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LupusPhase 1NCT05018858

Safety of Cultured Allogeneic Adult Umbilical Cord or Placental Derived Mesenchymal Stem Cell Intravenous Infusion for Lupus

A Phase 1 study testing cultured allogeneic adult umbilical cord or placental derived mesenchymal stem cells in people with Lupus, run by The Foundation for Orthopaedics and Regenerative Medicine at 2 sites in 2 countries.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

This trial will study the safety and efficacy of intravenous infusion of cultured allogeneic adult umbilical cord or placental derived mesenchymal stem cells for the treatment of Lupus Read more about this study

Who is it for?
Any age
Conditions the study is for
Lupus
What is being tested?
cultured allogeneic adult umbilical cord or placental derived mesenchymal stem cells
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
15 participants
Where
2 sitesin 2 countries
Study dates
Dec 2026to Oct 2028
Phase
Phase 1

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Diagnosis of Lupus
  • Understanding and willingness to sign a written informed consent document

Who cannot join

  • Active infection
  • Active cancer
  • Chronic multisystem organ failure
  • Pregnancy
  • Clinically significant Abnormalities on pre-treatment laboratory evaluation
  • Medical condition that would (based on the opinion of the investigator) compromise patient's safety.
Show all 10Show fewer
  • Continued drug abuse
  • Pre-menopausal women not using contraception
  • Previous organ transplant
  • Hypersensitivity to sulfur

Trial locations and contacts

2 sites in 2 countries. Contact the study team or a site near you to ask about taking part.

2 sites in 2 countries

United States1 site, 1 recruiting
  • Prodromos Stem Cell Institute

    Naples, Florida, 34102

    Chadwick Prodromos, MD, 847-699-6810 ext. 202, care@thepsci.com

    Recruiting

Other trials in United States

Greece1 site, 1 recruiting
  • Prodromos Stem Cell Institute

    Athens

    Chadwick Prodromos, MD, 847-699-6810 ext. 202, care@thepsci.com

    Recruiting

Other trials in Greece

About this study

Official title: Safety of Cultured Allogeneic Adult Umbilical Cord or Placental Derived Mesenchymal Stem Cell Intravenous Infusion for the Treatment of Lupus

This trial will study the safety and efficacy of intravenous infusion of cultured allogeneic adult umbilical cord or placental derived mesenchymal stem cells for the treatment of Lupus

Read the detailed description

Studies have shown that stem cell treatment is safe and efficacious for the treatment of Lupus. This patient funded trial aims to study the safety and efficacy of intravenous infusion of cultured allogeneic adult umbilical cord or placental derived mesenchymal stem cells (MSCs) for the treatment of Lupus. Patients with Lupus will receive a single intravenous infusion of MSCs. Patients will be evaluated within one month pre treatment and at 1, 6, 12, 24, 36, and 48 months post treatment for safety and efficacy.

Conditions
Lupus
Being tested
cultured allogeneic adult umbilical cord or placental derived mesenchymal stem cells
Keywords
Lupus, Lupus Arthritis, stem cell treatment

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • cultured allogeneic adult umbilical cord or placental derived mesenchymal stem cellsBiological

    cultured allogeneic adult umbilical cord or placental derived mesenchymal stem cells

Study groups in NCT05018858
Study groupRoleWhat they receive
Treatment GroupExperimentalSingle intravenous infusion
Receives: Biological: cultured allogeneic adult umbilical cord or placental derived mesenchymal stem cells

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Safety (adverse events)

    Clinical monitoring of possible adverse events or complications

    Measured: Four year follow-up

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Aug 2021
  2. Study startDec 2026 (estimated)
  3. Primary completionOct 2028 (estimated)
  4. Study completionOct 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
15 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05018858
Sponsor's protocol ID
SC-20-ATG-4
Status last verified
Oct 2026
First submitted
20 Aug 2021
Last updated
20 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No

Publications

  • Wang D, Li J, Zhang Y, Zhang M, Chen J, Li X, Hu X, Jiang S, Shi S, Sun L. Umbilical cord mesenchymal stem cell transplantation in active and refractory systemic lupus erythematosus: a multicenter clinical study. Arthritis Res Ther. 2014 Mar 25;16(2):R79. doi: 10.1186/ar4520.

    PubMed 24661633
  • Wang D, Zhang H, Liang J, Li X, Feng X, Wang H, Hua B, Liu B, Lu L, Gilkeson GS, Silver RM, Chen W, Shi S, Sun L. Allogeneic mesenchymal stem cell transplantation in severe and refractory systemic lupus erythematosus: 4 years of experience. Cell Transplant. 2013;22(12):2267-77. doi: 10.3727/096368911X582769c.

    PubMed 24388428
  • Sun L, Wang D, Liang J, Zhang H, Feng X, Wang H, Hua B, Liu B, Ye S, Hu X, Xu W, Zeng X, Hou Y, Gilkeson GS, Silver RM, Lu L, Shi S. Umbilical cord mesenchymal stem cell transplantation in severe and refractory systemic lupus erythematosus. Arthritis Rheum. 2010 Aug;62(8):2467-75. doi: 10.1002/art.27548.

    PubMed 20506343

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