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CD19 CAR-T Therapy for Refractory Pemphigus Vulgaris (RESET-PV-CART)

26. Juni 2026 aktualisiert von: Jinbo Chen

A Single-Arm, Open-Label Clinical Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of CD19 CAR-T Cell Therapy in Patients With Moderate-to-Severe Refractory Pemphigus Vulgaris

This is an investigator-initiated, single-center, single-arm, open-label exploratory clinical study designed to evaluate the safety, tolerability, and preliminary efficacy of autologous CD19 CAR-T cell therapy in patients with refractory pemphigus vulgaris.

Studienübersicht

Status

Rekrutierung

Bedingungen

Detaillierte Beschreibung

This is an investigator-initiated, open-label, single-center, single-arm exploratory interventional study designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, immune reconstitution, and preliminary clinical efficacy of autologous CD19 CAR-T cell therapy in adult patients with moderate-to-severe refractory pemphigus vulgaris.

Eligible participants are adults with refractory pemphigus vulgaris. After enrollment, participants will undergo leukapheresis for ex vivo manufacturing of autologous CD19 CAR-T cells. After product release, participants will receive lymphodepleting chemotherapy with fludarabine and cyclophosphamide within 2 to 7 days prior to CAR-T infusion.

Participants will receive a single intravenous infusion of autologous CD19 CAR-T cells at a protocol-defined dose (1 X 10^6 CAR-positive T cells per kilogram of body weight). Premedication may be administered at investigator discretion. No comparator group is included.

Participants will be followed for up to 96 weeks after infusion. Safety assessments include monitoring for cytokine release syndrome, immune effector cell-associated neurotoxicity syndrome, infections, cytopenias, organ toxicities, and other treatment-emergent adverse events.

Efficacy assessments include changes in PDAI score, disease control, Physician Global Assessment (PGA), Autoimmune Bullous Skin Disorder Intensity Score (ABSIS), relapse rate, time to relapse, and corticosteroid-sparing effects.

Translational assessments include peripheral CD19-positive B-cell depletion and reconstitution, B-cell subset dynamics, serum anti-desmoglein 1 and 3 antibody levels, and serum cytokine profiles. CAR-T pharmacokinetics will be evaluated through CAR transgene copy number and circulating CAR-positive T-cell detection, including expansion and persistence metrics.

Studientyp

Interventionell

Einschreibung (Geschätzt)

3

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

  • Name: Xiaoya Du
  • Telefonnummer: +86 27 8533 2028

Studieren Sie die Kontaktsicherung

  • Name: Jinbo Chen, MD, PhD
  • Telefonnummer: +86 188 2736 3048
  • E-Mail: chen999jb@163.com

Studienorte

    • Hubei
      • Wuhan, Hubei, China
        • Rekrutierung
        • Traditional Chinese and Western Medicine Hospital of Wuhan, Wuhan, Hubei
        • Kontakt:

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

Inclusion Criteria:

Participants must meet all of the following criteria:

  1. Ability to provide written informed consent.
  2. Age 18 to 70 years at screening, male or female.
  3. Diagnosis of pemphigus vulgaris confirmed by clinical presentation, histopathology, direct immunofluorescence (DIF), and positive anti-desmoglein 3 and/or anti-desmoglein 1 antibodies.
  4. Moderate-to-severe disease activity defined as Pemphigus Disease Area Index (PDAI) ≥ 15 at screening.
  5. Refractory pemphigus vulgaris is defined as inadequate response, disease relapse, or treatment dependence following systemic corticosteroids and rituximab-based therapy for at least 6 months, with persistent disease activity meeting at least one of the following criteria:

    1. Ongoing active disease with the appearance of new erythema, blisters, or erosions;
    2. Persistently elevated anti-desmoglein 1 or anti-desmoglein 3 antibody titers > 100 U/mL;
    3. Inability to taper systemic corticosteroids to < 20 mg/day prednisone equivalent (i.e., ≥ 4 tablets/day of standard prednisone dosing).
  6. Requirement for systemic therapy at screening due to active disease.
  7. Adequate vascular access for leukapheresis.
  8. Life expectancy greater than 6 months.
  9. Participants must have adequate organ function as defined below:

    1. Hematologic function: absolute neutrophil count ≥ 1.0 × 10⁹/L, platelet count ≥ 50 × 10⁹/L, hemoglobin ≥ 80 g/L.
    2. Renal function: Creatinine clearance ≥ 40 mL/min.
    3. Hepatic function: ALT and AST ≤ 2.5 × upper limit of normal; total bilirubin ≤ 1.5 × upper limit of normal.
    4. Cardiac function: Left ventricular ejection fraction (LVEF) ≥ 50% with no clinically significant cardiac dysfunction.
    5. Pulmonary function: Dyspnea ≤ Grade 1 (CTCAE v5.0) and oxygen saturation (SpO₂) ≥ 92% on room air.
    6. Coagulation function: international normalized ratio (INR) and activated partial thromboplastin time (aPTT) ≤ 1.5 × upper limit of normal, with no clinically significant coagulopathy.

9. No evidence of clinically significant active infection at baseline evaluation.

10. Reproductive Criteria: Women of childbearing potential must have a negative serum beta-human chorionic gonadotropin (β-hCG) test within 48 hours prior to initiation of lymphodepleting chemotherapy. Women of childbearing potential must agree to use effective contraception during study participation and for at least 12 months after CAR-T infusion. Male participants must agree to use effective contraception and avoid sperm donation during study participation and for at least 12 months after infusion.

Exclusion Criteria:

Participants meeting any of the following criteria will be excluded:

  1. Active uncontrolled infection at screening, requiring systemic antimicrobial therapy. Participants with active tuberculosis, hepatitis C virus (HCV), human immunodeficiency virus (HIV), or syphilis infection will be excluded. Participants with hepatitis B surface antigen and/or hepatitis B core antibody positivity may be eligible only if HBV DNA is below the lower limit of quantification and appropriate antiviral prophylaxis is provided at the investigator's discretion.
  2. History of other active autoimmune disease requiring systemic immunosuppression.
  3. Previous treatment with any gene-modified cellular therapy, including CAR-T or CAR-NK therapy.
  4. Prior allogeneic stem cell or solid organ transplantation.
  5. Severe or uncontrolled cardiovascular, pulmonary, hepatic, or renal disease that would increase risk associated with lymphodepleting chemotherapy or CAR-T cell infusion.
  6. Use of high-dose systemic corticosteroids (>1 mg/kg/day prednisone equivalent) within 7 days prior to leukapheresis.
  7. Use of rituximab or other B-cell-targeted biologics within protocol-defined washout period.
  8. Use of intravenous immunoglobulin, plasma exchange, or other intensive immunomodulatory therapy within 2 weeks prior to leukapheresis.
  9. Received live vaccine within 8 weeks prior to screening.
  10. History of malignancy within 5 years prior to enrollment, except adequately treated non-melanoma skin cancer or in situ carcinoma.
  11. Pregnancy or breastfeeding.
  12. Known hypersensitivity to any component of lymphodepleting chemotherapy or CAR-T cell product.
  13. Any condition that, in the investigator's judgment, would compromise patient safety or study integrity.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: CD19 CAR-T Therapy for Refractory Pemphigus Vulgaris
Participants with moderate-to-severe refractory pemphigus vulgaris will undergo leukapheresis for ex vivo manufacturing of autologous CD19 CAR-T cells. The CAR-T product is individually manufactured from each participant's own peripheral blood mononuclear cells and reinfused into the same participant; therefore, this is an autologous, patient-specific cellular therapy and not an allogeneic or off-the-shelf product. Following confirmation of product release, participants will receive protocol-defined lymphodepleting chemotherapy prior to CAR-T infusion, followed by a single intravenous infusion of autologous CD19 CAR-T cells. Participants will be monitored for safety, pharmacokinetics, pharmacodynamics, immune reconstitution, and preliminary clinical efficacy.
Autologous CD19 CAR-T cells are manufactured ex vivo using the participant's own T cells collected by leukapheresis. The CAR construct targets CD19-expressing B cells and consists of a single-chain variable fragment directed against CD19. Participants will receive lymphodepleting chemotherapy with fludarabine and cyclophosphamide prior to CAR-T cell infusion according to the protocol-defined schedule. Following completion of lymphodepletion, each participant will receive a single intravenous infusion of autologous CD19 CAR-T cells under inpatient monitoring. Premedication, including acetaminophen and diphenhydramine, may be administered prior to infusion at the investigator's discretion in accordance with institutional practice.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Incidence and Severity of Treatment-Emergent Adverse Events
Zeitfenster: From initiation of lymphodepleting chemotherapy through Day 90 after CAR-T cell infusion
Treatment-emergent adverse events, serious adverse events, dose-limiting toxicities, cytokine release syndrome, immune effector cell-associated neurotoxicity syndrome, infections, cytopenias, organ toxicities, infusion-related reactions, and clinically significant laboratory abnormalities will be assessed. Adverse events will be graded according to CTCAE v5.0, and immune effector cell-related toxicities will be assessed according to applicable consensus grading criteria.
From initiation of lymphodepleting chemotherapy through Day 90 after CAR-T cell infusion
Change From Baseline in PDAI Score at Week 12
Zeitfenster: Baseline and Week 12
The change from baseline in Pemphigus Disease Area Index (PDAI) score at Week 12 will be assessed to evaluate preliminary clinical efficacy of autologous CD19 CAR-T cell therapy in patients with refractory pemphigus vulgaris.
Baseline and Week 12
Proportion of participants achieving disease control at Week 4 after CAR-T infusion
Zeitfenster: Week 4
Disease control is defined as cessation of new active cutaneous or mucosal lesions with established lesion healing or no further progression of existing lesions, as assessed by the investigator. This endpoint evaluates the early clinical response following CD19 CAR-T cell therapy and reflects initial disease stabilization after B-cell depletion.
Week 4

