Clinical trials based on MSCs | ||||||
Date of registration/ Execution time | Study phase/Recruitment status | ID/URL | Title | Cell type | Number of total particpants/ Intervention or treatment | |
1 | 60 | |||||
14–02-2020/20-02-2020 to 20-02-2021 | 0/Not Recruiting | ChiCTR2000029816/http://www.chictr.org.cn/ showproj.aspx?proj=49389 | Clinical Study for Cord Blood Mesenchymal Stem Cells in the Treatment of Acute Novel Coronavirus Pneumonia (COVID- 19) | UCB- MSCs; UCB-NK | Experimental group: Conventional treatment followed by iv infusion UCB- MSCs Control group: Conventional treatment | |
2 | 60 | |||||
14-02-2020/20-02-2020 to 20-02-2021 | 0/ Not Recruiting | ChiCTR2000029817/http://www.chictr.org.cn/ showproj.aspx?proj=49384 | Clinical Study of Cord Blood NK Cells Combined with Cord Blood Mesenchymal Stem Cells in the Treatment of Acute Novel Coronavirus Pneumonia (COVID- 19) | NK and UCB- MSCs | Experimental group:High dose group: High-dose NK cells (>5×109) and MSCs (>5×109), iv infusion once, every 2 days for a total of 5 times Conventional dose group: Conventional dose NK cells (>3×109) and MSCs (>3×109), iv infusion once every 2 days for a total of 3 times Preventive dose group: Preventive dose NK cells (>3×109) and MSCs (>3×109), iv infusion once every week for a total of 1 time. | |
3 | 63 | |||||
07-02-2020/15-01-2020 to 31-12-2022 | 0/ Recruiting | ChiCTR2000029606/http://www.chictr.org.cn/ showproj.aspx?proj=49146 | Clinical Study for Human Menstrual Blood-Derived Stem Cells in the Treatment of Acute Novel Coronavirus Pneumonia (COVID-19) | MenSCs | Experimental group A: 1. Conventional treatment followed by iv infusion of MenSCs. Control group A: Conventional treatment Experimental group B: 1: Artificial liver therapy+conventional treatment 2: Artificial liver therapy followed by iv infusion of MenSCs +conventional treatment Control group A: Conventional treatment | |
4 | 10 | |||||
07-02-2020/06-02-2020 to 30-09-2020 | 2/ Recruiting | NCT04269525/https://clinicaltrials.gov/ show/NCT04269525 | Umbilical Cord(UC)-Derived Mesenchymal Stem Cells(MSCs) Treatment for the 2019-novel Coronavirus(nCOV) Pneumonia | UC- MSCs | Experimental group: UC-MSCs 3.3×107 cells/50 mL/bag, 3 bags each time. And UC-MSCs will be infused iv on the 1st, 3rd, 5th, and 7th days after enrollment, 1 time each day. Control group: None specified | |
5 | 70 | |||||
05-02-2020/31-01-2020 to 31-12-2020 | 0/ Recruiting | ChiCTR2000029580/http://www.chictr.org.cn/ showproj.aspx?proj=49088 | A prospective, single-blind, randomized controlled trial for Ruxolitinib combined with mesenchymal stem cell infusion in the treatment of patients with severe 2019-nCoV pneumonia (novel coronavirus pneumonia, NCP) | MSCs | Experimental group: Ruxolitinib combined with MSCs. Control group: Routine treatment. | |
6 | 20 | |||||
27-01-2020/21-01-2020 to 00-12 2021 | 1/Recruiting | NCT04252118/https://clinicaltrials.gov/ show/NCT04252118 | Mesenchymal Stem Cell Treatment for Pneumonia Patients Infected With 2019 Novel Coronavirus | MSCs | Experimental group: 3.0×107 MSCs iv at day 0, day 3, day 6 Control group: None specified | |
7 | 48 | |||||
14-02-2020/16-02-2020 to 15-02-2022 | NA/Not recruiting | NCT04273646/https://clinicaltrials.gov/ ct2/show/NCT04273646 | Study of Human Umbilical Cord Mesenchymal Stem Cells in the Treatment of Novel Coronavirus Severe Pneumonia | UC- MSCs | Experimental group: 4 times of UC-MSCs (0.5×106 UC-MSCs·kg−1 body weight iv at day 1, day 3, day 5, day 7) Control group: None specified | |
