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Epcoritamab and Pola-R-mini-CHP for the Treatment of Diffuse Large B Cell Lymphoma in Elderly or Unfit Patients

15. Juli 2026 aktualisiert von: Jonsson Comprehensive Cancer Center

A Phase I Study of Single Agent Epcoritamab Followed by Epcoritamab Plus Pola-R-Mini-CHP for Elderly/Unfit Patients With Previously Untreated DLBCL

This phase I trial tests the safety, side effects and best dose of epcoritamab alone and epcoritamab with polatuzumab vedotin, rituximab, cyclophosphamide, doxorubicin, and prednisone (pola-R- mini-CHP) for the treatment of diffuse large B cell lymphoma (DLBCL) in elderly or unfit patients. Epcoritamab is a monoclonal antibody that may interfere with the ability of cancer cells to grow and spread. A monoclonal antibody is a type of protein that can bind to certain targets in the body, such as molecules that cause the body to make an immune response (antigens). Polatuzumab vedotin is a monoclonal antibody, called polatuzumab, linked to a chemotherapy drug, called monomethyl auristatin E. Polatuzumab is a form of targeted therapy because it attaches to specific molecules (receptors) on the surface of cancer cells, known as B-cell receptors, and delivers monomethyl auristatin E to kill them. Rituximab is a monoclonal antibody. It binds to a protein called cluster of differentiation antigen 20 (CD20), which is found on B cells (a type of white blood cell) and some types of cancer cells. This may help the immune system kill cancer cells. Cyclophosphamide is in a class of medications called alkylating agents. It works by damaging the cell's DNA and may kill cancer cells. It may also lower the body's immune response. Doxorubicin is in a class of medications called anthracyclines. Doxorubicin damages the cell's DNA and may kill cancer cells. It also blocks a certain enzyme needed for cell division and deoxyribonucleic acid (DNA) repair. Prednisone is in a class of medications called corticosteroids. It is used to reduce inflammation and lower the body's immune response to help lessen the side effects of chemotherapy drugs. Epcoritamab alone and epcoritamab with pola-R-mini-CHP may be safe, tolerable and/or effective in treating DLBCL in elderly or unfit patients.

Studienübersicht

Detaillierte Beschreibung

PRIMARY OBJECTIVE:

I. To evaluate whether the addition of epcoritamab to 4- 6 cycles of standard Pola-R-mini-CHP preceded by 2 cycles of epcoritamab monotherapy (E + Pola-mini-CHP) is tolerable and effective.

EXPLORATORY OBJECTIVE:

I. To include the use of liquid biopsy techniques, specifically PhasED-seq, to assess treatment responses.

OUTLINE:

CYCLE 1: Patients receive polatuzumab vedotin intravenously (IV) and rituximab IV on day 1 and epcoritamab subcutaneously (SC) on day 1, 8, and 15 of the 21 day cycle, in the absence of disease progression or unacceptable toxicity.

CYCLE 2: Patients receive epcoritamab on day 1, 8 and 15 of the 21 day cycle, in the absence of disease progression or unacceptable toxicity.

CYCLE 3-4: Patients receive rituximab IV, polatuzumab vedotin IV, cyclophosphamide IV, doxorubicin IV on day 1, epcoritamab SC on days 1, 8 and 15 and prednisone orally (PO) on days 1-5 of each cycle. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity.

Patients then undergo disease assessment. Patients with complete remission receive cycles 5-6 and patients not in complete remission receive cycles 5-8.

CYCLES 5-8: Patients receive rituximab IV, polatuzumab vedotin IV, cyclophosphamide IV, doxorubicin IV and epcoritamab SC on day 1 and prednisone PO on days 1-5 of each cycle. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity.

Patients undergo urine sample collection and brain magnetic resonance imaging (MRI) during screening and positron emission tomography (PET)/computed tomography (CT) scan and blood sample collection throughout the study.

After completion of study treatment, patients are followed up week 36, week 48 then every 12 weeks through week 94, then every 24 weeks through week 240 then every 48 weeks until 6 years after the first dose of treatment. Patients who discontinue for treatment progression are followed up every every 6 months thereafter.

