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CompletedEUCTR 2020-003760-11

A phase III randomized, double-blind, placebo-controlled parallel group trial to examine the efficacy and safety of Iclepertin (BI 425809) once daily over 26 week treatment period in patients with ...

This historical record does not confirm current site availability.

Historical research recordMultiple countriesSchizophrenia
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
Germany · Italy and 3 more locations
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.

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Study clarity

Study information

Study start dateNot clearly listed
Recruitment status
Completed
Enrollment listed in the registry
586
Sponsor
Boehringer Ingelheim Pharma GmbH & Co. KG
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
Germany, Italy, Norway, ...
Age range
Not clearly listed
Official registry ID
EUCTR 2020-003760-11
Official title
Show the full official title

A phase III randomized, double-blind, placebo-controlled parallel group trial to examine the efficacy and safety of Iclepertin (BI 425809) once daily over 26 week treatment period in patients with ...

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Recruitment & locations

Completed

Germany · Italy · Norway

2 more locations
  • Poland
  • Sweden
Registry details
Historical country statuses
FAQ

Questions about this study

Who is behind this study?

The study sponsor is Boehringer Ingelheim Pharma GmbH & Co. KG, a pharmaceutical company.

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