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The objective of the study is to find the optimal dose of once daily oral neladenoson bialanate BAY when given in addition to appropriate therapy for specific comorbidities. E-mail: [email protected]. A multicenter, randomized, placebo-controlled, parallel group, double blind, dose-finding Phase II trial to study the efficacy, safety, pharmacokinetics and pharmacodynamic effects of the oral partial adenosine A1 receptor agonist neladenoson bialanate over 20 weeks in patients with chronic heart failure and preserved ejection fraction.
Compartir Facebook Twitter LinkedIn. Bayer Identifier: EudraCT Number: View results Ask a Question. Resumen del ensayo Enrollment Goal Trial Dates May June Phase 2.
Accepts Healthy Volunteers No. Ask a Question. Ubicaciones Ubicaciones. Intervention Type : Drug. Trial Purpose : Treatment. Allocation : Randomized. Assignment : Parallel Assignment. Trial Arms : 6. Secondary Outcome Absolute change in activity from baseline to 20 weeks. Activity is an important limitation in patients with preserved heart failure. This endpoint is to measure the in ability to exercise and improvement over 20 weeks. Click here and search for drug information provided by the FDA.
Click here and search for information on any recalls, market or product safety alerts by the FDA which might have occurred with this product.