Badanie bezpieczeństwa i skuteczności kombinacji epkoritamabu u pacjentów z chłoniakiem nieziarniczym z komórek B (B-NHL) (EPCORE™ NHL-2)
Otwarta próba fazy 1b/2 mająca na celu ocenę bezpieczeństwa i wstępnej skuteczności epkoritamabu (GEN3013; DuoBody®-CD3xCD20) w skojarzeniu z innymi lekami u pacjentów z chłoniakiem nieziarniczym z komórek B (B-NHL)
The purpose of this trial is to measure the safety and effectiveness of epcoritamab (EPKINLY™), either by itself or together with other therapies, when treating participants with B-cell non-Hodgkin Lymphoma (B-NHL). The aim of the first part of the trial is to identify the most appropriate dose of epcoritamab, and the aim of the second part of the trial is to assess the selected epcoritamab dose in a larger group of participants with B-NHL. All participants in this trial will receive either epcoritamab alone, or epcoritamab combined with another standard treatment regimen, with a total of 10 different treatment arms being studied.
Trial details include:
- The treatment duration for each participant depends upon which arm of treatment they are assigned to.
- The visit frequency for each participant depends upon which arm of treatment they are assigned to, but will be weekly to start for all participants, then will decrease to either: every 2 weeks, or every 3 weeks, or every 4 weeks, or every 8 weeks.
- All participants will receive active drug; no one will be given placebo.
Participants who receive treatment with epcoritamab will have it injected right under the skin. Participants will receive a different regimen of epcoritamab depending upon which arm of treatment they are assigned.
Participants who receive standard treatments will have intravenous (IV) infusions and/or oral administration of those treatments. Participants will receive a different standard treatment regimen depending upon which arm of treatment they are assigned.
Przegląd badań
Status
Status
Warunki
Warunki
Interwencja / Leczenie
Interwencja / Leczenie
- Lek: rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone
- Biologiczny: Epcoritamab
- Biologiczny: Epcoritamab
- Biologiczny: Epcoritamab
- Biologiczny: Epcoritamab
- Biologiczny: Epcoritamab
- Biologiczny: Epcoritamab
- Biologiczny: Epcoritamab
- Biologiczny: Epcoritamab
- Biologiczny: Epcoritamab
- Lek: Rituximab and Lenalidomide
- Lek: rituximab and bendamustine
- Lek: rituximab, cytarabine, dexamethasone, and oxaliplatin/carboplatin
- Lek: gemcitabine and oxaliplatin
- Lek: rituximab and lenalidomide
- Lek: rituximab, cyclophosphamide, reduced dose of doxorubicin, vincristine, and prednisone
- Lek: Lenalidomide
- Lek: rituximab, ifosfamide, carboplatin, and etoposide phosphate
Szczegółowy opis
A Phase 1b/2, open-label, multinational, interventional trial to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics/biomarkers, immunogenicity, and preliminary efficacy of epcoritamab in combination with other standard of care (SOC) agents in participants with B-NHL.
All participants in the trial will receive epcoritamab, as monotherapy or in combination. The following regimens will be investigated:
- Arm 1: epcoritamab + rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) in participants with previously untreated diffuse large B-cell lymphoma (DLBCL)
- Arm 2: epcoritamab + rituximab and lenalidomide (R2) in participants with relapsed/refractory (R/R) follicular lymphoma (FL)
- Arm 3: epcoritamab + rituximab and bendamustine (BR) in participants with previously untreated FL
- Arm 4: epcoritamab + rituximab, cytarabine, dexamethasone, and oxaliplatin/ carboplatin (R-DHAX/C) in participants with R/R DLBCL eligible for autologous stem cell transplant (ASCT)
- Arm 5: epcoritamab + gemcitabine and oxaliplatin (GemOx) in participants with R/R DLBCL ineligible for ASCT due to age, performance status (PS), or comorbidity
- Arm 6: epcoritamab + R2 in participants with previously untreated FL
- Arm 7: epcoritamab maintenance in participants with FL who achieve a complete response (CR) or a partial response (PR) following first or second line SOC treatment
- Arm 8: epcoritamab + reduced dose of R-CHOP (R mini-CHOP) in participants with previously untreated DLBCL who are ineligible to receive full-dose anthracycline
- Arm 9: epcoritamab + lenalidomide for second-line treatment in participants with R/R FL who progressed within 24 months of initiation of first-line anti-CD20-containing immunochemotherapy
- Arm 10: epcoritamab + rituximab, ifosfamide, carboplatin, and etoposide phosphate (R-ICE) in participants with R/R DLBCL eligible for ASCT
The trial consists of two parts: Part 1 ('Dose Escalation') and Part 2 ('Dose Expansion'). The primary objective of Part 1 is safety, and it includes Arm 1-5 and Arm 10. Part 2 includes all 10 arms (Arm 1-10) and the primary goal of all arms, except Arm 7, is preliminary efficacy. For Arm 7, the primary goal is safety. Participants in Arm 1-5 and Arm 10 can only participate in either Part 1 or Part 2. Dose Limiting Toxicities (DLTs) will be assessed in Part 1 and for a selected number of participants in Arm 8 during a 28-day period (safety run-in). The arms are conducted in parallel.
Typ studiów
Typ studiów
Zapisy (Rzeczywisty)
Zapisy
Faza
Faza
- Faza 2
- Faza 1
Rozszerzony dostęp
Rozszerzony dostęp
Zatwierdzony
- Dostępne: rozszerzony dostęp jest obecnie dostępny dla tego eksperymentalnego leczenia, a pacjenci, którzy nie biorą udziału w badaniu klinicznym, mogą uzyskać dostęp do leku, leku biologicznego lub urządzenia medycznego w trakcie badania.
- Nie jest już dostępny: rozszerzony dostęp był wcześniej dostępny dla tej interwencji, ale nie jest obecnie dostępny i nie będzie dostępny w przyszłości.
