Purpose

To investigate the efficacy, safety and tolerability of BI 409306 once daily compared to placebo given for 52 weeks to subjects with attenuated psychosis syndrome.

Category

IRB Number
20180639HU
NCT Number
-
Open to Enrollment
Yes
Sponsor
Boehringer Ingelheim -



Study Contact

Floyd Jones
+1 (210) 450-3158
jonesfa@uthscsa.edu

Amy Saklad
(210) 567-8229
saklada@uthscsa.edu

Mary Woolsey
(210) 567-8049
woolseym@uthscsa.edu

Principal Investigator
David Glahn

David Glahn
david.glahn@childrens.harvard.edu

Floyd Jones
+1 (210) 450-3158
jonesfa@uthscsa.edu

Amy Saklad
(210) 567-8229
saklada@uthscsa.edu

Mary Woolsey
(210) 567-8049
woolseym@uthscsa.edu



Eligibility

Eligible Ages
Between 16 Years and 30 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

    Exclusion Criteria


      Study Design

      Arm Groups