- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT06788964
Loncastuximab tesirine e rituximab come terapia a ponte prima della terapia a cellule T CD19 CD19 standard in pazienti con linfoma di grandi cellule a B (CORAL)
Uno studio di fase 2 su loncastuximab tesirine e rituximab come terapia a ponte prima della terapia a cellule T CD19 CD19 standard in pazienti con linfoma a grandi cellule di grandi dimensioni
The purpose of this clinical trial is to learn if the study treatment Loncastuximab tesirine and Rituximab is safe and efficient before standard of care chimeric antigen receptor T-cell (CAR-T) therapy in patients with relapsed or refractory large B-cell lymphoma.
Panoramica dello studio
Stato
Intervento / Trattamento
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 2
Contatti e Sedi
Contatto studio
- Nome: David Samuel
- Numero di telefono: 801-587-4713
- Email: david.samuel@hci.utah.edu
Backup dei contatti dello studio
- Nome: Narendranath Epperla, MD, MS, FACP
- Numero di telefono: 801-585-0255
- Email: naren.epperla@hci.utah.edu
Luoghi di studio
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North Carolina
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Chapel Hill, North Carolina, Stati Uniti, 27514
- Reclutamento
- UNC Lineberger Comprehensive Cancer Center
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Contatto:
- Kelsey Scheel
- Email: Kelsey_Scheel@med.unc.edu
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Utah
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Salt Lake City, Utah, Stati Uniti, 84112
- Reclutamento
- Huntsman Cancer Institute at University of Utah
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Contatto:
- David Samuel
- Numero di telefono: 801-587-4713
- Email: david.samuel@hci.utah.edu
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-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
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Subject aged ≥ 18 years.
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Intended to receive commercial CD19-directed CAR-T cell therapy (axi-cel and liso-cel).
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Need for bridging therapy as deemed clinically necessary by the treating physician.
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Relapsed or refractory DLBCL, tFL or PMBCL as defined by the 2016 World Health Organization classification (including patients with DLBCL transformed from indolent lymphoma), or high-grade B-cell lymphoma (HGBL), not otherwise specified, and HGBL with MYC and BCL2 and/or BCL6 rearrangements.
--Relapsed (disease that has recurred following a response) or refractory (disease that failed to respond to prior therapy) disease following at least one multi-agent systemic treatment regimen.
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Measurable disease as defined by the 2014 Lugano Classification as assessed by positron-emission tomography (PET)- computed tomography (CT) or by CT or magnetic resonance imaging (MRI) if the tumor is not fluorodeoxyglucose (FDG)-avid on screening PET-CT.
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ECOG Performance Status ≤ 2.
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Time between prior anticancer therapy and first dose of lonca-R as below
- Autologous hematopoietic cell transplantation - At least 30 days
- Allogeneic hematopoietic cell transplantation - At least 60 days
- Cytotoxic chemotherapy - At least 21 days
- Non-cytotoxic chemotherapy (e.g., small molecule inhibitor) - At least 14 days
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Adequate organ function as defined as:
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Hematologic:
- Absolute neutrophil count (ANC) ≥ 1000/mm3
- Platelet count ≥ 75,000/mm3
- Hemoglobin ≥ 8 g/dL
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Hepatic:
- Bilirubin ≤1.5 x upper limit of normal (ULN) or ≤3 x ULN with document liver involvement and/ or Gilbert's disease
- Transaminases (AST or ALT) ≤ 3 x ULN or ≤ 5 x ULN with documented liver involvement
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Renal:
- Estimated creatinine clearance ≥ 60 mL/min by Cockcroft-Gault formula.
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For female subjects: Negative pregnancy test or evidence of post-menopausal status. The post-menopausal status will be defined as having been amenorrheic for 12 months without an alternative medical cause or having undergone surgical sterilization (bilateral oophorectomy or hysterectomy). The following age-specific requirements apply:
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Women < 50 years of age:
- Amenorrheic for ≥ 12 months following cessation of exogenous hormonal treatments; and
- Luteinizing hormone and follicle-stimulating hormone levels in the post-menopausal range for the institution; or
- Underwent surgical sterilization (bilateral oophorectomy or hysterectomy).
