Expanded Access Program for Epcoritamab

Sponsor

Genmab (Industry)

Overall Status

Available

CT.gov ID

NCT05733650

Collaborator

AbbVie (Industry)

Study Details

Study Description

Brief Summary

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.

Condition or Disease	Intervention/Treatment	Phase
Large B-cell Lymphoma Diffuse Large B-Cell Lymphoma, Not Otherwise Specified Primary Mediastinal Large B-cell Lymphoma (PMBCL) High Grade B-cell Lymphoma (HGBCL) Grade 3B Follicular Lymphoma	Biological: Epcoritamab

Detailed Description

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.

Study Design

Study Type:

Expanded Access

Official Title:

Expanded Access Program (EAP) to Provide Epcoritamab (GEN3013) to Eligible Patients With Relapsed or Refractory Large B-cell Lymphoma

Outcome Measures

Primary Outcome Measures

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

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