Studientyp

Interventionell

Einschreibung (Geschätzt)

20

Phase

  • Phase 1

Kontakte und Standorte

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

Studienorte

    • California
      • Los Angeles, California, Vereinigte Staaten, 90095
        • UCLA / Jonsson Comprehensive Cancer Center
        • Kontakt:
        • Hauptermittler:
          • Sven De Vos

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

  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

Inclusion Criteria:

  • Previously untreated, histologically confirmed DLBCL according to World Health Organization (WHO) 2016 classification

    • Documented CD20+ mature B-cell neoplasm according to WHO classification (Swerdlow et al., 2016) or WHO classification (WHO, 2008) based on representative pathology report

      • Diffuse large B-cell lymphoma note: Other double-/triple-hit lymphomas are not eligible
    • Untreated patients who transform from low grade marginal zone lymphoma (MZL)
    • Other aggressive B-non-hodgkin lymphoma (NHL):

      • Primary mediastinal (thymic) large B-cell lymphoma (PMBCL)
      • High-grade B-cell lymphoma
      • Newly diagnosed follicular lymphoma grade 3B (FL 3B)
  • At least one bi-dimensionally measurable nodal lesion, defined as > 1.5 cm in its longest dimension, or one bi-dimensionally measurable extranodal lesion, defined as > 1.0 cm in its longest diameter
  • Age > 80 years, or age 70-79 years and not considered a candidate for full-dose aggressive chemotherapy (R-CHOP) with at least one of the following:

    • Impairment in > 2 activity of daily living (ADL) component and/or
    • Impairment in > 2 instrumental activity of daily living (IADL) component and/or
    • Cumulative Illness Rating Scale for Geriatrics (CIRS-G) score of at least 1 comorbidity with a severity score of 3-4 (not including lymphoma and hematologic deficiencies due to lymphoma) or a score of 2 in > 8 comorbidities.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2
  • Life expectancy of at least 24 weeks
  • No significant pulmonary comorbidities (e.g., history of pneumonitis, severe chronic obstructive pulmonary disease [COPD])
  • Left ventricular ejection fraction ≥ 45%
  • Creatinine clearance > 40 mL/min

    • Exceptions may be made for patients with creatinine clearance < 40 mL/min, provided creatinine is within normal range
  • Hemoglobin > 9 g/dL
  • Absolute neutrophil counts ≥ 1.0 × 10^9/L; growth factor support allowed in case of bone marrow involvement
  • Platelet counts ≥ 75 × 10^9/L or, in the presence of bone marrow involvement or splenomegaly, ≥ 50 × 10^9/L
  • Lymphocyte counts < 5 × 10^9/L
  • If receiving glucocorticoid treatment at screening, must be a maximum daily dose of prednisone 100 mg (or equivalent) and a total of no more than 140 mg over the last 14 days prior to the first dose of epcoritamab, unless for disease control
  • Before the first dose of epcoritamab, during the trial and for 12 months after last administration of epcoritamab, a woman must be either:

    • Not of childbearing potential: premenarchal; postmenopausal (> 45 years of age with amenorrhea for at least 12 months or any age with amenorrhea for at least 6 months and a serum follicle stimulating hormone [FSH] level > 40 IU/L or milli-International unit mIU/mL); permanently sterilized (e.g., bilateral tubal occlusion [which includes tubal ligation procedures as consistent with local regulations], hysterectomy, bilateral salpingectomy, bilateral oophorectomy); or otherwise be incapable of pregnancy
  • A man who is sexually active with a woman of childbearing potential must agree to use a barrier method of birth control (that is the use of condom) during the trial and for 12 months after receiving the last dose of epcoritamab
  • COVID-19 ELIGIBILITY CRITERIA: Subject has no known active severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection
  • COVID-19 ELIGIBILITY CRITERIA: If a subject has signs/symptoms suggestive of SARS-CoV-2 infection or have had recent known exposure to someone with SARS-CoV-2 infection, the subject must have a negative molecular (e.g., polymerase chain reaction [PCR]) test, or 2 negative antigen test results at least 24 hours apart, to rule out SARS-CoV-2 infection.

    • Note: SARS-CoV-2 diagnostic tests should be applied following local requirements/recommendations
  • COVID-19 ELIGIBILITY CRITERIA: Subjects who do not meet SARS-CoV-2 infection eligibility criteria must be screen failed and may only rescreen after they meet the following SARS-CoV-2 infection viral clearance criteria:

