Can reprogrammed immune cells silence lupus? a small trial aims to find out.
NCT ID NCT07720310
First seen Jul 22, 2026 · Last updated Jul 23, 2026 · Updated 1 time
Summary
This trial tests whether anti-CD19 CAR-T cell therapy can put severe lupus into remission. The treatment involves taking a patient's own immune cells, engineering them to target and destroy faulty B cells, and infusing them back. The study enrolls 12 adults with refractory systemic lupus erythematosus who have not responded to at least two prior therapies. Researchers will measure disease activity and serologic remission to see if this one-time cell therapy can replace lifelong medication.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- anti-CD19 CAR-T cells (academic CAR-T product made with a lentiviral vector)
- What this could lead to
- If successful, this could offer a durable, drug-free remission for people with severe lupus that hasn't responded to standard treatments.
- What could go wrong
- This is a very early, small trial with only 12 participants. CAR-T therapy carries risks like cytokine release syndrome and neurotoxicity, and it may not work for everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 12 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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Jun 2030
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with refractory SLE treated in N.N. Alexandrov National Cancer Center
- Ages
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18 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. A confirmed diagnosis of SLE according to the 2019 EULAR/ACR criteria. 2. Subacute or acute SLE. 3. SLE activity according to the SELENA-SLEDAI disease activity index screening score ≥6 and/or the requirement for prednisolone (or equivalent doses of methylprednisolone) at a dose greater than 7.5 mg/day (6 mg/day for methylprednisolone) to maintain lower disease activity. 4. A history of two or more prior therapies (one of the drugs mycophenolate mofetil or cyclophosphamide, or the development of side effects/intolerance to these drugs). 5. Patients aged 18 years or older. 6. A medical consultation on the need for this treatment method using cell therapy. 7. Written informed consent from the patient for treatment. 8. Patient compliance with the treatment protocol. 9. Adequate organ function. Exclusion Criteria: 1. Any change in therapy within 90 days prior to the planned administration of CAR-T cell therapy. 2. Patient requiring renal replacement therapy. 3. Active hepatitis B or active hepatitis C (HCV RNA positive). 4. HIV-infected patients. 5. Uncontrolled acute life-threatening bacterial, viral, or fungal infection (e.g., positive blood culture ≤ 72 hours before infusion). 6. Unstable angina and/or myocardial infarction within 6 months prior to screening. 7. Previous or concomitant malignancy with the exception of: * basal cell or squamous cell carcinoma (adequate wound healing is required before study entry); * In situ carcinoma of the cervix or breast, without evidence of recurrence for at least 3 years prior to study entry; * A primary malignant tumor that has been completely resected and in complete remission for ≥ 5 years. 8. Pregnant and lactating women. 9. Intolerance to the excipients of the cell product. 10. Cardiac arrhythmia not controlled by medical therapy. 11. Patients with active neurological autoimmune or inflammatory disorders (e.g., Guillain-Barré syndrome, amyotrophic lateral sclerosis). 12. The presence of any primary immunodeficiency. 13. Socioeconomic or geographic circumstances that cannot guarantee adequate compliance with the protocol requirements for treatment and follow-up. \-
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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NN Alexandrov National Cancer Centre of Belarus
Lyasny, Minsk Oblast, 223040, Belarus
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