8 | 9 | |||||
28-02-2020/19-02-2020 to 20-02-2021 | 1/ Recruiting | ChiCTR2000030300/http://www.chictr.org.cn/ showprojen.aspx?proj=50022 | Umbilical cord mesenchymal stem cells (hucMSCs) in the treatment of high risk novel coronavirus pneumonia (COVID-19) patients | UC- MSCs | Experimental group: MSCs Control group: None specified | |
9 | 32 | |||||
26-02-2020/14-02-2020 to 31-05-2020 | NA/Not recruiting | ChiCTR2000030224/http://www.chictr.org.cn/ showprojen.aspx?proj=49968 | Clinical study of mesenchymal stem cells in treating severe novel coronavirus pneumonia (COVID- 19) | MSCs | Experimental group 1: critical group Intervention, injecting MSCs Experimental group 2: severe group, Intervention, injecting MSCs Control group 3: Control of the critical group, intervention, injecting normal saline Control group 4: Control of the severe group, intervention, injecting normal saline | |
10 | 60 | |||||
24-02-2020/17-02-2020 to 17-04-2020 | 0/Not recruiting | ChiCTR2000030173/http://www.chictr.org.cn/ showprojen.aspx?proj=49229 | Key techniques of umbilical cord mesenchymal stem cells for the treatment of novel coronavirus pneumonia (COVID-19) and clinical application demonstration | UC- MSCs | Experimental group: UC-MSCs Control group: Convention treatment | |
11 | 60 | |||||
24-02-2020/24-02-2020 to 31-05-2020 | 2/Not recruiting | ChiCTR2000030138/http://www.chictr.org.cn/ showproj.aspx?proj=50004 | Clinical Trial for Human Mesenchymal Stem Cells in the Treatment of Severe Novel Coronavirus Pneumonia (COVID- 19) | UC- MSCs | Experimental group: Iv injection of UC-MSCs Control group: Routine treatment+placebo | |
12 | 16 | |||||
23-02-2020/01-02-2020 to 31-08-2020 | NA/ Recruiting | ChiCTR2000030116/http://www.chictr.org.cn/ showproj.aspx?proj=49901 | Safety and effectiveness of human umbilical cord mesenchymal stem cells in the treatment of acute respiratory distress syndrome of severe novel coronavirus pneumonia (COVID-19) | UC- MSCs | Experimental group: Different stem cell doses Control group: None specified | |
13 | 40 | |||||
22-02-2020/01-03-2020 to 31-12-2021 | 0/Not recruiting | ChiCTR2000030088/http://www.chictr.org.cn/ showproj.aspx?proj=49902 | Umbilical cord Wharton's Jelly derived mesenchymal stem cells in the treatment of severe novel coronavirus pneumonia (COVID- 19) | UC-Whartons Jellys MSCs | Experimental group: Iv injection of Wharton's Jelly MSCs (1×106/kg), cell suspension volume: 40 mL Control group: Iv 40 mL saline | |
14 | 20 | |||||
20-02-2020/06-02-2020 to 05-02-2022 | NA/ Recruiting | ChiCTR2000030020/http://www.chictr.org.cn/ showproj.aspx?proj=49812 | The clinical application and basic research related to mesenchymal stem cells to treat novel coronavirus pneumonia (COVID- 19) | MSCs | Experimental group: Case series: MSCs therapy Control group: None specified | |
15 | 120 | |||||
18-02-2020/30-01-2020 to 31-03-2020 | 1-2/Recruiting | ChiCTR2000029990/http://www.chictr.org.cn/sho wproj.aspx?proj=49674 | Clinical trials of mesenchymal stem cells for the treatment of pneumonitis caused by novel coronavirus pneumonia (COVID- 19) | MSCs | Experimental group: MSCs Control group: Saline | |
16 | 45 | |||||