- Tymczasowo niedostępny: rozszerzony dostęp nie jest obecnie dostępny dla tej interwencji, ale oczekuje się, że będzie dostępny w przyszłości.
- Zatwierdzono do celów marketingowych: interwencja został zatwierdzony przez amerykańską Agencję ds. Żywności i Leków do użytku publicznego.
Kontakty i lokalizacje
Lokalizacje studiów
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Heidelberg, Australia, VIC 3084
- Austin Health
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Nedlands, Australia, 6009
- Linear Clinical Research Limited
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Bruges, Belgia, 8000
- AZ Sint-Jan
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Ghent, Belgia, 9000
- Universitair Ziekenhuis Gent
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Yvoir, Belgia, 5530
- CHU UCL Namur Site Godinne
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Hradec Králové, Czechy
- Fakultni nemocnice Hradec Kralove
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Ostrava - Poruba, Czechy
- Fakultni nemocnice Ostrava
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Prague, Czechy, 15006
- Fakultni nemocnice v Motole
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Prague, Czechy
- Vseobecna Fakultni Nemocnice
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Aarhus, Dania
- Århus Hospital
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Copenhagen, Dania, 2100
- Rigshospitalet
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Odense, Dania
- Odense University Hospital
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Vejle, Dania
- Vejle Sygehus
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Kuopio, Finlandia, 70210
- Kuopio University Hospital
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Lahti, Finlandia, 15850
- HUS Cancer Center
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Lille, Francja, 59037
- Hopital Claude Huriez - CHRU Lille
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Marseille, Francja, 13005
- Hôpital de la Timone
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Paris, Francja, 75475
- Hôpital Saint-Louis
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Pierre-Bénite, Francja, 69495
- Centre Hospitalier Lyon Sud
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Barcelona, Hiszpania, 8035
- Hospital Universitari Vall d'Hebron
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Barcelona, Hiszpania, 08908
- ICO l Hospitalet
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Madrid, Hiszpania, 28046
- Hospital Universitario La Paz
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Madrid, Hiszpania, 28040
- Hospital Universitario Fundacion Jimenez Diaz
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Salamanca, Hiszpania, 37007
- Hospital Universitario de Salamanca
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Amsterdam, Holandia, 1105 AZ
- Amsterdam UMC, Locatie VUMC
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Groningen, Holandia, 9713
- Universitair Medisch Centrum Groningen (UMCG)
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Leiden, Holandia, 2333 ZA
- Leids Universitair Medisch Centrum
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Maastricht, Holandia, 6229 HX
- Maastricht University Medical Center
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Rotterdam, Holandia
- Erasmus Medisch Centrum
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Utrecht, Holandia, 3584
- UMC Utrecht
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Oslo, Norwegia, 310
- Oslo Universitetssykehus HF, Radiumhospitalet
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Alabama
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Birmingham, Alabama, Stany Zjednoczone, 35294
- University of Alabama at Birmingham
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California
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Los Angeles, California, Stany Zjednoczone, 90048
- Cedars-Sinai Medical Center
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Los Angeles, California, Stany Zjednoczone, 90095
- David Geffen School of Medicine at UCLA
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San Francisco, California, Stany Zjednoczone, 94143
- University of California San Francisco
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Massachusetts
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Boston, Massachusetts, Stany Zjednoczone, 02215
- Dana Farber Cancer Institute
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Michigan
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Ann Arbor, Michigan, Stany Zjednoczone, 48109
- University of Michigan Comprehensive Cancer Center Michigan Medicine
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New Jersey
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Hackensack, New Jersey, Stany Zjednoczone, 07601
- Hackensack University Medical Center
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New York
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New York, New York, Stany Zjednoczone, 10029
- Mount Sinai
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New York, New York, Stany Zjednoczone, 10065
- Memorial Sloan Kettering CC
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North Carolina
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Charlotte, North Carolina, Stany Zjednoczone, 28204
- Levine Cancer Center
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Texas
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Dallas, Texas, Stany Zjednoczone, 75390
- Southwestern Medical Center
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Borås, Szwecja
- Södra Älvsborgs Sjukhus
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Gothenburg, Szwecja, 413 45
- Sahlgrenska Sjukhuset
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Lund, Szwecja
- Skånes Universitetssjukhus
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Solna, Szwecja
- Karolinska Universitetssjukhuset
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Uppsala, Szwecja
- Akademiska Sjukhuset
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Bergamo, Włochy, 24127
- Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII (Presidio Papa Giovanni XXIII)
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Bologna, Włochy
- Azienda Ospedaliera Universitaria Policlinico Sant'Orsola Malpighi IRCCS
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Candiolo, Włochy, 10060
- Fondazione del Piemonte per l Oncologia Istituto di Candiolo IRCCS
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Meldola, Włochy, 47014
- IRCCS Istituto Scientifico Romagnolo Per Lo Studio Dei Tumori Dino Amadori IRST
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Milan, Włochy, 20122
- Fondazione IRCCS CA' Granda Ospedale Maggiore Policlinico
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Pavia, Włochy, 27100
- Fondazione IRCCS Policlinico San Matteo
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Reggio Emilia, Włochy, 42123
- Arcispedale S. Maria Nuova Azienda Ospedaliera di Reggio Emilia
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Manchester, Zjednoczone Królestwo
- The Christie Hospital
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Newcastle upon Tyne, Zjednoczone Królestwo, NE7 7D
- Freeman Hospital
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Plymouth, Zjednoczone Królestwo, PL6 8DH
- Derriford Hospital
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Kryteria uczestnictwa
Kryteria kwalifikacji
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Key Inclusion Criteria
- Measurable disease defined as ≥1 measurable nodal lesion (long axis >1.5 cm and short axis >1.0 cm) or ≥1 measurable extra-nodal lesion (long axis >1.0 cm) on computed tomography (CT) or magnetic resonance imaging (MRI). Applies to all arms except arm 7.
