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

No results posted yet for this study

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

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

More Related Trials

Entities

Companies

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 NCT00550849 on ClinicalTrials.gov