Glofit and Obin in Follicular Lymphoma and Marginal Zone Lymphoma

NCT ID: NCT05783596

Last Updated: 2025-09-17

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 47 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-07-18
• Study Completion Date: 2029-03-31

Brief Summary

The purpose of this study is to determine how effective and safe the combination of glofitamab and obinutuzumab is in treating patients with Follicular Lymphoma (FL) and Marginal Zone Lymphoma (MZL) who have not received other treatments for their lymphoma.

The names of the study drugs involved in this study are:

• Glofitamab (a type of immunotherapy)
• Obinutuzumab (a type of immunotherapy)

Detailed Description

This is an open-label, multicenter, phase II study to evaluate the efficacy and safety of obinutuzumab and glofitamab for patients with untreated follicular lymphoma (FL) or marginal zone lymphoma (MZL). Obinutuzumab and Glofitamab use the immune system to target and attack cancer cells.

The research study procedures include screening for eligibility, study treatment visits, bone marrow biopsies, blood tests, Computerized Tomography (CT) scans, and Positron Emission Tomography (PET) scans.

The U.S. Food and Drug Administration (FDA) has not approved glofitamab as a treatment for any disease.

The U.S. FDA has approved obinutuzumab in combination with chemotherapy for patients with follicular lymphoma.

Participants will receive study treatment for approximately 9 months and will be followed for 10 years.

It is expected that about 45-50 people will take part in this research study.

Genentech and Roche are supporting this research study by providing the study drugs, glofitamab and obinutuzumab, and funding for the study.

Conditions

Follicular Lymphoma; Marginal Zone Lymphoma; Indolent Non-hodgkin Lymphoma

Study Design

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

Study Groups

Obinutuzumab + Glofitamab for Follicular Lymphoma

Participants will undergo study procedures as outlined:

• Imaging scans (CT or PET) at screening and after cycles 3, 7, and 12 of treatment.
• Bone marrow biopsy at baseline.
• Cycle 1

• Days -21, -14, -7, 0 of 36 day cycle: Predetermined dose of Obinutuzumab.
• Days 1 and 8 of 36 day cycle: Predetermined dose of Glofitamab. (First dose will be administered in the hospital.)
• Cycles 2 - 12:

o Day 1 of 21 day cycle: Predetermined dose of Glofitamab.

• Bone marrow biopsy within 2 weeks of end of treatment.
• Imaging scans (CT or PET) at 12, 18, and 24 months after treatment initiation.
• Follow up visits up to 5 years after treatment completion.

Group Type: EXPERIMENTAL

Obinutuzumab

Intervention Type: DRUG

Humanized glycoengineered type II anti-CD20 monoclonal antibody, via IV infusion.

Glofitamab

Intervention Type: DRUG

T-cell bispecific humanized monoclonal antibody, via IV infusion.

Obinutuzumab + Glofitamab for Marginal Zone Lymphoma

Participants will undergo study procedures as outlined:

• Imaging scans (CT or PET) at screening and after cycles 3, 7, and 12 of treatment.
• Bone marrow biopsy at baseline.
• Cycle 1

• Days -21, -14, -7, 0 of 36 day cycle: Predetermined dose of Obinutuzumab.
• Days 1 and 8 of 36 day cycle: Predetermined dose of Glofitamab. (First dose will be administered in the hospital.)
• Cycles 2 - 12:

o Day 1 of 21 day cycle: Predetermined dose of Glofitamab.

• Bone marrow biopsy within 2 weeks of end of treatment.
• Imaging scans (CT or PET) at 12, 18, and 24 months after treatment initiation.
• Follow up visits up to 5 years after treatment completion.

Group Type: EXPERIMENTAL

Obinutuzumab

Intervention Type: DRUG

Humanized glycoengineered type II anti-CD20 monoclonal antibody, via IV infusion.

Glofitamab

Intervention Type: DRUG

T-cell bispecific humanized monoclonal antibody, via IV infusion.

Interventions

Obinutuzumab

Humanized glycoengineered type II anti-CD20 monoclonal antibody, via IV infusion.

Intervention Type: DRUG

Glofitamab

T-cell bispecific humanized monoclonal antibody, via IV infusion.

