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Completed Phase 2 Interventional

Efficacy, Safety and Tolerability of XBD173 in Patients With Generalized Anxiety Disorder

ClinicalTrials.gov ID: NCT00108836

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT00108836. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 15, 2026, 9:17 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will test the efficacy, safety and tolerability of XBD173 in the treatment of generalized anxiety disorder in patients.

Study identification

NCT ID
NCT00108836
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
400 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 2005 (Type not available)
Primary completion
Not listed
Completion
May 2006 (Actual)
Last update posted
May 20, 2010

2005 – 2006

United States locations

U.S. sites
16
U.S. states
8
U.S. cities
16
Facility City State ZIP Site status
Investigational Site Anaheim California 92801 —
Investigational Site Los Angeles California 90024 —
Investigational Site Newport Beach California 92660 —
Investigational Site Redlands California 92374 —
Investigational Site San Diego California 92108 —
Investigational Site Fort Meyers Florida 33712 —
Investigational Site St. Petersburg Florida 33702 —
Investigational Site West Palm Beach Florida 33407 —
Investigational Site Atlanta Georgia 30308 —
Investigational Site Hoffman Estates Illinois 60194 —
Investigational Site Oak Brook Illinois 60523 —
Investigational Site Overland Park Kansas 66211 —
Investigational Site Dayton Ohio 45408 —
Investigational Site Portland Oregon 97239 —
Investigational Site Madison Tennessee 37115 —
Investigational Site Memphis Tennessee 38119 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00108836, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 20, 2010 · Synced Nov 15, 2026

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