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

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Amgen

Status and phase

Completed
Phase 4

Conditions

Anemia

Treatments

Drug: Aranesp

Study type

Interventional

Funder types

Industry

Identifiers

NCT00117117
20020132

Details and patient eligibility

About

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®.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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