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Clinical Trial Summary

This is a multicenter, international, prospective, observational study of patients who are receiving systemic chemotherapy for solid tumour cancers (breast, colorectal, ovarian, prostate, lung, bladder, endometrial, renal, pancreatic, esophageal or gastric) and who are receiving darbepoetin alfa (Aranesp®) or other erythropoiesis-stimulating agent (ESA) to treat symptomatic anaemia.

Quality of Life will be assessed electronically with the aim of estimating improvement in quality of life for those patients receiving darbepoetin alfa (Aranesp®) who also have an increase in haemoglobin (Hb) of ≥1 g/dL


Clinical Trial Description

Before enrolling participants, each country was assigned to either cohort 1 (patients receiving only darbepoetin alfa) or cohort 2 (patients receiving any ESA). Cohort 2 was assigned only to those countries in which local regulations did not permit observational study participation by patients receiving a specific agent in a drug class. ;


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Anemia
  • Bladder Cancer
  • Breast Cancer
  • Cancer
  • Carcinoma, Renal Cell
  • Colorectal Cancer
  • Colorectal Neoplasms
  • Endometrial Cancer
  • Esophageal Cancer
  • Esophageal Neoplasms
  • Gastric Cancer
  • Kidney Neoplasms
  • Lung Cancer
  • Ovarian Cancer
  • Ovarian Neoplasms
  • Pancreatic Cancer
  • Pancreatic Neoplasms
  • Prostate Cancer
  • Prostatic Neoplasms
  • Renal Cancer
  • Solid Tumors
  • Stomach Neoplasms
  • Urinary Bladder Neoplasms

NCT number NCT01444456
Study type Observational
Source Amgen
Contact
Status Completed
Phase N/A
Start date October 2011
Completion date October 2013

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