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Clinical Trials/EUCTR2005-005464-92-DE
EUCTR2005-005464-92-DE
Active, not recruiting
Not Applicable

A randomized phase II study of docetaxel in combination with oxaliplatin with or without 5-FU or capecitabine in metastatic or locally recurrent gastric cancer previously untreated with chemotherapy for advanced disease. - DOCOX GASTRIC (Docetaxel-Oxaliplatin in Gastric Cancer)

Sanofi-aventis groupe0 sites270 target enrollmentSeptember 14, 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Sanofi-aventis groupe
Enrollment
270
Status
Active, not recruiting
Last Updated
13 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 14, 2006
End Date
TBD
Last Updated
13 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\.Patient’s consent form obtained, signed and dated before beginning specific protocol procedures.
  • 2\.Histologically proven gastric adenocarcinoma, including adenocarcinoma of the gastro\-oesophageal junction,
  • 3\.Metastatic or locally recurrent disease
  • 4\.Prior adjuvant (and/or neo\-adjuvant) chemotherapy with 5\-FU, CDDP, epirubicin is allowed provided that the patient has relapsed \> 12 months after the end of the chemotherapy.
  • 5\.At least 4 weeks from prior radiotherapy for palliation of metastases and 3 weeks from surgery.
  • 6\.Patient age \= 18
  • 7\.Performance status Karnofsky index \> 70
  • 8\.Hematology within 7 days before randomization:
  • Hb \=10g/dl, ANC \=2\.0 109/L, platelets \=100 x 109/L
  • 9\.Blood chemistry within 7 days before randomization:

Exclusion Criteria

  • Patients will be excluded from this study if they meet any of the following criteria:
  • 1\.Other tumor type than adenocarcinoma
  • 2\.Any prior palliative chemotherapy.
  • 3\.Any prior adjuvant (and/or neo\-adjuvant) chemotherapy other than those specified in inclusion criterion \#4\.
  • 4\.No prior Taxotere® or Eloxatin® or Xeloda®
  • 5\.Neurosensory symptoms NCI\-CTCAE grade\=2
  • 6\.Prior radiotherapy other than (neo) adjuvant. In case of (neo)adjuvant radiotherapy, the relapse must be outside the radiotherapy fields
  • 7\.Previous or other current malignancies, with the exception of adequately treated in situ carcinoma of the cervix uteri or non melanoma skin cancer and of (any) cancers cured more than 5 years before study entry
  • 8\.Other serious illness or medical conditions:
  • \-unstable cardiac disease despite treatment, myocardial infarction within 6 months prior to study entry,

Outcomes

Primary Outcomes

Not specified

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