None listed
Conditions
Interventions
Paclitaxel, UFT and Leucovorin, days 1,8 and 15 every 4 weeks, until disease progression or clinical decision.
Sponsors
CTRG initiated study
Study design
Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Open (masking not used)
Eligibility
Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
No
Inclusion criteria
First line metastatic, female, adequate haematological, renal and hepatic function.
Exclusion criteria
No exclusion criteria
Outcome results
None listed