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 ...
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Historical research recordMultiple countriesSchizophrenia
Understand this study
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.
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 ...
Looking for a study you can join?
Explore recruiting studiesRecruitment & locations
CompletedGermany · Italy · Norway
2 more locations
- Poland
- Sweden
Questions about this study
Who is behind this study?
The study sponsor is Boehringer Ingelheim Pharma GmbH & Co. KG, a pharmaceutical company.
