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NCT00265551 · ClinicalTrials.gov registry record · Phase 2

Study Evaluating SCA-136 in Subjects With Acute Exacerbations of Schizophrenia

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

Completed
Registry status
Phase 2
Development phase
300
Enrollment target

NCT00265551: Completed Phase 2 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

NCT00265551 is a Phase 2 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 300 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (126% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00265551, a Phase 2 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

COMPLETED
Registry status
Phase 2
Development phase
300 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether a low dose and a high dose of the study drug SCA-136 are effective and safe in the treatment of schizophrenia requiring hospitalization.

Interventions

  • DRUG placebo
  • DRUG SCA-136 (200 mg)
  • DRUG SCA-136 (400 mg)
  • DRUG olanzapine (15 mg)

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2006-01
Est. Completion 2007-01
Phase Phase 2

What the finished NCT00265551 record still lists

NCT00265551 is an interventional study that assigns participants to a tested intervention. The registered 300 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 (126% higher).

The record links to 0 conditions, and to 4 interventions - of which placebo is the first listed.

NCT00265551 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00265551 about?

NCT00265551 is a clinical study titled "Study Evaluating SCA-136 in Subjects With Acute Exacerbations of Schizophrenia". The purpose of this study is to determine whether a low dose and a high dose of the study drug SCA-136 are effective and safe in the treatment of schizophrenia requiring hospitalization.

What is the current status of trial NCT00265551?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 300 participants. The study started on 2006-01. Estimated completion is 2007-01.

What interventions are being tested in trial NCT00265551?

The interventions under investigation include: placebo (DRUG), SCA-136 (200 mg) (DRUG), SCA-136 (400 mg) (DRUG), olanzapine (15 mg) (DRUG).

Who is sponsoring clinical trial NCT00265551?

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 NCT00265551's enrollment target sits among peer trials

300 167th of 2000 higher than 1,813 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 NCT00265551, the US trial registry maintained by the National Library of Medicine. NCT00265551 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.