Phase I/II Study to Evaluate the Efficacy and Safety of a Combination Chemotherapy

PHASE1TerminatedINTERVENTIONAL
Enrollment

12

Participants

Timeline

Start Date

June 30, 2006

Primary Completion Date

March 31, 2014

Study Completion Date

March 31, 2014

Conditions
Lung Cancer
Interventions
DRUG

Bortezomib 1.3 mg/m2

"Level I (every 21 day cycle, D8), 1.3 mg/m2:~Day 1: bevacizumab 15 mg/kg ,carboplatin Area Under the Curve (AUC 6) 900mg, bortezomib 1.3 mg/m2 Day 8 : bortezomib 1.3 mg/m2~Level II (every 21 day cycle):~Day 1: bevacizumab 15 mg/kg, carboplatin Area Under the Curve (AUC 6) 900mg, bortezomib 1.6 mg/m2 Day 8 : bortezomib 1.6 mg/m2~Level III(every 21 day cycle):~Day 1: bevacizumab 15 mg/kg, carboplatin Area Under the Curve (AUC 6) 900mg, bortezomib 1.8 mg/m2 Day 8 : bortezomib 1.8 mg/m2"

DRUG

Bortezomib 1.6 mg/m2

Level II (every 21 day cycle, D8), 1.6 mg/m2

DRUG

Bortezomib 1.8 mg/m2

Level III (every 21 day cycle, D8) 1.8 mg/m2

DRUG

Carboplatin AUC 6

Carboplatin AUC6

DRUG

Bevacizumab

Bevacizumab 15 mg/kg

DRUG

Taxotere

Taxotere 70 + G-CSF

Trial Locations (1)

01655-0002

University of Massachusetts Medical School, Worcester

All Listed Sponsors
collaborator

Millennium Pharmaceuticals, Inc.

INDUSTRY

collaborator

Genentech, Inc.

INDUSTRY

lead

University of Massachusetts, Worcester

OTHER