Home >  Registry
     
 
Protocol Registry Trial Results IFPMA Background Links
About this Registry

This registry serves as a global repository for information on ongoing Roche Pharmaceuticals Phase II to Phase IV clinical studies, Phase I studies in patients and Roche Diagnostics interventional studies on advanced diagnostic products.

For More Information 

Common Questions
More Frequently Asked Questions 
Overview of Clinical Trials 
Glossary of Terms 
Phase Definitions 
Field Definitions 
Roche Clinical Trial Global Policy 
Site Provided by Thomson CenterWatch

Trial information

A Study of Management of Tarceva - Induced Rash in Patients With Non-Small Cell Lung Cancer.

Status: Recruiting

Protocol number: ML20829

Sponsor: Hoffmann-La Roche

Company division: Pharmaceutical

Official Scientific Title: A randomized, open label study to evaluate the effect of doxycycline on Tarceva-induced skin rash in patients with non-small cell lung cancer after failure of first line chemotherapy

Brief summary: This 2 arm study will evaluate the management of Tarceva-induced skin rash in patients with non-small cell lung cancer who have failed first-line chemotherapy for advanced disease. Eligible patients will be randomized to receive a)doxycycline 100mg po daily or b)no preventative treatment; all patients will receive Tarceva 150mg/kg po daily. The anticipated time on study treatment is until disease progression or intolerable toxicity, and the target sample size is 100-500 individuals. Target sample size is 120.

Study phase: II

Study type: Interventional; Treatment; Randomized; Open Label; Active; Parallel; Safety/Efficacy study

Condition: Non-Small Cell Lung Cancer

Intervention type: Drug

Intervention name: erlotinib [Tarceva]

Primary outcome: 1. Incidence of skin rash Time frame: First 4 months of treatment

Key secondary outcomes: 1. Response rate, rate of disease control, PFS, 1 year survival. Time frame: Event driven 2. Specific skin toxicity assessment, AEs, laboratory parameters. Time frame: Throughout study

Inclusion criteria:

  • adult patients, 18-75 years of age;
  • confirmed non-small cell lung cancer;
  • failure after first line chemotherapy for advanced disease, and scheduled for second line therapy with Tarceva.

Exclusion criteria:

  • rash of any etiology at study entry;
  • history of significant heart disease;
  • any other malignancies (other than adequately treated squamous cell skin cancer, or in situ cancer of the cervix);
  • history of allergic reactions to tetracyclines.

Gender: Males or Females

Age limits: Min: 18 Years Max: 75 Years

Accepts healthy volunteers: No

Anticipated start date: November, 2007

Trial registration date: 09/17/2007

Date last updated: 8/19/2008


Link to trial result

This trial is being conducted at the following locations:

France

  • Angers
  • Antibes
  • Bobigny
  • Bordeaux
  • Brest
  • Caen
  • Chalon Sur Saone
  • Chartres
  • Draguignan
  • Gap
  • Gleize
  • Le Mans
  • Levallois Perret
  • Limoges
  • Metz
  • Nimes
  • Paris
  • Perigueux
  • Perpignan
  • Pierre Benite
  • Pontoise
  • Rennes
  • Rouen
  • Tours
  • Vannes

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.

Country*
Are you a:*
Subject*
Last Name*
First Name*
Telephone
E-mail*

your email address is needed for us to reply