Breast Cancer Clinical Trial

Lapatinib In Chemotherapy-Naive Or Metastatic Breast Cancer

Summary

This phase II study will evaluate and compare the efficacy and tolerability of two dose schedules (1500 mg QD and 500 mg BID) of oral Lapatinib as treatment for patients with advanced or metastatic breast cancer.

View Eligibility Criteria

Eligibility Criteria

Inclusion criteria:

Histologically confirmed invasive breast cancer with incurable stage IIIB, IIIC with T4 lesion or stage IV disease at primary diagnosis or at relapse after curative intent surgery.
Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1.
Documented amplification of ErbB2 by Fluorescence in situ hybridization (FISH)
Measurable disease by Response Evaluation Criteria In Solid Tumors (RECIST)
Adequate renal, hepatic and cardiac function

Exclusion criteria:

Prior chemotherapy, immunotherapy, biologic therapy or anti-ErbB1/ErbB2 therapy other than adjuvant therapy. [Prior neo-adjuvant or adjuvant therapy (including trastuzumab) will be allowed provided it was stopped at least 12 months before study entry.
Patients with active brain metastases
Patients with bilateral breast cancer, bone metastases as the only disease site or metastases to more than 30% of the hepatic parenchyma.

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

138

Study ID:

NCT00089999

Recruitment Status:

Completed

Sponsor:

GlaxoSmithKline

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There are 23 Locations for this study

See Locations Near You

GSK Investigational Site
Hollywood Florida, 33021, United States
GSK Investigational Site
Santiago Región Metro De Santiago, 75009, Chile
GSK Investigational Site
Santiago Región Metro De Santiago, 83804, Chile
GSK Investigational Site
Santiago Región Metro De Santiago, , Chile
GSK Investigational Site
Pokfulam , , Hong Kong
GSK Investigational Site
Delhi , 11008, India
GSK Investigational Site
Hyderabad, Andhra Pradesh , 50048, India
GSK Investigational Site
Pune , 41100, India
GSK Investigational Site
Bandar Tun Razak, Cheras , 59100, Malaysia
GSK Investigational Site
Kubang Kerian , 16150, Malaysia
GSK Investigational Site
Tanjong Bungah , 10450, Malaysia
GSK Investigational Site
Tanjong Bungah , 11200, Malaysia
GSK Investigational Site
Ixtaltepec / Espinal Oaxaca, 70140, Mexico
GSK Investigational Site
Merida Yucatán, 97500, Mexico
GSK Investigational Site
Mexico , , Mexico
GSK Investigational Site
Karachi , 54000, Pakistan
GSK Investigational Site
Karachi , 74800, Pakistan
GSK Investigational Site
Karachi , , Pakistan
GSK Investigational Site
Lahore , , Pakistan
GSK Investigational Site
Rawalpindi , , Pakistan
GSK Investigational Site
Callao , Calla, Peru
GSK Investigational Site
Lima , Lima , Peru
GSK Investigational Site
Lima , Lima , Peru
GSK Investigational Site
Lima , Lima , Peru
GSK Investigational Site
Bydogoszcz , 85-79, Poland
GSK Investigational Site
Krakow , 31-11, Poland
GSK Investigational Site
Olsztyn , 10-22, Poland
GSK Investigational Site
Singapore , 16961, Singapore
GSK Investigational Site
Singapore , 25850, Singapore
GSK Investigational Site
Taipei , 100, Taiwan
GSK Investigational Site
Taipei , 114, Taiwan

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

138

Study ID:

NCT00089999

Recruitment Status:

Completed

Sponsor:


GlaxoSmithKline

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