Last updated on September 2017

Phase II Study of BNC210 in PTSD


Brief description of study

This is a randomized, double-blind, placebo-controlled study, evaluating the effects of BNC210 versus placebo on the symptoms of Post-Traumatic Stress Disorder, as measured by the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5). The secondary objectives of the study are to evaluate the effects of BNC210 on anxiety, depression, global functioning and patient reported outcomes in patients with PTSD. Safety and tolerability of BNC210 will also be assessed. Study participants will receive 12 weeks of blinded treatment followed by a 3 week follow-up period.

Clinical Study Identifier: NCT02933606

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Michael Meade, BSc

Oceanside, CA United States
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Michael Meade, BSc

Rancho Mirage, CA United States
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Michael Meade, BSc

Redlands, CA United States
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Michael Meade, BSc

Riverside, CA United States
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Michael Meade, BSc

Gainesville, FL United States
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Michael Meade, BSc

Jacksonville, FL United States
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Michael Meade, BSc

Lauderhill, FL United States
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Michael Meade, BSc

North Miami, FL United States
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Michael Meade, BSc

Oakland Park, FL United States
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Michael Meade, BSc

Orlando, FL United States
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Michael Meade, BSc

Hoffman Estates, IL United States
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Michael Meade, BSc

Overland Park, KS United States
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Michael Meade, BSc

New Bedford, MA United States
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Michael Meade, BSc

Lincoln, NE United States
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Michael Meade, BSc

Las Vegas, NV United States
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Michael Meade, BSc

Berlin, NJ United States
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Michael Meade, BSc

Canton, OH United States
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Michael Meade, BSc

Memphis, TN United States
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Michael Meade, BSc

Dallas, TX United States
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Michael Meade, BSc

San Antonio, TX United States
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Michael Meade, BSc

Maroubra, Australia
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Michael Meade, BSc

Auchenflower, Australia
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Michael Meade, BSc

Elizabeth Vale, Australia
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Michael Meade, BSc

St Kilda, Australia
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