Status:

COMPLETED

Study of IV YM087 to Assess Efficacy and Safety in Patients With Euvolemic or Hypervolemic Hyponatremia

Lead Sponsor:

Cumberland Pharmaceuticals

Collaborating Sponsors:

Astellas Pharma US, Inc.

Conditions:

Hyponatremia

Eligibility:

All Genders

18+ years

Phase:

PHASE3

Brief Summary

This study will investigate the application of a vasopressin antagonist in the treatment of hyponatremia most likely caused by inappropriate AVP secretion. The population studied will include patients...

Eligibility Criteria

Inclusion

  • Serum sodium levels 115 to \< 130mEq/L
  • Euvolemic or Hypervolemic hyponatremia

Exclusion

  • Clinical evidence of volume depletion or dehydration
  • Untreated severe hypothyroidism, hyperthyroidism, or adrenal insufficiency
  • Uncontrolled brady-or tachyarrhythmias requiring pacemaker placement or treatment

Key Trial Info

Start Date :

August 1 2000

Trial Type :

INTERVENTIONAL

End Date :

February 1 2003

Estimated Enrollment :

84 Patients enrolled

Trial Details

Trial ID

NCT00380575

Start Date

August 1 2000

End Date

February 1 2003

Last Update

May 2 2014

Active Locations (47)

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Page 1 of 12 (47 locations)

1

Mobile, Alabama, United States

2

Phoenix, Arizona, United States

3

Tuscon, Arizona, United States

4

La Jolla, California, United States

Study of IV YM087 to Assess Efficacy and Safety in Patients With Euvolemic or Hypervolemic Hyponatremia | DecenTrialz