Ozmosi | Tedisamil Drug Profile

Product Description

Mechanisms of Action: Voltage-Gated Potassium Channel Blocker

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: N/A

FDA Designation: *

Approval Status: Not Approved

Approved Countries: Sweden

Approved Indications: None

Known Adverse Events: None

Company: Solvay Pharmaceuticals
Company Location:
Company Founding Year: None
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Atrial Fibrillation|Atrial Flutter

Trial ID	Trial	Phase	Trial Status	Disease	Primary Completion Date	Latest Trial Update Date	Data Updated
NCT00126022	S219.3.116	P3	Completed	Atrial Flutter\|Atrial Fibrillation	2006-03-01	2019-03-21	Treatments
NCT00126074	S219.3.118	P3	Completed	Atrial Fibrillation\|Atrial Flutter	2006-03-01	2019-03-21	Treatments
NCT00126061	S219.3.117	P3	Completed	Atrial Flutter\|Atrial Fibrillation	2006-01-01	2019-03-21	Treatments
2004-000346-21	2004-000346-21	P3	Active, not recruiting	Atrial Flutter\|Atrial Fibrillation	2005-03-06	2022-03-12	Treatments

Recent News Events

Date	Type	Title
07/01/2023	PubMed	Bayesian Network Meta-analysis of Randomized Controlled Trials on the Efficacy of Antiarrhythmics in the Pharmacological Cardioversion of Paroxysmal Atrial Fibrillation.
04/11/2022	PubMed	Effect of Early Pharmacologic Cardioversion vs. Non-early Cardioversion in the Patients With Recent-Onset Atrial Fibrillation Within 4-Week Follow-Up Period: A Systematic Review and Network Meta-Analysis.
07/01/2020	PubMed	Pharmacologic Cardioversion of Recent-Onset Atrial Fibrillation and Flutter in the Emergency Department: A Systematic Review and Network Meta-analysis.

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Tedisamil

Alternative Names: tedisamil Clinical Status: Inactive Latest Update: 2023-07-01 Latest Update Note: PubMed Publication