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Clinical Trial Summary

This trial is comprised of a 4-week randomized, double-blind, placebo-controlled treatment period followed by an optional 8-week open-label extension (OLE) period. This trial will evaluate the efficacy and safety of oral PRAX-114 flexibly dosed at 40 to 60 mg for 4 weeks compared to placebo in adults with PTSD. The OLE period consisting of treatment with 40 mg PRAX-114 for 8 weeks will provide additional efficacy and safety data.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05260541
Study type Interventional
Source Praxis Precision Medicines
Contact
Status Terminated
Phase Phase 2
Start date January 25, 2022
Completion date September 23, 2022

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