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The AURORA study will be conducted to confirm the efficacy and safety of cenicriviroc (CVC) for the treatment of liver fibrosis in adult subjects with NASH.
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and ...
Eligibility: - People who are documented exceptional responders to cancer treatment. They must have given a tumor sample that is available to researchers.
The purposes of this study are to investigate the level of correspondence between the most severe and most bothersome symptoms, and to examine discordant ...
About this study. This study seeks to define normal values and repeatability of the deltoid muscle in healthy volunteers and to establish scanning ...
About this study. The Valchlor PROVe study is a multi-center, prospective, observational, US-based drug study that longitudinally follows patients with ...
The purpose of this study is to determine if fluticasone furoate/vilanterol improves survival in patients with chronic obstructive pulmonary disease with a ...
The primary aims of the study include determining the patient's experience with colon capsule endoscopy (CCE) and the associated bowel preparation. In addition, ...
The main aim of this pilot study is to evaluate treatment-related toxicity and clinical indicators of QOL in HCT patients, and to integrate these into a ...
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