Epcoritamab-CAR T Cells for Large B-cell Lymphomas

NCT ID: NCT06458439

Last Updated: 2025-03-27

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 31 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-09-24
• Study Completion Date: 2027-12-31

Brief Summary

This study investigates the feasibility and efficacy of epcoritamab treatment before CAR T cells. This study also investigates if, when patients have residual lymphoma after CAR T cells, epcoritamab can help to effectively treat that lymphoma.

Conditions

Lymphoma, Non-Hodgkin; Relapsed Diffuse Large B Cell Lymphoma; Refractory Diffuse Large B-cell Lymphoma; High-grade B-cell Lymphoma; Transformed Indolent Non-Hodgkin Lymphoma to Diffuse Large B-Cell Lymphoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Epcoritamab

Study participants will bridging epcoritamab on Cycles 1-3, Days 1, 8, 15, and 22 (once weekly).

Group Type: EXPERIMENTAL

Epcoritamab

Intervention Type: DRUG

• C1D1: fixed priming dose of 0.16 mg subcutaneous injection
• C1D8: fixed intermediate dose of 0.8 mg subcutaneous injection
• C1D15 onward: fixed full dose of 48 mg subcutaneous injection

Interventions

Epcoritamab

• C1D1: fixed priming dose of 0.16 mg subcutaneous injection
• C1D8: fixed intermediate dose of 0.8 mg subcutaneous injection
• C1D15 onward: fixed full dose of 48 mg subcutaneous injection

Intervention Type: DRUG

Other Intervention Names

GEN3013; DuoBody -CD3xCD20

Eligibility Criteria

Inclusion Criteria

• Age > 18 years
• Subject must be able and willing to provide informed consent. In the case where the patient is incapacitated or not otherwise capable, a legally authorized representative (or decision maker when there is not an advanced directive in place) must be willing to provide informed consent on behalf of the patient.
• Able to comply with the study protocol, in the investigator's judgment
• ECOG PS of 0 - 2
• Pathology report confirming eligible diagnosis
• Documented CD20+ tumor cells on most recent biopsy
• Patients will have failed to respond to frontline standard of care therapy containing an anthracycline and anti-CD20 antibody
• Patients will be eligible and consent to be treated with a "commercially available" anti-CD19, 4-1BB, CD3zeta CAR-T cell therapy or anti-CD19, CD28, CD3zeta CAR T cell therapy (for example, tisagenlecleucel, lisocabtagene maraleucel, or axicabtagene maraleucel)
• Patients must have a PET/CT scan (preferred), diagnostic CT scan, or MRI with at least one bi-dimensionally measurable lesion (≥ 1.5 cm for nodal lesions or ≥ 1cm for extra-nodal lesions in largest dimension by low-dose computerized tomography [CT] scan with FDG-uptake ≥ liver)
• Adequate laboratory studies
• Resolution of toxicities from prior therapy to a grade that does not contraindicate trial participation in the opinion of the investigator
• Ability and willingness to take proper contraceptive precautions

Exclusion Criteria

• Inability or unwillingness of the patient or legally authorized representative (or decision-maker when there is not an advanced directive in place) to provide informed consent.
• Prior solid organ transplantation
• Primary central nervous system (CNS) lymphoma or active secondary CNS involvement by lymphoma at screening as confirmed by magnetic resonance imaging (MRI)/computed tomography (CT) scan (brain) or, if clinically indicated, by lumbar puncture.

1. Patients with a history of autoimmune-related hypothyroidism on a stable dose of thyroid replacement hormone

2. Patients with a history of lymphoma-related immune thrombocytopenic purpura or autoimmune hemolytic anemia in remission may be eligible for this study if approved by the Regulatory Sponsor and Principal Investigator

3. Patients with eczema, psoriasis, lichen simplex chronicus, or vitiligo with dermatologic manifestations only (e.g., patients with psoriatic arthritis are excluded) are eligible for the study provided all of following conditions are met:

i. Rash must cover < 10% of body surface area ii. Disease is well controlled at baseline and requires only low-potency topical corticosteroid iii. No occurrence of acute exacerbations of the underlying condition requiring psoralen plus ultraviolet A radiation, methotrexate, retinoids, biologic agents, oral calcineurin inhibitors, or corticosteroids (> 20 mg/day prednisone or equivalent for > 2 weeks) within the previous 3 months d. rheumatoid arthritis or similar autoimmune/rheumatic conditions

• Systemic immunosuppressive medications (including but not limited to cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-tumor necrosis factor agents). However, the following are permitted:

1. If receiving glucocorticoid treatment at screening, must be a maximum daily dose of prednisone 10 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.