28-02-2020/28-02-2020 to 31-12-2021 | 1-2/Not recruiting | NCT04288102/https://clinicaltrials.gov/ct2/ show/NCT04288102 | Treatment With Mesenchymal Stem Cells for Severe Corona Virus Disease 2019 (COVID-19) | MSCs | Experimental group: 3 times of MSCs ((body weight≥70 kg, 4.0×107 cells per time; body weight <70 kg, 3.0×107 cells per time) iv at day 0, day 3, day 6). Control group: Saline containing 1% human serum albumin (solution of MSCs)3 times of placebo(iv at day 0, day 3, day 6) | |
17 | 48 | |||||
24-02-2020/24-02-2020 to 01-02-2021 | NA/ Recruiting | NCT04293692/https://clinicaltrials.gov/ show/NCT04293692 | Therapy for Pneumonia Patients Infected by 2019 Novel Coronavirus | UC- MSCs | Experimental group: Participants will receive conventional treatment plus 4 times of 0.5×106 UC-MSCs·kg−1 body weight suspended in 100 mL saline containing 1% human albumin iv, at day 1, day 3, day 5, day 7. Control group: Participants will receive conventional treatment plus 4 times of placebo (100 mL saline containing 1% human albumin) iv at day 1, day 3, day 5, day 7. | |
Clinical trials based on MSCs-derivatives | ||||||
Date of registration/ Execution time | Study phase/ Recruitment status | ID/ URL | Title | Cell type | Number of total participants/ Intervention or treatment | |
1 | 30 | |||||
04-02-2020 /5-02-2020 to 30-04-2021 | 0/ Not Recruiting | ChiCTR2000029569/http://www.chictr.org.cn/ showproj.aspx?proj=49062 | Safety and efficacy of umbilical cord blood mononuclear cells conditioned medium in the treatment of severe and critically novel coronavirus pneumonia (COVID-19): a randomized controlled trial | UC- MSCs CM | Experimental group: Conventional treatment combined with UC-MSCs CM Control group: Conventional treatment | |
2 | 30 | |||||
19-02-2020/15-02-2020 to 31-07-2020 | 1/ Not Recruiting | NCT04276987/https://clinicaltrials.gov/ct2/ show/NCT04276987 | A Pilot Clinical Study on Inhalation of Mesenchymal Stem Cells Exosomes Treating Severe Novel Coronavirus Pneumonia | AT- MSCsExo | Experimental group: 5 times aerosol inhalation of MSCs-derived exosomes (2.0×108 nano vesicles/3 mL at day 1, day 2, day 3, day 4, day 5). Control group: None specified | |
3 | 26 | |||||
2020-02-26/28-02-2020 to 31-05-2020 | 0/ Not Recruiting | ChiCTR2000030261/http://www.chictr.org.cn/ showprojen.aspx?proj=49963 | A study for the key technology of mesenchymal stem cells exosomes atomization in the treatment of novel coronavirus pneumonia (COVID-19) | MSCs Exo | Experimental group: Aerosol inhalation of exosomes Control group: Blank | |
4 | 90 | |||||
03-03-2020/31-01-2020 to 31-01-2021 | NA/ Not Recruiting | ChiCTR2000030484/http://www.chictr.org.cn/ showproj.aspx?proj=50263 | HUMSCs and Exosomes Treating Patients with Lung Injury following Novel Coronavirus Pneumonia (COVID-19) | UC- MSCs and Exo | Experimental group: Group 1: HUMSCs iv, 5×107 cells/ time, once / week, twice/course Group 2: HUMSCs iv infusion, 5×107 cells / time, 1 time / week, 2 times / course, a total of 2 courses; Exosomes: iv administration, 180 mg / time, 1 time / day, 7 days / course, 2 courses in total Control group: Same amount of placebo (stem cell solvent) | |
Clinical trials based on other cell types | ||||||
Date of registration/ Execution time | Study phase/ Recruitment status | ID/ URL | Title | Cell type | Number of participants/ Intervention or treatment | |
1 | 60 | |||||
14-02-2020 /20-02-2020 to 20-02-2021 | 0 / Not Recruiting | ChiCTR2000029812/http://www.chictr.org.cn/ showproj.aspx?proj=49374 | Clinical Study for Umbilical Cord Blood Mononuclear Cells in the Treatment of Acute Novel Coronavirus Pneumonia (COVID- 19) | UCBMC | Experimental group: Conventional treatment followed by iv of UCBMC preparations Control group: Conventional treatment | |
2 | 30 | |||||
05-02-2020 /05-02-2020 to 30-04-2021 | 0 / Recruiting | ChiCTR2000029572/http://www.chictr.org.cn/ showproj.aspx?proj=41760 | Safety and efficacy of umbilical cord blood mononuclear cells in the treatment of severe and critically novel coronavirus pneumonia (COVID-19): a randomized controlled clinical trial | UCBMC | Experimental group: Conventional treatment combined with UCBMC Control group: Conventional treatment | |
3 | 100 | |||||
17-02-2020 /24-02-2020 to 31-12-2024 | 1-2 /Recruiting | NCT04276896/https://clinicaltrials.gov/ show/NCT04276896 | Function and Safety Study of SARS-CoV-2 Synthetic Minigene Vaccines | autologo us LV- DC vaccine or antigen- specific cytotoxic T Cells | Experimental group: Patients will receive approximately 5×106 LV-DC vaccine or 1×108 CTLs as a single infusion via sub- cutaneous fluids / Iv injection and may receive additional infusions. Control group: None specified | |
4 | 30 | |||||
13-02-2020 /20-02-2020 to 30-12-2020 | 1 / Recruiting | NCT04280224/https://clinicaltrials.gov/ show/NCT04280224 | NK Cells Treatment for Novel Coronavirus Pneumonia | NK cells | Experimental group: Conventional treatment plus twice a week of NK cells (0.1-2×107 NK cells·kg−1 body weight) Control group: Conventional treatment | |
5 | 20 | |||||
06-03-2020/10-04-2020 to 10-11- 2020 | 2 /Not recruiting | NCT04299152/https://clinicaltrials.gov/ct2/s how/NCT04299152 | Clinical Application of Stem Cell Educator Therapy for the Treatment of Viral Inflammation Caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) | CB-SC | Experimental group: Combination Product: Stem Cell Educator-Treated Mononuclear Cells Apheresis SCE therapy circulates a patient's blood through a blood cell separator, briefly cocultures the patient's immune cells with adherent CB-SC in vitro, and returns the “educated” autologous immune cells to the patient's circulation. Control group: Conventional treatment of patients with SARS-CoV-2. Patients will receive the regular treatments by only addressing their symptoms such as reducing fever and cough. | |
6 | 90 | |||||
28-02-2020 /01-03-2020 to 17-02-2021 | 0 /Not recruiting | ChiCTR2000030088/http://www.chictr.org.cn/ showproj.aspx?proj=49779 | Clinical trial for umbilical cord blood CIK and NK cells in the treatment of mild and general patients infected with novel coronavirus pneumonia (COVID- 19) | CIK and NK | Experimental group: CIK group: UCB CIK cells (1.6×108/kg) were injected twice every other day. NK group: UCB NK cells (1.6×108/kg) were injected twice every other day. Control group: Conventional therapy |
CB-MSCs: Umbilical cord blood derived-mesenchymal stem cells; UCB-NK: Umbilical cord blood derived-natural killer; MenSCs: mesenchymal stem cells derived from menstrual uid; UC-MSCs: umbilical cord derived mesenchymal stem cells; UC-MSCs CM: umbilical cord derived mesenchymal stem cells-conditioned médium; AT-MSCs Exo: Adipose tissue xosomes; MSCs Exo: mesenchymal stem cells exosomes; UCBMC: umbilical cord blood derived mononuclear cells; CTL: cytotoxic T cells; LV: lentivirus; DC: dendritic cells; NK: atural killer cells; CB-SC: cord blood stem cells; CIK: Cytokine-induced killer cells; Iv: intravenous.