enrollment target is 33 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (45% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00770978, a Phase 1 study, has completed, sponsored by Basilea Pharmaceutica.

COMPLETED
Registry status
Phase 1
Development phase
33 participants
Enrollment target

Study Summary

The purpose of this research study is to measure the levels of ceftobiprole in the blood and urine during and after administration of four doses of ceftobiprole. Safety of the drug will also be evaluated.

Interventions

  • DRUG ceftobiprole q12h
  • DRUG ceftobiprole q8h

Trial Details

FieldValue
Enrollment Target 33 participants
Start Date 2008-11
Est. Completion 2010-09
Phase Phase 1
Basilea Pharmaceutica

21 total trials

What the finished NCT00770978 record still lists

NCT00770978 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 33 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (45% lower).

The record links to 0 conditions, and to 2 interventions - of which ceftobiprole q12h is the first listed.

NCT00770978 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00770978 about?

NCT00770978 is a clinical study titled "Open Label Study of Ceftobiprole to Evaluate Pharmacokinetics in Adults Hospitalized in the ICU". The purpose of this research study is to measure the levels of ceftobiprole in the blood and urine during and after administration of four doses of ceftobiprole. Safety of the drug will also be evaluated.

What is the current status of trial NCT00770978?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 33 participants. The study started on 2008-11. Estimated completion is 2010-09.

What interventions are being tested in trial NCT00770978?

The interventions under investigation include: ceftobiprole q12h (DRUG), ceftobiprole q8h (DRUG).

Who is sponsoring clinical trial NCT00770978?

This trial is sponsored by Basilea Pharmaceutica, which has 21 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00770978's enrollment target sits among peer trials

33 1280th of 2000 higher than 705 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00770978, the US trial registry maintained by the National Library of Medicine. NCT00770978 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.