- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07599280
Universal STAR-T Cell Injection in R/R Autoimmune Diseases.
An Exploratory Clinical Study of Universal STAR-T Cell Injection in Subjects With Relapsed/Refractory Autoimmune Diseases
This is a Phase I, single-arm, open-label, dose-escalation and dose-expansion study.
This study evaluates the safety and efficacy of universal STAR-T cells in patients with R/R CTD-associated Immune Thrombocytopenia (CTD-ITP). Approximately 9 patients aged 18-65 will receive infusion of universal STAR-T cells at the starting dose of 3E6 STAR+T cells/kg. The main purpose of exploratory clinical research is to explore the efficacy and safety of universal STAR-T cell and the lymphodepletion regimen. The primary endpoint is observations of types, severity, and frequency of adverse events (AEs) and efficacy assessment. This single-arm, open-label trial will enroll patients across Chinese People's Liberation Army (PLA) General Hospital.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Background: Connective Tissue Disease-associated Immune Thrombocytopenia (CTD-ITP) is a severe complication of autoimmune disorders, including Systemic Lupus Erythematosus (SLE), Sjögren's Syndrome (pSS), and Antiphospholipid Syndrome (APS). Thrombocytopenia occurs in 20%-40% of SLE patients and up to 50% of APS patients. While often mild, severe cases lead to significant bleeding risk, poor quality of life, and increased mortality.
Current standard therapies-glucocorticoids, intravenous immunoglobulin (IVIG), and immunosuppressants (e.g., cyclophosphamide, mycophenolate mofetil)-often fail in refractory or relapsing cases. Long-term dependence on high-dose steroids results in severe adverse events (infections, osteoporosis) and poor prognosis.
B cells play a central role in autoantibody production and immune dysregulation in CTD-ITP. Novel strategies focusing on deep B-cell depletion or immune reconstitution offer a promising new approach for patients who have exhausted conventional treatments.
This study aims to evaluate the safety and preliminary efficacy of universal STAR-T cell in patients with relapsed/refractory CTD-ITP. Approximately 3~6 patients aged 18-65 will be enrolled in the dose-escalation phase to receive infusion of universal STAR-T cells at the starting dose of 3E6 STAR+T cells/kg.
In patients with relapsed/refractory connective tissue disease-associated immune thrombocytopenia, the primary efficacy endpoint is the complete response rate at week 12, while the secondary efficacy endpoints include the complete response rate at week 24; the partial response rate, overall response rate, and change in platelet count from baseline at both weeks 12 and 24; as well as time to response, drug-free remission duration, and response duration.
Study endpoints include primary endpoints such as dose - limiting toxicity (DLT), the type, severity, and frequency of adverse events (AE), and efficacy endpoints; secondary endpoints encompass the in - vivo expansion and persistence of universal STAR - T cells, main pharmacokinetic (PK) parameters (including peak expansion (Cₘₐₓ), time to peak (Tₘₐₓ), area under the blood concentration - time curve (AUC), and studies on cell subtypes and dominant clones), main pharmacodynamic (PD) parameters (such as changes in cytokines and the level and characteristics of immune cell reconstitution like CD19 - positive B cells), and immunogenicity - related studies (including the production of anti - drug antibodies (ADA) against universal STAR - T cells and replication - competent associated virus (RCA) in peripheral blood).
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 1
Contatti e Sedi
Contatto studio
- Nome: Jian Zhu
- Numero di telefono: 8610-66937166
- Email: jian_jzhu@126.com
Luoghi di studio
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Beijing Municipality
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Haidian, Beijing Municipality, Cina
- No. 28, Fuxing Road, Haidian District, Beijing, China.
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
Inclusion Criteria:
- Age ranges from 18 to 65 years old (including threshold), regardless of gender.
