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Zilovertamab Vedotin and Lenalidomide (ZiVLen) Therapy for Relapsed/Refractory Peripheral T-Cell Lymphoma (ZiVLen)

27 ottobre 2026 aggiornato da: Olivia Newton-John Cancer Research Institute

This study will test whether a combination of two medicines, zilovertamab vedotin (ZV) and lenalidomide, can help people with peripheral T-cell lymphoma that has come back after treatment or has not responded to previous treatment. The combination, called "ZiVLen", is designed to provide an alternative treatment approach that may use less chemotherapy than standard regimens. Researchers will evaluate how well this treatment works in controlling the lymphoma and will also assess its safety and side effects. The study will collect research biospecimens (archival tissue, and onstudy blood and stool samples) to investigate whether there are any immune system changes in participants who's lymphoma responds to the treatment compared to those who do not. In addition, health related quality of life surveys (patient reported outcome measures [PROMS]) will be collected to better understand whether the treatment and/or trial has impacted the health related quality of life of participants in their own voice. The results of this study will help determine whether ZiVLen should be studied further in larger clinical trials.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

25

Fase

  • Fase 2

Contatti e Sedi

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

Luoghi di studio

    • New South Wales
      • Sydney, New South Wales, Australia, 2139
        • Concord Repatriation General Hospital
        • Contatto:
        • Investigatore principale:
          • Janlyn Falconer, MBBS
    • Queensland
    • Victoria
    • Washington
      • Nedlands, Washington, Australia, 6009
        • Sir Charles Gairdner Hospital
        • Contatto:
        • Investigatore principale:
          • Dejan Radeski, MBBS FRACP FRCPA

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

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  1. Histologically confirmed R/R nodal PTCL which include subtypes T-follicular helper cell lymphoma (angioimmunoblastic T-cell lymphoma, follicular T-helper cell lymphoma, T-follicular helper cell lymphoma-not otherwise specified), anaplastic large cell lymphoma (ALCL; both ALK+ and ALK-) and peripheral T-cell lymphoma-not otherwise specified (PTCL-NOS). In the absence of a fresh biopsy, the most recent archival tumour tissue should be used and obtained between the last dose of the last prior cancer regimen and C1D1.

  2. Confirmed R/R disease after at least one prior line of therapy containing a combination chemotherapy regimen. Monotherapies, such as corticosteroids are excluded. Prior exposure to an ADC (including brentuximab vedotin) is permitted, provided all ADC-related toxicities, including but not limited to peripheral neuropathy, have resolved to Grade ≤1 prior to study entry.

  3. Is an individual of any sex/gender, ≥18 years of age at the time of providing documented informed consent.

  4. Patients of childbearing potential willing to adhere to the contraceptive precautions.

  5. The participant (or legally acceptable representative) has provided documented informed consent for the study.

    Additional Categories

  6. Has an ECOG performance status of 0 to 1 (unless attributable to lymphoma, in which case patients of performance status 2 are eligible) assessed within 7 days before registration.

  7. Has an ejection fraction ≥45% as determined by either ECHO or GCBP.

  8. HIV infected participants must have well controlled HIV on ART.

  9. Participants who are HBsAg positive are eligible if they have received HBV antiviral therapy and have undetectable HBV viral load prior to enrolment.

11. Participants with history of HCV infection are eligible if HCV viral load is undetectable at screening.

12. Participants with a prior allogeneic haematopoietic stem cell transplant are eligible provided they are >90 days post-transplant, have no evidence of acute or chronic graft-versus-host disease, and are not receiving systemic immunosuppressive therapy (except for low-dose corticosteroids equivalent to <10 mg/day of prednisolone). Participants with a prior autologous haematopoietic stem cell transplant are eligible provided they are >90 days post-transplant and meet organ function and haematological parameter criteria unsupported by growth factors or transfusions.

13. Life expectancy > 12 weeks. 14. Adequate organ function

Exclusion Criteria:

  1. Any other type of lymphoma except nodal PTCL as listed above.

  2. Has clinically significant (ie, active) cardiovascular disease: cerebral vascular accident/stroke (<6 months prior to enrollment), myocardial infarction (<6 months prior to enrollment), unstable angina, congestive heart failure (New York Heart Association Classification Class ≥II), or serious cardiac arrhythmia requiring medication.

  3. Has QTcF prolongation of >480 msec.

  4. Has ongoing Grade >1 peripheral neuropathy.

  5. Has a demyelinating form of Charcot-Marie-Tooth disease.

  6. HIV-infected participants with a history of Kaposi's sarcoma and/or Multicentric Castleman's Disease.

  7. Patients with a current or past history of venous thromboembolism (VTE; pulmonary embolism/deep venous thrombosis) are permitted to study inclusion provided that there is no contraindication to receive VTE prophylaxis with either anticoagulation or antiplatelet therapy.

  8. Has ongoing corticosteroid therapy (exceeding 10 mg daily of prednisone equivalent). Prednisone equivalent dosing must have been stable for at least 28 days prior to enrolment.

  9. Received a live or live-attenuated vaccine within 30 days before the first dose of study intervention. Administration of killed vaccines is allowed.

    Refer to Section 6.5 for information on COVID-19 vaccines.

  10. Known intolerance to any of the study interventions and/or their excipients.

  11. Received a strong inhibitor or inducer of CYP3A4 within 14 days prior to randomization or is expected to require chronic use of a strong CYP3A4 inhibitor or inducer during treatment with study intervention until 30 days after the last dose.

