A Study of BMS-833923 With Cisplatin and Capecitabine in Inoperable, Metastatic Gastric, Gastroesophageal, or Esophageal Adenocarcinomas

PHASE1CompletedINTERVENTIONAL
Enrollment

39

Participants

Timeline

Start Date

November 30, 2009

Primary Completion Date

November 30, 2012

Study Completion Date

November 30, 2012

Conditions
Stomach NeoplasmsEsophageal Neoplasms
Interventions
DRUG

BMS-833923

Capsule, Oral, Starting dose 30 mg, Once daily, continuous until discontinuation from study

DRUG

Cisplatin

Vial, intravenous (IV), 80 mg/m² IV, Once every 21 days, 1 day per cycle until discontinuation from study

DRUG

Capecitabine

Tablets, Oral, 1000 mg/m², twice a day (BID), 14 days per cycle, until discontinuation from study

Trial Locations (6)

90033

Usc/Norris Comprehensive Cancer Center, Los Angeles

94805

Local Institution, Villejuif

91010-3012

City Of Hope National Medical Center, Duarte

77030-4009

The University Of Texas Md Anderson Cancer Center, Houston

M5G 2M9

Local Institution, Toronto

1105 AZ

Local Institution, Amsterdam

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Exelixis

INDUSTRY

lead

Bristol-Myers Squibb

INDUSTRY

NCT00909402 - A Study of BMS-833923 With Cisplatin and Capecitabine in Inoperable, Metastatic Gastric, Gastroesophageal, or Esophageal Adenocarcinomas | Biotech Hunter | Biotech Hunter