Status:
COMPLETED
A Study to Investigate the Effect of ASP1517 After Intermittent Oral Dosing in Dialysis Chronic Kidney Disease Patients With Anemia Compared With Darbepoetin as a Reference Drug
Lead Sponsor:
Astellas Pharma Inc
Conditions:
Renal Anemia Associated With Chronic Renal Failure (CRF)
Eligibility:
All Genders
20-75 years
Phase:
PHASE2
Brief Summary
This study is to evaluate safety and efficacy of intermittent oral dosing of ASP1517 in dialysis chronic kidney disease patients with anemia.
Detailed Description
To evaluate the safety and the dose-response of ASP1517 on hemoglobin (Hb) correction when ASP1517 is applied intermittently in dialysis chronic kidney disease patients with anemia. To evaluate the t...
Eligibility Criteria
Inclusion
- Patients who diagnosed as a end-stage kidney disease (ESKD) and are receiving stable chronic maintenance dialysis 3 times per week for ≥ 12 weeks
- Patients who are receiving ESA for at least 8 weeks and the dose of ESA is within the dose range of ESA label
- Hb value at screening test is ≥10.0 g/dL
- Receiving hemodialysis via arteriovenous fistula (AVF) or arteriovenous graft (AVG) or via permanent catheter
- Most recent two Hb values before dialysis during washout period must be both \<9.5 g/dL and one of two Hb values must be tested on first visit of the week
Exclusion
- Proliferative retinopathy, age-related macular degeneration, retinal vein occlusion and/or macular edema that is considered to require treatment
- Immunological disease with severe inflammation as assessed by the Investigator; even if the inflammation is in remission, the subject is excluded (e.g. lupus erythematosus, rheumatoid arthritis, Sjogren's syndrome, celiac disease, etc)
- Having a history of gastric/intestinal resection considered influential on the absorption of the drug in the gastrointestinal tract or active gastroparesis
- Uncontrollable hypertension (SBP ≥160 mmHg and DBP ≥110 mmHg, before dialysis, at screening test)
- Congestive heart failure (NYHA classification III or higher)
- Having a history of hospitalization for stroke, myocardial infarction or lung infarction within 24 weeks before 1st registration
- Positive for any of the following: human immunodeficiency virus (HIV); hepatitis B surface antigen (HBsAg); or anti-hepatitis C virus antibody (anti-HCV Ab)
- Anemia other than anemia due to low/absent renal production of EPO (e.g., iron deficiency anemia, hemolytic anemia, pancytopenia, etc)
- Pure red cell aplasia
- Using anabolic androgenic steroid, testosterone enanthate or mepitiostane within 6 weeks before 1st registration
Key Trial Info
Start Date :
March 28 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 15 2014
Estimated Enrollment :
130 Patients enrolled
Trial Details
Trial ID
NCT01888445
Start Date
March 28 2013
End Date
September 15 2014
Last Update
October 30 2024
Active Locations (8)
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1
Chugoku, Japan
2
Chūbu, Japan
3
Hokuriku, Japan
4
Kansai, Japan