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Clinical Trial Summary

The purpose of this open-label phase IIa clinical trial study is to evaluate the safety and preliminary efficacy of hBMMSC intravenous treatment in patients with aPAP.


Clinical Trial Description

Autoimmune pulmonary alveolar proteinosis (aPAP) is a rare lung disease for which there is no specific drug treatment. Currently, the standard treatment strategy for PAP is whole-lung lavage (WLL), which is invasive and has limited therapeutic efficacy. The purpose of this study is to evaluate the safety and preliminary efficacy of hBMMSC intravenous treatment in patients with aPAP. The clinical trial intends to involve 10 participants. The trial is expected to last approximately 2 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06111846
Study type Interventional
Source Jiuzhitang Maker (Beijing) Cell Technology Co.,Ltd.
Contact
Status Not yet recruiting
Phase Phase 2
Start date November 1, 2023
Completion date August 30, 2026

See also
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Recruiting NCT02243228 - Inhalation of Granulocyte-macrophage Colony-stimulating Factor (GM-CSF) for Autoimmune Pulmonary Alveolar Proteinosis (PAP) Phase 2
Completed NCT03231033 - Pioglitazone Therapy of Autoimmune Pulmonary Alveolar Proteinosis Autoimmune Pulmonary Alveolar Proteinosis Phase 1
Completed NCT03531996 - The Longitudinal Evaluation of Autoimmune Pulmonary Alveolar Proteinosis
Completed NCT03482752 - Safety Extension Trial of Inhaled Molgramostim in Autoimmune Pulmonary Alveolar Proteinosis Phase 3