Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

Loncastuximab Tesirine and Rituximab as First-line Therapy in Patients With Post-transplant Lymphoproliferative Disorder (PLUTO) (PLUTO)

5 agosto 2026 aggiornato da: University of Utah

A Phase 1/2 Study of Loncastuximab Tesirine and Rituximab as First-line Therapy in Patients With Post-transplant Lymphoproliferative Disorder (PLUTO)

The purpose of phase I of this clinical trial is to learn the recommended dose of the drugs loncastuximab tesirine and rituximab in participants with post-transplant lymphoproliferative disorders (PTLD).

The purpose of phase II of this clinical trial is to learn if the drugs loncastuximab tesirine and rituximab are effective in participants with post-transplant lymphoproliferative disorders (PTLD).

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

23

Fase

  • Fase 2
  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Utah
      • Salt Lake City, Utah, Stati Uniti, 84112
        • Huntsman Cancer Institute at University of Utah
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • Subject aged ≥ 18 years.
  • Histologically confirmed B-cell PTLD (monomorphic and polymorphic) following solid organ transplantation; with or without EBV association.

    --Note: Subjects with classic Hodgkin-like PTLD are excluded.

  • 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
  • ECOG Performance Status ≤ 2.
  • Adequate organ function as defined as:

    • Hematologic:

      • Absolute neutrophil count (ANC) ≥ 1000/mm3
      • Platelet count ≥ 75,000/mm3
      • Hemoglobin ≥ 8 g/dL
    • 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
    • Renal:

      • Estimated creatinine clearance ≥ 60 mL/min by Cockcroft-Gault formula.
  • 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. The following age-specific requirements apply:

    • 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).
    • 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).
  • 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 5.4.1 and 5.4.2.
  • Subjects or their legal representatives must be able to read, understand, and provide informed consent to participate in the trial.
  • 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:

  • PTLD following liquid transplantation
  • CNS involvement
  • Prior treatment for PTLD with the exception of radiation, antivirals, steroids and reduced immunosuppression
  • Human immunodeficiency virus (HIV) infection
  • Major surgery within 4 weeks prior to enrolment
  • History of bleeding diathesis (e.g., von Willebrand's disease), hemophilia, or active bleeding.
  • Subjects with chronic liver disease with hepatic impairment Child-Pugh class C
  • Pregnant or lactating or intending to become pregnant during the study
  • Active autoimmune disease which, in the opinion of the investigator, may negatively impact subject safety or interfere with study participation.
  • The diagnosis of another malignancy which, in the opinion of the investigator, is likely to negatively impact subject safety or interfere with study participation.
  • 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:

    • 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).
      • Grade 2 or higher edema (peripheral, pleural or ascites)
      • Grade 1 or higher pericardial effusion
    • Severe pulmonary disease
    • Uncontrolled diabetes mellitus
    • Severely immunocompromised state
    • 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.
  • Active systemic bacterial, viral, fungal, or other infection requiring systemic treatment at time of screening
  • 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
  • Active hepatitis C infection
  • Grade 2 or higher rash
  • Clinically significant fluid accumulation in the third space
  • 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

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Non randomizzato
  • Modello interventistico: Assegnazione sequenziale
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Dose Level 1 (starting dose): SD or PD

Dose Level 1:

  • Loncastuximab tesirine: 0.075 mg/kg IV every 3 weeks
  • Rituximab: 375 mg/m2 IV

This arm included participants who had SD (Stable Disease) or PD (Progressive Disease) after the first 6 weeks of treatment.

Lonca-R will be administered for 4 cycles with response assessment at 6 weeks (+/- 1 week) following the last Lonca-R treatment. If they do not achieve a response, they will come off the study but will be monitored for survival.

Lonca will be administered by IV at 75µg/kg every 3 weeks (DL1).
Rituximab or rituximab biosimilar will be administered by IV at 375 mg/m2 on Day 1 of every cycle. Lonca will be administered first, followed by rituximab (with a 30 min wait time between the two agents)
Altri nomi:
  • Riabni
  • Ruxienza
  • Truxima
  • RITUXAN
Sperimentale: Dose Level 1 (starting dose): PR

Dose Level 1:

  • Loncastuximab tesirine: 0.075 mg/kg IV every 3 weeks
  • Rituximab: 375 mg/m2 IV

This arm included participants who had a Partial Response (PR) after the first 6 weeks of treatment.

Lonca-R will be administered for 4 cycles with response assessment at 6 weeks (+/- 1 week) following the last Lonca-R treatment. If they achieve PR, they will have the option to receive either rituximab consolidation or R-CHOP (at the physician's discretion).

Lonca will be administered by IV at 75µg/kg every 3 weeks (DL1).
Rituximab or rituximab biosimilar will be administered by IV at 375 mg/m2 on Day 1 of every cycle. Lonca will be administered first, followed by rituximab (with a 30 min wait time between the two agents)
Altri nomi:
  • Riabni
  • Ruxienza
  • Truxima
  • RITUXAN
Sperimentale: Dose Level 1 (starting dose): CR

Dose Level 1:

  • Loncastuximab tesirine: 0.075 mg/kg IV every 3 weeks
  • Rituximab: 375 mg/m2 IV

This arm included participants who had a Complete Response (CR) after the first 6 weeks of treatment.

Lonca-R will be administered for 4 cycles with response assessment at 6 weeks (+/- 1 week) following the last Lonca-R treatment. If they achieve a CR after 4 cycles of Lonca-R, they will receive rituximab consolidation (SOC).