- Eastern Cooperative Oncology Group (ECOG) PS score of 0, 1 or 2
- Acceptable organ function at screening
- CD20-positive non-Hodgkin lymphoma (NHL) at most recent representative tumor biopsy
- If of childbearing potential participant must practicing a highly effective method of birth control
- A man who is sexually active with a woman of childbearing potential must agree to use a barrier method of birth control
Arm 1:
- Newly diagnosed DLBCL
- DLBCL, not otherwise specified (NOS)
- "Double-hit" or "triple-hit" DLBCL
- FL Grade 3B
Arm 2: R/R FL
Arm 3: Newly diagnosed, previously untreated FL grade 1-3A
Arm 4:
- Documented R/R DLBCL and eligible for HDT-ASCT
- DLBCL, NOS
- "Double-hit" or "triple-hit" DLBCL
- FL Grade 3B
Arm 5:
- Documented R/R DLBCL and ineligible for HDT-ASCT
- DLBCL, NOS
- "Double-hit" or "triple-hit" DLBCL
- FL Grade 3B
Arm 6: Newly diagnosed, previously untreated FL grade 1-3A
Arm 7:
- FL Grade 1-3A
- If PR or CR per Lugano criteria following first-line or second-line treatment with SOC regimen, and last dose of SOC within 6 months prior to enrollment.
Arm 8:
- Newly diagnosed DLBCL who are not fit to receive full-dose anthracycline
- T-cell/histiocyte rich DLBCL
- "Double-hit" or "triple-hit" DLBCL
- FL Grade 3B
Arm 9:
- R/R FL
- Progressed within 24 months of initiating first-line treatment
Arm 10:
- Documented R/R DLBCL and eligible for HDT-ASCT
- DLBCL, NOS
- "Double-hit" or "triple-hit" DLBCL
- FL Grade 3B
Key Exclusion Criteria
- Chemotherapy, radiation therapy, or major surgery within 4 weeks prior to the first dose of epcoritamab
- Any prior treatment with a bispecific antibody targeting CD3 and CD20.
- Treatment with CAR-T therapy within 100 days prior to first dose of epcoritamab
- Clinically significant cardiovascular disease
- Evidence of significant, uncontrolled concomitant diseases that could affect compliance with the protocol or interpretation of results
- CNS lymphoma or known CNS involvement by lymphoma at screening as confirmed by MRI/CT scan of the brain and, if clinically indicated, by lumbar puncture
- Positive tests for hepatitis B virus or hepatitis C virus indicating acute or chronic infection
- Known history of seropositivity of human immunodeficiency virus (HIV)
- Active tuberculosis or history of completed treatment for active tuberculosis within the past 12 months
- Neuropathy > grade 1
- Receiving immunostimulatory agent
- Prior allogeneic HSCT
- Current seizure disorder requiring anti-epileptic therapy
NOTE: Other protocol defined Inclusion/Exclusion criteria may apply.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Nielosowe
- Model interwencyjny: Przydział równoległy
- Maskowanie: Brak (otwarta etykieta)
Liczba ramion
Broń i interwencje
Grupa uczestników / ArmGrupa uczestników / Arm |
Interwencja / LeczenieInterwencja / Leczenie |
|---|---|
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Eksperymentalny: Arm 1 - Epcoritamab + R-CHOP
In participants with previously untreated DLBCL. |
6 cycles (21-day cycles)
Inne nazwy:
Every week in cycle 1-4, every 3 weeks in cycle 5 and 6, followed by every 4 weeks in cycle 7 for a total of 1 year.
Inne nazwy:
Every week in cycle 1-3, every 2 weeks in cycle 4-9, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and 2, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and then every 8 weeks for a total of 2 years.
Inne nazwy:
Every week in cycles 1 and 2, then every 3 weeks in cycles 3 to 6 and then every 4 weeks for cycles 7 and 8.
Inne nazwy:
Every week in cycle 1-3 and then every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1-4, every 2 weeks in cycle 5-9 followed by every 4 weeks until ASCT or disease progression.
Inne nazwy:
Eligible participants will receive subcutaneous (SC) epcoritamab in 28-day cycles. Fixed-treatment epcoritamab will be administered following a 2-Set Up Dosing regimen in Cycle 1. There will be 2 cohorts, 2a and 2b with different dosing schedules. Cohort 2a will be dosed weekly (QW) in Cycles 1-3, once every 2 weeks (Q2W) in Cycles 4-9, and once every 4 weeks (Q4W) in Cycle 10 and beyond for up to 2 years. In cohort 2b, an alternate dosing schedule for epcoritamab will be explored: epcoritamab administered QW for Cycles 1-2 only, then Q4W in Cycle 3 and beyond for up to 2 years.
Inne nazwy:
Cycle 1-3 every week, every other week Cycle 4-9 and then Q4W until progression or unacceptable toxicity.
Inne nazwy:
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Eksperymentalny: Arm 2 - Epcoritamab + R2
In participants with R/R FL. |
Every week in cycle 1-4, every 3 weeks in cycle 5 and 6, followed by every 4 weeks in cycle 7 for a total of 1 year.
Inne nazwy:
Every week in cycle 1-3, every 2 weeks in cycle 4-9, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and 2, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and then every 8 weeks for a total of 2 years.
Inne nazwy:
Every week in cycles 1 and 2, then every 3 weeks in cycles 3 to 6 and then every 4 weeks for cycles 7 and 8.
Inne nazwy:
Every week in cycle 1-3 and then every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1-4, every 2 weeks in cycle 5-9 followed by every 4 weeks until ASCT or disease progression.
Inne nazwy:
Eligible participants will receive subcutaneous (SC) epcoritamab in 28-day cycles. Fixed-treatment epcoritamab will be administered following a 2-Set Up Dosing regimen in Cycle 1. There will be 2 cohorts, 2a and 2b with different dosing schedules. Cohort 2a will be dosed weekly (QW) in Cycles 1-3, once every 2 weeks (Q2W) in Cycles 4-9, and once every 4 weeks (Q4W) in Cycle 10 and beyond for up to 2 years. In cohort 2b, an alternate dosing schedule for epcoritamab will be explored: epcoritamab administered QW for Cycles 1-2 only, then Q4W in Cycle 3 and beyond for up to 2 years.
