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NCT00387686 · ClinicalTrials.gov registry record · Phase 2

A Phase 2/3 Multicenter, Controlled Trial Of rhBMP-2/CPM In Tibial Fractures

A Phase 2 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

Terminated
Registry status
Phase 2
Development phase
367
Enrollment target

NCT00387686: Clinical Trial Phase 2 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

NCT00387686 is a Phase 2 study that was terminated before completion, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 367 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (176% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00387686, a Phase 2 study, was terminated before completion, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

TERMINATED
Registry status
Phase 2
Development phase
367 participants
Enrollment target

Study Summary

The primary objective of this study is to assess whether a single dose of rhBMP-2/CPM administered at the fracture site via percutaneous injection, in combination with standard of care, accelerates fracture union and return to normal function in subjects who have a closed diaphyseal tibial fracture when compared to standard of care alone.

Interventions

  • DRUG rhBMP-2/CPM

Trial Details

FieldValue
Enrollment Target 367 participants
Start Date 2006-11
Est. Completion 2010-03
Phase Phase 2

Why NCT00387686 stopped before completion

NCT00387686 is an interventional study that assigns participants to a tested intervention. The registered 367 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (176% higher).

The record links to 0 conditions, and to 1 intervention - of which rhBMP-2/CPM is the first listed.

NCT00387686 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00387686 about?

NCT00387686 is a clinical study titled "A Phase 2/3 Multicenter, Controlled Trial Of rhBMP-2/CPM In Tibial Fractures". The primary objective of this study is to assess whether a single dose of rhBMP-2/CPM administered at the fracture site via percutaneous injection, in combination with standard of care, accelerates fracture union and return to normal function in subjects who have a closed diaphyseal tibial fracture ...

What is the current status of trial NCT00387686?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 367 participants. The study started on 2006-11. Estimated completion is 2010-03.

What interventions are being tested in trial NCT00387686?

The interventions under investigation include: rhBMP-2/CPM (DRUG).

Who is sponsoring clinical trial NCT00387686?

This trial is sponsored by Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00387686's enrollment target sits among peer trials

367 121st of 2000 higher than 1,880 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 NCT00387686, the US trial registry maintained by the National Library of Medicine. NCT00387686 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.