99
Participants
Start Date
December 16, 2010
Primary Completion Date
September 11, 2013
Study Completion Date
September 11, 2013
Carboplatin
Carboplatin (carboplatin area under the plasma concentration-time curve \[AUC\] of 6 milligram per milliliter into minute \[mg/mL\*min\] administered as an intravenous (IV) infusion once every 21 days on Day 1, for a total of 6 doses (cycles) until unacceptable toxicity, disease progression, or other reasons for participant withdrawal.
Paclitaxel
Paclitaxel 200 milligram per square meter (mg/m\^2) administered as an intravenous (IV) infusion once every 21 days on Day 1, for a total of 6 doses (cycles) until unacceptable toxicity, disease progression, or other reasons for participant withdrawal.
MEDI-575
MEDI-575 at a dose of 25 milligram per kilogram (mg/kg) administered as an IV infusion once every 21 days on Day 1 for a total of 6 cycles until unacceptable toxicity, disease progression, initiation of alternative anticancer therapy, or other reasons for participant withdrawal. MEDI-575 alone continued in those participants who achieved stable disease or better at the completion of carboplatin/paclitaxel therapy and did not demonstrate toxicity to MEDI-575.
Research Site, Szombathely
Research Site, Lake Success
Research Site, Berlin
Research Site, Marseille
Research Site, Baltimore
Research Site, Baltimore
Research Site, Annapolis
Research Site, Hilton Head Island
Research Site, Chattanooga
Research Site, Canton
Research Site, Lafayette
Research Site, Detroit
Research Site, Chicago
Research Site, Omaha
Research Site, Baton Rouge
Research Site, Houston
Research Site, Corpus Christi
Research Site, Fountain Valley
Research Site, Oxnard
Research Site, Boston
Research Site, Danvers
Research Site, Hershey
Research Site, Ottawa
Research Site, Fukuoka
Research Site, Sunto-gun
Research Site, Gdansk
Research Site, Lodz
Research Site, Mrozy
Research Site, Szczecin
Lead Sponsor
MedImmune LLC
INDUSTRY