2. Patients who received a single dose of a systemic immunosuppressant medications (e.g., single dose of dexamethasone for nausea or B symptoms) may be enrolled

3. The use of inhaled corticosteroids is permitted

4. The use of mineralocorticoids for management of orthostatic hypotension is permitted

5. The use of physiologic doses of corticosteroids (< 20 mg/day of prednisone or equivalent) for uses such as management of adrenal insufficiency is permitted

• Known past or current malignancy, other than inclusion diagnoses, except for:

1. Cervical carcinoma of Stage 1B or less.

2. Adequately resected, non-metastatic basal cell or squamous cell skin carcinoma.

3. Non-invasive, superficial bladder cancer.

4. Prostate cancer with a current PSA level <0.1 ng/mL.

5. Patients with a malignancy that has been treated with curative intent will also be enrolled if that malignancy is in remission prior to first dose of epcoritamab

• Known clinically significant cardiovascular disease
• Patients with the following active infection(s) could have increased risks for toxicity if treated with bispecific antibody therapy, thus patient will be excluded if:

1. Positive serologic or PCR test results for acute or chronic HBV infection. Patients whose HBV infection status cannot be determined by serologic test results (www.cdc.gov/hepatitis/hbv/pdfs/serologicchartv8.pdf) must be negative for HBV by PCR to be eligible for study participation. Patients with a history of hepatitis B who are negative for HBV by PCR, will not be excluded but will be placed on suppressive antiviral therapy

2. Acute or chronic HCV infection. Patients who are positive for HCV antibody must be negative for HCV by PCR to be eligible for study participation. Patients with a history of hepatitis C who have been adequately treated (negative PCR) will not be excluded.

3. Positive serologic or RT-PCR test results for HIV infection.

• Known active bacterial, viral, fungal, mycobacterial, parasitic, or other infection (excluding fungal infections of nail beds) at study enrollment, or any major documented infection requiring treatment with IV antibiotics or hospitalization within 2 weeks of enrollment. Empiric or prophylactic antibiotics administered during neutropenia or neutropenic fever without microbiologic evidence of infection do not exclude patients.
• Clinically significant pulmonary disease (e.g., bronchospasm and/or obstructive pulmonary disease) that requires chronic oxygen or corticosteroid use > 20 mg mg/day prednisone or equivalent
• Uncontrolled seizure disorder
• Exposure to live or live attenuated vaccine within 4 weeks prior to signing ICF
• Pregnancy or breast feeding
• Any serious medical condition or abnormality in clinical laboratory tests that, in the investigator's judgment, precludes the patient's safe participation in and completion of the study, or which could affect compliance with the protocol or interpretation of results

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Genmab

INDUSTRY

Sponsor Role: collaborator

Abramson Cancer Center at Penn Medicine

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Elise Chong, MD

Role: PRINCIPAL_INVESTIGATOR

Abramson Cancer Center at the University of Pennsylvania

Locations

Abramson Cancer Center at the University of Pennsylvania

Philadelphia, Pennsylvania, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Brittany Koch

Role: CONTACT

Brittany.Koch@pennmedicine.upenn.edu

215-776-5548

Kaitlin Kennard

Role: CONTACT

Kaitlin.Kennard@pennmedicine.upenn.edu

Facility Contacts

Brittany Koch

Role: primary

Brittany.Koch@pennmedicine.upenn.edu

215-776-5548

Kaitlin Kennard

Role: backup

Kaitlin.Kennard@pennmedicine.upenn.edu

Other Identifiers

IRB#855865

Identifier Type: OTHER

Identifier Source: secondary_id

UPCC 03424

Identifier Type: -

Identifier Source: org_study_id