Diese Seite wurde automatisch übersetzt und die Genauigkeit der Übersetzung wird nicht garantiert. Bitte wende dich an die englische Version für einen Quelltext.

Disulfiram for Preventing Treatment Complications in Patients Undergoing CAR T-cell Therapy for Relapsed or Refractory Diffuse Large B-cell Lymphoma

5. November 2026 aktualisiert von: University of Michigan Rogel Cancer Center

A Single Center, Phase I/II Study of Disulfiram for the Prevention of Immunotoxicity in Patients Undergoing CAR T-Cell Therapy

This phase I/II trial tests the safety, best dose, and effectiveness of disulfiram for preventing treatment complications in patients with large B-cell lymphoma that has come back after a period of improvement (relapsed) or that does not respond to treatment (refractory) and who are undergoing chimeric antigen receptor (CAR) T-cell therapy. Two major complications of CAR T-cell therapy include cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS). CRS results from inflammation in the body when the immune system responds too aggressively to the modified T cells working to attack cancer cells. ICANS is inflammation of the brain or nerves. CRS is most often a prelude to ICANS, and both of these toxicities currently require immunosuppression for treatment, which can inhibit CAR T-cell response. Disulfiram has been found to impact several biologic pathways that cause CRS. Disulfiram may be safe and effective for reducing the incidence and severity of reactions to CAR T-cell therapy without inhibiting CAR T-cell response.

Studienübersicht

Status

Noch keine Rekrutierung

Bedingungen

Intervention / Behandlung

Studientyp

Interventionell

Einschreibung (Geschätzt)

12

Phase

  • Phase 2
  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studienorte

    • Michigan
      • Ann Arbor, Michigan, Vereinigte Staaten, 48109
        • University of Michigan Rogel Cancer Center
        • Kontakt:
        • Hauptermittler:
          • Marcus Geer

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • Histologic diagnosis of relapsed/refractory large B-cell lymphoma
  • >= 18 years of age at the time of signing informed consent (ICF)
  • Understands and voluntarily signs the ICF prior to conduct of any study-related assessments or procedures
  • Willing to adhere to the study visit schedule and other protocol requirements
  • Willing/able to abstain from any drug/substance at risk for reaction with disulfiram for the duration of treatment
  • Eastern Cooperative Oncology Group (ECOG) performance status =< 2
  • Eligible for therapy with axicabtagene ciloleucel per institutional criteria
  • Confirmation of a manufactured CAR T-cell product within clinical specifications for axicabtagene ciloleucel
  • Females and males of childbearing potential must be willing to use effective methods of contraception from the time of informed consent until 12 months (female) or 4 months (males with female partners of reproductive potential) after the cyclophosphamide infusion
  • Willingness to consent / co-enroll on the University of Michigan cellular therapy long-term follow-up study - HUM00043287 (UMCC2001-0234)

Exclusion Criteria:

  • Serious or uncontrolled infection defined as not having cleared infection despite being on appropriate antimicrobial therapy for 5 days would be excluded. Also any infection which, in the opinion of the investigator, places the patient at an unacceptable risk for treatment-related complications, could impede the ability to safely administer therapy, or could interfere with evaluation of study intervention

  • Active hepatitis B or C (latent hepatitis B will not be excluded), or HIV. Entecavir prophylaxis can be used for latent hepatitis B. A patient's viral load must be undetectable per quantitative polymerase chain reaction (PCR) and/or nucleic acid testing at screening

  • Total bilirubin of >= 1.5 x upper limit of normal (ULN) unless attributed to Gilbert's syndrome or underlying primary malignancy. Patients with Gilbert syndrome or underlying primary malignancy involving the liver with total bilirubin >= 2.5 x ULN (or absolute total bilirubin >= 3 mg/dL) should be excluded. Aspartate aminotransferase (AST): >= 2.5 x ULN, alanine aminotransferase (ALT): >= 2.5 x ULN

  • Active concurrent autoimmune disease requiring systemic immunosuppression

  • Active primary or secondary central nervous system (CNS) lymphoma

  • Active clinically relevant central nervous system disease including but not limited to:

    • Seizures/Epilepsy
    • Stroke or unstable neurologic deficits within the past 12 months prior to enrollment
    • Cerebral edema
    • Aphasia
    • Severe brain injury
    • Cerebellar disease
    • Documented history of dementia as confirmed by neuropsychiatric testing
    • Parkinson's disease
    • Psychosis
  • Any other significant medical condition (including neurological or psychiatric) which, in the opinion of the investigator, places the participant at an unacceptable risk for treatment-related complications, could interfere with the successful or safe delivery of therapy, or could interfere with evaluation of study intervention or interpretation of participant safety or study results. Including but not limited to:

    • Diabetes with associated autonomic dysfunction
    • Uncontrolled Hypothyroidism
    • Chronic or acute nephritis
    • Hepatic cirrhosis/insufficiency
  • Pregnant or nursing females

  • Current or previous treatment with any other agents explicitly for prophylaxis of CRS or ICANS, including corticosteroids and investigational agents during the study enrollment period. Corticosteroids given for disease treatment should have a washout of at least 5 half-lives prior to cell infusion. Use of prophylactic antiseizure medications is not contraindicated

  • History of, or a concurrent, clinically significant illness, medical condition or laboratory abnormality that, in the investigator's opinion, could affect the conduct of the study

  • Concurrent use of prohibited medications or substances at risk of precipitating a disulfiram reaction

  • Hypersensitivity to disulfiram or to other thiuram derivatives used in pesticides and rubber vulcanization

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Unterstützende Pflege
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Supportive care (disulfiram)

Patients receive disulfiram PO QD on days -5 to +21. Patients receive cyclophosphamide IV and fludarabine IV on days -5 to -3 and then receive axi-cel IV on day 0. Patients also undergo CT or PET/CT at screening and follow-up and undergo collection of blood samples throughout the trial.