    • No signs/symptoms suggestive of active SARS-CoV-2 infection
    • Negative molecular (e.g., PCR) result or 2 negative antigen test results at least 24 hours apart
  • COVID-19 ELIGIBILITY CRITERIA: Patients with SARS-CoV-2 antigen or PCR testing positivity within 30 days prior to cycle 1 day 1 are not eligible
  • COVID-19 ELIGIBILITY CRITERIA: Any patient with documented SARS-CoV-2 infection within 6 months prior to planned cycle 1 day 1 must have no persistent respiratory symptoms, no evidence of residual sequelae, and a negative PCR test for SARS-CoV-2
  • COVID-19 ELIGIBILITY CRITERIA: Ongoing active bacterial, viral, fungal, mycobacterial, parasitic, or other infection requiring systemic treatment (excluding prophylactic treatment) at the time of enrollment or within the previous 2 weeks prior to the first dose of epcoritamab, including COVID-19 infection. Note that a past COVID-19 infection may be a risk factor, but if resolved and the subject is vaccinated, it may be allowable to enroll the subject

Exclusion Criteria:

  • Prior treatment for DLBCL with chemotherapy, immunotherapy, and biologic therapy

    • Exception: patients who are treated with prednisone as part of pre-phase treatment
  • Current grade > 1 peripheral neuropathy by clinical examination
  • Known or suspected chronic active Epstein-Barr virus infection
  • Subjects that have transformed from indolent (i) NHL, who have previously been treated with an anthracycline-containing regimen or a CD3-CD20 bispecific antibody
  • Patients with known history or suspected history of hemophagocytic lymphohistiocytosis (HLH)
  • Primary central nervous system (CNS) lymphoma or CNS involvement by lymphoma at screening as confirmed by mandatory magnetic resonance imaging (MRI)/computed tomography (CT) scan (brain) and, if clinically indicated, by lumbar puncture
  • Aspartate aminotransferase (AST), and/or alanine aminotransferase (ALT) > 3 × upper limit of normal (within 14 days of initiation of study treatment)
  • Total bilirubin > 1.5 × upper limit of normal, unless bilirubin rise is due to Gilbert's syndrome or of non-hepatic origin (within 14 days of initiation of study treatment)

    • Patients with a documented history of Gilbert syndrome and in whom total bilirubin elevations are accompanied by elevated indirect bilirubin are eligible
  • International normalization ratio (INR) > 1.5 x upper limit of normal (ULN) in the absence of therapeutic anticoagulation (within 14 days of initiation of study treatment)
  • Partial thromboplastin time (PTT) or activated partial thromboplastin time (aPTT) > 1.5 x ULN in the absence of a lupus anticoagulant or therapeutic anticoagulant (within 14 days of initiation of study treatment)
  • Estimated creatinine clearance (CrCl) < 40 mL/min (within 14 days of initiation of study treatment)
  • Known clinically significant cardiovascular disease or significant pulmonary disease (including obstructive pulmonary disease and history of bronchospasm) including:

    • Unstable arrhythmias
    • Onset of unstable angina pectoris within 6 months of signing informed consent form (ICF)
    • Acute myocardial infarction within 6 months of signing ICF
    • Congestive heart failure (New York Heart Association Class III or IV cardiac disease and/or known decrease ejection fraction of < 45%)
    • Stroke or intracranial hemorrhage within 6 months prior to signing ICF
    • In case of any history of cardiovascular disease, a cardiology consult is required within 60 days of enrollment.
    • For patients who are ≥ 75 years old, 2 or more active cardiovascular diseases (any type, ≥ grade 2)
  • Confirmed history or current autoimmune disease or other diseases resulting in permanent immunosuppression or requiring permanent immunosuppressive therapy including, but not limited to, myocarditis, pneumonitis, myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, vascular thrombosis associated with antiphospholipid syndrome, Wegener granulomatosis, Sjögren syndrome, Guillain-Barré syndrome, multiple sclerosis, vasculitis, or glomerulonephritis
  • Low-dose (≤ 10 mg/day) prednisolone (or equivalent) for rheumatoid arthritis or similar conditions is allowed
  • Received systemic immunosuppressive medications (including, but not limited to, cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-tumor necrosis factor agents) with the exception of corticosteroid treatment < 10 mg/day prednisone or equivalent within 2 weeks prior to first the dose of study drug
  • Positive test results for chronic hepatitis B infection (defined as positive hepatitis B surface antigen [HBsAg] serology)

    • Patients with occult or prior hepatitis B infection (defined as positive total hepatitis B core antibody and negative HBsAg) may be included if hepatitis B virus DNA is undetectable at the time of screening. These patients must be willing to undergo monthly DNA testing and appropriate antiviral therapy as indicated
  • Acute or chronic hepatitis C virus (HCV) infection

    • Patients who are positive for HCV antibody must be negative for HCV by polymerase chain reaction
  • Known human immunodeficiency virus (HIV) infection with a cluster of differentiation 4 (CD4) count greater than 200 cells/µL; HIV testing is required at screening only if required per local health authorities or institutional standards
  • History of other malignancy that could affect compliance with the protocol or interpretation of results

