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Completed Phase 2 Interventional

Study to Evaluate the Safety and Efficacy of DR-3001 Versus Placebo in Women With Overactive Bladder

ClinicalTrials.gov ID: NCT00196404

Public ClinicalTrials.gov record NCT00196404. 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 Oct 22, 2026, 8:43 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

A Multicenter, Randomized, Double-blind Study to Evaluate the Safety and Efficacy of DR-3001 Versus Placebo in Women With Overactive Bladder

Brief summary

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

This is a placebo-controlled, double-blind study to evaluate the safety and efficacy of two doses of DR-3001 in women with overactive bladder who have symptoms of predominant or pure urge incontinence, urinary urgency and elevated urinary frequency

Study identification

NCT ID
NCT00196404
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Duramed Research
Industry
Enrollment
800 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
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
Oct 2004 (Type not available)
Primary completion
Dec 2006 (Actual)
Completion
Dec 2006 (Actual)
Last update posted
Aug 20, 2012

2004 – 2006

United States locations

U.S. sites
46
U.S. states
24
U.S. cities
45
Facility City State ZIP Site status
Duramed Investigational Site Birmingham Alabama 35209 —
Duramed Investigational Site Huntsville Alabama 35801 —
Duramed Investigational Site Mobile Alabama 36608 —
Duramed Research Site Phoenix Arizona 85015 —
Duramed Research Site Tucson Arizona 85712 —
Duramed Investigational Site Little Rock Arkansas 72205 —
Duramed Investigational Site San Diego California 92108 —
Duremed Research Site San Diego California 92108 —
Duramed Investigational Site Aurora Colorado 80012 —
Duramed Research Site Colorado Springs Colorado 80909 —
Duramed Investigational Site Denver Colorado 80220 —
Duramed Investigational Site Waterbury Connecticut 06708 —
Duramed Investigational Site Aventura Florida 33180 —
Duramed Research Site Gainesville Florida 32607 —
Duramed Investigational Site Decatur Georgia 30034 —
Duramed Research Site Sandy Springs Georgia 30328 —
Duramed Investigational Site Boise Idaho 83712 —
Duramed Investigational Site Boise Indiana 83705 —
Duramed Investigational Site Evansville Indiana 47714 —
Duramed Investigational Site Fort Wayne Indiana 46825 —
Duramed Investigational Site Indianapolis Indiana 46202 —
Duramed Investigational Site Jeffersonville Indiana 47130 —
Duramed Investigational Site Meridian Indiana 83642 —
Duramed Investigational Site Shreveport Louisiana 71106 —
Duramed Investigational Site Jackson Mississippi 39202 —
Duramed Investigational Site Lebanon New Hampshire 03756 —
Duramed Investigational Site Edison New Jersey 08837 —
Duramed Investigational Site Livingston New Jersey 07039 —
Duramed Investigational Site Moorestown New Jersey 08057 —
Duramed Investigational Site Williamsville New York 14221 —
Duramed Investigational Site Portland Oregon 97210 —
Duramed Investigational Site Lancaster Pennsylvania 17604 —
Duramed Investigational Site Philadelphia Pennsylvania 19114 —
Duramed Investigational Site Providence Rhode Island 02904 —
Duramed Investigational Site Charleston South Carolina 29425 —
Duramed Investigational Site Jackson Tennessee 38305 —
Duramed Investigational Site Memphis Tennessee 38120 —
Duramed Investigational Site Nashville Tennessee 37232 —
Duramed Investigational Site Dallas Texas 75234 —
Duramed Research Site Houston Texas 77024 —
Duramed Investigational Site San Antonio Texas 78229 —
Duramed Research Site Waco Texas 76712 —
Duramed Investigational Site Salt Lake City Utah 84124 —
Duramed Investigational Site Seattle Washington 98105 —
Duramed Research Site Tacoma Washington 98405 —
Duramed Investigational Site Milwaukee Wisconsin 53209 —

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00196404, 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 Aug 20, 2012 · Synced Oct 22, 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 public registry record, listed eligibility criteria, and available contact information for NCT00196404 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →