Status:

COMPLETED

Effects Of Nadroparin In Patients With Lung, Pancreas Or Prostate Cancer

Lead Sponsor:

GlaxoSmithKline

Conditions:

Thrombosis, Venous

Eligibility:

All Genders

18+ years

Phase:

PHASE3

Brief Summary

This study will evaluate the effects of nadroparin on survival and disease progression in patients with hormone-refractory prostate cancer (HRPC), locally advanced pancreatic cancer or non-small-cell ...

Eligibility Criteria

Inclusion

  • Inclusion criteria:
  • Hormone refractory prostate cancer within 6 months of diagnosis, OR locally advanced (non-metastasized) pancreatic cancer within 3 months of diagnosis, OR non-small-cell lung cancer within 3 months of stage IIIB.
  • Exclusion criteria:
  • Life expectancy of \<3 months.
  • Poor performance status (Karnofsky \<60).
  • Need to be on anticoagulants.
  • Use of nadroparin (a low molecular weight heparin) for any reason including a history of heparin-induced thrombocytopenia.
  • Have brain metastasis.
  • At a high risk of bleeding or have a platelet count \<50,000/mm3.
  • Have very poor kidney function.

Exclusion

    Key Trial Info

    Start Date :

    May 1 2006

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    July 1 2009

    Estimated Enrollment :

    503 Patients enrolled

    Trial Details

    Trial ID

    NCT00312013

    Start Date

    May 1 2006

    End Date

    July 1 2009

    Last Update

    March 23 2017

    Active Locations (95)

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    Page 1 of 24 (95 locations)

    1

    GSK Investigational Site

    Aalst, Belgium, 9300

    2

    GSK Investigational Site

    Antwerp, Belgium, 2020

    3

    GSK Investigational Site

    Brasschaat, Belgium, 2930

    4

    GSK Investigational Site

    Brussels, Belgium, 1070