- Confirmed diagnosis of a connective tissue disease (CTD) according to the latest international classification criteria, including but not limited to Systemic Lupus Erythematosus (SLE), Primary Sjögren's Syndrome (pSS), Antiphospholipid Syndrome (APS), and Undifferentiated Connective Tissue Disease (UCTD).
Confirmed diagnosis of CTD-associated immune thrombocytopenia meeting one of the following:
Platelet count < 30 × 10⁹/L; Platelet count < 50 × 10⁹/L accompanied by bleeding tendency.
- Bone marrow morphology consistent with the characteristics of immune thrombocytopenia (ITP).
- Prior Treatment History: Failure to achieve partial remission (PR) after receiving at least one of the following regimens continuously for ≥ 3 months, or inability to maintain efficacy during glucocorticoid tapering:
At least one course of glucocorticoid pulse therapy; Or high-dose glucocorticoids combined with one or more immunosuppressants (including biologics).
6. Essential Organ Function Criteria:
Bone marrow: Neutrophils ≥1×10^9/L (within 2 weeks, excluding granulocyte colony-stimulating factor use).
Hemoglobin ≥60 g/L.
Liver: ALT/AST ≤3×ULN (disease-related elevations permitted). TBIL
≤1.5×ULN (disease-related elevations permitted).
- Renal: CrCl≥30mL/min (Cockcroft-Gault formula, excluding acute declines).
- Coagulation: INR/PT ≤1.5×ULN.
- Cardiovascular: Hemodynamic stability. 7. Fertile females or males with partners of childbearing age must use medically approved contraception or abstain during and ≥12 months post- treatment. Negative serum HCG test (within 7 days pre-enrollment) for fertile females; non-lactating.
8. Voluntary participation with signed informed consent and compliance.
Exclusion Criteria:
Subjects who meet any of the following exclusion criteria will not be admitted to the study:
- Individuals with a severe history of drug allergies or those with an allergic constitution;
- Individuals with existing or suspected uncontrolled or treatable fungal, bacterial, viral, or other infections;
- Subjects with central nervous system diseases (excluding those with a history of epilepsy, psychiatric disorders, organic brain disease syndromes, cerebrovascular accidents, encephalitis, or central nervous system vasculitis resulting from the underlying disease);
- Subjects whose cardiac function cannot tolerate the study interventions;
- Subjects with congenital immunoglobulin deficiencies;
- Subjects with a history of malignant tumors within the past five years;
- Subjects with end-stage renal failure;
- Subjects who are positive for hepatitis B surface antigen (HBsAg) and hepatitis B core antibody (HBcAb) with peripheral blood HBV DNA titers exceeding the upper limit of detection; subjects who are positive for hepatitis C virus (HCV) antibody and peripheral blood HCV RNA; subjects who are positive for human immunodeficiency virus (HIV) antibody; and subjects who are positive for syphilis testing;
- Subjects with psychiatric disorders or severe cognitive dysfunction;
- Subjects who have participated in other clinical trials within the past three months prior to enrollment;
- Subjects who have received immunosuppressive agents with therapeutic effects on the disease within five half-lives prior to enrollment or biological agents within four weeks prior to enrollment;
- Pregnant women or women planning to become pregnant;
- Subjects whom the investigator believes have other reasons that preclude their inclusion in this study.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: Universal STAR-T Cell
Subjects will receive infusion of Universal STAR-T Cells at the starting dose of 3E6 STAR+T cells/kg.
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Subjects will receive infusion of Universal STAR-T Cells at the starting dose of 3E6 STAR+T cells/kg.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Incidence of Dose-Limiting Toxicities (DLTs).
Lasso di tempo: Within 28 days after infusion
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To assess the safety and tolerability of [Drug Name] and determine the Maximum Tolerated Dose (MTD) or Recommended Phase 2 Dose (RP2D).
DLTs are defined according to the NCI Common Terminology Criteria for Adverse Events (CTCAE) v5.0
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Within 28 days after infusion
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Preliminary assessment of efficacy.
