- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT05900401
Tolleranza ritardata attraverso il chimerismo misto
This study will examine the safety and effectiveness of a bone marrow transplant after kidney transplant (from either a living or deceased donor). An investigational medication and other treatments will be given prior to and after the transplant to help protect the transplanted kidney from being attacked by the body's immune system
Panoramica dello studio
Stato
Descrizione dettagliata
Recipients of previous living donor (LD) or deceased donor (DD) kidney transplants that were maintained on conventional immunosuppression (I.S.), will receive a conditioning regimen that includes rituximab on study day -6, fludarabine 15 mg/m2/day on days -5 to -3 (3 doses), Cyclophosphamide (30 mg/kg/day) on days -5 and -4, followed by local thymic irradiation (7 Gy) on day -1 and Siplizumab (anti-CD2 mAb) on days, -2, -1, 0 and +1. Donor hematopoetic stem cells (HSCs) will be infused on study day 0. Methylprednisolone 250mg/day will be started on day 0 and tapered off by day 20 (Fig. 2). Prophylaxis will be provided for hemorrhagic cystitis, PCP, fungal infection, CMV, and perioperative infection. All patients who require any blood transfusion will receive only leukocyte-depleted and irradiated blood products for a period of at least 12 months following HSC Transplant. The recipients will undergo renal allograft biopsy at 6 months after HSCT. If the I.S. withdrawal criteria are met, I.S. will be slowly tapered off by 9-12 months
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 2
- Fase 1
Contatti e Sedi
Contatto studio
- Nome: Tatsuo Kawai
- Numero di telefono: 617-726-0289
- Email: tkawai@mgh.harvard.edu
Backup dei contatti dello studio
- Nome: Gabriel Impreso Baysa
- Email: gimpresobaysa@mgh.harvard.edu
Luoghi di studio
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Massachusetts
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Boston, Massachusetts, Stati Uniti, 02114
- Reclutamento
- Massachusetts General Hospital
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Investigatore principale:
- Tatsuo Kawai, MD, PhD
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Contatto:
- Tatsuo Kawai, MD, PhD
- Numero di telefono: 617.726.0289
- Email: tkawai@mgh.harvard.edu
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Recipient Inclusion Criteria
- Male or female 18-65 years of age.
- Kidney transplant recipients from either LD or DD, with cryo-preserved HSCs available, good renal function (GFR>60 ml/min/1.73m2), normal current allograft biopsy, and no history of documented rejection episodes.
- First or second renal transplant.
- Use of FDA-approved methods of contraception (those with less than a 3% failure rate) by all recipients from the time that study treatment begins until 104 weeks (24 months) after renal transplantation. (For further information on FDA- approved methods of contraception, see https://www.fda.gov/media/150299/download
- Ability to understand and provide informed consent.
- Negative COVID-19 test during screening and two days prior to HSC transplantation (HSCT).
Deceased Donor (DD)
- Male or female 18-70 years of age.
- Consent to donate vertebral bones is obtained from the donor family.
- HSCs are successfully cryopreserved and saved >2X106/kg (CD34+ cells) of the recipient.
- Acceptable laboratory parameters (hematology in normal or near-normal range. Liver function <2 times the upper limit of normal, and normal creatinine)
- Negative for viral infection with HbsAg, HIV, HCV, or HTLV-1
- Negative COVID-19 test at the time of HSC procurement.
Living Donor (LD)
- Willingness to provide HSCs by leukapheresis or bone marrow aspiration.
- Negative serologic pregnancy test for females of childbearing potential
- Good general health as per conventional evaluation for kidney donation.
- Acceptable laboratory parameters (hematology in normal or near normal range. Liver function <2 times the upper limit of normal, and normal creatinine)
- Negative for viral infection with HbsAg, HIV, HCV, or HTLV-1.
- Cardiac/pulmonary function within normal limits (CXR, ECG).
- Ability to understand and provide informed consent.
- Meets standard institutional criteria for PBSC collection.
- Negative COVID-19 test during screening and two days prior to PBSC collection.
Recipient Exclusion Criteria
- ABO blood group-incompatible renal allograft.
- Evidence of anti-HLA antibody (donor specific with an MFI >1000) as assessed by routine methodology (Luminex)
- Previous history of biopsy proven rejection.
- Persistent Leukopenia (WBC less than 2,000/mm3) or thrombocytopenia (<100,000/mm3).
- Seropositivity for HIV-1, hepatitis B surface or core antigen, or hepatitis C virus (confirmed by hepatitis C virus RNA).
- Active infection
- Left ventricular ejection fraction < 40% as determined by TTE or clinical evidence of heart failure.
- Forced expiratory volume FEV1 or DLCO < 50% of predicted.
- Lactation or pregnancy.
- History of cancer (following the American Transplant Society Guidelines)
- Underlying renal disease etiology with high risk of disease recurrence in the transplanted kidney (such as focal segmental glomerulosclerosis). Autoimmune diseases such as Lupus and Thrombotic Thrombocytopenic Purpura.
- Enrollment in other investigational drug studies within 30 days prior to enrollment.
- Abnormal (>2 times lab normal) values for (a) liver function chemistries (ALT, AST, AP), (b) bilirubin, (c) coagulation studies (PT, PTT), or any patients on chronic anticoagulation therapy.
- Allergy or sensitivity to any component of Siplizumab, fludarabine, CP, tacrolimus, MMF or rituximab.
