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Completed Phase 2 Interventional Results available

SMP-986 Phase 2 Proof of Concept in Patients With Overactive Bladder Syndrome (OABS)

ClinicalTrials.gov ID: NCT00409539

Public ClinicalTrials.gov record NCT00409539. 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 Nov 6, 2026, 8:40 AM EST

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Official title

A 10-week Randomised, DB, PG, PC Phase 2 Study to Investigate the Extent of Symptom Relief and the Safety and Tolerability of SMP-986 (20, 40, 80 and 120 mg) Administered Once Daily for 8 Weeks to Patients With Overactive Bladder Syndrome

Brief summary

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

SMP-986 is a compound being developed for the treatment of overactive bladder syndrome (OABS). This clinical study is designed to test the hypothesis that SMP-986 at doses of 20mg, 40mg, 80mg or 120mg provides greater symptom relief in OABS compared to placebo. The hypothesis will be tested by measuring the change in mean voids/24 hrs after treatment with SMP-986 compared to placebo, as well comparing the change in: the severity of urgency episodes, mean number of urgency episodes/24 hr, mean number of incontinence episodes/24 hr and the mean void volume/void between SMP-986 and placebo.

Study identification

NCT ID
NCT00409539
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Sumitomo Pharma America, Inc.
Industry
Enrollment
550 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
20 Years to 80 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
Dec 2006 (Type not available)
Primary completion
Jun 2008 (Actual)
Completion
Jul 2008 (Actual)
Last update posted
Dec 10, 2014

2006 – 2008

United States locations

U.S. sites
21
U.S. states
13
U.S. cities
21
Facility City State ZIP Site status
Visions Clinical Research Tuscon Arizona 85712 —
Peninsula Urology Center Atherton California 94027 —
San Bernadino Urological Association Medical Group San Bernadino California 92404 —
9040 Friars Road San Diego California 92108 —
South Florida Medical Research Aventura Florida 33180 —
Visions Clinical Research Boynton Beach Florida 33437 —
Florida Healthcare Research Ocala Florida 34474 —
Southern Research Group, Centre Point Boulevard Tallahassee Florida 32308 —
Atlanta Medical Research Alpharetta Georgia 30005 —
Urological Surgeons of IL Kankakee Illinois 60901 —
Regional Urology Shreveport Louisiana 71106 —
Accumed Research Associate Garden City New York 11530 —
Hudson Valley Urology Kingston New York 12401 —
New York Urological Associates, PC New York New York 10022 —
Hudson Valley Urology Poughkeepsie New York 12601 —
Unifour Medical Research Hickory North Carolina 28601 —
University of Pittsburg, Dept Urology Pittsburgh Pennsylvania 15213 —
Volunteer Research Group Knoxville Tennessee 37920 —
5920 Saratoga Boulevard Corpus Christi Texas 78414 —
National Clinical Research Inc Richmond Virginia 23294 —
801 W. 5th Avenue Spokane Washington 99202 —

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 48 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00409539, 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 Dec 10, 2014 · Synced Nov 6, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00409539 live on ClinicalTrials.gov.

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