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Trial information

A Study of Herceptin (Trastuzumab) Monotherapy in Women With Metastatic Breast Cancer

Status: Completed

Protocol number: WO16229

Sponsor: Hoffmann-La Roche AG

Company division: Pharmaceutical

Official Scientific Title: An open-label study of the effect of Herceptin monotherapy on tumor response in women with metastatic breast cancer with HER2 overexpression/amplification

Brief summary: This study will assess the efficacy of treatment with intravenous Herceptin in patients with metastatic breast cancer who demonstrate overexpression of HER2. The anticipated time on study treatment is until disease progression and the target sample size is <100 individuals. Target sample size is 80.

Study phase: II

Study type: Interventional; Treatment; Non-Randomized; Open Label; Uncontrolled; Single Group; Safety/Efficacy study

Condition: Breast Cancer

Intervention type: Drug

Intervention name: trastuzumab[Herceptin]

Primary outcome: 1. Efficacy: Tumor response rate and progression

Key secondary outcomes: 1. Efficacy: Time to progression, clinical benefit rate. Safety: Adverse events, LVEF measurement, hematologic and biochemical parameters

Inclusion criteria:

  • female patients >=18 years of age;
  • metastatic breast cancer;
  • HER2 overexpression.

Exclusion criteria:

  • other invasive malignancy in the past 5 years;
  • prior cytotoxic chemotherapy, or >=2 hormone therapies for treatment of metastatic breast cancer.

Gender: Females

Age limits: Min: 18 Years Max: N/A (No limit)

Accepts healthy volunteers: No

Trial registration date: 06/24/2005

Date last updated: 8/19/2008


Link to trial result

This trial was conducted at the following locations:

Australia

  • Brisbane
  • Geelong
  • Parkville
  • Perth

Brazil

  • Porto Alegre

Canada

  • Calgary, AB
  • Winnipeg, MB
  • Ottawa, ON
  • Toronto, ON
  • Montreal, QC
  • Quebec City, QC

China

  • Hong Kong

Denmark

  • Århus
  • København

Germany

  • Stralsund
  • Trier

Italy

  • Milano
  • Parma
  • Treviglio

Mexico

  • Guadalajara
  • Mexico City

New Zealand

  • Auckland
  • Christchurch

Spain

  • Barcelona
  • Lleida
  • Madrid
  • Oviedo
  • Palma de Mallorca
  • San Juan
  • San Sebastian
  • Sevilla
  • Valencia

Sweden

  • Lund
  • Uppsala

Taiwan

  • Taipei

United Kingdom

  • Bedford
  • Cardiff
  • Glasgow
  • Leeds
  • Manchester
  • Oxford
  • Sutton

To contact Roche for more information on this trial please complete the email form below. Treatment decisions and/or suitability for a specific trial are decisions only your healthcare provider can make. If you are patient interested in any of the studies, please have your healthcare provider contact us via this website, and they will be provided with the relevant clinical trial information.

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