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Vasospastic Angina clinical trials

View clinical trials related to Vasospastic Angina.

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NCT ID: NCT02094469 Completed - Vasospastic Angina Clinical Trials

Safety and Efficacy Study of Cilostazol to Treat Vasospastic Angina

STELLA_Ext
Start date: December 2013
Phase: Phase 3
Study type: Interventional

This study will be conducted in accordance with the local regulation of New Drug Application. Overall duration of this trial will be 3 years after approval of MFDS. Each subject will participate around 26 weeks, which include the 24 weeks treatment period and 2 weeks safety follow up period. Withdrawn subjects due to efficacy after 4 weeks treatment will participate in 6 weeks in total including 2 weeks safety follow up. Withdrawn subjects with other reason also have 2 weeks follow up period.

NCT ID: NCT02087007 Completed - Vasospastic Angina Clinical Trials

A Therapeutic Confirmatory Study to Evaluate the Efficacy and Safety of Cilostazol in Subjects With Vasospastic Angina

STELLA
Start date: November 2013
Phase: Phase 3
Study type: Interventional

This study will be conducted in accordance with the local regulation of New Drug Application. Overall duration of this trial will be 3 years after approval of KFDA. Each subject will participate around 7 weeks, which include the 2 weeks Amlodipine run-in period, 4 weeks double blind period and 1 week safety follow up period

NCT ID: NCT00602017 Completed - Hypertension Clinical Trials

Bioequivalency Study of Amlodipine Tablets Under Fasting Conditions

Start date: April 2004
Phase: N/A
Study type: Interventional

The objective of this study was the bioequivalence of a Roxane Laboratories' Amlodipine Besylate tablets, 10 mg, to Norvasc® Tablets, 10 mg (Pfizer) under fasting conditions using a single-dose, randomized, 2-treatment, 2-period, 2-sequence crossover design.

NCT ID: NCT00601302 Completed - Hypertension Clinical Trials

Bioequivalency Study of Amlodipine Tablets Under Fed Conditions

Start date: April 2004
Phase: N/A
Study type: Interventional

The objective of this study was the bioequivalence of a Roxane Laboratories' Amlodipine Besylate tablets, 10 mg, to Norvasc® Tablets, 10 mg (Pfizer) under fed conditions using a single-dose, randomized, 2-treatment, 2-period, 2-sequence crossover design.