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Clinical Trial Summary

The purpose of this study is to determine the safety and efficacy of HB-1 versus placebo in male and female adult patients aged 18 to 60 years, inclusive, with Panic Disorder.

Clinical Trial Description

This is a multicenter, randomized, double-blind, placebo-controlled trial. All patients with Panic Disorder, with or without specified co-morbidities, who meet all of the inclusion and none of the exclusion criteria will be eligible. Patients and researchers will be blinded to their treatment group. The study will enroll approximately 80 adult patients who meet the diagnosis of panic disorder. The patients will be treated for 12 weeks including a 1 week safety follow up visit following the last dose of study drug. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT05071430
Study type Interventional
Source Honeybrains Biotech LLC
Contact Alon Seifan
Phone 786-620-3204
Email [email protected]
Status Not yet recruiting
Phase Phase 2
Start date October 6, 2021
Completion date October 29, 2022

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