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Clinical Trials/NCT00701753
NCT00701753
Terminated
Not Applicable

A Pharmacogenetic Investigation of Antipsychotics in Schizophrenia and Schizophrenia-Like Psychoses

TheraGenetics Limited1 site in 1 country24 target enrollmentMay 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Schizophrenia
Sponsor
TheraGenetics Limited
Enrollment
24
Locations
1
Status
Terminated
Last Updated
17 years ago

Overview

Brief Summary

An individual's genetic make-up is known to determine their response to antipsychotic medication. Genetic markers that determine efficacy and side effects of medication may be identified and used to predict treatment outcome.

The study is a naturalistic study of routinely prescribed antipsychotics using outcome measures undertaken as part of the routine clinical care of the cohort. These clinical data are linked with genetic information obtained from DNA and RNA from blood samples undertaken as part of the study.

No alteration is made to the subjects treatment regime or medication.

The study is a two stage investigation:

  • The first stage involves the collection of a databank of clinical information and blood samples for DNA and RNA extraction from patients treated with antipsychotic medication.
  • The second stage is a molecular genetic investigation of treatment-related genetic factors that may contribute to response prediction and predisposition to side effects.

From these genetic studies pharmacogenetic prediction tests will be validated and/or developed.

Registry
clinicaltrials.gov
Start Date
May 2008
End Date
March 2009
Last Updated
17 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
TheraGenetics Limited

Eligibility Criteria

Inclusion Criteria

  • Written informed consent must be obtained
  • DSM-IV diagnosis must be one of:
  • schizophrenia
  • schizophreniform
  • schizoaffective
  • delusional disorder
  • brief reactive psychosis
  • psychosis not otherwise specified
  • Ethnic origin of both parents must be known
  • A minimum of 6 weeks continuous treatment completed with the given antipsychotic, prescribed at least at minimum recommended doses

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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