Study of Sorafenib With or Without VT-122 in Patients With Hepatocellular Carcinoma (HCC)
Public ClinicalTrials.gov record NCT01265576. 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.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Randomized, Double Blind, Placebo Controlled, Multicenter Phase 2 Study of VT-122 in Combination With Sorafenib Compared to Sorafenib With Placebo in Patients With Hepatocellular Carcinoma and Systemic Inflammation at Risk for Cachexia
Study identification
- NCT ID
- NCT01265576
- Recruitment status
- Not listed
- Study type
- Interventional
- Phase
- Phase 2
- Lead sponsor
- Vicus Therapeutics
- Industry
- Enrollment
- 20 participants
Conditions and interventions
Conditions
Interventions
- Placebo Drug
- Sorafenib Drug
- VT-122 (propranolol plus etodolac) Drug
Drug
Eligibility (public fields only)
- Age range
- 18 Years and older
- 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
- Nov 30, 2010
- Primary completion
- Jan 31, 2014
- Completion
- Mar 31, 2016
- Last update posted
- Dec 8, 2015
2010 – 2016
United States locations
- U.S. sites
- 10
- U.S. states
- 6
- U.S. cities
- 9
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Vicus Clinical Site | Berkeley | California | 94704 | — |
| Vicus Clinical Site | Atlanta | Georgia | 30318 | — |
| Vicus Clinical Site | New Brunswick | New Jersey | — | — |
| Vicus Clinical Site | Newark | New Jersey | 07103 | — |
| Vicus Clinical Site | Paterson | New Jersey | 07503 | — |
| Vicus Clinical Site | Buffalo | New York | 14263 | — |
| Vicus Clinical Site | New York | New York | 10016 | — |
| Vicus Clinical Site | Philadelphia | Pennsylvania | — | — |
| Vicus Clinical Site | Houston | Texas | 77024 | — |
| Vicus Clinical Site | Houston | Texas | 77030 | — |
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 NCT01265576, 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 8, 2015 · Synced May 8, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT01265576 live on ClinicalTrials.gov.