Status:

UNKNOWN

Residual Plasma Concentration of Sorafenib and Adverse Events in CHC

Lead Sponsor:

University Hospital, Caen

Conditions:

Advanced or Metastatic Hepatocellular Carcinoma

Eligibility:

All Genders

18+ years

Brief Summary

To date, Sorafenib is the only drug therapy to have demonstrated a benefit in overall survival in patients with advanced or metastatic hepatocellular carcinoma. However, this treatment causes many adv...

Eligibility Criteria

Inclusion

  • Major Patients.
  • Patients with hepatocellular carcinoma on cirrhosis.
  • Patients treated for the first time with sorafenib for hepatocellular carcinoma.
  • Informed information about the study.

Exclusion

  • Patients with contraindications to sorafenib.
  • Pregnant or lactating woman

Key Trial Info

Start Date :

January 1 2018

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

March 1 2019

Estimated Enrollment :

60 Patients enrolled

Trial Details

Trial ID

NCT03340636

Start Date

January 1 2018

End Date

March 1 2019

Last Update

November 13 2017

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Caen University Hospital

Caen, France

Residual Plasma Concentration of Sorafenib and Adverse Events in CHC | DecenTrialz