Clinical trial

Efficacy and Safety of SR121463B in Patients With Syndrome of Inappropriate…

NCT00264927 · Sanofi, Industry · Completed

Key facts

NCT number NCT00264927
Title Efficacy and Safety of SR121463B in Patients With Syndrome of Inappropriate Antidiuretic Hormone Secretion
Official title A Randomized, Double-Blind, Placebo-Group, Multicenter Study Evaluating the Efficacy and Safety of SR121463B in Patients With Syndrome of Inappropriate Antidiuretic Hormone Secretion
Acronym SIADH
Lead sponsor Sanofi, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Inappropriate ADH Syndrome, Hyponatremia
Intervention type Drug
Interventions SR121463B
Enrollment 77
Start date May 1, 2004
Primary completion Sep 1, 2007
Completion Sep 1, 2007
First posted Dec 13, 2005
Last update posted Dec 10, 2008
Countries Belgium, Brazil, Canada, Croatia, Germany, Hong Kong, Hungary, Netherlands, Portugal, Spain, United States

At a glance

  • 10–99 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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