Inne nazwy:
Cycle 1-3 every week, every other week Cycle 4-9 and then Q4W until progression or unacceptable toxicity.
Inne nazwy:
Rituximab 375 milligrams per meter squared (mg/m^2) will be administered intravenously QW in Cycle 1 and Q4W in Cycles 2-5. Lenalidomide 20 mg will be administered orally daily for 21 days for 12 cycles.
Inne nazwy:
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Eksperymentalny: Arm 3 - Epcoritamab + BR
In participants with previously untreated FL. |
Every week in cycle 1-4, every 3 weeks in cycle 5 and 6, followed by every 4 weeks in cycle 7 for a total of 1 year.
Inne nazwy:
Every week in cycle 1-3, every 2 weeks in cycle 4-9, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and 2, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and then every 8 weeks for a total of 2 years.
Inne nazwy:
Every week in cycles 1 and 2, then every 3 weeks in cycles 3 to 6 and then every 4 weeks for cycles 7 and 8.
Inne nazwy:
Every week in cycle 1-3 and then every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1-4, every 2 weeks in cycle 5-9 followed by every 4 weeks until ASCT or disease progression.
Inne nazwy:
Eligible participants will receive subcutaneous (SC) epcoritamab in 28-day cycles. Fixed-treatment epcoritamab will be administered following a 2-Set Up Dosing regimen in Cycle 1. There will be 2 cohorts, 2a and 2b with different dosing schedules. Cohort 2a will be dosed weekly (QW) in Cycles 1-3, once every 2 weeks (Q2W) in Cycles 4-9, and once every 4 weeks (Q4W) in Cycle 10 and beyond for up to 2 years. In cohort 2b, an alternate dosing schedule for epcoritamab will be explored: epcoritamab administered QW for Cycles 1-2 only, then Q4W in Cycle 3 and beyond for up to 2 years.
Inne nazwy:
Cycle 1-3 every week, every other week Cycle 4-9 and then Q4W until progression or unacceptable toxicity.
Inne nazwy:
6 cycles (28-day cycles)
Inne nazwy:
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Eksperymentalny: Arm 4 - Epcoritamab + R-DHAX/C
In participants with R/R DLBCL eligible for ASCT. |
Every week in cycle 1-4, every 3 weeks in cycle 5 and 6, followed by every 4 weeks in cycle 7 for a total of 1 year.
Inne nazwy:
Every week in cycle 1-3, every 2 weeks in cycle 4-9, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and 2, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and then every 8 weeks for a total of 2 years.
Inne nazwy:
Every week in cycles 1 and 2, then every 3 weeks in cycles 3 to 6 and then every 4 weeks for cycles 7 and 8.
Inne nazwy:
Every week in cycle 1-3 and then every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1-4, every 2 weeks in cycle 5-9 followed by every 4 weeks until ASCT or disease progression.
Inne nazwy:
Eligible participants will receive subcutaneous (SC) epcoritamab in 28-day cycles. Fixed-treatment epcoritamab will be administered following a 2-Set Up Dosing regimen in Cycle 1. There will be 2 cohorts, 2a and 2b with different dosing schedules. Cohort 2a will be dosed weekly (QW) in Cycles 1-3, once every 2 weeks (Q2W) in Cycles 4-9, and once every 4 weeks (Q4W) in Cycle 10 and beyond for up to 2 years. In cohort 2b, an alternate dosing schedule for epcoritamab will be explored: epcoritamab administered QW for Cycles 1-2 only, then Q4W in Cycle 3 and beyond for up to 2 years.
Inne nazwy:
Cycle 1-3 every week, every other week Cycle 4-9 and then Q4W until progression or unacceptable toxicity.
Inne nazwy:
3 cycles (21-day cycles)
Inne nazwy:
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Eksperymentalny: Arm 5 - Epcoritamab + GemOx
In participants with R/R DLBCL ineligible ASCT. |
Every week in cycle 1-4, every 3 weeks in cycle 5 and 6, followed by every 4 weeks in cycle 7 for a total of 1 year.
Inne nazwy:
Every week in cycle 1-3, every 2 weeks in cycle 4-9, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and 2, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and then every 8 weeks for a total of 2 years.
Inne nazwy:
Every week in cycles 1 and 2, then every 3 weeks in cycles 3 to 6 and then every 4 weeks for cycles 7 and 8.
Inne nazwy:
Every week in cycle 1-3 and then every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1-4, every 2 weeks in cycle 5-9 followed by every 4 weeks until ASCT or disease progression.
Inne nazwy:
Eligible participants will receive subcutaneous (SC) epcoritamab in 28-day cycles. Fixed-treatment epcoritamab will be administered following a 2-Set Up Dosing regimen in Cycle 1. There will be 2 cohorts, 2a and 2b with different dosing schedules. Cohort 2a will be dosed weekly (QW) in Cycles 1-3, once every 2 weeks (Q2W) in Cycles 4-9, and once every 4 weeks (Q4W) in Cycle 10 and beyond for up to 2 years. In cohort 2b, an alternate dosing schedule for epcoritamab will be explored: epcoritamab administered QW for Cycles 1-2 only, then Q4W in Cycle 3 and beyond for up to 2 years.
Inne nazwy:
Cycle 1-3 every week, every other week Cycle 4-9 and then Q4W until progression or unacceptable toxicity.
Inne nazwy:
4 cycles (28-day cycles)
Inne nazwy:
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Eksperymentalny: Arm 6 - Epcoritamab + R2
In participants with previously untreated FL. |
Every week in cycle 1-4, every 3 weeks in cycle 5 and 6, followed by every 4 weeks in cycle 7 for a total of 1 year.
Inne nazwy:
Every week in cycle 1-3, every 2 weeks in cycle 4-9, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and 2, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and then every 8 weeks for a total of 2 years.
