A Study to Assess Symptom Burden in Subjects With Nonmyeloid Malignancies Receiving Chemotherapy and Aranesp®

The purpose of this trial is to prospectively assess the relationship between changes in hemoglobin (hgb) and changes in symptom burden associated with anemia in cancer patients receiving chemotherapy supported with Aranesp®.

Completed

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Key information

Conditions

Anemia Hematologic Diseases Hemic and Lymphatic Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Subjects with nonmyeloid malignancy(ies)
Anemia (hgb less than or equal to 11.0 g/dL) due to cancer and chemotherapy

Exclusion criteria

Subjects with acute myelogenous leukemia (AML), chronic myelogenous leukemia (CML), myelodysplastic syndromes (MDS)
Unstable cardiac disease or anemia due to other causes

Treatment and study plan

Aranesp

Drug

Primary outcomes

Patient reported outcomes

Secondary outcomes

Changes in hemoglobin endpoints and RBC transfusion requirements

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Completed

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Sponsors and collaborators

Lead sponsor

Amgen

Industry

Registry information

Important dates

Study start: 2002
Study completion: 2003
First posted: Jul 4, 2005
Registry last updated: Mar 25, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed