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NCT01669980 · ClinicalTrials.gov registry record · Phase 4

Safety and Efficacy Study of Ceftaroline Versus a Comparator in Pediatric Subjects With Complicated Community Acquired Pneumonia (CABP)

A Phase 4 study, sponsored by Forest Laboratories.

Completed
Registry status
Phase 4
Development phase
40
Enrollment target

NCT01669980: Completed Phase 4 study, sponsored by Forest Laboratories.

NCT01669980 is a Phase 4 study that has completed, run by Forest Laboratories. The registered enrollment target is 40 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01669980, a Phase 4 study, has completed, sponsored by Forest Laboratories.

COMPLETED
Registry status
Phase 4
Development phase
40 participants
Enrollment target

Study Summary

This is a study of safety and effectiveness of ceftaroline fosamil in children with Complicated Community-acquired Pneumonia receiving antibiotic therapy in the hospital.

Primary Outcome

Evaluate the safety and tolerability of IV administered ceftaroline fosamil in children with complicated CABP. Summaries of patient AEs, SAEs, deaths, discontinuations due to AEs, laboratory evaluations (hematology studies, comprehensive and metabolic panel), and vital signs will be provided for each treatment group.

Interventions

  • DRUG Ceftaroline fosamil
  • DRUG IV Ceftriaxone and Vancomycin

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2012-10
Est. Completion 2014-08
Phase Phase 4
Forest Laboratories

145 total trials

What the finished NCT01669980 record still lists

NCT01669980 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (92% lower).

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

NCT01669980 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01669980 about?

NCT01669980 is a clinical study titled "Safety and Efficacy Study of Ceftaroline Versus a Comparator in Pediatric Subjects With Complicated Community Acquired Pneumonia (CABP)". This is a study of safety and effectiveness of ceftaroline fosamil in children with Complicated Community-acquired Pneumonia receiving antibiotic therapy in the hospital.

What is the current status of trial NCT01669980?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 40 participants. The study started on 2012-10. Estimated completion is 2014-08.

What interventions are being tested in trial NCT01669980?

The interventions under investigation include: Ceftaroline fosamil (DRUG), IV Ceftriaxone and Vancomycin (DRUG).

Who is sponsoring clinical trial NCT01669980?

This trial is sponsored by Forest Laboratories, which has 145 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01669980's enrollment target sits among peer trials

40 1397th of 2000 higher than 533 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT01669980, the US trial registry maintained by the National Library of Medicine. NCT01669980 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.