Given IV

Andere Namen:
  • Cytoxan
  • CTX
  • (-)-Cyclophosphamid
  • 2H-1,3,2-Oxazaphosphorin, 2-[Bis(2-chlorethyl)amino]tetrahydro-, 2-Oxid, Monohydrat
  • Carloxan
  • Ciclofosfamida
  • Ciclofosfamid
  • Cicloxal
  • Clafen
  • Claphene
  • CP-Monohydrat
  • CYCLO-Zelle
  • Cycloblastin
  • Cyclophospham
  • Cyclophosphamid-Monohydrat
  • Cyclophosphamid
  • Cyclophosphan
  • Cyclophosphanum
  • Cyclostin
  • Cytophosphan
  • Fosfaseron
  • Genoxal
  • Genuxal
  • Ledoxina
  • Mitoxan
  • Neosar
  • Revimmun
  • Syklofosfamid
  • WR-138719
  • Asta B 518
  • B-518
  • B 518
  • B518
  • WR 138719
  • WR138719
  • Frindovyx

Undergo collection of blood samples

Andere Namen:
  • Biologische Probensammlung
  • Bioprobe gesammelt
  • Probenentnahme
  • Beispielsammlung

Undergo CT or PET/CT

Andere Namen:
  • CT
  • KATZE
  • Computertomographie
  • Computergestützte axiale Tomographie
  • CT-Scan
  • Tomographie
  • Computerisierte Axialtomographie (Verfahren)
  • Computertomographie (CT)-Scan
  • Diagnosekatze Scan
  • Diagnose -Katzen -Scan -Service -Typ

Undergo PET/CT

Andere Namen:
  • Medizinische Bildgebung, Positronen-Emissions-Tomographie
  • HAUSTIER
  • PET-Scan
  • Positronen-Emissions-Tomographie-Scan
  • Positronen-Emissions-Tomographie
  • Pt
  • Positronen-Emissions-Tomographie (Verfahren)

Given IV

Andere Namen:
  • Fluradosa

Given IV

Andere Namen:
  • Yescarta
  • KTE C19
  • KTE-C19
  • KTE-C19 AUTO
  • Axi-cel
  • Axikel
  • KTEC19

Given PO

Andere Namen:
  • Antabus
  • DS
  • Teturamin
  • TTD
  • Tetraethylthioperoxydicarbonsäurediamid

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Incidence of dose-limiting toxicities
Zeitfenster: Within day +35 post-chimeric antigen receptor (CAR) T-cell therapy

At the end of the trial, will report number of patients assigned to each dose, as well as the number of patients experiencing toxicity at each dose.

Within day +35 post-chimeric antigen receptor (CAR) T-cell therapy
Proportion of patients that are alive and free from grade 2-4 cytokine release syndrome (CRS) with no intervening treatment of CRS
Zeitfenster: Through day +28 post-CAR T-cell therapy

At the end of the trial, will report number of patients assigned to each dose, as well as the number of patients experiencing efficacy outcomes at each dose.

Through day +28 post-CAR T-cell therapy

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Incidence of grade 2-4 CRS
Zeitfenster: By day +28 post-CAR T-cell therapy

The occurrence of severe CRS will be considered binary, and the rate will be defined as number of patients with severe CRS divided by the number of evaluable patients. The rate will be reported along with the 95% exact binomial confidence interval.

By day +28 post-CAR T-cell therapy
Incidence of all-grade CRS
Zeitfenster: By day +28 post-CAR T-cell therapy

The occurrence of CRS will be considered binary, and the rate will be defined as number of patients with CRS divided by the number of evaluable patients. The rate will be reported along with the 95% exact binomial confidence interval.

By day +28 post-CAR T-cell therapy
Incidence of all-grade immune effector cell associated neurotoxicity syndrome (ICANS)
Zeitfenster: By day +28 post-CAR T-cell therapy

The occurrence of severe ICANS will be considered binary and the rate will be defined as number of patients with severe ICANS divided by the number of evaluable patients. The rate will be reported along with the 95% exact binomial confidence interval.

By day +28 post-CAR T-cell therapy
Incidence of disulfiram-related grade 2 to 5 non-hematologic toxicity
Zeitfenster: By day +28 post-CAR T-cell therapy

Will be assessed by Common Terminology Criteria for Adverse Events, version 5.0. The occurrence of drug related grade 2-5 non-hematologic toxicity with at least a 'possible' attribution to disulfiram will be considered binary, and the rate will be defined as number of patients experiencing toxicity divided by the number of evaluable patients. The rate will be reported along with the 95% exact binomial confidence interval.

By day +28 post-CAR T-cell therapy

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Ermittler

  • Hauptermittler: Marcus Geer, University of Michigan Rogel Cancer Center

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. November 2026

Primärer Abschluss (Geschätzt)

1. Mai 2028

Studienabschluss (Geschätzt)

1. Mai 2028

Studienanmeldedaten

Zuerst eingereicht

5. November 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

5. November 2026

Zuerst gepostet (Tatsächlich)

12. November 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

12. November 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

5. November 2026

Zuletzt verifiziert

1. November 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • UMCC 2025.132
  • NCI-2026-05448 (Registrierungskennung: CTRP (Clinical Trial Reporting Program))
  • HUM00287270 (Andere Kennung: University of Michigan Rogel Cancer Center)

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Ja

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Produkt, das in den USA hergestellt und aus den USA exportiert wird

Ja

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .