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Last Updated: December 22, 2024

CLINICAL TRIALS PROFILE FOR VERELAN PM

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All Clinical Trials for VERELAN PM

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Trial ID	Title	Status	Sponsor	Phase	Start Date	Summary
NCT00589303 ↗	AV Node Ablation and Pacemaker Therapy Compared to Drug Therapy for Atrial Fibrillation - Pilot Study	Terminated	Medtronic	Phase 3	2007-12-01	The purpose of this study is to determine whether early atrioventricular node (AVN) ablation with pacing device therapy will reduce death and hospitalization when compared to the conventional drug therapy in elderly patients with recurrent and symptomatic atrial fibrillation (AF).
NCT00589303 ↗	AV Node Ablation and Pacemaker Therapy Compared to Drug Therapy for Atrial Fibrillation - Pilot Study	Terminated	Mayo Clinic	Phase 3	2007-12-01	The purpose of this study is to determine whether early atrioventricular node (AVN) ablation with pacing device therapy will reduce death and hospitalization when compared to the conventional drug therapy in elderly patients with recurrent and symptomatic atrial fibrillation (AF).
NCT00647673 ↗	Fasting Study of Verapamil HCl Extended-Release Capsules 300 mg and Verelan® PM Extended-Release Capsules 300 mg	Completed	Mylan Pharmaceuticals	Phase 1	2006-01-01	The objective of this study was to investigate the bioequivalence of Mylan's verapamil HCl extended-release 300 mg capsules to Schwarz's Verelan® PM extended-release 300 mg capsules following evening administration of a single, oral 300 mg (1 x 300 mg) dose under fasting conditions.
NCT00648050 ↗	Fasting Study of Verapamil HCl Extended-Release Capsules 300 mg to Verelan® PM Extended-Release Capsules 300 mg	Completed	Mylan Pharmaceuticals	Phase 1	2006-03-01	The objective for this study was to investigate the bioequivalence of Mylan's verapamil HCl extended-release 300 mg capsules to Schwarz's Verelan® PM extended-release 300 mg capsules following evening administration of a single, oral 300 mg (1 x 300 mg) dose administration under fasting conditions.
NCT00648401 ↗	Food Study of Verapamil HCl Extended-Release Capsules 300 mg and Verelan® PM Extended-Release Capsules 300 mg	Completed	Mylan Pharmaceuticals	Phase 1	2006-01-01	The objective for this study was to investigate the bioequivalence of Mylan's verapamil HCl extended-release 300 mg capsules to Schwarz's Verelan® PM extended-release 300 mg capsules following a single, oral 300 mg (1 x 300 mg) dose administration under fed conditions.
>Trial ID	>Title	>Status	>Sponsor	>Phase	>Start Date	>Summary

Clinical Trial Conditions for VERELAN PM

Condition Name

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Condition Name for VERELAN PM
Intervention	Trials
Healthy	5
FESS	1
Heart Failure	1
Heart Rate	1
[disabled in preview]	0
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Condition MeSH

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Condition MeSH for VERELAN PM
Intervention	Trials
Blood Loss, Surgical	1
Heart Failure	1
Ischemic Stroke	1
Hemorrhage	1
[disabled in preview]	0
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Clinical Trial Locations for VERELAN PM

Trials by Country

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Trials by Country for VERELAN PM
Location	Trials
United States	15
Canada	1
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Trials by US State

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Trials by US State for VERELAN PM
Location	Trials
North Dakota	4
Minnesota	2
New Hampshire	1
Illinois	1
Tennessee	1
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Clinical Trial Progress for VERELAN PM

Clinical Trial Phase

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Clinical Trial Phase for VERELAN PM
Clinical Trial Phase	Trials
Phase 3	1
Phase 2	1
Phase 1	8
[disabled in preview]	2
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Clinical Trial Status

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Clinical Trial Status for VERELAN PM
Clinical Trial Phase	Trials
Completed	8
Not yet recruiting	2
Recruiting	1
[disabled in preview]	1
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Clinical Trial Sponsors for VERELAN PM

Sponsor Name

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Sponsor Name for VERELAN PM
Sponsor	Trials
Mylan Pharmaceuticals	4
Mayo Clinic	2
Assiut University	2
[disabled in preview]	2
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Sponsor Type

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Sponsor Type for VERELAN PM
Sponsor	Trials
Other	11
Industry	7
NIH	1
[disabled in preview]	0
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