Phase IIa Efficacy and Safety Trial of capadenoson in Patients with Chronic Stable Angina

Mise à jour : Il y a 4 ans
Référence : EUCTR2007-000425-22

Femme et Homme

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Extrait

The main objective of this study is to demonstrate that chronic administration of BAY 68-4986 for 28 days at doses of 1 mg, 2 mg and 4 mg, is efficacious in a patient population with chronic stable angina and documented coronary heart disease. The primary efficacy parameter will be the total exercise time.


Critère d'inclusion

  • Patients with Chronic Stable Angina

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