Federal Research Clinical Center FMBA of Russia
Moscow, 115682, Russia
NCT Number: NCT02594839
The study evaluates the safety and the efficacy of the addition of intravenous transplantation of donor bone marrow mesenchymal stem cells in patients with idiopathic interstitial pneumonia or connective tissue disease associated with interstitial lung disease, which have actively progressing disease with rapid loss of pulmonary function on the background of routine treatment.
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Notify Me20 year–80 year
All sexes
Interventional
Phase 1 / Phase 2
Moscow, 115682, Russia
Despite significant progress in the treatment of interstitial lung disease, achieved thanks to new drugs, such as pirfenidone and nintedanib, there are many patients for whom these drugs are not available or poorly tolerated. In addition significant evidence of their effectiveness and safety is valid only for idiopathic pulmonary fibrosis. The transplantation of allogeneic stem cells is a promising direction in the modern medicine with the proven safety for different diseases. But the effectiveness of this therapy is still under research. We believe that in most severe cases of a rapidly progressive interstitial lung disease the transplantation of mesenchymal stem cells may be an effective technology due to their immunomodulatory properties.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Bone marrow will be harvested in healthy donors followed by separation and cultivation of MSCs. Before infusion cells will be suspended in 400 mL saline
intravenous infusion of 400 mL saline
Time frame: 12 months
registration of adverse events related to infusion and 12 months follow-up
Time frame: 12 months
Assessment of the diffusing lung capacity at 3, 6, 9, 12 months of treatment
Time frame: 12 months
Assessment of spirometry at 3, 6, 9, 12 months of treatment
Time frame: 12 months
Assessment of 6MWD at 3, 6, 9, 12 months of treatment
Federal Research Clinical Center of Federal Medical & Biological Agency, Russia
Other Gov
A Phase I-II Study to Evaluate Safety and Efficacy of Allogeneic Bone-Marrow Mesenchymal Stem Cells in Patients With Rapidly Progressive Interstitial Lung Disease
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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