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CompletedEUCTR 2008-006738-85

A Single Dose, Open-Label, Randomized, Two-Way Crossover Food Effect Study Comparing 12.5 mg FazaClo™ (clozapine) ODT under Fasted and Fed Conditions in Healthy Male Volunteers.

This historical record does not confirm current site availability.

Historical research recordUnited KingdomSchizophrenia
The study in practice

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What did researchers investigate?

This EU register entry describes an interventional medicine trial, designed to assign participants a study treatment. The protocol sets out the treatment, eligibility criteria and assessments. Check the source details below for country statuses and any transfer to CTIS.

Listed locations
United Kingdom
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Study clarity

Study information

Study start dateNot clearly listed
Recruitment status
Completed
Enrollment listed in the registry
24
Sponsor
Azur Pharma, Ltd.
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
United Kingdom
Age range
Not clearly listed
Official registry ID
EUCTR 2008-006738-85
Official title
Show the full official title

A Single Dose, Open-Label, Randomized, Two-Way Crossover Food Effect Study Comparing 12.5 mg FazaClo™ (clozapine) ODT under Fasted and Fed Conditions in Healthy Male Volunteers.

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Recruitment & locations

Completed

United Kingdom

Registry details
Historical country statuses
FAQ

Questions about this study

Who is behind this study?

The study sponsor is Azur Pharma, Ltd., a pharmaceutical company.

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