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Clinical Trial Summary

This study will evaluate the efficacy, safety, and pharmacokinetics of 10 mg of oral administration balovaptan once a day (QD) compared with matching placebo in adults (18 years and older) with autism spectrum disorder (ASD).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03504917
Study type Interventional
Source Hoffmann-La Roche
Contact
Status Terminated
Phase Phase 3
Start date August 8, 2018
Completion date July 1, 2020

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