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Trial information

A Study to Optimize the Dose of PEGASYS (Peginterferon alfa-2a (40KD)) in Patients With Metastatic Malignant Melanoma

Status: Completed

Protocol number: NO16007

Sponsor: Hoffmann-La Roche Inc

Company division: Pharmaceutical

Official Scientific Title: A randomized, open-label, dose finding study of the effect of subcutaneous administration of PEGASYS on tumor response in patients with metastatic malignant melanoma.

Brief summary: This study will evaluate the safety and efficacy of different doses of PEGASYS in patients with metastatic malignant melanoma. The anticipated time on study treatment is 3-12 months and the target sample size is 100-500 individuals. Target sample size is 135.

Study phase: II

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

Condition: Malignant Melanoma

Intervention type: Drug

Intervention name: peginterferonalfa-2a (40KD) [PEGASYS]

Primary outcome: 1. Efficacy: Measurements of visible and palpable tumor, disease response

Key secondary outcomes: 1. Safety: AEs, laboratory tests results, vital signs

Inclusion criteria:

  • male or female patients, 18-75 years of age;
  • confirmed metastatic melanoma;
  • bidimensionally measurable disease.

Exclusion criteria:

  • fertile men or women, unless surgically sterile or using adequate contraceptive methods, and pregnant or lactating women;
  • patients who have received previous interferon therapy, chemotherapy or immunotherapy, investigational agents, or vaccines for stage IV melanoma.

Gender: Males or Females

Age limits: Min: 18 Years Max: 75 Years

Accepts healthy volunteers: No

Trial registration date: 07/26/2005

Date last updated: 9/29/2008


Link to trial result

This trial was conducted at the following locations:

Austria

  • Wien

Canada

  • Calgary, AB
  • Edmonton, AB
  • Montreal, QC

France

  • Bordeaux
  • Marseille
  • Nantes

Germany

  • Kiel
  • Mannheim
  • Tübingen

Italy

  • Milano

Netherlands

  • Rotterdam

Spain

  • Madrid
  • Valencia

Switzerland

  • Zürich

United Kingdom

  • Glasgow
  • Northwood

United States

  • San Diego , CA
  • San Francisco, CA
  • Vallejo, CA
  • Denver, CO
  • Miami, FL
  • Orlando, FL
  • Rochester, MN
  • Columbia , MO
  • St. Louis, MO
  • Albuquerque, NM
  • New York, NY
  • Rochester, NY
  • Pittsburgh, PA
  • Providence, RI
  • Memphis , TN
  • Seattle, WA

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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