Know Cancer

or
forgot password

QUALITY OF LIFE BENEFIT IN ANEMIC CANCER PATIENTS TREATED WITH NEORECORMON (EPOETIN BETA): QUALITY OF LIFE TREATMENT RESPONSE AND CLINICAL EVALUATION OF ONCE-WEEKLY DOSING


Phase 4
18 Years
N/A
Not Enrolling
Both
Anemia

Thank you

Trial Information

QUALITY OF LIFE BENEFIT IN ANEMIC CANCER PATIENTS TREATED WITH NEORECORMON (EPOETIN BETA): QUALITY OF LIFE TREATMENT RESPONSE AND CLINICAL EVALUATION OF ONCE-WEEKLY DOSING


Inclusion Criteria:



- male and female patients;

- >=18 years of age;

- anemia and prescribed treatment with NeoRecormon;

- confirmed diagnosis of a solid or lymphoid hematologic malignancy;

- receiving or scheduled to receive chemotherapy;

- life expectancy of >=6 months.

Exclusion Criteria:

- anemia after bleeding, hemolytic anemia, megaloblastic anemia, anemia in chronic
kidney failure, lever and endocrinology diseases;

- contraindications to NeoRecormon;

- administration of NeoRecormon during chemotherapy (e.g. on the third day after
chemotherapy cycle start);

- bleeding within one month before and/or during study;

- severe infection within one month before and/or during study;

- inability of patient to fill the questionnaires in.

Type of Study:

Interventional

Study Design:

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Clinical: Hematological response - increase in hemoglobin of at least 2 g/dL within the previous 6 weeks.

Outcome Time Frame:

Baseline, 3-4 weeks, 6-8 weeks, 10-12 weeks and 14-16 weeks after study start

Safety Issue:

No

Principal Investigator

Clinical Trials

Investigator Role:

Study Director

Investigator Affiliation:

Hoffmann-La Roche

Authority:

Russia: Ministry of Health of Russian Federation

Study ID:

ML20197

NCT ID:

NCT00776425

Start Date:

March 2007

Completion Date:

January 2011

Related Keywords:

  • Anemia
  • Anemia

Name

Location