    • Patients with a history of curatively treated basal or squamous cell carcinoma or melanoma of the skin or in situ carcinoma of the cervix, or early-stage localized prostate cancer (Gleason score < 6 or below, Stage I or II) with no requirement for therapy at any time prior to study are eligible.
    • Patients with a malignancy that has been treated with curative intent will also be excluded unless the malignancy has been in documented remission without treatment for > 2 years before enrollment. Exception will be made for patients with a history of breast cancer that is estrogen receptor-/progesterone receptor-positive for more than 2 years before enrollment who are treated with adjuvant hormonal therapy
  • Evidence of significant, uncontrolled concomitant diseases that could affect compliance with the protocol or interpretation of results or that could increase risk to the patient
  • Known active bacterial, viral, fungal, mycobacterial, parasitic, or other infection (excluding fungal infections of nail beds) at study enrollment or any major episode of infection requiring treatment with IV antibiotics or hospitalization (relating to the completion of the course of antibiotics) within 4 weeks before cycle 1 day 1 (C1D1)
  • Clinically significant history of liver disease, including viral or other hepatitis, current alcohol abuse, or cirrhosis
  • Recent major surgery within 4 weeks before the start of C1D1
  • Superficial lymph node biopsies for diagnosis is allowed

Studienplan

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

Wie ist die Studie aufgebaut?

Designdetails

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

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Treatment (epcoritamab, pola-r-mini-CHP)
See Detailed Description
Gegeben 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
PO gegeben
Andere Namen:
  • Deltason
  • Orason
  • Δ1-Cortison
  • 1, 2-Dehydrocortison
  • Adamon
  • Cortancyl
  • Dacortin
  • DeCortin
  • Decortisyl
  • Decorton
  • Delta 1-Cortison
  • Delta-Kuppel
  • Deltacorten
  • Deltacortison
  • Deltadehydrocortison
  • Deltison
  • Delta
  • Econoson
  • Lisacort
  • Meprosona-F
  • Metacortandracin
  • Meticorten
  • Ofisolona
  • Panafcort
  • Panasol-S
  • Parakort
  • Perrigo Prednison
  • PRED
  • Prädiktor
  • Prädicorten
  • Prednicen-M
  • Prednikort
  • Prednidib
  • Prednilonga
  • Vorurteil
  • Prednison Intensol
  • Prednisonum
  • Predniton
  • Promifen
  • Strahlen
  • Service
  • SK-Prednison
Gegeben IV
Andere Namen:
  • Rituxan
  • MabThera
  • AB 798
  • BI 695500
  • C2B8 monoklonaler Antikörper
  • Chimärer Anti-CD20-Antikörper
  • CT-P10
  • IDEC-102
  • IDEC-C2B8
  • IDEC-C2B8 monoklonaler Antikörper
  • Monoklonaler Antikörper IDEC-C2B8
  • PF-05280586
  • Riabni
  • Rituximab ABBS
  • Rituximab ARRX
  • Rituximab-Biosimilar ABP 798
  • Rituximab-Biosimilar BI 695500
  • Rituximab-Biosimilar CT-P10
  • Rituximab-Biosimilar GB241
  • Rituximab-Biosimilar IBI301
  • Rituximab-Biosimilar JHL1101
  • Rituximab-Biosimilar PF-05280586
  • Rituximab-Biosimilar RTXM83
  • Rituximab-Biosimilar SAIT101
  • Rituximab-Biosimilar SIBP-02
  • Rituximab-Biosimilar TQB2303
  • Rituximab PVVR
  • Rituximab-arrx
  • Rituximab-pvvr
  • RTXM83
  • Ruhe
  • Truxima
  • Rixathon
  • Ikgdar
  • Mabtas
  • Rituximab-abbs
  • BI-695500
  • BI695500
  • Blitzima
  • IDEC 102
  • IDEC102
  • PF 05280586
  • PF05280586
  • Ritemvia
  • Rituximab-Blit
  • Rituximab-Ritus
  • Rituximab-rixa
  • Rituximab-rixi
  • Riximyo
  • RTXM 83
  • RTXM-83
  • ABP-798
  • ABP798
  • CT P10
  • CTP10
  • GP 2013
  • GP-2013
  • GP2013
  • Rituximab Biosimilar GP2013
Gegeben IV
Andere Namen:
  • Adriablastin
  • Hydroxydaunomycin
  • Hydroxyl-Daunorubicin
  • Hydroxyldaunorubicin
Unterziehe dich einem PET-Scan
Andere Namen:
  • Medizinische Bildgebung, Positronen-Emissions-Tomographie
  • HAUSTIER
  • PET-Scan
  • Positronen-Emissions-Tomographie-Scan
  • Positronen-Emissions-Tomographie
  • Pt
  • Positronen-Emissions-Tomographie (Verfahren)
Unterziehe dich einem CT-Scan
Andere Namen:
  • CT
  • KATZE
  • Computertomographie
  • Computergestützte axiale Tomographie
  • CT-Scan
  • Tomographie
  • Computerisierte Axialtomographie (Verfahren)
  • Computertomographie (CT)-Scan
  • Diagnosekatze Scan
  • Diagnose -Katzen -Scan -Service -Typ
Lassen Sie sich Blut- und Urinproben entnehmen
Andere Namen:
  • Biologische Probensammlung
  • Bioprobe gesammelt
  • Probenentnahme
  • Beispielsammlung
Gegeben IV
Andere Namen:
  • DCDS4501A
  • ADC DCDS4501A
  • Antikörper-Wirkstoff-Konjugat DCDS4501A
  • FCU2711
  • Polatuzumab Vedotin-piiq
  • Polivy
  • RG7596
  • Ro 5541077-000
  • FCU-2711
  • RG 7596
  • RG-7596
Unterziehe dich einer MRT des Gehirns
Andere Namen:
  • MRT
  • Magnetresonanz
  • Magnetresonanztomographie-Scan
  • Medizinische Bildgebung, Magnetresonanz / Kernspinresonanz
  • HERR
  • MR-Bildgebung
  • MRT-Untersuchung
  • NMR-Bildgebung
  • NMRI
  • Kernspinresonanztomographie
  • Magnetresonanztomographie (MRT)
  • sMRT
  • Magnetresonanztomographie (Verfahren)
  • MRTs
  • Strukturelle MRT
Gegeben SC
Andere Namen:
  • GEN3013
  • Bispezifischer Anti-CD20/CD3-Antikörper GEN3013
  • DuoBody-CD3xCD20
  • Epcoritamab-bysp
  • Epkinly
  • GEN 3013
  • GEN-3013
  • Tepkinly