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change From Baseline in Pemphigus Disease Area Index (PDAI) Score Over Time (Range 0-263)
Zeitfenster: Baseline through Week 96 after CAR-T cell infusion
Changes from baseline in Pemphigus Disease Area Index (PDAI) score will be assessed at scheduled follow-up visits to evaluate the durability of clinical response. The total PDAI score ranges from 0 to 263, with higher scores indicating more severe disease.
Baseline through Week 96 after CAR-T cell infusion
Change From Baseline in Physician Global Assessment Score (PGA) (Range 0-10)
Zeitfenster: Baseline through Week 96 after CAR-T cell infusion
Change from baseline in PGA score will be assessed at scheduled follow-up visits. PGA is a physician-rated global assessment of pemphigus disease severity, with higher scores indicating more severe disease activity.
Baseline through Week 96 after CAR-T cell infusion
Change from Baseline in Autoimmune Bullous Skin Disorder Intensity Score (ABSIS) (Range 0-206)
Zeitfenster: Baseline through Week 96 after CAR-T cell infusion
Change from baseline in ABSIS will be assessed at scheduled follow-up visits. ABSIS is used to evaluate autoimmune bullous disease activity, with higher scores indicating more severe disease activity.
Baseline through Week 96 after CAR-T cell infusion
Proportion of participants achieving disease control at Week 12
Zeitfenster: Week 12
Disease control is defined as cessation of new active cutaneous or mucosal lesions with healing or stabilization of existing lesions, as assessed by the investigator. This endpoint evaluates the durability and consolidation of clinical response following CD19 CAR-T cell therapy in patients with refractory pemphigus vulgaris.
Week 12
Change From Baseline in Anti-Desmoglein 1 and Anti-Desmoglein 3 Antibody Levels
Zeitfenster: Baseline through Week 96 after CAR-T cell infusion
Serum anti-desmoglein 1 and anti-desmoglein 3 antibody levels will be measured to evaluate changes in pemphigus-related autoantibody responses after CD19 CAR-T cell therapy.
Baseline through Week 96 after CAR-T cell infusion
Peripheral CD19-Positive B-Cell Depletion and Reconstitution
Zeitfenster: Baseline through Week 96 after CAR-T cell infusion
Peripheral CD19-positive B-cell counts and B-cell subset dynamics will be assessed to evaluate the pharmacodynamic effect of CD19 CAR-T cell therapy, including B-cell depletion, time to B-cell aplasia, duration of B-cell depletion, and B-cell reconstitution.
Baseline through Week 96 after CAR-T cell infusion
Number of Circulating CAR-Positive T Cells in Peripheral Blood
Zeitfenster: From CAR-T cell infusion through Week 96
The number of circulating CAR-positive T cells in peripheral blood will be measured by flow cytometry at scheduled time points after CAR-T cell infusion to assess in vivo CAR-T cell expansion.
From CAR-T cell infusion through Week 96
CAR Transgene Copy Number in Peripheral Blood
Zeitfenster: From CAR-T cell infusion through Week 96
CAR transgene copy number in peripheral blood will be measured by quantitative polymerase chain reaction or digital PCR at scheduled time points after CAR-T cell infusion to assess CAR-T cell expansion and persistence.
From CAR-T cell infusion through Week 96
Duration of Detectable CAR-T Cells in Peripheral Blood
Zeitfenster: From CAR-T cell infusion through Week 96
The duration of detectable CAR-T cells in peripheral blood will be assessed based on the time from CAR-T cell infusion to the last time point at which CAR-positive T cells or CAR transgene copies remain detectable.
From CAR-T cell infusion through Week 96
Change From Baseline in Serum Cytokine Levels
Zeitfenster: Baseline through Week 96 after CAR-T cell infusion
