- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT05733650
Udvidet adgangsprogram til Epcoritamab
Expanded Access Program (EAP) til at give Epcoritamab (GEN3013) til kvalificerede patienter med recidiverende eller refraktær storcellet B-celle lymfom
The purpose of this program is to provide investigational epcoritamab, an antibody also known as GEN3013 (DuoBody-CD3xCD20), in an expanded access setting for eligible patients with relapsed and/or refractory (R/R) large B-cell lymphoma (LBCL) who have a high unmet medical need with no other treatment options. It is a requirement that patients do not qualify for an ongoing epcoritamab clinical program or are unable to participate due to logistical reasons.
Access to investigational epcoritamab can be requested by contacting preapprovalaccessprograms@genmab.com.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This is a multicenter program conducted within the United States. The program will consist of screening, treatment (Cycle 1 Day 1 until epcoritamab discontinuation), safety follow-up, post-treatment and/or survival follow-up.
Undersøgelsestype
Udvidet adgangstype
- Behandling IND/Protokol
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Must be 18 years of age or older
- R/R CD20+ mature B-cell neoplasm
- Eastern Cooperative Oncology Group Performance Status (ECOG PS) 0, 1, or 2
- ≥ 2 prior lines of antineoplastic therapy, including ≥ 1 anti-CD20 monoclonal antibody (mAb)
- Fluorodeoxyglucose (FDG) positron emission tomography (PET)-avid and measurable disease by computed tomography/magnetic resonance imaging (CT/MRI)
- Patients considering the EAP should have no other available therapeutic option and cannot be eligible for other epcoritamab trials.
- Patients considering the EAP must be located in proximity to a US site given that the EAP is currently available only in the United States.
- Prior to initiating any program-related assessments or procedures, patients (or their legally acceptable representative) must sign an informed consent form (ICF), which indicates the purpose of the program, the procedures required for the program, and confirms the patient's willingness to participate in the program.
Exclusion Criteria:
- Any prior therapy with an investigational bispecific antibody targeting CD3 and CD20
- Prior treatment with CAR-T therapy within 100 days prior to first epcoritamab administration
- Primary central nervous system (CNS) lymphoma or known CNS involvement by lymphoma
- Confirmed history of or current autoimmune disease or other diseases resulting in permanent immunosuppression or requiring permanent immunosuppressive therapy. Low-dose prednisolone for rheumatoid arthritis or similar conditions is allowed.
- Active hepatitis B or hepatitis C
- Known clinically significant cardiac disease
- Pregnancy or breastfeeding
- Known hypersensitivity to allopurinol or rasburicase
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Samarbejdspartnere og efterforskere
Datoer for undersøgelser
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- GCT3013-101
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