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Completed Phase 3 Interventional Results available

Pipamperone/Citalopram (PNB01) Versus Citalopram (CIT) and Versus Pipamperone (PIP) in Major Depressive Disorder (MDD)

ClinicalTrials.gov ID: NCT01312922

Public ClinicalTrials.gov record NCT01312922. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 10:14 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Pipamperone/Citalopram (PNB01) Versus Citalopram (CIT) and Versus Pipamperone (PIP) in the Treatment of Moderate to Severe Major Depressive Disorder (MDD): a Randomized, Double-blind Phase III Study of 10 Weeks

Study identification

NCT ID
NCT01312922
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
PharmaNeuroBoost N.V.
Industry
Enrollment
555 participants

Conditions and interventions

Interventions

  • PNB01 fixed dose combination of pipamperone and citalopram Drug
  • Citalopram Drug
  • Pipamperone Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Aug 31, 2011
Primary completion
Oct 31, 2012
Completion
Nov 30, 2012
Last update posted
Apr 6, 2022

2011 – 2012

United States locations

U.S. sites
26
U.S. states
11
U.S. cities
25
Facility City State ZIP Site status
Site 103 Glendale California
Site 101 National City California
Site 113 Riverside California
Site 106 San Diego California
Site 116 San Diego California
Site 112 Fort Myers Florida
Site 135 Miami Florida
Site 108 Winter Park Florida
Site 133 Atlanta Georgia
Site 128 Smyrna Georgia
Site 132 Libertyville Illinois
Site 117 Schaumburg Illinois
Site 110 Baltimore Maryland
Site 109 Flowood Mississippi
Site 115 New York New York
Site 126 Beachwood Ohio
Site 127 Cincinnati Ohio
Site 124 Middleburg Heights Ohio
Site 105 Allentown Pennsylvania
Site 123 Media Pennsylvania
Site 122 Philadelphia Pennsylvania
Site 119 Austin Texas
Site 104 Dallas Texas
Site 102 Wichita Falls Texas
Site 107 Kirkland Washington
Site 134 Seattle Washington

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01312922, 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 Apr 6, 2022 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01312922 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →