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Completed

NCT Number: NCT02594839

Safety and Efficacy of Allogeneic Mesenchymal Stem Cells in Patients With Rapidly Progressive Interstitial Lung Disease

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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Key information

Age range

20 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Federal Research Clinical Center FMBA of Russia

Moscow, 115682, Russia

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and female patients 20-80 years old
  • Diagnosis of idiopathic interstitial pneumonia or secondary to connective tissue diseases interstitial lung disease, based on:
  • Clinical symptoms > 12 months duration,
  • Histologically diagnosed or diagnostic chest HRCT features of interstitial pneumonia
  • Forced Vital Capacity (FVC) ≥ 40% predicted and Diffusing Lung Capacity (DLCO) ≥20%
  • Loss more than 10% of FVC (L) and DLCO during the last 12 months
  • Signed informed consent.

Exclusion criteria

  • Diagnosis of an interstitial lung disease other than idiopathic interstitial pneumonia or connective tissue disease associated with interstitial lung disease (sarcoidosis, pulmonary alveolar proteinosis, lymphangioleiomyomatosis, pulmonary amyloidosis, exposure-related lung disease etc)
  • Obstructive lung disease: FEV1/FVC < 0.70
  • Clinically significant medical condition, in the opinion of the investigator, may compromise the results of the study
  • Evidence of active infection within 4 week prior to enrollment
  • History of malignancy < 5 years prior to enrollment
  • Unable to cooperate with any study procedures
  • Pregnant or breast-feeding
  • Treatment with antiinflammatory or antifibrotic drugs including oral steroids, cytostatic drugs, pirfenidone, D penicillamine, colchicine, tumor necrosis factor α blockers, imatinib, interferon γ, monoclonal antibodies < 6 months prior to randomization.
  • Active listing for transplant of any organ.
  • Known history of alcohol abuse within 1 year prior to enrollment
  • Participation in another clinical trial

Treatment and study plan

Bone marrow mesenchymal stem cells

Drug

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

Placebo

Drug

intravenous infusion of 400 mL saline

Primary outcomes

  1. Safety: Number of serious adverse events

    Time frame: 12 months

    registration of adverse events related to infusion and 12 months follow-up

Secondary outcomes

  1. DLCO changes from baseline

    Time frame: 12 months

    Assessment of the diffusing lung capacity at 3, 6, 9, 12 months of treatment

  2. FVC changes from baseline

    Time frame: 12 months

    Assessment of spirometry at 3, 6, 9, 12 months of treatment

  3. exercise capacity changes

    Time frame: 12 months

    Assessment of 6MWD at 3, 6, 9, 12 months of treatment

Sponsors and collaborators

Lead sponsor

Federal Research Clinical Center of Federal Medical & Biological Agency, Russia

Other Gov

Registry information

Official study title

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

Important dates

Study start
2013
Primary completion
2018
Study completion
2018
First posted
Nov 3, 2015
Registry last updated
Jan 9, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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