Inne nazwy:
Every week in cycles 1 and 2, then every 3 weeks in cycles 3 to 6 and then every 4 weeks for cycles 7 and 8.
Inne nazwy:
Every week in cycle 1-3 and then every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1-4, every 2 weeks in cycle 5-9 followed by every 4 weeks until ASCT or disease progression.
Inne nazwy:
Eligible participants will receive subcutaneous (SC) epcoritamab in 28-day cycles. Fixed-treatment epcoritamab will be administered following a 2-Set Up Dosing regimen in Cycle 1. There will be 2 cohorts, 2a and 2b with different dosing schedules. Cohort 2a will be dosed weekly (QW) in Cycles 1-3, once every 2 weeks (Q2W) in Cycles 4-9, and once every 4 weeks (Q4W) in Cycle 10 and beyond for up to 2 years. In cohort 2b, an alternate dosing schedule for epcoritamab will be explored: epcoritamab administered QW for Cycles 1-2 only, then Q4W in Cycle 3 and beyond for up to 2 years.
Inne nazwy:
Cycle 1-3 every week, every other week Cycle 4-9 and then Q4W until progression or unacceptable toxicity.
Inne nazwy:
rituximab 6 cycles and lenalidomide 12 cycles (28-day cycles)
Inne nazwy:
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Eksperymentalny: Arm 7 - Epcoritamab maintenance
In participants with FL who achieved a CR or PR after receiving SOC treatment in 1L or 2L. |
Every week in cycle 1-4, every 3 weeks in cycle 5 and 6, followed by every 4 weeks in cycle 7 for a total of 1 year.
Inne nazwy:
Every week in cycle 1-3, every 2 weeks in cycle 4-9, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and 2, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and then every 8 weeks for a total of 2 years.
Inne nazwy:
Every week in cycles 1 and 2, then every 3 weeks in cycles 3 to 6 and then every 4 weeks for cycles 7 and 8.
Inne nazwy:
Every week in cycle 1-3 and then every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1-4, every 2 weeks in cycle 5-9 followed by every 4 weeks until ASCT or disease progression.
Inne nazwy:
Eligible participants will receive subcutaneous (SC) epcoritamab in 28-day cycles. Fixed-treatment epcoritamab will be administered following a 2-Set Up Dosing regimen in Cycle 1. There will be 2 cohorts, 2a and 2b with different dosing schedules. Cohort 2a will be dosed weekly (QW) in Cycles 1-3, once every 2 weeks (Q2W) in Cycles 4-9, and once every 4 weeks (Q4W) in Cycle 10 and beyond for up to 2 years. In cohort 2b, an alternate dosing schedule for epcoritamab will be explored: epcoritamab administered QW for Cycles 1-2 only, then Q4W in Cycle 3 and beyond for up to 2 years.
Inne nazwy:
Cycle 1-3 every week, every other week Cycle 4-9 and then Q4W until progression or unacceptable toxicity.
Inne nazwy:
|
|
Eksperymentalny: Arm 8 - Epcoritamab + R mini-CHOP
In participants with previously untreated DLBCL who are ineligible to receive full-dose anthracycline. |
Every week in cycle 1-4, every 3 weeks in cycle 5 and 6, followed by every 4 weeks in cycle 7 for a total of 1 year.
Inne nazwy:
Every week in cycle 1-3, every 2 weeks in cycle 4-9, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and 2, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and then every 8 weeks for a total of 2 years.
Inne nazwy:
Every week in cycles 1 and 2, then every 3 weeks in cycles 3 to 6 and then every 4 weeks for cycles 7 and 8.
Inne nazwy:
Every week in cycle 1-3 and then every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1-4, every 2 weeks in cycle 5-9 followed by every 4 weeks until ASCT or disease progression.
Inne nazwy:
Eligible participants will receive subcutaneous (SC) epcoritamab in 28-day cycles. Fixed-treatment epcoritamab will be administered following a 2-Set Up Dosing regimen in Cycle 1. There will be 2 cohorts, 2a and 2b with different dosing schedules. Cohort 2a will be dosed weekly (QW) in Cycles 1-3, once every 2 weeks (Q2W) in Cycles 4-9, and once every 4 weeks (Q4W) in Cycle 10 and beyond for up to 2 years. In cohort 2b, an alternate dosing schedule for epcoritamab will be explored: epcoritamab administered QW for Cycles 1-2 only, then Q4W in Cycle 3 and beyond for up to 2 years.
Inne nazwy:
Cycle 1-3 every week, every other week Cycle 4-9 and then Q4W until progression or unacceptable toxicity.
Inne nazwy:
6 cycles (21-day cycles)
Inne nazwy:
|
|
Eksperymentalny: Arm 9 - Epcoritamab + Lenalidomide
In participants with R/R FL who progressed within 24 months of initiation of first-line anti-CD20-containing immunochemotherapy. |
Every week in cycle 1-4, every 3 weeks in cycle 5 and 6, followed by every 4 weeks in cycle 7 for a total of 1 year.
Inne nazwy:
Every week in cycle 1-3, every 2 weeks in cycle 4-9, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and 2, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and then every 8 weeks for a total of 2 years.
Inne nazwy:
Every week in cycles 1 and 2, then every 3 weeks in cycles 3 to 6 and then every 4 weeks for cycles 7 and 8.
Inne nazwy:
Every week in cycle 1-3 and then every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1-4, every 2 weeks in cycle 5-9 followed by every 4 weeks until ASCT or disease progression.
Inne nazwy:
Eligible participants will receive subcutaneous (SC) epcoritamab in 28-day cycles. Fixed-treatment epcoritamab will be administered following a 2-Set Up Dosing regimen in Cycle 1. There will be 2 cohorts, 2a and 2b with different dosing schedules. Cohort 2a will be dosed weekly (QW) in Cycles 1-3, once every 2 weeks (Q2W) in Cycles 4-9, and once every 4 weeks (Q4W) in Cycle 10 and beyond for up to 2 years. In cohort 2b, an alternate dosing schedule for epcoritamab will be explored: epcoritamab administered QW for Cycles 1-2 only, then Q4W in Cycle 3 and beyond for up to 2 years.
