WHO ICTRP trial

Pragmatic randomized trial of Risperdal Consta versus oral atypical…

EUCTR2005-004383-23-GB · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2005-004383-23-GB
Public title Pragmatic randomized trial of Risperdal Consta versus oral atypical antipsychotics in poorly adherent subjects with schizophrenia ina routine care setting. Protocol RISSCH4055; Phase IV (risperidone microspheres) - Pragmatic randomized trial of Risperdal Consta versus oral atypical antipsychotics
Scientific title Pragmatic randomized trial of Risperdal Consta versus oral atypical antipsychotics in poorly adherent subjects with schizophrenia ina routine care setting. Protocol RISSCH4055; Phase IV (risperidone microspheres) - Pragmatic randomized trial of Risperdal Consta versus oral atypical antipsychotics
Primary sponsor Janssen Cilag Ltd
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): yes
Countries Ireland;United Kingdom
Conditions Schizophrenia
Interventions Trade Name: Risperdal Consta 25mg Product Name: RISPERDAL Consta/25mg Product Code: F109 Pharmaceutical Form: Suspension for injection Trade Name: Risperdal Consta 37.5 mg Product Name: RISPERDAL Consta/37,5mg Product Code: F109…
Registration date Oct 26, 2005
Target size 260
Secondary IDs RISSCH4055
Registry page clinicaltrialsregister.eu

At a glance

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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