- Any medical condition that the investigator deems incompatible with participation in the trial. This includes a history of alcohol abuse or illicit drug use/dependence.
- Non-insulin dependent diabetes (NIDDM) without good blood glucose control (HbA1c<7). Severe retinopathy, gastroparesis, or severe neuropathy which prevent subject's normal independent daily activities.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Non randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Separare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: Kidney and Stem Cell Recipients
Months-Years after standard transplant, patients will undergo bone marrow transplant (either from prospective collection of stem cells from their living donor, or from bone marrow collected at the time of deceased donation) |
Months-Years after standard transplant, patients will undergo bone marrow transplant (either from prospective collection of stem cells from their living donor, or from bone marrow collected at the time of deceased donation) Fludarabine 15 mg/m2/day on days -5 to -3 (3 doses) Cyclophosphamide (CP) 30 mg/kg/day on days -5 and -4 Rituximab on study day -6 Siplizumab (anti-CD2 mAb) on days, -2, -1, 0 and +1. |
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Sperimentale: Kidney and Stem Cell Donors
PBSC will be collected from the LD via leukapheresis 1-4 weeks before the scheduled HSCT. The donor will first undergo standard GCSF mobilization: GCSF (can be TBO-GCSF) dosed at 10 mcg/kg/d (rounded to nearest pre-filled syringe) administered subcutaneously daily for 5 consecutive days. On the 5th day, the donor will undergo standard large volume leukapheresis. The target yield will be 2-3 x 106 CD34+ cells / kg of actual recipient body weight. A maximum of 3 days of pheresis will be allowed. A minimum of 2 x 106 CD34+ cells / kg of actual recipient body weight will be required to proceed |
PBSC will be collected from the LD via leukapheresis 1-4 weeks before the scheduled HSCT. The donor will first undergo standard GCSF mobilization: GCSF (can be TBO-GCSF) dosed at 10 mcg/kg/d (rounded to nearest pre-filled syringe) administered subcutaneously daily for 5 consecutive days. On the 5th day, the donor will undergo standard large volume leukapheresis. The target yield will be 2-3 x 106 CD34+ cells / kg of actual recipient body weight. A maximum of 3 days of pheresis will be allowed. A minimum of 2 x 106 CD34+ cells / kg of actual recipient body weight will be required to proceed. |
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
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Incidenza del chimerismo misto transitorio
Lasso di tempo: 3 mesi
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3 mesi
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Incidenza della tolleranza del trapianto renale
Lasso di tempo: 2 anni dopo la sospensione dell'immunosoppressione
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2 anni dopo la sospensione dell'immunosoppressione
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Incidenza della sopravvivenza dei partecipanti
Lasso di tempo: 2 anni dopo la sospensione dell'immunosoppressione
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2 anni dopo la sospensione dell'immunosoppressione
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Incidenza della sopravvivenza del trapianto
Lasso di tempo: 2 anni dopo la sospensione dell'immunosoppressione
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2 anni dopo la sospensione dell'immunosoppressione
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Incidenza della sindrome di transizione chimerica
Lasso di tempo: 3 mesi
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3 mesi
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Incidenza di DSA
Lasso di tempo: 2 anni dopo la sospensione dell'immunosoppressione
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2 anni dopo la sospensione dell'immunosoppressione
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Incidenza di GvHD
Lasso di tempo: 2 anni dopo la sospensione dell'immunosoppressione
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2 anni dopo la sospensione dell'immunosoppressione
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Incidenza di tossicità da irradiazione timica
Lasso di tempo: 2 anni dopo la sospensione dell'immunosoppressione
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2 anni dopo la sospensione dell'immunosoppressione
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Incidence of Allograft Rejection
Lasso di tempo: 2 years after immunosuppression withdrawal
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Measuring incidence of acute or chronic rejection free survival |
2 years after immunosuppression withdrawal
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Incidence of infections
Lasso di tempo: 2 years after immunosuppression withdrawal
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Clinically significant, invasive or resistant opportunistic infection |
2 years after immunosuppression withdrawal
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Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Tatsuo Kawai, Massachusetts General Hospital
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
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
- Malattie urogenitali
- Malattie urogenitali maschili
- Malattie renali
- Malattie urologiche
- Malattie urogenitali femminili
- Malattie urogenitali femminili e complicanze della gravidanza
- Insufficienza renale
- Aminoacidi, peptidi e proteine
- Proteine
- Prodotti chimici organici
- Terapie
- Procedure chirurgiche, operative
- Idrocarburi
- Trapianto
- Anticorpi, monoclonali
- Anticorpi
- Immunoglobuline
- Immunoproteine
- Proteine del sangue
- Globuline sieriche
- Globuline
- Senape di fosforamide
- Composti di senape di azoto
- Composti di senape
- Idrocarburi, alogenati
- Fosforamidi
- Composti organofosfori
- Anticorpi, monoclonali, derivati da murina
- Terapia a base di cellule e tessuti
- Terapia biologica
- Trapianto di tessuto
- Rituximab
- Ciclofosfamide
- fludarabina
- Trapianto di midollo osseo
- siplizumab
Altri numeri di identificazione dello studio
- 2023P000486
Piano per i dati dei singoli partecipanti (IPD)
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Informazioni su farmaci e dispositivi, documenti di studio
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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 .