Study to Evaluate sUA-Lowering Activity, Safety & PK Interaction of Oral BCX4208 & Allopurinol Admin. in Subjects w/Gout

NCT01129648 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 87

Last updated 2012-01-23

No results posted yet for this study

Summary

To evaluate safety and efficacy of BCX4208 alone and in combination with allopurinol in subjects with gout.

Conditions

Interventions

DRUG

Placebo

Administered daily for 21 days

DRUG

Allopurinol

Administered daily for 21 days.

DRUG

Allopurinol

Administered daily for 21 days.

DRUG

Allopurinol

Administered daily for 21 days.

DRUG

BCX4208

Administered daily for 21 days.

DRUG

Allopurinol

Administered daily for 21 days.

DRUG

Allopurinol

Administered daily for 21 days.

DRUG

Allopurinol

Administered daily for 21 days.

DRUG

BCX4208

Administered daily for 21 days.

DRUG

Allopurinol

Administered daily for 21 days.

DRUG

Allopurinol

Administered daily for 21 days.

DRUG

Allopurinol

Administered daily for 21 days.

DRUG

BCX4208

Administered daily for 21 days.

DRUG

Allopurinol

Administered daily for 21 days.

DRUG

Allopurinol

Administered daily for 21 days.

DRUG

Allopurinol

Administered daily for 21 days.

DRUG

BCX4208

Adminstered daily for 21 days

Sponsors & Collaborators

  • BioCryst Pharmaceuticals

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Max Age
69 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-05-31
Primary Completion
2010-11-30
Completion
2010-11-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Drugs
Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01129648 on ClinicalTrials.gov