Taxotere, Cisplatin, and CPT-11 in Advanced Solid Tumor Malignancies

PHASE1CompletedINTERVENTIONAL
Enrollment

46

Participants

Timeline

Start Date

September 30, 1999

Primary Completion Date

January 31, 2003

Study Completion Date

April 30, 2009

Conditions
Solid Tumor
Interventions
DRUG

Taxotere

Given intravenously on days 1 and 8 of a 21-day cycle. Participants can continue to receive study drug as long as there disease does not worsen and they do not experience serious side effects.

DRUG

Cisplatin

Given intravenously on days 1 and 8 of a 21-day cycle. Participants can continue to receive study drug as long as there disease does not worsen and they do not experience serious side effects.

DRUG

CPT-11

Given intravenously on days 1 and 8 of a 21-day cycle. Participants can continue to receive study drug as long as there disease does not worsen and they do not experience serious side effects.

Trial Locations (3)

02114

Massachusetts General Hospital, Boston

02115

Brigham and Women's Hospital, Boston

Dana-Farber Cancer Institute, Boston

All Listed Sponsors
collaborator

Brigham and Women's Hospital

OTHER

collaborator

Massachusetts General Hospital

OTHER

lead

Dana-Farber Cancer Institute

OTHER

NCT00251407 - Taxotere, Cisplatin, and CPT-11 in Advanced Solid Tumor Malignancies | Biotech Hunter | Biotech Hunter