Table 2

Clinical trials investigating MSCs for COPD treatment

NCT numberStudy designNo.Cell typeRouteFUPrimary outcomeStudy completionRemarks
NCT00683722
(USA)81
Placebo-ctrl
Randomised
Double-blind
62Allog.
BM-MSC
Intravenous2  ySafety/efficacy
(phase II)
2010 December
NCT01306513
(The Netherlands)82
Single group
Open label
10Autol.
BM-MSC
Intravenous1 ySafety (phase I)2012 NovemberWith LVRS
NCT01758055
(Iran)90
Single group
Open label
12Autol.
BM-MSC
Endobronchialn.s.Safety
(phase I)
2014 January
NCT01872624
(Brazil)83
Placebo-ctrl
Non-randomised Open label
10Allog.
BM-MSC
Endobronchial4 moSafety
(phase I)
2015 MarchWith EB valves
NCT02645305
(Vietnam)90
Single group
Open label
20Autol.
AT-MSC
Intravenous1 ySafety/efficacy
(phase II)
2016 DecemberWith APRP
NCT02041000
(USA)90
Single group
Open label
100Autol.
AT-MSC
Intravenous6 moSafety/efficacy
(phase II)
2017 JanuaryCommercial (Bioheart)
NCT02412332
(Brazil)90
Placebo-ctrl
Randomised Open label
20Autol.
AT-MSC, BMMC or both
Intravenous1 ySafety/efficacy
(phase II)
2017 April
NCT01849159
(Russia)90
Placebo-ctrl
Randomised
Open label
30Allog.
BM-MSC
Intravenous2 ySafety/efficacy
(phase II)
2017 JuneHypoxia-cultured
NCT02216630
(USA)90
Single group
Open label
200Autol.
AT-MSC
Intravenous1 ySafety/efficacy
(phase II)
2017 AugustCommercial (Kimera)
NCT02161744
(USA)90
Single group
Open label
60Autol.
AT-MSC
Intravenous1 ySafety/efficacy
(phase I)
2017 August
NCT01559051
(USA)90
Single group
Open label
100Autol.
AT-MSC
Intravenous/
endobronchial
6 moSafety/efficacy
(phase II)
2017 NovemberCommercial (Ageless Regenerative Institute)
NCT02348060
(USA)90
Single group
Open label
75Autol.
AT-MSC
n.s.1 yQuality of life2018 FebruaryCommercial (StemGenex)
  • Allog., allogeneic; APRP, activated platelet-rich plasma (from peripheral blood); AT-MSC, adipose tissue-derived stem cells; Autol., autologous; BM-MSC, bone marrow-derived mesenchymal stromal cells; BMMCs, bone marrow-derived mononuclear cells; Ctrl, controlled; d, day; FU, follow-up; LVRS, lung volume reduction surgery; mo, month; n.s., not specified; NCT, ClinicalTrials.gov Identifier number; No., number of participants enrolled; route, route of administration; y, year.