Last updated on May 2019

Riociguat in Children With Pulmonary Arterial Hypertension (PAH)

Brief description of study

This study is designed to evaluate the safety, tolerability, pharmacodynamics and pharmacokinetics of riociguat at age-, sex- and body-weight-adjusted doses of 0.5 mg, 1.0 mg, 1.5 mg, 2.0 mg and 2.5 mg TID in children from 6 to less than 18 years with pulmonary arterial hypertension (PAH) group 1. The study consists of two phases: titration phase up to 8 weeks and a maintenance phase up to 16 weeks.

Clinical Study Identifier: NCT02562235

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The Children's Hospital

Aurora, CO United States
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East Carolina University

Greenville, NC United States
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UZ Gent

Gent, Belgium
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H pital des Enfants

TOULOUSE Cedex 9, France
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Recruitment Status: Open

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