A Phase I / II Trial of Nintedanib in Asian Hepatocellular Carcinoma Patients

NCT00987935 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 134

Last updated 2016-03-10

Study results available
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Summary

This study is to evaluate the safety, appropriate dose, and efficacy of BIBF 1120 in liver cancer patients

Conditions

  • Carcinoma, Hepatocellular

Interventions

DRUG

Sorafenib

400 mg twice daily

DRUG

BIBF 1120

Twice daily

Sponsors & Collaborators

Principal Investigators

  • Boehringer Ingelheim · Boehringer Ingelheim

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-10-31
Primary Completion
2014-07-31
Completion
2016-01-31

Countries

  • South Korea
  • Taiwan

Study Locations

More Related Trials

Entities

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 NCT00987935 on ClinicalTrials.gov