A Safety, Tolerability, and Pharmacokinetics Study of Onartuzumab as Single Agent or in Combination With Sorafenib in Participants With Advanced Hepatocellular Carcinoma

PHASE1CompletedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

September 30, 2013

Primary Completion Date

March 31, 2015

Study Completion Date

March 31, 2015

Conditions
Carcinoma, Hepatocellular
Interventions
DRUG

Onartuzumab

Onartuzumab intravenous infusion at a starting dose of 10 or 15 milligram per kilogram body weight administered every 3 weeks (Q3W) until disease progression or unacceptable toxicity occurs (maximum up to 31 months).

DRUG

Sorafenib

Sorafenib 400 milligram (mg) tablets (2 tablets of 200 mg each) orally once daily or twice daily depending on the cohort assigned until disease progression or unacceptable toxicity occurs (maximum up to 31 months).

Trial Locations (10)

100

Taipei

10065

New York

21231

Baltimore

34232

Sarasota

37203

Nashville

77030

Houston

119228

Singapore

169610

Singapore

Unknown

Pokfulam

00704

Tainan City

All Listed Sponsors
lead

Hoffmann-La Roche

INDUSTRY

NCT01897038 - A Safety, Tolerability, and Pharmacokinetics Study of Onartuzumab as Single Agent or in Combination With Sorafenib in Participants With Advanced Hepatocellular Carcinoma | Biotech Hunter | Biotech Hunter