  12. Received a strong modulator of CYP2D6 or P-gp within 14 days prior to randomization or is expected to require chronic use of a strong modulator of CYP2D6 or P-gp during treatment with study intervention until 30 days after the last dose

  13. Is receiving an investigational agent or has received an investigational agent or has used an investigational device within 4 weeks prior to study intervention administration.

  14. Known additional malignancy that is progressing or has required active treatment within the past 2 years.

  15. Known active CNS lymphoma. CNS staging at diagnosis with MRI brain/spine and CSF analysis is not mandatory and only required if there is a clinical suspicion of CNS involvement.

  16. Active infection requiring systemic therapy.

  17. Concurrent active HBV (defined as HBsAg positive and detectable HBV DNA) and HCV (defined as anti-HCV antibody positive and detectable HCV RNA) infection.

  18. History or current evidence of any condition, therapy, laboratory abnormality, or other circumstance that might confound the results of the study or interfere with the participant's ability to cooperate with the requirements of the study, such that it is not in the best interest of the participant to participate, in the opinion of the treating investigator.

  19. History of solid organ transplant within 2 years of study enrollment.

  20. Participants who have not adequately recovered from major surgery or have ongoing surgical complications.

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: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Zilovertamab vedotin (1.75mg/kg) Q3W + Lenalidomide (15mg p.o. 14 days)

Induction phase:

Zilovertamab vedotin (1.75mg/kg) will be administered using a 30-minute IV infusion on Day 1 of Cycle 1, and then on Day 1 of each 3-week (21-day) cycle, for up to 6 cycles. Capsules of lenalidomide (15mg) will be administered orally (p.o) on planned dosing days (14 days per cycle) for up to 6 cycles.

Participants will have FDG PET/CT scans at the start of the study, prior to induction treatment and following cycle 2 and 6. Response assessments will be undertaken according to Lugano criteria. Participants achieving an objective response will continue onto maintenance phase.

Maintenance phase:

Lenalidomide treatment (15mg p.o, 14 days of a 21 day cycle) for up to 6 additional cycles.

After finishing treatment, participants will attend follow-up visits every 3 months for up to 24 months.

Zilovertamab vedotin Intravenous (IV) Infusion - 1.75 mg/kg will be administered every 3 weeks for 6 cycles

Lenalidomide (15mg) will be administered by mouth for 14 days of each 21 day cycle. 6 cycles will be administered in combination with zilovertamab vedotin, in participants with an objective response, a further 6 cycles will be administered (maximum of 12 cycles)

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Rate of complete response to up to 6 cycles of combination zilovertamab vedotin and lenalidomide
Lasso di tempo: Up to 18 weeks.

Rate of complete response to up to 6 cycles of combination zilovertamab vedotin and lenalidomide as determined by first documented disease progression per Lugano response criteria.

Up to 18 weeks.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Number of participants who experienced an adverse event (AE)
Lasso di tempo: Up to 110 days after the last dose of investigational product.

An AE is any unfavorable and unintended sign, symptom, or disease temporally associated with the use of a medicinal product or protocol-specified procedure, whether or not considered related to the medicinal product or protocol-specified procedure. Any worsening of a preexisting condition that is temporally associated with the use of the investigational products, is also an AE. The number of participants who experienced an AE will be reported.

Up to 110 days after the last dose of investigational product.
Overall survival (OS)
Lasso di tempo: Up to 33 months

As defined as the time from enrolment until death, due to any cause, will be reported.

Up to 33 months
Duration of response
Lasso di tempo: Up to 33 months

DOR, defined as the time from the first documented evidence of CR or PR until disease progression or death due to any cause, whichever occurs first, will be reported.

Up to 33 months
Progression Free Survival
Lasso di tempo: Up to 33 months

PFS, defined as the time from enrolment to the first documented disease progression per Lugano response criteria as assessed by PET/CT or death due to any cause, whichever occurs first will be presented.

Up to 33 months
Change from baseline of health related quality of life
Lasso di tempo: Up to 9 months

EORTC-QLQ-C30 (baseline and end of treatment) and PRO-CTCAE (baseline and prior to each cycle of treatment and end of treatment) responses will be collected from participants to examine any changes in health related quality of life.

Up to 9 months

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Blood and tissue markers linked to treatment response and side effects
Lasso di tempo: 2 years

Blood and tissue samples will be used for biomarker analysis, which will include but is not limited to: minimum residual disease (MRD) in blood using cfDNA assessments, tumour microenvironment, peripheral blood immune portrait correlate potential biomarkers with treatment responses and toxicity.

2 years
Gut bacteria changes linked to treatment response and side effects
Lasso di tempo: 2 years

Studying whether changes in gut bacteria are associated with how patients respond to treatment and their risk of side effects.

2 years

Collaboratori e investigatori

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

Collaboratori

Investigatori

  • Investigatore principale: Eliza A Hawkes, MBBS DMedSc, Austin Health

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 gennaio 2027

Completamento primario (Stimato)

31 dicembre 2028

Completamento dello studio (Stimato)

31 dicembre 2030

Date di iscrizione allo studio

Primo inviato

27 ottobre 2026

Primo inviato che soddisfa i criteri di controllo qualità

27 ottobre 2026

Primo Inserito (Effettivo)

3 novembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

3 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

27 ottobre 2026

Ultimo verificato

1 ottobre 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

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

prodotto fabbricato ed esportato dagli 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 .

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