Drug Search Results

Satavaptan

Alternative Names: satavaptan, sr121463b
Latest Update: 2023-08-24
Latest Update Note: PubMed Publication

Product Description

Mechanisms of Action: V2 Antagonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Sanofi
Company Location: PARIS I0 75008
Company CEO: Paul Hudson
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Satavaptan

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 3: Liver Cirrhosis|Inappropriate ADH Syndrome|Hyponatremia|Diabetes Insipidus|Heart Failure

Phase 2: Liver Cirrhosis|Hyponatremia|Inappropriate ADH Syndrome|Diabetes Insipidus

Trial	Phase	Trial Status	Disease	Primary Completion Date
SPARe-2	P3	Completed	Liver Cirrhosis	2009-03-03
CATS	P3	Completed	Liver Cirrhosis	2008-12-30
PASCCAL-1	P2	Completed	Liver Cirrhosis	2008-12-03
AQUARIST1	P3	Terminated	Hyponatremia\|Inappropriate ADH Syndrome	2008-12-01

Recent News Events

Date	Type	Title
08/24/2023	PubMed	Safety and Efficacy of Vaptans in the Treatment of Hyponatremia from Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH): A Systematic Review and Meta-Analysis.
06/21/2023	PubMed	Non-Selective Beta-Blockers and Risk of Sepsis in Patients with Cirrhosis and Ascites: Results from a Large Observational Study.
11/01/2022	PubMed	Development and validation of the Cirrhotic Ascites Severity model-A patient-reported outcome-based model to predict 1-year mortality.

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