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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03345316
Other study ID # FFI-1010-004
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date November 1, 2017
Est. completion date November 1, 2019

Study information

Verified date December 2019
Source Fuji Yakuhin Co., Ltd.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is revealing that the ratio of creatinine clearance (Ccr) to inulin clearance (Cin) measuring at the same time is more than 1.2.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date November 1, 2019
Est. primary completion date November 1, 2019
Accepts healthy volunteers No
Gender All
Age group N/A to 18 Years
Eligibility Inclusion Criteria:

- Kidney disease patients requiring exact evaluation of kidney function

- eGFR: >=30 and <=89 mL/min/1.73m^2

Exclusion Criteria:

- Edema on the day before start of study treatment

- Oliguria on the day before start of study treatment

- Dehydration on the day before start of study treatment

- Infection or inflammatory disease before administration

- History of epilepsy or organic brain disorder

- History of, clinically significant cardiac, hematologic, hepatic and pancreatic disease

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
FFI-1010
Intravenous single dosing

Locations

Country Name City State
Japan Fuji Yakuhin Investigational sites Tokyo

Sponsors (1)

Lead Sponsor Collaborator
Fuji Yakuhin Co., Ltd.

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ratio of Cin to Ccr measuring at the same time Demonstrating usability of inulin clearance by comparison between inulin clearance and creatinine clearance at the same time after the start of FFI-1010 administration 120 minutes