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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01964196
Other study ID # 1517-CL-0303
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date September 17, 2013
Est. completion date December 1, 2015

Study information

Verified date April 2021
Source Astellas Pharma Inc
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is to evaluate the safety and the dose-response of ASP1517 in the treatment of anemia in non-dialysis Chronic Kidney Disease (CKD) patients when ASP1517 is applied intermittently.


Description:

To evaluate the safety and the dose-response of ASP1517 on Hemoglobin (Hb) correction in the treatment of anemia in non-dialysis Chronic Kidney Disease (CKD) patients when ASP1517 is applied intermittently. Patients will receive ASP1517 three times a week (TIW) for first 6weeks. Patients may have the second-randomization to TIW dosing or once-a-week (QW) dosing at Week 6, 8, 10, 12, 14 or 16 if patients meet the criteria.


Recruitment information / eligibility

Status Completed
Enrollment 107
Est. completion date December 1, 2015
Est. primary completion date July 6, 2015
Accepts healthy volunteers No
Gender All
Age group 20 Years to 74 Years
Eligibility Inclusion Criteria: - Chronic kidney disease with an estimated glomerular filtration rate (as calculated by the Japanese GFR estimation equation) of =<89 mL/min/1.73 m2, and not required dialysis for 3 months since study completion - The mean of two Hb values at screening test and Hb test (at least one week apart form the screening test) is <10.0 g/dL, with a difference of =1.0 g/dL between the two values - Both TSAT>=5% and ferritin >=30 ng/mL at screening test - Serum folate =4.0 ng/mL and Vitamin B12 =180 pg/mL at screening test Exclusion Criteria: - 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 evidence of active gastroparesis. - Uncontrollable hypertension (more than one third blood pressure values of diastolic BP >100 mmHg within 16 weeks prior to screening test including) - Congestive heart failure (NYHA classification III or higher) - Having a history of hospitalization for stroke, myocardial infarction or lung infarction within 24 weeks before screening test - Positive for any of the following: anti-hepatitis C virus antibody (anti-HCV Ab); hepatitis B surface antigen (HBsAg); or human immunodeficiency virus (HIV) - Anemia other than anemia due to low/absent renal production of EPO (e.g., iron deficiency anemia, hemolytic anemia, pancytopenia, etc) - Using ESA, anabolic androgenic steroid, testosterone enanthate or mepitiostane within 6 weeks before screening test

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
ASP1517
Oral administration
Placebo
Oral

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Astellas Pharma Inc

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of rise in Hb (g/dL/week) at Week 6 Baseline and at 6 weeks after dosing
Secondary Percentage of cumulative number of responder patients responder is defined as a Hb =10.0 g/dL and an increase in Hb by =1.0 g/dL for 28 weeks after dosing
Secondary Percentage of visits at which patients maintain Hb between 10.0-12.0 g/dL after achieving Hb =10.0 g/dL for each patients for 28 weeks after dosing
Secondary Percentage of patients who maintain Hb between 10.0-12.0 g/dL at each visit Before and Week-2, -3, -4, -6, -8, -10, -12, -14, -16, -18, -20, -22, -24 and -28
Secondary Change from baseline in Hb Before and Week-2, -3, -4, -6, -8, -10, -12, -14, -16, -18, -20, -22, -24 and -28
Secondary Safety assessed as the incidence of adverse events, vital signs, 12-lead ECGs and lab-tests for 28 weeks after dosing
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