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TerminatedEUCTR 2011-004494-81

Proof-of-Concept Study of Pipamperone 15mg added to Stable Treatment with Risperidone or Paliperidone in Chronic Schizophrenic and Schizoaffective Patients with Residual Symptoms: a phase I/IIa, r...

This historical record does not confirm current site availability.

Historical research recordBelgiumSchizophrenia
The study in practice

Understand this study

What is this study about?

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
Belgium
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.

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What to know before participating

A point to clarify

This is historical registry information. What is the current study status and protocol?

Study clarity

Things to check before joining

Study start dateNot clearly listed
Recruitment status
Terminated
Enrollment listed in the registry
Not clearly listed
Sponsor
Pharmaneuroboost N.V.
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
Belgium
Age range
Not clearly listed
Official registry ID
EUCTR 2011-004494-81
Official title
Show the full official title

Proof-of-Concept Study of Pipamperone 15mg added to Stable Treatment with Risperidone or Paliperidone in Chronic Schizophrenic and Schizoaffective Patients with Residual Symptoms: a phase I/IIa, r...

Recruitment & locations

Terminated

Belgium

Registry details
Historical country statuses

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Pharmaneuroboost N.V.

Is this study still recruiting?

The historical registry lists this study as terminated.

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