Trial · NCT00265551
Study Evaluating SCA-136 in Subjects With Acute Exacerbations of Schizophrenia
NCT00265551, Phase 2, Completed, Wyeth is now a wholly owned subsidiary of Pfizer
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Study Evaluating SCA-136 in Subjects With Acute Exacerbations of Schizophrenia. Trials, record NCT00265551. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00265551
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Study Evaluating SCA-136 in Subjects With Acute Exacerbations of Schizophrenia
- NCT number
- NCT00265551
- Status
- Completed
- Phases
- Phase 2
- Enrollment
- 300 participants
- Lead sponsor
- Wyeth is now a wholly owned subsidiary of Pfizer
- Conditions
- Schizophrenia
- Interventions
- SCA-136 (200 mg), SCA-136 (400 mg), olanzapine (15 mg), placebo
- First posted
- 2005-12-14
- Last updated
- 2007-12-10
Source ClinicalTrials.gov
Registered outcomes10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change from baseline to day 42 on the positive subscale of the SCI-PANNS | ||
| Secondary | Change from baseline to day 42 on: | ||
| Secondary | SCI-PANNS total score | ||
| Secondary | negative symptom sub-scale score of SCI-PANNS | ||
| Secondary | general psychopathology subscale score of SCI-PANNS | ||
| Secondary | response rate based upon SCI-PANNS total score | ||
| Secondary | BPRS score | ||
| Secondary | CGI-S score | ||
| Secondary | CGI-I score | ||
| Secondary | Cognitive assessments scores |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 24613032 | DERIVED |
Source PubMed
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT00265551
GET https://conductscience.org/api/trials/v1/NCT00265551/registered