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Terminated Phase 2 Interventional Results available

Effect of Febuxostat Compared to Placebo on Exercise Tolerance in Participants With Chronic Stable Angina

ClinicalTrials.gov ID: NCT01549977

Public ClinicalTrials.gov record NCT01549977. 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 21, 2026, 11:24 AM 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 Phase 2, Double-Blind, Placebo-Controlled Study to Assess the Effect of Febuxostat 80 mg Once Daily Compared to Placebo on Exercise Tolerance in Subjects With Chronic Stable Angina

Brief summary

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

The purpose of this study is to evaluate the effect of febuxostat, once daily (QD), compared to placebo as an add on to stable anti-anginal therapy, on the total exercise time of participants with Chronic Stable Angina.

Study identification

NCT ID
NCT01549977
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Takeda
Industry
Enrollment
1 participant

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 85 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
Jul 2012 (Type not available)
Primary completion
Nov 2012 (Actual)
Completion
Nov 2012 (Actual)
Last update posted
Dec 20, 2013

2012

United States locations

U.S. sites
21
U.S. states
13
U.S. cities
21
Facility City State ZIP Site status
Not listed Carmichael California — —
Not listed Fresno California — —
Not listed Irvine California — —
Not listed Paramount California — —
Not listed Sacramento California — —
Not listed San Diego California — —
Not listed Tampa Florida — —
Not listed Dunwoody Georgia — —
Not listed Suwanee Georgia — —
Not listed Lexington Kentucky — —
Not listed City of Saint Peters Missouri — —
Not listed St Louis Missouri — —
Not listed Salisbury North Carolina — —
Not listed Columbus Ohio — —
Not listed Lyndhurst Ohio — —
Not listed Oklahoma City Oklahoma — —
Not listed Tipton Pennsylvania — —
Not listed San Antonio Texas — —
Not listed Manassas Virginia — —
Not listed Port Orchard Washington — —
Not listed Madison Wisconsin — —

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 NCT01549977, 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 20, 2013 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01549977 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →