Viewing StudyNCT00341055



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Last Modification Date: 2024-10-26 @ 9:25 AM
Study NCT ID: NCT00341055
Status: COMPLETED
Last Update Posted: 2011-06-10
First Post: 2006-06-19

Brief Title: A Study to Evaluate the Hematologic Response Rate the Rate at Which the Hemoglobin Level Rises of PROCRIT Epoetin Alfa Given at a Dose of 80000 Units Once Weekly to Cancer Patients With Anemia Who Are Receiving Chemotherapy
Sponsor:
Organization: Johnson Johnson Pharmaceutical Research Development LLC

Study Design

Study Type: INTERVENTIONAL
Expanded Access Type Individual: None
Expanded Access Type Intermediate: None
Expanded Access Type Treatment: None
Patient Registry: None
Target Duration: None
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention: None
Bio Spec Description: None
Enrollment Count: 69
Enrollment Type: ACTUAL
Design Primary Purpose:
Design Masking:
Phases:
Name
PHASE3
Observational Models:
Time Perspective List:
Who Masked List: