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

5. august 2026 opdateret af: 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).

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

23

Fase

  • Fase 2
  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Studiesteder

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

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.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Ikke-randomiseret
  • Interventionel model: Sekventiel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: 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)
Andre navne:
  • Riabni
  • Ruxience
  • Truxima
  • RITUXAN
Eksperimentel: 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)
Andre navne:
  • Riabni
  • Ruxience
  • Truxima
  • RITUXAN
Eksperimentel: 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)
Andre navne:
  • Riabni
  • Ruxience
  • Truxima
  • RITUXAN
Eksperimentel: 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)
Andre navne:
  • Riabni
  • Ruxience
  • Truxima
  • RITUXAN
Eksperimentel: 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)
Andre navne:
  • Riabni
  • Ruxience
  • Truxima
  • RITUXAN
Eksperimentel: 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)
Andre navne:
  • Riabni
  • Ruxience
  • Truxima
  • RITUXAN

Hvad måler undersøgelsen?

Primære resultatmål

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

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
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.
Tidsramme: 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.
Tidsramme: 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.
Tidsramme: 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.
Tidsramme: 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.
Tidsramme: 4 years
To assess OS.
4 years

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Samarbejdspartnere

Efterforskere

  • Ledende efterforsker: Narendranath Epperla, MD, Huntsman Cancer Institute

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

1. august 2026

Primær færdiggørelse (Anslået)

1. juni 2030

Studieafslutning (Anslået)

1. juni 2031

Datoer for studieregistrering

Først indsendt

30. april 2026

Først indsendt, der opfyldte QC-kriterier

30. april 2026

Først opslået (Faktiske)

7. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

6. august 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

5. august 2026

Sidst verificeret

1. april 2026

Mere information

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Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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