A Study to Investigate the Efficacy, Safety and Tolerability of Four Different Doses of BI 409306 Compared to Placebo Given for 12 Weeks in Patients With Schizophrenia on Stable Antipsychotic Treatment.

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE II RANDOMISED, DOUBLE-BLINDED, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY, SAFETY, AND TOLERABILITY OF FOUR ORALLY ADMINISTRATED DOSES OF BI 409306 ONCE DAILY DURING A 12-WEEK TREATMENT PERIOD IN PATIENTS WITH SCHIZOPHRENIA ON STABLE ANTIPSYCHOTIC TREATMENT

Intervention/treatment:
BI 409306
Medical condition:
SCHIZOPHRENIA
Protocol code:
1289.6
Control number:
176563
Status:
Closed
Approved:
August 15, 2014
Date Completed:
Trial phase:
Phase 2
For more information:
ClinicalTrials.gov - NCT02281773
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years to 55 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Boehringer Ingelheim, Call Center
Organization
Boehringer Ingelheim
Phone:
1-800-243-0127
Sponsor
BOEHRINGER INGELHEIM (CANADA) LTD LTEE

Locations

British Columbia

Dr. Alexander McIntyre Inc.
Penticton, British Columbia, V2A 4M4

Ontario

Depression, Mood Disorders and Schizophrenia Treatment Centr
Burlington, Ontario, L7R4E2

Results

See the results from the trial NCT02281773. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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