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

5 sierpnia 2026 zaktualizowane przez: 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).

Przegląd badań

Typ studiów

Interwencyjne

Zapisy (Szacowany)

23

Faza

  • Faza 2
  • Faza 1

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Kopia zapasowa kontaktu do badania

Lokalizacje studiów

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Opis

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.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Nielosowe
  • Model interwencyjny: Zadanie sekwencyjne
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: 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)
Inne nazwy:
  • Riabni
  • Ruxience
  • Truxima
  • RYTUKSAN
Eksperymentalny: 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)
Inne nazwy:
  • Riabni
  • Ruxience
  • Truxima
  • RYTUKSAN
Eksperymentalny: 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)
Inne nazwy:
  • Riabni
  • Ruxience
  • Truxima
  • RYTUKSAN
Eksperymentalny: 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)
Inne nazwy:
  • Riabni
  • Ruxience
  • Truxima
  • RYTUKSAN
Eksperymentalny: 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)
Inne nazwy:
  • Riabni
  • Ruxience
  • Truxima
  • RYTUKSAN
Eksperymentalny: 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)
Inne nazwy:
  • Riabni
  • Ruxience
  • Truxima
  • RYTUKSAN

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Phase I: Define Maximum Tolerated Dose (MTD) based on the rate of dose-limiting toxicities (DLTs) during the DLT evaluation period.
Ramy czasowe: 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.
Ramy czasowe: 4 years
To assess the efficacy of the combination of lonca-R based on CR rate after 4 cycles.
4 years

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 4 years
To assess OS.
4 years

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Współpracownicy

Śledczy

  • Główny śledczy: Narendranath Epperla, MD, Huntsman Cancer Institute

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

1 sierpnia 2026

Zakończenie podstawowe (Szacowany)

1 czerwca 2030

Ukończenie studiów (Szacowany)

1 czerwca 2031

Daty rejestracji na studia

Pierwszy przesłany

30 kwietnia 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

30 kwietnia 2026

Pierwszy wysłany (Rzeczywisty)

7 maja 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

6 sierpnia 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

5 sierpnia 2026

Ostatnia weryfikacja

1 kwietnia 2026

Więcej informacji

Terminy związane z tym badaniem

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Tak

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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