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Women ≥ 50 years of age:
- Amenorrheic for 12 months or more following cessation of all exogenous hormonal treatments; or
- Had radiation-induced menopause with last menses >1 year ago; or
- Had chemotherapy-induced menopause with last menses >1 year ago; or
- Underwent surgical sterilization (bilateral oophorectomy, bilateral salpingectomy, or hysterectomy).
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Female subjects of childbearing potential and male subjects with a sexual partner of childbearing potential must agree to use a highly effective method of contraception and the lactation requirements as described in Sections 5.41.1 and 5.4.2.
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Subjects or their legal representatives must be able to read, understand, and provide informed consent to participate in the trial.
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Willing and capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in the protocol
Exclusion Criteria:
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Previous treatment with any anti-CD19 therapy including lonca or prior CD19 CAR T-cell therapy
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Subjects receiving investigational CAR-T products
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Major surgery within 4 weeks prior to starting study therapy.
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History of bleeding diathesis (e.g., von Willebrand's disease), hemophilia, or active bleeding.
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Subjects with chronic liver disease with hepatic impairment Child-Pugh class C
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Pregnant or lactating or intending to become pregnant during the study
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Active graft-versus-host disease
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Post-transplantation lymphoproliferative disorders
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Active autoimmune disease which, in the opinion of the investigator, may negatively impact subject safety or interfere with study participation.
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The diagnosis of another malignancy which, in the opinion of the investigator, is likely to negatively impact subject safety or interfere with study participation.
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Subjects with known CNS involvement.
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Significant medical diseases or conditions including those requiring substantial changes in concomitant medications, as assessed by the investigator, that would substantially increase the risk-to-benefit ratio of participating in the study. This includes, but is not limited to the following conditions:
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Cardiovascular disorders:
- Congestive heart failure New York Heart Association Class III or IV, unstable angina pectoris, serious cardiac arrhythmias.
- Myocardial infarction (MI) within 6 months before the first dose.
- QTc prolongation defined as a QTcF > 480 ms.
- Congenital long QT syndrome or a corrected QT measure (QTc) interval of >480 ms at screening (unless secondary to pacemaker or bundle branch block).
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Severe pulmonary disease
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Uncontrolled diabetes mellitus
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Severely immunocompromised state
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Any other condition that would, in the Investigator's judgment, contraindicate the subject's participation in the clinical study due to safety concerns or compliance with clinical study procedures.
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Active systemic bacterial, viral, fungal, or other infection requiring systemic treatment at time of screening
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HIV infection.
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Subjects with evidence of active hepatitis B infection, based on positive surface antigen or Hepatitis B DNA PCR are excluded. Subjects who are Hepatitis B core antibody positive must take prophylaxis with entecavir or equivalent and be willing to undergo monthly Hepatitis B DNA PCR testing. Subjects with active Hep C patients may be enrolled if other parameters precluding hepatic impairment are met and they are not undergoing active therapy for hepatitis C.
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Known prior severe hypersensitivity to a CD19 antibody, lonca (including SG3249) or any of its excipients, or history of positive serum human ADA to a CD19 antibody.
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Subjects taking prohibited medications as described in Section 6.8.1. A washout period of prohibited medications for a period of at least five half-lives or as clinically indicated should occur before the start of treatment.
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 |
|---|---|
|
Sperimentale: Treatment: All Patients
The study will investigate the effectiveness of Loncastuximab tesirine and Rituximab (Lonca-R) prior to standard of care CAR-T cell therapy. |
Patients will receive Loncastuximab Tesirine intravenously for 1-6 cycles (every 21 days) prior to standard of care CAR-T cell therapy.
