Clinical TrialID 1423

Sorafenib Plus Tegafur/Uracil (UFUR®) for Hepatocellular Carcinoma (HCC)

NCT00464919

Hepatocellular Carcinoma

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
1423
Evidence Id
1423
Core Evidence Id
1423
Source Clinical Trial Id
1403
Herb2 Clinical Trial Id
HBCT001403
Nct Id
NCT00464919
Title
Sorafenib Plus Tegafur/Uracil (UFUR®) for Hepatocellular Carcinoma (HCC)
Status
Completed
Phase
Phase 2
Study Result
No
Study Condition
Hepatocellular Carcinoma
Study Type
Interventional
Study Design
Allocation: NON_RANDOMIZED|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
Intervention
DRUG: Sorafenib|DRUG: tegafur/uracil (UFUR®)
Intervention Allocation
Non_Randomized
Intervention Model
Single_Group
Intervention Mask
Intervention Purpose
Treatment
Gender
All
Age
Adult, Older_Adult
Enrollment
50
Outcome Measure
To determine the progression- free survival of sorafenib plus tegafur/uracil (UFUR®) for the treatment of advanced or metastatic HCC., 2007~2008
Sponsor Collaborator
National Taiwan University Hospital
Funded By
OTHER
Location
National Taiwan University Hospital, Taipei, 100, Taiwan
Other Id
950914
Start Date
2007-04
Primary Completion Date
Completion Date
2009-03
First Posted
2007-04-24
Results First Posted
Last Update Posted
2009-07-07
Study Document
Study Url
https://clinicaltrials.gov/study/NCT00464919
Title Cn
Title En
Sorafenib Plus Tegafur/Uracil (UFUR®) for Hepatocellular Carcinoma (HCC)
Bilingual Status
semi_complete