Erythropoietin Alfa in Elderly Subjects With Unexplained Anemia

Eligible subjects will be recruited out of the companion study "Anemia in the Elderly"
(NCT00640172), after active participation in that study is complete. Subjects will have had
a full hematologic evaluation, and unexplained anemia will have been previously defined.

Subjects will provide baseline physical function testing, including exercise testing on a
treadmill and testing how far patients can walk in 6 minutes (walk test), as well as quality
of life; activity level; and mental functioning.

Study visits will be weekly, and the dose level may be adjusted to achieve the target
hemoglobin level within 16 weeks. Once at target, the drug will be taken for a total of 12
additional weeks. The maximum time on the study drug could be 28 weeks, and the minimum time
be on the 14 weeks.

The walk tests and questionnaires will be repeated when the target hemoglobin level is
reached, and when treatment is completed. The tests about quality of life, activity level,
and mental functioning will be repeated at the end of treatment. Follow-up visits will be
every 4 weeks for 12 weeks to check for side effects.

INCLUSION CRITERIA:

- Aged ≥ 65

- Hb ≤ 11 g/dL

- Outpatient at either the VA Palo Alto Health Care Systems (VAPAHCS) or Stanford
Hospital and Clinics (SHC)

- Independently living in the community (ie, not institutionalized or living in a group
home)

- Ability to understand and the willingness to sign a written informed consent document

- Performance level ECOG 2 or better

- Diagnosis of unexplained anemia

EXCLUSION CRITERIA:

- Substance abuse or mental health or other problems that would affect compliance with
the protocol

- Predicted mortality based on co-morbidities of less than 3 months

- On any erythropoiesis-stimulating agent in the prior 3 months

- Known HIV; hepatitis B; or hepatitis C chronic infection

- Clinically significant and uncontrolled medical condition considered a high risk for
participation in an investigational study

- Serum albumin < 3 g/dL

- Use of an investigational medication or participation in an investigational study
within 4 weeks prior to enrollment in the trial

- Liver disease as defined as total bilirubin ≥ 2 g/dL or AST/ALT ≥ 2 times the upper
limit of normal

- Allergy to recombinant human erythropoietin

- Estimated glomerular filtration rate by Modification of Diet in Renal Disease (MDRD)
equation of < 30 mL/min/1.73 m2 or dialysis

- History of proximal deep venous thrombosis or pulmonary embolism within the past 12
months

- Known contraindication to exercise testing