Inne nazwy:
Cycle 1-3 every week, every other week Cycle 4-9 and then Q4W until progression or unacceptable toxicity.
Inne nazwy:
12 cycles (28-day cycles) |
|
Eksperymentalny: Arm 10 - Epcoritamab + R-ICE
In participants with R/R DLBCL eligible for ASCT. |
Every week in cycle 1-4, every 3 weeks in cycle 5 and 6, followed by every 4 weeks in cycle 7 for a total of 1 year.
Inne nazwy:
Every week in cycle 1-3, every 2 weeks in cycle 4-9, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and 2, followed by every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1 and then every 8 weeks for a total of 2 years.
Inne nazwy:
Every week in cycles 1 and 2, then every 3 weeks in cycles 3 to 6 and then every 4 weeks for cycles 7 and 8.
Inne nazwy:
Every week in cycle 1-3 and then every 4 weeks for a total of 2 years.
Inne nazwy:
Every week in cycle 1-4, every 2 weeks in cycle 5-9 followed by every 4 weeks until ASCT or disease progression.
Inne nazwy:
Eligible participants will receive subcutaneous (SC) epcoritamab in 28-day cycles. Fixed-treatment epcoritamab will be administered following a 2-Set Up Dosing regimen in Cycle 1. There will be 2 cohorts, 2a and 2b with different dosing schedules. Cohort 2a will be dosed weekly (QW) in Cycles 1-3, once every 2 weeks (Q2W) in Cycles 4-9, and once every 4 weeks (Q4W) in Cycle 10 and beyond for up to 2 years. In cohort 2b, an alternate dosing schedule for epcoritamab will be explored: epcoritamab administered QW for Cycles 1-2 only, then Q4W in Cycle 3 and beyond for up to 2 years.
Inne nazwy:
Cycle 1-3 every week, every other week Cycle 4-9 and then Q4W until progression or unacceptable toxicity.
Inne nazwy:
3 cycles (21-day cycles)
Inne nazwy:
|
Co mierzy badanie?
Podstawowe miary wyniku
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Part 1: Number of Participants With Dose limiting Toxicities (DLTs)
Ramy czasowe: During the first cycle (Cycle length= 28 days) in each cohort
|
DLT events are defined as clinically significant adverse events (AEs) or abnormal laboratory values assessed as unrelated to disease progression, underlying disease, intercurrent illness, or concomitant medications as assessed per Common Terminology Criteria for Adverse Events (NCI-CTCAE) criteria version 5.0. |
During the first cycle (Cycle length= 28 days) in each cohort
|
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Part 1 and Part 2 (Arms 1-5, 7 and 10): Number of Participants With Adverse Events (AEs)
Ramy czasowe: From first dose of drug until either 60 days after last dose, date participant withdraws consent, date participant starts a new systemic anticancer therapy, or date participant dies, whichever occurs first (up to approximately 3 years)
|
An AE is any untoward medical occurrence in a participant or clinical investigation participant administered a pharmaceutical product and that does not necessarily have a causal relationship with this treatment. An AE can therefore be any unfavorable and unintended sign. (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal (investigational) product, whether or not related to the medicinal (investigational) product. |
From first dose of drug until either 60 days after last dose, date participant withdraws consent, date participant starts a new systemic anticancer therapy, or date participant dies, whichever occurs first (up to approximately 3 years)
|
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Part 2 (Except Arm 7): Overall Response Rate (ORR)
Ramy czasowe: Up to 3 years
|
ORR is defined as the percentage of participants achieving complete response (CR) or partial response (PR) based on Lugano criteria. |
Up to 3 years
|
Miary wyników drugorzędnych
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Część 1 i 2: Klirens (CL) epkoritamabu
Ramy czasowe: Przed i po podaniu dawki w wielu punktach czasowych, aż do przerwania leczenia (do 3 lat)
|
Przed i po podaniu dawki w wielu punktach czasowych, aż do przerwania leczenia (do 3 lat)
|
|
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Część 1 i 2: Maksymalne (szczytowe) stężenie epkoritamabu w osoczu (Cmax)
Ramy czasowe: Przed i po podaniu dawki w wielu punktach czasowych, aż do przerwania leczenia (do 3 lat)
|
Przed i po podaniu dawki w wielu punktach czasowych, aż do przerwania leczenia (do 3 lat)
|
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Część 1 i 2: Czas do osiągnięcia Cmax (Tmax) epkoritamabu
Ramy czasowe: Przed i po podaniu dawki w wielu punktach czasowych, aż do przerwania leczenia (do 3 lat)
|
Przed i po podaniu dawki w wielu punktach czasowych, aż do przerwania leczenia (do 3 lat)
|
|
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Część 1 i 2: Końcowy okres półtrwania w fazie eliminacji (t1/2) epkoritamabu
Ramy czasowe: Przed i po podaniu dawki w wielu punktach czasowych, aż do przerwania leczenia (do 3 lat)
|
Przed i po podaniu dawki w wielu punktach czasowych, aż do przerwania leczenia (do 3 lat)
|
|
|
Część 1 i 2: Liczba uczestników z przeciwciałami przeciwlekowymi (ADA) przeciw epkoritamabowi
Ramy czasowe: Do 3 lat
|
Do 3 lat
|
|
|
Część 1 i 2: Czas trwania ujemnego wyniku minimalnej choroby resztkowej (MRD).
