Study to Assess the Safety, Tolerability, and Pharmacodynamics of RTA 402 in Patients With Hepatic Dysfunction
NCT00550849 · Status: TERMINATED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 16
Last updated 2025-05-30
Summary
This study assesses the safety and tolerability of RTA 402 in patients with liver disease.
Conditions
Interventions
- DRUG
-
RTA 402
5 mg oral capsules
- DRUG
-
RTA 402
25 mg oral capsules
- DRUG
-
RTA 402
50 mg oral capsules
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Thomas C. Marbury, MD · Orlando Clinical Research Center
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2007-04-30
- Primary Completion
- 2007-11-30
- Completion
- 2007-11-30
Countries
- United States
Study Locations
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