Safety Study of an Antipsychotic, Sertindole, to Treat Schizophrenia
Status and phase
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Details and patient eligibility
About
The purpose of this study is to permit the patients with schizophrenia who received Sertindole during a previous randomised trial, study 99824, to continue with this treatment.
Full description
Schizophrenia is a disabling and often chronic disorder that may require long-term treatment. This protocol is an extension study of a randomised study comparing the safety of Sertindole versus Risperidone. Patients who were randomised to Sertindole and who completed the previous study have the possibility to receive continued Sertindole treatment in this open one-arm study. Sertindole is generally well tolerated and is approved in the EU, but not yet marketed in France. The follow-up of the patients will be similar to that in the previous study and requires quarterly visits. Patient management reflects routine clinical practice in accordance with the Sertindole label. Any severe safety issue is reported to the company.
Enrollment
Sex
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Volunteers
Inclusion criteria
- Participation in the previous SCoP study, 99824
- Still fulfils the EU SPC requirements for Sertindole
Exclusion criteria
- Withdrawn before the end of the SCoP study, 99824
- Become homeless
- Participation in another clinical trial at the same time
- Unlikely to comply with the clinical study protocol or is unsuitable for any reason
Trial design
Primary purpose
Allocation
Interventional model
Masking
18 participants in 1 patient group
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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