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Created Extension study - This study was no longer feasible
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| Name | Class |
|---|---|
| Cardiokine Biopharma, LLC | INDUSTRY |
| Biogen | INDUSTRY |
To demonstrate that after 12 weeks of open-label lixivaptan treatment, serum sodium is maintained in hyponatremic patients continuing to receive lixivaptan compared to placebo during the 4 week double blind treatment period.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Placebo QD or BID | Placebo Comparator | Placebo QD or BID |
|
| Lixivaptan QD or BID | Experimental | Lixivaptan QD or BID |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Lixivaptan | Drug | Capsules containing 25, or 50 mg doses of oral lixivaptan to be administered BID or QD Lixivaptan will be administered for 12 weeks in the Open-Label Period which will be followed by a 4 week Randomized, Placebo-Controlled period. |
| Measure | Description | Time Frame |
|---|---|---|
| To demonstrate that after 12 weeks of open-label lixivaptan treatment, serum sodium is maintained in hyponatremic patients continuing to receive lixivaptan compared to placebo during the 4 week double blind treatment period. | 12 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| To demonstrate that after 12 weeks of open-label lixivaptan treatment, improvements in the time to complete the Trail Making Test (Part B) will be maintained in patients continuing to receive lixivaptan. | 20 weeks |
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Inclusion Criteria:
Men and Women with age greater than or equal to 18 years.
Prior successful participation in a randomized, blinded, placebo-controlled Phase 3 lixivaptan study of hyponatremia in Heart Failure (Protocol CK-LX3401) with evidence of continued need for therapy as follows:
The patient has clinical evidence of volume overload with at least one of the following:
Exclusion Criteria:
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| ID | Term |
|---|---|
| D004487 | Edema |
| ID | Term |
|---|---|
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| ID | Term |
|---|---|
| C409452 | lixivaptan |
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