Ramy czasowe: Do 3 lat
|
Do 3 lat
|
|
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Część 2 (Ramię 7): Odsetek uczestników, którzy przeszli z pozytywnego na MRD na negatywny na MRD
Ramy czasowe: Do 3 lat
|
Do 3 lat
|
|
|
Część 2 (z wyjątkiem Grupy 7): Odsetek uczestników z całkowitą odpowiedzią (CR) w Grupach 1 do 10
Ramy czasowe: Do 3 lat
|
Do 3 lat
|
|
|
Część 1 i 2: Obszar pod krzywą czasu koncentracji (AUC) epcoritamabu
Ramy czasowe: Przedstawić i po daniu w wielu punktach czasowych do czasu przerwania leczenia (do 3 lat)
|
Przedstawić i po daniu w wielu punktach czasowych do czasu przerwania leczenia (do 3 lat)
|
|
|
Part 1 and 2: Number of Immune Cell Populations
Ramy czasowe: Up to 2 years
|
Immune cell populations in peripheral blood and tumor biopsies will be assessed. |
Up to 2 years
|
|
Part 1 and 2: Percentage of Immune Cell Populations
Ramy czasowe: Up to 2 years
|
Immune cell populations in peripheral blood and tumor biopsies will be assessed. |
Up to 2 years
|
|
Part 1 and 2: Change From Baseline in Cytokine Levels up to Cycle 3
Ramy czasowe: Up to Cycle 3 (cycle length = 21 days for Arms 1, 4, 8 and 10; cycle length = 28 days for Arms 2, 3, 5, 6 and 9; cycle length = 28 days (Cycle 1) and 56 days (Cycles 2, 3) for Arm 7)
|
Change in cytokine levels in peripheral blood samples will be assessed. |
Up to Cycle 3 (cycle length = 21 days for Arms 1, 4, 8 and 10; cycle length = 28 days for Arms 2, 3, 5, 6 and 9; cycle length = 28 days (Cycle 1) and 56 days (Cycles 2, 3) for Arm 7)
|
|
Part 1 and 2: Change From Baseline in Circulating Tumor Deoxyribonucleic Acid (DNA) Level up to End of Treatment (up to 2 Years)
Ramy czasowe: Up to 2 years
|
Change in circulating tumor DNA levels will be assessed. |
Up to 2 years
|
|
Part 1: ORR
Ramy czasowe: Up to 3 years
|
ORR is defined as the percentage of participants achieving CR or PR based on Lugano criteria. |
Up to 3 years
|
|
Part 1 and 2: Duration of Response (DOR)
Ramy czasowe: Up to 3 years
|
DOR: the time from the first documentation of objective tumor response (CR or PR) to the date of first PD or death, whichever occurs earlier, based on Lugano criteria. |
Up to 3 years
|
|
Part 1 and 2: Time to Response (TTR)
Ramy czasowe: Up to 3 years
|
TTR is defined as the time from Day 1 of Cycle 1 to first documentation of objective tumor response (CR or PR). |
Up to 3 years
|
|
Part 1 and 2: Progression Free Survival (PFS)
Ramy czasowe: Up to 3 years
|
PFS is defined as the time from Day 1 of Cycle 1 to first documented PD or death due to any cause, whichever occurs earlier, based on Lugano criteria. |
Up to 3 years
|
|
Part 1 and 2: Overall Survival (OS)
Ramy czasowe: Up to 3 years
|
OS is defined as the time from the date of first dose, to the date of death due to any cause. |
Up to 3 years
|
|
Part 1 and 2: Time to Next Anti-lymphoma Therapy (TTNT)
Ramy czasowe: Up to 3 years
|
TTNT is defined as the time from Day 1 of Cycle 1 to first documented administration of subsequent anti-lymphoma therapy. |
Up to 3 years
|
|
Part 1 and 2: Percentage of Participants With Minimal Residual Disease (MRD) Negativity
Ramy czasowe: Up to 3 years
|
It is defined as the percentage of participants with at least 1 MRD negative result. |
Up to 3 years
|
|
Part 2 (Arm 7): Percentage of Participants With CR
Ramy czasowe: Week 24, Week 48, and Week 96
|
It is defined as the percentage of participants who remain in complete remission or converting to complete remission after first trial drug administration. |
Week 24, Week 48, and Week 96
|
|
Part 1 and 2: Time to Complete Response (TTCR)
Ramy czasowe: Up to 3 years
|
TTCR is defined as the time from first trial drug administration to the date of first documented complete response post-treatment. |
Up to 3 years
|
|
Part 1 and 2: Duration of Complete Response (DoCR)
Ramy czasowe: Up to 3 years
|
DoCR is defined as the time from the first documentation of CR to the date of PD or death, whichever occurs first based on Lugano criteria. |
Up to 3 years
|
|
Part 2: Number of Participants with AEs (Except Arm 7)
Ramy czasowe: From first dose of drug until either 60 days after last dose, date participant withdraws consent, date participant starts a new systemic anticancer therapy, or date participant dies, whichever occurs first (up to approximately 3 years)
|
An AE is any untoward medical occurrence in a participant or clinical investigation participant administered a pharmaceutical product and that does not necessarily have a causal relationship with this treatment. An AE can therefore be any unfavorable and unintended sign. (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal (investigational) product, whether or not related to the medicinal (investigational) product. |
From first dose of drug until either 60 days after last dose, date participant withdraws consent, date participant starts a new systemic anticancer therapy, or date participant dies, whichever occurs first (up to approximately 3 years)
|
Współpracownicy i badacze
Sponsor
Sponsor
Współpracownicy
Współpracownicy
Publikacje i pomocne linki
Publikacje ogólne
- Brody JD, Jorgensen J, Belada D, Costello R, Trneny M, Vitolo U, Lewis DJ, Karimi YH, Sureda A, Andre M, Wahlin BE, Lugtenburg PJ, Jiang T, Karagoz K, Steele AJ, Abbas A, Wang L, Risum M, Cordoba R. Epcoritamab plus GemOx in transplant-ineligible relapsed/refractory DLBCL: results from the EPCORE NHL-2 trial. Blood. 2025 Apr 10;145(15):1621-1631. doi: 10.1182/blood.2024026830.
