A Study of the Efficacy and Safety of MK2578 for the Treatment of Anemia in Patients With Kidney Disease (MK2578-003-AM03-EXT12)

• Status: Terminated
• Trial end date: 2010-05-01
• Target enrollment: 0
• Participant gender: All

Summary

This study will evaluate the efficacy and safety of intravenous MK2578, given as maintenance treatment for renal anemia in chronic kidney disease patients on dialysis who were previously receiving erythropoietin stimulating agents.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Merck Sharp & Dohme Corp.
• Treatments: Epoetin Alfa

Criteria

Inclusion Criteria:

Base Study:

• Patient is male or is a female who either cannot have children or who agrees to use appropriate contraceptive measures

• Patient has been on hemodialysis for at least 6 months when informed consent is signed

• Patient has received intravenous epoetin alfa or epoetin beta for a least 6 months when the informed consent is signed

Extension Study:

• Patient completed the base study through Week 12

• Patient tolerated MK2578 and demonstrated compliance with study procedures

Exclusion Criteria:

• Patient has a life expectancy of less than 6 months

• Patient is scheduled for a kidney transplant within the next 6 months

• Patient has had a blood transfusion within 12 weeks of screening

• Patient has had major surgery within 12 weeks of screening or plans to have surgery

• Patient has Human Immunodeficiency Virus (HIV)

• Patient has history of blood dyscrasia, hematologic disorders or any other disease known to cause anemia

• Patient has severe congestive heart failure (CHF)

• Patient has a history of malignant cancer, except certain skin or cervical cancers

• Patient has a history of grand mal seizures within the last 6 months