Lasso di tempo: The efficacy endpoint evaluation for 104 weeks.
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1. Evaluation of preliminary efficacy based on relevant disease activity indices or response criteria.
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The efficacy endpoint evaluation for 104 weeks.
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Type, severity, and frequency of Adverse Events (AEs) and Serious Adverse Events (SAEs).
Lasso di tempo: AEs observation will be follow-up for 24 weeks. The observation period is extended to 104 weeks.
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Serious Adverse Events (SAEs).
Description: Characterization of treatment-emergent adverse events (TEAEs) graded by NCI-CTCAE v5.0, including laboratory abnormalities, vital sign changes, and infusion-related reactions.
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AEs observation will be follow-up for 24 weeks. The observation period is extended to 104 weeks.
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Maximum Plasma Concentration of YTS109 (Cmax) .
Lasso di tempo: Up to 24 weeks (Core Analysis Period); Extended observation up to 104 weeks.
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To evaluate the maximum observed plasma concentration of YTS109.
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Up to 24 weeks (Core Analysis Period); Extended observation up to 104 weeks.
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Time to Reach Maximum Plasma Concentration (Tmax) of YTS109
Lasso di tempo: Up to 24 weeks (Core Analysis Period); Extended observation up to 104 weeks.
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To evaluate the time to reach the maximum observed plasma concentration of YTS109
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Up to 24 weeks (Core Analysis Period); Extended observation up to 104 weeks.
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Area Under the Plasma Concentration-Time Curve (AUC) of YTS109
Lasso di tempo: Up to 24 weeks (Core Analysis Period); Extended observation up to 104 weeks.
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To evaluate the total systemic exposure to YTS109 over time.
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Up to 24 weeks (Core Analysis Period); Extended observation up to 104 weeks.
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PD Biomarker Level Change (Cytokines Concentration).
Lasso di tempo: Up to 24 weeks (Core Analysis Period); Extended observation up to 104 weeks.
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Evaluate the Pharmacodynamic (PD) effects of YTS109 cells.
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Up to 24 weeks (Core Analysis Period); Extended observation up to 104 weeks.
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PD Biomarker Level Change (B cells Quantification and Phenotypic).
Lasso di tempo: Up to 24 weeks (Core Analysis Period); Extended observation up to 104 weeks.
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Evaluate the Pharmacodynamic (PD) effects of YTS109 cells.
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Up to 24 weeks (Core Analysis Period); Extended observation up to 104 weeks.
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Immunogenicity: Anti-Drug Antibodies (ADA) against universal STAR-T cells
Lasso di tempo: Up to 24 weeks (Core Analysis Period); Extended observation up to 104 weeks.
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To evaluate the development of anti-drug antibodies (ADA) against allogeneic universal STAR-T cells in peripheral blood.
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Up to 24 weeks (Core Analysis Period); Extended observation up to 104 weeks.
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Replication-Competent Adeno-Associated Virus (RCA) Detection
Lasso di tempo: Up to 24 weeks (Core Analysis Period); Extended observation up to 104 weeks.
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To evaluate the presence of replication-competent adeno-associated virus (RCA) in peripheral blood.
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Up to 24 weeks (Core Analysis Period); Extended observation up to 104 weeks.
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Collaboratori e investigatori
Sponsor
Collaboratori
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Citopenia
- Processi patologici
- Malattie autoimmuni
- Malattie del sistema immunitario
- Emorragia
- Manifestazioni cutanee
- Malattie ematologiche
- Disturbi della coagulazione del sangue
- Disturbi emorragici
- Disturbi delle piastrine del sangue
- Microangiopatie trombotiche
- Porpora, Trombocitopenica
- Porpora
- Trombocitopenia
- Condizioni patologiche, segni e sintomi
- Segni e sintomi
- Malattie emiche e linfatiche
- Porpora, Trombocitopenica, Idiopatica
Altri numeri di identificazione dello studio
- YTS109-006
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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