ClinicalTrials.gov record
Terminated Phase 2Phase 3 Interventional

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

ClinicalTrials.gov ID: NCT00387686

Public ClinicalTrials.gov record NCT00387686. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 19, 2026, 10:59 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2/3, Multicenter, Double-Blind, Randomized, Controlled Study Of Recombinant Human Bone Morphogenetic Protein-2 (rhBMP-2)/Calcium Phosphate Matrix (CPM) In Closed Diaphyseal Tibial Fracture

Study identification

NCT ID
NCT00387686
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Industry
Enrollment
367 participants

Conditions and interventions

Conditions

Interventions

  • rhBMP-2/CPM Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2006
Primary completion
Jun 30, 2009
Completion
Feb 28, 2010
Last update posted
Feb 27, 2013

2006 – 2010

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Pfizer Investigational Site Birmingham Alabama 35294-3708
Pfizer Investigational Site Birmingham Alabama 35294
Pfizer Investigational Site Aurora Colorado 80012
Pfizer Investigational Site Denver Colorado 80204
Pfizer Investigational Site New Haven Connecticut 06519
Pfizer Investigational Site Pinellas Park Florida 33781
Pfizer Investigational Site Fort Wayne Indiana 46804
Pfizer Investigational Site Indianapolis Indiana 46202
Pfizer Investigational Site Baltimore Maryland 21201-1595
Pfizer Investigational Site Kalamazoo Michigan 49007
Pfizer Investigational Site Portage Michigan 49002
Pfizer Investigational Site Lebanon New Hampshire 03756
Pfizer Investigational Site New Brunswick New Jersey 08901
Pfizer Investigational Site Brooklyn New York 11220
Pfizer Investigational Site Elmhurst New York 11373
Pfizer Investigational Site Charlotte North Carolina 28203-5871
Pfizer Investigational Site Memphis Tennessee 38103

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 51 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00387686, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 27, 2013 · Synced May 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00387686 live on ClinicalTrials.gov.

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