ClinicalTrials.Veeva

Menu

Combination Weekly Taxotere™ With Iressa™ /Placebo in Metastatic Breast Cancer

AstraZeneca logo

AstraZeneca

Status and phase

Completed
Phase 2

Conditions

Metastatic Breast Cancer

Treatments

Drug: Docetaxel
Drug: Gefitinib

Study type

Interventional

Funder types

Industry

Identifiers

NCT00319618
1839IL/0128

Details and patient eligibility

About

The purpose of this study is to determine if combination therapy of weekly Taxotere™ with Iressa™ will increase the objective responses in measurable leasions in metastatic breast cancer

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Histologically confirmed mammary carcinoma

Exclusion criteria

  • prior taxane chemotherapy for metastatic disease or prior treatment with tyrosine kinase inhibitors inhibiting the EGF receptor.
  • Prior hormone treatment or one type of anthracycline based treatment regimen without taxane for metastatic disease is allowed prior to inclusion.
  • If the patient has been treated in the adjuvant or neoadjuvant setting with taxanes, inclusion is allowed when the first cycle of trial medication is started 12 months after the last course of adjuvant treatment

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems