Overview
Clinical Pharmacology Trial to Investigate the Dose of OPC-61815 Injection Equivalent to Tolvaptan 15-mg Tablet in Patients With Congestive Heart Failure
Status:
Completed
Completed
Trial end date:
2018-04-24
2018-04-24
Target enrollment:
0
0
Participant gender:
All
All
Summary
The dose for intravenous administration of OPC-61815 achieving tolvaptan exposure equivalent to that for oral administration of tolvaptan 15-mg tablet will be investigated by administering OPC-61815 injection 2 to 16mg or tolvaptan 15-mg oral tablet to subjects with congestive heart failure.Phase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Otsuka Pharmaceutical Co., Ltd.Treatments:
Tolvaptan
Criteria
Inclusion Criteria:1. Subjects who are currently on treatment with any of the following diuretics
- Loop diuretics equivalent to furosemide tablet or fine granules at a dose of 40
mg/day or higher
- Concomitant use of a loop diuretic and a thiazide diuretic (including thiazide
analogs) at any dose
- Concomitant use of a loop diuretic and an aldosterone antagonist or
potassium-sparing diuretic agent at any dose
2. Subjects with congestive heart failure in whom lower limb edema, pulmonary congestion,
and/or jugular venous distension due to volume overload is present
3. Subjects who are currently hospitalized or who are able to be hospitalized during the
trial
Exclusion Criteria:
1. Subjects with acute heart failure
2. Subjects with a history of hypersensitivity to any of ingredients of OPC-61815 or
tolvaptan
3. Subjects who are unable to sense thirst or who have difficulty with fluid intake