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Completed Phase 2 Interventional

Tranilast Plus Allopurinol in Patients With Moderate to Severe Gout (TAnGO)

ClinicalTrials.gov ID: NCT01109121

Public ClinicalTrials.gov record NCT01109121. 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 23, 2026, 12:02 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 Randomized, Double-Blind, Parallel Group Study to Evaluate the Safety and Efficacy of Tranilast in Combination With Allopurinol in Patients With Moderate to Severe Gout (TAnGO)

Study identification

NCT ID
NCT01109121
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Nuon Therapeutics, Inc.
Industry
Enrollment
112 participants

Conditions and interventions

Interventions

  • Combination 400 Drug
  • Allopurinol Drug
  • Combination 600 Drug

Drug

Eligibility (public fields only)

Age range
18 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
May 31, 2010
Primary completion
Nov 30, 2010
Completion
Dec 31, 2010
Last update posted
Jan 5, 2011

2010 – 2011

United States locations

U.S. sites
24
U.S. states
20
U.S. cities
24
Facility City State ZIP Site status
Nuon Investigative Site La Jolla California
Nuon Investigative Site Santa Maria California
Nuon Investigative Site Washington D.C. District of Columbia
Nuon Investigative Site New Port Richey Florida
Nuon Investigative Site Honolulu Hawaii
Nuon Investigative Site Boise Idaho
Nuon Investigative Site Bloomington Indiana
Nuon Investigative Site Owensboro Kentucky
Nuon Investigative Site Baltimore Maryland
Nuon Investigative Site Wheaton Maryland
Nuon Investigative Site Billings Montana
Nuon Investigative Site Omaha Nebraska
Nuon Investigative Site Reno Nevada
Nuon Investigative Site Teaneck New Jersey
Nuon Investigative Site Durham North Carolina
Nuon Investigative Site Cincinnati Ohio
Nuon Investigative Site Oklahoma City Oklahoma
Nuon Investigative Site Lake Oswego Oregon
Nuon Investigative Site Duncansville Pennsylvania
Nuon Investigative Site West Reading Pennsylvania
Nuon Investigative Site Charleston South Carolina
Nuon Investigative Site Greenville South Carolina
Nuon Investigative Site Waco Texas
Nuon Investigative Site Spokane Washington

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01109121, 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 Jan 5, 2011 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01109121 live on ClinicalTrials.gov.

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