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Progression free survival
Zeitfenster: From initiation of treatment to disease progression based on the investigator-based assessments per Lugano criteria or death due to any causes, up to 6 years
Kaplan-Meier estimates will be provided. 95% confidence intervals will be generated.
From initiation of treatment to disease progression based on the investigator-based assessments per Lugano criteria or death due to any causes, up to 6 years

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Overall response rate
Zeitfenster: Up to 6 years
Defined as the proportion of patients achieving a complete response (CR) or partial response (PR) based on Lugano criteria. CR defined as the disappearance of all evidence of disease based on Lugano critera. PR defined as a ≥ 50% reduction in tumor burden based on Lugano criteria. Kaplan-Meier estimates will be provided. 95% confidence intervals will be generated.
Up to 6 years
Duration of response
Zeitfenster: From the first documentation of CR or PR to disease progression or death, up to 6 years
Kaplan-Meier estimates will be provided. 95% confidence intervals will be generated.
From the first documentation of CR or PR to disease progression or death, up to 6 years
Overall survival
Zeitfenster: From enrollment until death due to any cause, up to 6 years
Kaplan-Meier estimates will be provided. 95% confidence intervals will be generated.
From enrollment until death due to any cause, up to 6 years
Incidence and severity of adverse events
Zeitfenster: Up to 6 years
95% confidence intervals will be generated.
Up to 6 years
Incidence and severity of changes in laboratory values
Zeitfenster: Up to 6 years
95% confidence intervals will be generated.
Up to 6 years
Incidence of dose interruptions, delays, and discontinuations
Zeitfenster: Up to 6 years
95% confidence intervals will be generated.
Up to 6 years

Mitarbeiter und Ermittler

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

Mitarbeiter

Ermittler

  • Hauptermittler: Sven De Vos, UCLA / Jonsson Comprehensive 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)

8. Dezember 2026

Primärer Abschluss (Geschätzt)

8. Oktober 2030

Studienabschluss (Geschätzt)

8. Oktober 2031

Studienanmeldedaten

Zuerst eingereicht

15. Juli 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

15. Juli 2026

Zuerst gepostet (Tatsächlich)

20. Juli 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

20. Juli 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

15. Juli 2026

Zuletzt verifiziert

1. Juli 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

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

Nein

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 .

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