Change from baseline in serum cytokine levels will be measured to characterize immune activation after CAR-T cell infusion and to support evaluation of cytokine release syndrome. Cytokines include interleukin-6 (IL-6), interferon-gamma (IFN-γ), tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β), interleukin-2 (IL-2), interleukin-10 (IL-10), and interleukin-17A (IL-17A).
Baseline through Week 96 after CAR-T cell infusion
Change From Baseline in Lymphocyte Subset Counts
Zeitfenster: Baseline through Week 96 after CAR-T cell infusion
Change from baseline in lymphocyte subset counts will be assessed at scheduled follow-up visits by flow cytometry to characterize immune reconstitution after CD19 CAR-T cell therapy. Lymphocyte subsets include CD3-positive T cells, CD4-positive T cells, CD8-positive T cells, CD19-positive B cells, and natural killer cells.
Baseline through Week 96 after CAR-T cell infusion
Change From Baseline in B-Cell Subset Counts
Zeitfenster: Baseline through Week 96 after CAR-T cell infusion
Change from baseline in B-cell subset counts will be assessed at scheduled follow-up visits by flow cytometry to characterize B-cell depletion and reconstitution after CD19 CAR-T cell therapy. B-cell subsets may include naïve B cells, non-switched memory B cells, switched memory B cells, and plasmablasts.
Baseline through Week 96 after CAR-T cell infusion
Relapse Rate Through Week 96
Zeitfenster: From disease control through Week 96 after CAR-T cell infusion
Relapse rate will be assessed as the proportion of participants who experience relapse after achieving disease control. Relapse is defined as the occurrence of three or more new lesions within one month that do not heal spontaneously within one week, or extension of established lesions.
From disease control through Week 96 after CAR-T cell infusion
Time to First Relapse
Zeitfenster: From disease control through Week 96 after CAR-T cell infusion
Time to first relapse will be assessed as the time from achievement of disease control to the first documented relapse.
From disease control through Week 96 after CAR-T cell infusion
Change From Baseline in Daily Prednisone-Equivalent Corticosteroid Dose
Zeitfenster: Baseline through Week 96 after CAR-T cell infusion
Change from baseline in daily systemic corticosteroid use will be assessed using prednisone-equivalent dose in milligrams per day at scheduled follow-up visits. A lower prednisone-equivalent daily dose indicates reduced corticosteroid requirement after CAR-T cell therapy.
Baseline through Week 96 after CAR-T cell infusion
Incidence of Serious Adverse Events and Long-Term Safety Events
Zeitfenster: From informed consent through Week 96 after CAR-T cell infusion
Serious adverse events, infections, prolonged cytopenias, organ dysfunction, secondary malignancies, and other clinically significant long-term safety events will be recorded throughout the study follow-up period.
From informed consent through Week 96 after CAR-T cell infusion

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

15. Januar 2026

Primärer Abschluss (Geschätzt)

30. Dezember 2026

Studienabschluss (Geschätzt)

30. Dezember 2028

Studienanmeldedaten

Zuerst eingereicht

19. Juni 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

26. Juni 2026

Zuerst gepostet (Tatsächlich)

2. Juli 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

2. Juli 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

26. Juni 2026

Zuletzt verifiziert

1. Juni 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • WuhanITCWMH-XS-2025139

Plan für individuelle Teilnehmerdaten (IPD)

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Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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