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Terminated Phase 3 Interventional

Compare the Effects of Bifeprunox and Quetiapine on Weight Changes in Stable Schizophrenic Patients

ClinicalTrials.gov ID: NCT00396214

Public ClinicalTrials.gov record NCT00396214. 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 Sep 1, 2026, 7:46 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 Randomized, Multicenter, Double-Blind, Parallel Group Study To Compare the Effects of Bifeprunox and Quetiapine on Weight Changes in Stable Schizophrenic Patients

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of the study is to evaluate changes in weight short and long term with bifeprunox and quetiapine. Study participation for the subject is 57 weeks.

Study identification

NCT ID
NCT00396214
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Solvay Pharmaceuticals
Industry
Enrollment
83 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
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
Mar 31, 2007
Primary completion
Dec 31, 2007
Completion
Dec 31, 2007
Last update posted
Jun 3, 2008

2007 – 2008

United States locations

U.S. sites
69
U.S. states
24
U.S. cities
55
Facility City State ZIP Site status
Site 313 Anaheim California
Site 333 Anaheim California
Site 323 Cerritos California
Site 374 Costa Mesa California
Site 326 Culver City California
Site 300 Glendale California
Site 343 Long Beach California
Site 356 Los Angeles California
Site 367 Los Angeles California
Site 322 Oceanside California
Site 316 Pasadena California
Site 302 Sacramento California
Site 315 San Diego California
Site 331 San Diego California
Site 340 San Diego California
Site 311 Santa Ana California
Site 336 Santa Ana California
Site 344 Torrance California
Site 318 Denver Colorado
Site 371 Darien Connecticut
Site 358 Hartford Connecticut
Site 360 New Britain Connecticut
Site 317 Hialeah Florida
Site 362 Largo Florida
Site 327 Miami Florida
Site 373 Miami Florida
Site 334 North Miami Florida
Site 351 North Miami Florida
Site 338 Orange City Florida
Site 332 Tampa Florida
Site 330 Atlanta Georgia
Site 308 Augusta Georgia
Site 370 Decatur Georgia
Site 366 Smyma Georgia
Site 337 Chicago Illinois
Site 361 Oakbrook Terrace Illinois
Site 335 Indianapolis Indiana
Site 341 Lake Charles Louisiana
Site 304 Shreveport Louisiana
Site 301 Glen Burnie Maryland
Site 342 Towson Maryland
Site 328 Detroit Michigan
Site 357 Minneapolis Minnesota
Site 309 St Louis Missouri
Site 369 Omaha Nebraska
Site 320 Clementon New Jersey
Site 347 Clementon New Jersey
Site 310 Buffalo New York
Site 312 Buffalo New York
Site 306 Cedarhurst New York
Site 321 New York New York
Site 353 New York New York
Site 372 New York New York
Site 324 Staten Island New York
Site 329 Cincinnati Ohio
Site 345 Oklahoma City Oklahoma
Site 368 Oklahoma City Oklahoma
Site 354 Portland Oregon
Site 314 Philadelphia Pennsylvania
Site 346 Philadelphia Pennsylvania
Site 348 Philadelphia Pennsylvania
Site 350 Sioux Falls South Dakota
Site 352 Memphis Tennessee
Site 307 Austin Texas
Site 303 Conroe Texas
Site 305 Houston Texas
Site 325 San Antonio Texas
Site 319 Richmond Virginia
Site 349 Spokane Washington

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 82 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00396214, 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 Jun 3, 2008 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00396214 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →