Study of Efficacy & Safety of Oral YM087 in Subjects With Euvolemic or Hypervolemic Hyponatremia
NCT00492037 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 83
Last updated 2014-05-02
Summary
Study of efficacy \& safety of oral YM087 in subjects with euvolemic or hypervolemic hyponatremia
Conditions
Interventions
- DRUG
-
YM087 oral
Sponsors & Collaborators
-
Parke-Davis
collaborator INDUSTRY -
Cumberland Pharmaceuticals
lead INDUSTRY
Principal Investigators
-
Art Wheeler, MD · Cumberland Pharmaceuticals, Inc.
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 85 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2000-01-31
- Completion
- 2002-02-28
Countries
- Belgium
- Finland
- France
- Germany
- Italy
- Netherlands
- Poland
- Spain
- United Kingdom
Study Locations
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