c-Met Second-Line Hepatocellular Carcinoma

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

66

Participants

Timeline

Start Date

May 18, 2014

Primary Completion Date

February 14, 2018

Study Completion Date

February 14, 2018

Conditions
Carcinoma, Hepatocellular
Interventions
DRUG

Tepotinib

Participants received a single oral dose of Tepotinib 300 milligram (mg) in each 21 days treatment cycle until progressive disease, intolerable toxicity, death, or withdrawal from treatment.

DRUG

Tepotinib

Participants received a single oral dose of Tepotinib 500 mg daily in each 21 days treatment cycle until progressive disease, intolerable toxicity, death, or withdrawal from treatment.

Trial Locations (1)

Unknown

Please contact the Merck KGaA Communication Center located in, Darmstadt

All Listed Sponsors
lead

Merck KGaA, Darmstadt, Germany

INDUSTRY

NCT02115373 - c-Met Second-Line Hepatocellular Carcinoma | Biotech Hunter | Biotech Hunter