Trials / Completed
CompletedNCT00925990
CTS-1027 in Interferon-Naive Hepatitis C Patients
A Trial of CTS-1027 in Interferon-Naive Hepatitis C Patients
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 70 (actual)
- Sponsor
- Conatus Pharmaceuticals Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The study is intended to determine whether CTS-1027 either alone or in combination with ribavirin is safe and effective in Hepatitis C patients who have not previously been treated with interferon.
Detailed description
There are approximately 1 million Hepatitis C (HCV) patients in the US who have failed to respond to, or cannot tolerate, interferon or interferon plus ribavirin therapy. Significant adverse effects of interferon therapy include bone marrow depression (with reduced white blood cell and platelet counts) and major psychiatric disorders (especially depression). Ribavirin is associated with hemolytic anemia in a minority of patients who are treated with it. Patients with chronic HCV infection have a very low incidence of spontaneous viral clearance, have progressive disease, and have a continuing medical need for more efficacious and safer therapy. There is a significant unmet medical need for therapy in HCV patients who cannot (or will not) tolerate interferon-based treatment. This trial will evaluate the effects of CTS-1027 with or without ribavirin in patients who are previously untreated with interferon including patients with major psychiatric disorders, uncontrolled autoimmune disease, and patients who simply decline treatment.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | ribavirin | 200 mg capsules, either 1000 or 1200 mg taken twice daily for up to 24 weeks |
| DRUG | CTS-1027 | 5 and 10 mg tablets, 15 mg taken twice daily, for up to 24 weeks |
| DRUG | Placebo for ribavirin | Capsules identical to ribavirin in appearance containing inactive ingredients |
Timeline
- Start date
- 2009-06-01
- Primary completion
- 2010-05-01
- Completion
- 2010-07-01
- First posted
- 2009-06-23
- Last updated
- 2012-03-27
- Results posted
- 2012-03-27
Locations
21 sites across 2 countries: United States, Puerto Rico
Source: ClinicalTrials.gov record NCT00925990. Inclusion in this directory is not an endorsement.