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Completed Phase 3 Interventional Results available

Sorafenib as Adjuvant Treatment in the Prevention Of Recurrence of Hepatocellular Carcinoma (STORM)

ClinicalTrials.gov ID: NCT00692770

Public ClinicalTrials.gov record NCT00692770. 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.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 12:39 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III Randomized, Double-blind, Placebo-controlled Study of Sorafenib as Adjuvant Treatment for Hepatocellular Carcinoma After Surgical Resection or Local Ablation.

Study identification

NCT ID
NCT00692770
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bayer
Industry
Enrollment
1,114 participants

Conditions and interventions

Interventions

  • Nexavar (Sorafenib, BAY43-9006) Drug
  • Placebo 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
Aug 14, 2008
Primary completion
Nov 28, 2013
Completion
Nov 27, 2014
Last update posted
Aug 7, 2018

2008 – 2014

United States locations

U.S. sites
29
U.S. states
20
U.S. cities
23
Facility City State ZIP Site status
Not listed Birmingham Alabama 35294-3300
Not listed Phoenix Arizona 85054
Not listed Los Angeles California 90033
Not listed Los Angeles California 90095-7077
Not listed San Francisco California 94115
Not listed Washington D.C. District of Columbia 20007
Not listed Miami Florida 33136
Not listed Atlanta Georgia 30322
Not listed Indianapolis Indiana 46202
Not listed Louisville Kentucky 40202
Not listed New Orleans Louisiana 70112
Not listed Baltimore Maryland 21287
Not listed Boston Massachusetts 02114
Not listed Boston Massachusetts 02215
Not listed Burlington Massachusetts 01805
Not listed Ann Arbor Michigan 48109
Not listed Minneapolis Minnesota 55407
Not listed Minneapolis Minnesota 55455
Not listed New York New York 10029
Not listed Cleveland Ohio 44106
Not listed Cleveland Ohio 44195
Not listed Columbus Ohio 43210
Providence Portland Medical Center Portland Oregon 97213
Not listed Portland Oregon 97239
Not listed Pittsburgh Pennsylvania 15213
Not listed Houston Texas 77030
Not listed Richmond Virginia 23249
Not listed Seattle Washington 98101
Not listed Seattle Washington 98109

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 170 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00692770, 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 Aug 7, 2018 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00692770 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →