Study to Evaluate Effectiveness of Aranesp®
NCT00117130 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL
Last updated 2011-01-21
Summary
The purpose of this study was to evaluate subject preference for Aranesp® administered once monthly (i.e., every 4 weeks (Q4W)) or Procrit® administered once weekly (QW).
Conditions
Interventions
- DRUG
-
Aranesp®
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
MD · Amgen
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
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