Lonca will be administered by IV at 75µg/kg every 3 weeks (DL1).
Rituximab or rituximab biosimilar will be administered by IV at 375 mg/m2 on Day 1 of every cycle. Lonca will be administered first, followed by rituximab (with a 30 min wait time between the two agents)
Altri nomi:
  • Riabni
  • Ruxienza
  • Truxima
  • RITUXAN
Sperimentale: Dose Level 2: SD or PD

Dose Level 2:

  • Loncastuximab tesirine: 0.15 mg/kg IV every 3 weeks for the first 2 cycles, then 0.075 mg/kg starting C3
  • Rituximab: 375 mg/m2 IV

This arm included participants who had SD (Stable Disease) or PD (Progressive Disease) after the first 6 weeks of treatment.

Lonca-R will be administered for 4 cycles with response assessment at 6 weeks (+/- 1 week) following the last Lonca-R treatment. If they do not achieve a response, they will come off the study but will be monitored for survival.

Lonca will be administered by IV at 75µg/kg every 3 weeks (DL1).
Rituximab or rituximab biosimilar will be administered by IV at 375 mg/m2 on Day 1 of every cycle. Lonca will be administered first, followed by rituximab (with a 30 min wait time between the two agents)
Altri nomi:
  • Riabni
  • Ruxienza
  • Truxima
  • RITUXAN
Sperimentale: Dose Level 2: PR

Dose Level 2:

  • Loncastuximab tesirine: 0.15 mg/kg IV every 3 weeks for the first 2 cycles, then 0.075 mg/kg starting C3
  • Rituximab: 375 mg/m2 IV

This arm included participants who had a Partial Response (PR) after the first 6 weeks of treatment.

Lonca-R will be administered for 4 cycles with response assessment at 6 weeks (+/- 1 week) following the last Lonca-R treatment. If they achieve PR, they will have the option to receive either rituximab consolidation or R-CHOP (at the physician's discretion).

Lonca will be administered by IV at 75µg/kg every 3 weeks (DL1).
Rituximab or rituximab biosimilar will be administered by IV at 375 mg/m2 on Day 1 of every cycle. Lonca will be administered first, followed by rituximab (with a 30 min wait time between the two agents)
Altri nomi:
  • Riabni
  • Ruxienza
  • Truxima
  • RITUXAN
Sperimentale: Dose Level 2: CR

Dose Level 2:

  • Loncastuximab tesirine: 0.15 mg/kg IV every 3 weeks for the first 2 cycles, then 0.075 mg/kg starting C3
  • Rituximab: 375 mg/m2 IV

This arm included participants who had a Complete Response (CR) after the first 6 weeks of treatment.

Lonca-R will be administered for 4 cycles with response assessment at 6 weeks (+/- 1 week) following the last Lonca-R treatment. If they achieve a CR after 4 cycles of Lonca-R, they will receive rituximab consolidation (SOC).

Lonca will be administered by IV at 75µg/kg every 3 weeks (DL1).
Rituximab or rituximab biosimilar will be administered by IV at 375 mg/m2 on Day 1 of every cycle. Lonca will be administered first, followed by rituximab (with a 30 min wait time between the two agents)
Altri nomi:
  • Riabni
  • Ruxienza
  • Truxima
  • RITUXAN

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Phase I: Define Maximum Tolerated Dose (MTD) based on the rate of dose-limiting toxicities (DLTs) during the DLT evaluation period.
Lasso di tempo: 4 years
To assess the Recommended Phase 2 Dose (RP2D) of loncastuximab tesirine and rituximab in participants with post-transplant lymphoproliferative disorders (PTLD).
4 years
Phase II: The complete response (CR) rate after 4 cycles of lonca-R per Lugano 2014 criteria1.
Lasso di tempo: 4 years
To assess the efficacy of the combination of lonca-R based on CR rate after 4 cycles.
4 years

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
The frequency of adverse events (AEs) and serious adverse events (SAEs) characterized by type, severity (as defined by the NIH CTCAE, version 6.0), seriousness, duration, and relationship to study treatment.
Lasso di tempo: 4 years
To assess the safety and tolerability of lonca-R in subjects with B-cell PTLD.
4 years
The overall response rate (ORR) after 4 cycles of lonca-R.
Lasso di tempo: 4 years
To determine ORR after 4 cycles of lonca-R in subjects with B-cell PTLD.
4 years
The best complete response (CR) rate is defined as CR at the completion of 4 cycles of lonca-R or 4 cycles of lonca-R and 4 cycles of consolidation of rituximab monotherapy (every 3 weeks) in subjects with B-cell PTLD.
Lasso di tempo: 4 years
To determine the best CR rate in subjects with B-cell PTLD.
4 years
Median and two year progression-free survival (PFS). PFS will be as defined as the time from study drug initiation to the time of documented disease progression (as assessed by Lugano Criteria), or death from any cause.
Lasso di tempo: 4 years
To assess PFS.
4 years
Median and two year overall survival (OS). OS is defined as the time from initiation of treatment until death from any cause.
Lasso di tempo: 4 years
To assess OS.
4 years

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Collaboratori

Investigatori

  • Investigatore principale: Narendranath Epperla, MD, Huntsman Cancer Institute

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 agosto 2026

Completamento primario (Stimato)

1 giugno 2030

Completamento dello studio (Stimato)

1 giugno 2031

Date di iscrizione allo studio

Primo inviato

30 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

30 aprile 2026

Primo Inserito (Effettivo)

7 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

6 agosto 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

5 agosto 2026

Ultimo verificato

1 aprile 2026

Maggiori informazioni

Termini relativi a questo studio

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Sì

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

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 .

Sottoscrivi