- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07720310
Anti-CD19 CAR-T Cell Therapy for Patients With Refractory Systemic Lupus Erythematosus
Studieoversikt
Status
Intervensjon / Behandling
Studietype
Registrering (Antatt)
Kontakter og plasseringer
Studiesteder
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Minsk Oblast
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Lyasny, Minsk Oblast, Hviterussland, 223040
- NN Alexandrov National Cancer Centre of Belarus
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Prøvetakingsmetode
Studiepopulasjon
Beskrivelse
Inclusion Criteria:
- A confirmed diagnosis of SLE according to the 2019 EULAR/ACR criteria.
- Subacute or acute SLE.
- 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.
- 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).
- Patients aged 18 years or older.
- A medical consultation on the need for this treatment method using cell therapy.
- Written informed consent from the patient for treatment.
- Patient compliance with the treatment protocol.
- Adequate organ function.
Exclusion Criteria:
- Any change in therapy within 90 days prior to the planned administration of CAR-T cell therapy.
- Patient requiring renal replacement therapy.
- Active hepatitis B or active hepatitis C (HCV RNA positive).
- HIV-infected patients.
- Uncontrolled acute life-threatening bacterial, viral, or fungal infection (e.g., positive blood culture ≤ 72 hours before infusion).
- Unstable angina and/or myocardial infarction within 6 months prior to screening.
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.
- Pregnant and lactating women.
- Intolerance to the excipients of the cell product.
- Cardiac arrhythmia not controlled by medical therapy.
- Patients with active neurological autoimmune or inflammatory disorders (e.g., Guillain-Barré syndrome, amyotrophic lateral sclerosis).
- The presence of any primary immunodeficiency.
Socioeconomic or geographic circumstances that cannot guarantee adequate compliance with the protocol requirements for treatment and follow-up.
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Studieplan
Hvordan er studiet utformet?
Designdetaljer
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
SELENA-SLEDAI activity index assessment and serologic remission (defined as normal level of primary (dsDNA and/or antiSm) and antiphospholipid antibodies (lupus anticoagulant (LA), AT to cardiolipinanti-dsDNA and normal complement C3 and C4 levels)
Tidsramme: 36 months after CAR-T cells infusion
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SELENA-SLEDAI (Safety of Estrogens in Lupus Erythematosus National Assessment - Systemic Lupus Erythematosus Disease Activity Index) Score Interpretation: 0 points: Remission / no activity 1-4 points: Low activity 5-10 points: Moderate activity > 10 points: High activity (Scores ≥ 6 typically indicate active disease requiring treatment) |
36 months after CAR-T cells infusion
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Evaluation of CAR T-Cell-Related Toxicities
Tidsramme: Start from 0 day up to 30 days after CAR-T cells infusion
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Evaluation of Cytokine Release Syndrom (CRS) according NCCN guidelines version 2.2026. Immune Effector cell-associated Neurotoxicity Syndrom (ICANS) accordin NCCN guidelines version 2.2026. |
Start from 0 day up to 30 days after CAR-T cells infusion
|
Samarbeidspartnere og etterforskere
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 20251677
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
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