Clinical Trial: Safety and Efficacy of PMT Therapy of hPAP
Study Status: Completed
Recruit Status: RECRUITING
Condition: Hereditary Pulmonary Alveolar Proteinosis
Study Type: INTERVENTIONAL
Official Title: A First-In-Human Clinical Trial of Lentiviral-mediated CSF2RA Gene Transfer/Pulmonary Macrophage Transplantation Therapy of Hereditary Pulmonary Alveolar Proteinosis
Brief Summary:
The major goal of this study is to evaluate a new type of cell transplantation therapy for individuals with hereditary PAP, study a new treatment that may be useful for treatment of other diseases, and research mechanisms that drive the development and function of lung macrophages.
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