Status:

COMPLETED

A Phase II Study of Oxaliplatin in Association With 5FU and Folinic Acid in the Treatment of Subjects With Non-Surgical or Advanced Metastatic Gastric Cancer

Lead Sponsor:

Sanofi

Conditions:

Stomach Neoplasms

Eligibility:

All Genders

18+ years

Phase:

PHASE2

Brief Summary

This phase II trial will evaluate, in first line advanced or metastatic gastric cancer, the efficacy and tolerance of another oxaliplatin, 5FU bolus combination already tested in advanced colorectal c...

Eligibility Criteria

Inclusion

  • Histologically proven gastric or gastroesophagic junction adenocarcinoma
  • Measurable disease at least in a unidimensional manner. If a unique metastasis constitutes the only disease symptom, histological confirmation will be required
  • Metastatic or locally non-surgical primary gastric cancer
  • Recurrent gastric cancer after local and/or systemic treatment with a post-surgical period of at least 4 weeks, a post-adjuvant chemotherapy period or a neo-adjuvant chemo-radiotherapy of at least 6 months
  • Serum bilirubin\< 2 mg/dl
  • Serum creatinine \< or =to 2 times normal superior limit
  • Absolute neutrophil count \> or =to 2000/dl
  • Platelet count \> or =to 100000/dl
  • Hemoglobin \> or =to 10 g/dl
  • AST/ALT \< or =to 2.5 times normal superior institutional limit
  • Alkaline phosphatase \< or =to 5 times the normal superior institutional limit
  • Age \> 18 years
  • Performance Status ECOG 0-2
  • Written informed consent signed and dated

Exclusion

  • Symptomatic sensory peripheral neuropathy
  • Uncontrolled concomitant disease.(e.g. severe diabetes mellitus, arterial hypertension)
  • Any other malignancy diagnosed within 5 years previous to the gastric cancer, with the exception of " in situ " cervix carcinoma or non-melanoma skin cancer
  • Concomitant anti-tumoral treatment
  • Cerebral metastases
  • Unstable heart disease, even though under treatment
  • Myocardial infarction within the last 6 months
  • Pregnancy or nursing (or women in reproductive life without adequate contraception)
  • Significant neurological or psychiatric disorders

Key Trial Info

Start Date :

November 1 2002

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

April 1 2004

Estimated Enrollment :

21 Patients enrolled

Trial Details

Trial ID

NCT00611507

Start Date

November 1 2002

End Date

April 1 2004

Last Update

March 25 2008

Active Locations (1)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (1 locations)

1

Sanofi-Aventis

Bogotá, Colombia