Open Label Extension Study of Conatumumab and Ganitumab (AMG 479)

PHASE2CompletedINTERVENTIONAL
Enrollment

12

Participants

Timeline

Start Date

March 3, 2011

Primary Completion Date

February 5, 2020

Study Completion Date

February 5, 2020

Conditions
Advanced Solid TumorsCarcinoidColorectal CancerLocally AdvancedLymphomaMetastatic CancerNon-Small Cell Lung CancerSarcomaSolid Tumors
Interventions
DRUG

Modified FOLFOX6

The mFOLFOX6 regimen is a combination therapy of oxaliplatin 85 mg/m² administered as a 2-hour intravenous (IV) infusion on day 1 and leucovorin 400 mg/m² racemate or 200 mg/m² levo-leucovorin administered as a 2-hour infusion on day 1, followed by a loading dose of 5-fluorouracil (5-FU) 400 mg/m² IV bolus administered on day 1, then 5-FU 2400 mg/m² via ambulatory pump administered for a period of 46 to 48 hours every 14 days.

BIOLOGICAL

Conatumumab

Administered by intravenous infusion Q2W or Q3W.

BIOLOGICAL

Ganitumab

Administered by intravenous infusion Q3W or Q4W.

BIOLOGICAL

Bevacizumab

Administered at a dose of 5 mg/kg by intravenous infusion on day 1 of each 14 day cycle.

Trial Locations (12)

14263

Research Site, Buffalo

33612

Research Site, Tampa

38120

Research Site, Memphis

48109

Research Site, Ann Arbor

77030

Research Site, Houston

78229

Research Site, San Antonio

80218

Research Site, Denver

84403

Research Site, Ogden

91010

Research Site, Duarte

92093-0957

Research Site, La Jolla

70-891

Research Site, Szczecin

08035

Research Site, Barcelona

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Amgen

INDUSTRY