- Falchi L, Sureda A, Leppa S, Vermaat JSP, Nijland M, Christensen JH, de Vos S, Holte H, Merryman RW, Lugtenburg PJ, Abrisqueta P, Linton KM, Sunkersett G, Hoehn D, Rana A, Abbas A, Marek J, Hao Y, Steele AJ, Morehouse C, Hutchings M, Belada D. Fixed-duration epcoritamab plus R2 drives favorable outcomes in relapsed or refractory follicular lymphoma. Blood. 2025 Nov 27;146(22):2629-2640. doi: 10.1182/blood.2025029909.
- Falchi L, Vermaat JSP, Brody JD, Leslie L, Offner F, Christensen JH, Nijland M, Belada D, Wahlin BE, Drott K, Gomez Prieto P, Kopeckova K, Garcia-Sancho AM, Mei JP, Altintas I, Risum M, Reilly A, Zou J, Abrisqueta P. Epcoritamab with rituximab and lenalidomide as first-line treatment for follicular lymphoma (EPCORE NHL-2): an open-label, multicentre, phase 1/2 b trial. Lancet Haematol. 2026 Sep;13(9):e614-e625. doi: 10.1016/S2352-3026(26)00198-5.
- Falchi L, Offner F, de Vos S, Brody JD, Morillo D, Linton K, Snauwaert S, Roost Clausen M, Karimi YH, Thieblemont C, Vitolo U, Leslie LA, Narkhede MS, Cordoba R, Oki T, Wielgos-Bonvallet M, Khoshdeli M, Hao Y, Archer K, Risum M, Belada D. Fixed-duration epcoritamab plus R-CHOP in newly diagnosed LBCL with IPI score 3-5: results from the EPCORE NHL-2 trial. Blood. 2026 Aug 11:blood.2026033839. doi: 10.1182/blood.2026033839. Online ahead of print.
- Abrisqueta P, Karimi YH, Morillo D, Cordoba R, Phillips T, De Vos S, Nijland M, Offner F, Andersson PO, Brody J, Cheah CY, Prieto PG, Hellstrom M, Jorgensen JM, Lewis D, Linton KM, Musuraca G, Wang L, Marek J, Osei-Bonsu K, Risum M, Falchi L. Epcoritamab plus rituximab, dexamethasone, cytarabine, oxaliplatin/carboplatin induces deep and durable responses in transplant-eligible patients with relapsed or refractory diffuse large B-cell lymphoma: results from the EPCORE NHL-2 trial. Haematologica. 2026 Oct 1;111(10):3346-3357. doi: 10.3324/haematol.2025.300086. Epub 2026 Mar 5.
Przydatne linki
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Rozpoczęcie studiów
Zakończenie podstawowe (Szacowany)
Zakończenie podstawowe
Ukończenie studiów (Szacowany)
Ukończenie studiów
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Pierwszy wysłany
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia wysłana aktualizacja
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
- Nowotwory
- Choroby układu odpornościowego
- Nowotwory według typu histologicznego
- Choroby limfatyczne
- Zaburzenia limfoproliferacyjne
- Zaburzenia immunoproliferacyjne
- Chłoniak nieziarniczy
- Chłoniak z komórek B
- Chłoniak
- Choroby hemowe i limfatyczne
- Chłoniak, duże komórki B, rozlany
- Chłoniak, Pęcherzykowy
- Aminokwasy, peptydy i białka
- Białka
- Organiczne chemikalia
- Związki heterocykliczne, 1-ring
- Związki heterocykliczne
- Benzimidazoleles
- Związki heterocykliczne, 2-ring
- Związki heterocykliczne, sterowanie stopieniem
- Kwasy nukleinowe, nukleotydy i nukleozydy
- Węglowodory
- Węglowodory, cykliczne
- Węglowodany
- Kwasy, acykliczne
- Kwasy karboksylowe
- Alkaloidy
- Policykliczne aromatyczne węglowodory
- Węglowodory, aromatyczne
- Związki policykliczne
- Glikozydy
- Piperydyny
- Indole
- Przeciwciała, monoklonalne
- Przeciwciała
- Immunoglobuliny
- Immunoproteiny
- Białka krwi
- Globuliny w surowicy
- Globuliny
- Kompleksy koordynacyjne
- Deoksycytydyna
- Cytydyna
- Nukleozydy pirymidynowe
- Pirymidyn
- Ciąży
- Ciężarne
- Steroidy
- Związki sterownika
- Sterydy, fluorowane
- Mostki fosforamidu
- Związki musztardy azotu
- Związki musztardy
- Węglowodory, uboczne
- Fosforamidy
- Związki okorosfosforowe
- Nukleozydy
- Ciąży
- Ciąży
- Vinca alkaloidy
- Sesologanina alkaloidy tryptaminy
- Alkaloidy indole
- Indolizicyny
- Indolizyny
- Arabinonukleozydy
- Antracykliny
- Naftaceny
- Aminoglikozydy
- Maślany
- Przeciwciała, monoklonalne, mysie
- Daunorubicyna
- Oksazyny
- Ftalimidy
- Kwasy ftaliczne
- Kwasy, karbocykliczne
- Piperidones
- Izoindoles
- Lenalidomid
- Oksaliplatyna
- Chlorowodorek bendamustyny
- Rytuksymab
- Gemcytabina
- Deksametazon
- Prednizon
- Cyklofosfamid
- Cytarabina
- Karboplatyna
- Doksorubicyna
- Winkrystyna
- Ifosfamid
- Fosforan etopozydowy
- Protokół R-Chop
Inne numery identyfikacyjne badania
Inne numery identyfikacyjne badania
- GCT3013-02
- 2020-000845-15 (Numer EudraCT)
- NL74222.056.20 (Identyfikator rejestru: CCMO)
- 283235 (Inny identyfikator: IRAS ID; UK Research Summaries Database)
- RECF4377 (Inny identyfikator: The French National Cancer Institute)
- 2023 (Grant/umowa NIH USA)
- 2023-504805-35-00 (Ctis)
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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 .