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Last Updated: March 29, 2024

CLINICAL TRIALS PROFILE FOR VERELAN PM


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All Clinical Trials for VERELAN PM

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.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for VERELAN PM

Condition Name

Condition Name for VERELAN PM
Intervention Trials
Healthy 5
Refractory Hodgkin Lymphoma 1
Blood Loss 1
Type 2 Diabetes Mellitus 1
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Condition MeSH

Condition MeSH for VERELAN PM
Intervention Trials
Blood Loss, Surgical 1
Heart Failure 1
Ischemic Stroke 1
Hemorrhage 1
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Clinical Trial Locations for VERELAN PM

Trials by Country

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

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

Clinical Trial Phase for VERELAN PM
Clinical Trial Phase Trials
Phase 3 1
Phase 2 1
Phase 1 8
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Clinical Trial Status

Clinical Trial Status for VERELAN PM
Clinical Trial Phase Trials
Completed 8
Not yet recruiting 2
Terminated 1
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Clinical Trial Sponsors for VERELAN PM

Sponsor Name

Sponsor Name for VERELAN PM
Sponsor Trials
Mylan Pharmaceuticals 4
Mayo Clinic 2
Assiut University 2
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Sponsor Type

Sponsor Type for VERELAN PM
Sponsor Trials
Other 11
Industry 7
NIH 1
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