Altri nomi:
Rituximab is administered intravenously for 1-6 cycles (every 21 days) prior to standard of care CAR-T cell therapy.
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
The complete response (CR) rate at D30 post CAR-T(+/- 7 days) post CAR-T administration per Lugano 2014 criteria.
Lasso di tempo: 1 month
|
To evaluate the efficacy of SOC CAR T-cell therapy in patients with R/R large B-cell lymphoma following bridging with lonca-R. |
1 month
|
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Duration of cytopenias post CAR-T (as defined by the NIH CTCAE, version 5.0) D30 post CAR-T (+/- 7 days).
Lasso di tempo: 1 month
|
To evaluate toxicities post CAR-T |
1 month
|
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Severity of cytopenias post CAR-T (as defined by the NIH CTCAE, version 5.0) D30 (+/- 7 days).
Lasso di tempo: 1 month
|
To evaluate toxicities post CAR-T |
1 month
|
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Rate of infections D30 (+/- 7 days).
Lasso di tempo: 1 month
|
To evaluate toxicities post CAR-T |
1 month
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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CD19 expression as measured by flow cytometry and IHC on biopsies obtained pre- and post-lonca-R (optional) and post-CAR-T (optional but strongly recommended)
Lasso di tempo: 5 years
|
To determine whether CD19 expression is reduced in patients who receive bridging with lonca-R prior to CAR-T. |
5 years
|
|
ORR defined as the proportion of subjects achieving a confirmed PR or CR at D30 (+/- 7 days) post CAR-T per Lugano 2014 criteria1.
Lasso di tempo: 1 month
|
To evaluate the level of disease control provided by bridging lonca-R |
1 month
|
|
Best response rate per Lugano 2014 criteria following CAR-T (based on imaging up until D90 post CAR-T)
Lasso di tempo: 3 months
|
To evaluate the level of disease control provided by bridging lonca-R |
3 months
|
|
ORR defined as the proportion of subjects achieving a confirmed PR or CR post lonca-R (pre-CAR-T)
Lasso di tempo: 5 years
|
To evaluate the level of disease control provided by bridging lonca-R |
5 years
|
|
Level of disease control (measured as percentage) with lonca-R as evaluated by CT measurements and metabolic tumor volume on PET pre and post Lonca-R
Lasso di tempo: 5 years
|
To evaluate the level of disease control provided by bridging lonca-R |
5 years
|
|
The frequency of adverse events (AEs) and serious adverse events (SAEs) characterized by severity (as defined by the NIH CTCAE, version 5.0)
Lasso di tempo: 5 years
|
To assess the safety and tolerability of lonca-R in the study population. |
5 years
|
|
The frequency of adverse events (AEs) and serious adverse events (SAEs) characterized by seriousness.
Lasso di tempo: 5 years
|
To assess the safety and tolerability of lonca-R in the study population. |
5 years
|
|
The frequency of adverse events (AEs) and serious adverse events (SAEs) characterized by duration.
Lasso di tempo: 5 years
|
To assess the safety and tolerability of lonca-R in the study population. |
5 years
|
|
The frequency of adverse events (AEs) and serious adverse events (SAEs) characterized by relationship to study treatment.
Lasso di tempo: 5 years
|
To assess the safety and tolerability of lonca-R in the study population. |
5 years
|
Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Investigatore principale: Narendranath Epperla, MD, MS, FACP, Huntsman Cancer Institute
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
Termini MeSH pertinenti aggiuntivi
- Processi patologici
- Attributi della malattia
- Condizioni patologiche, segni e sintomi
- Ricorrenza
- Aminoacidi, peptidi e proteine
- Proteine
- Anticorpi, monoclonali
- Anticorpi
- Immunoglobuline
- Immunoproteine
- Proteine del sangue
- Globuline sieriche
- Globuline
- Anticorpi, monoclonali, derivati da murina
- Rituximab
- loncastuximab tesiine
Altri numeri di identificazione dello studio
- HCI184585
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
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 .