Intervention Type: DRUG

Other Intervention Names

RO5072759, GA101, GAZYVA, GAZYVARO; RO7082859

Eligibility Criteria

Inclusion Criteria

• Histologically confirmed diagnosis of either FL (grade 1-3A) or MZL (any subtype) with review of the diagnostic pathology specimen at one of the participating institutions. Patients with active histologic transformation are excluded.
• No prior systemic therapy for FL or MZL. Prior treatment with radiation therapy or short course steroids is allowed.
• Meets at least one criterion to begin treatment based on the modified GELF criteria:

• Symptomatic adenopathy
• Organ function impairment due to disease involvement, including cytopenias due to marrow involvement (WBC <1.5x109/L; absolute neutrophil count [ANC] <1.0x109/L, Hgb <10g/dL; or platelets <100x109/L)
• Constitutional symptoms
• Maximum diameter of disease > 7cm
• >3 nodal sites of involvement
• Risk of local compressive symptoms
• Splenomegaly (craniocaudal diameter > 16cm on CT imaging)
• Clinically significant pleural or peritoneal effusion
• Leukemic phase (>5x109/L circulating malignant cells)
• Rapid generalized disease progression
• Renal infiltration
• Bone lesions
• Patients cannot be in need of urgent cytoreductive chemotherapy in the opinion of the treating investigator.
• Eastern Cooperative Oncology Group (ECOG) performance status of 0-2. (Appendix A)
• Age ≥18 years.
• Adequate hematologic and organ function:

• Absolute neutrophil count > 1.0x109/L unless due to marrow involvement by lymphoma in which case ANC must be >0.5x109/L
• Platelets > 75 x109/L, unless due to marrow involvement by lymphoma, in which case platelets must be >50 x109/L
• Creatinine clearance > 40ml/min (by Cockcroft-Gault Formula)
• Total bilirubin < 1.5 X ULN, unless Gilbert syndrome, in which case direct bilirubin must be < 1.5 x ULN
• AST/ALT < 2.5 X ULN, unless documented liver involvement by lymphoma, in which case AST/ALT must be <5 x ULN
• Ability to understand and the willingness to sign a written informed consent document.
• Willingness to provide a pre-treatment tumor sample by core needle or excisional surgical biopsy. A fresh biopsy is strongly encouraged, but an archival sample is acceptable if the following provisions are met: 1) availability of a tumor-containing formalin-fixed, paraffin-embedded (FFPE) tissue block, 2) if the tumor containing FFPE tissue block cannot be provided in total, sections from this block should be provided that are freshly cut and mounted on positively-charged glass slides (SuperFrost Plus are recommended). Preferably, 25 slides should be provided; if not possible, a minimum of 15 slides is required. Exceptions to this criterion may be made with approval of the sponsor-investigator.
• Willingness to remain abstinent or to use two effective contraceptive methods that result in a failure rate of <1% per year from screening until: (a) at least 3 months after pre-treatment with obinutuzumab or 2 months after the last dose of glofitamab, whichever is longer, if the patient is a male or (b) until at least 18 months after pre-treatment with obinutuzumab or 2 months after the last dose of glofitamab, whichever is longer, if patient is a female. Examples of contraceptive methods with a failure rate of <1% per year include:

• Tubal ligation, male sterilization, hormonal implants, established proper use of hormonal contraceptives that inhibit ovulation, hormone-releasing intrauterine devices, and copper intrauterine devices.
• Alternatively, two methods (e.g., two barrier methods such as a condom and a cervical cap) may be combined to achieve a failure rate of <1% per year. Barrier methods must always be supplemented with the use of a spermicide.

Exclusion Criteria

• Patients who require systemic immunosuppressive therapy for an ongoing medical condition will be excluded. For corticosteroids, patients receiving a prednisone dose of >10 mg daily (or equivalent) will not be eligible. A short course of steroids (up to 14 days, not exceeding 40 mg dexamethasone or equivalent in a single day) for symptom palliation is allowed, in which case patients should be off steroids at least 7 days prior to treatment start.
• Patients with bulky cervical adenopathy that is 1) compressing the upper airway or 2) in close proximity to the upper airway and could result in airway compression during a tumor flare event).
• History of severe allergic or anaphylactic reactions to monoclonal antibody therapy unless in consultation with an allergy specialist they are deemed eligible for retreatment with desensitization.
• Patients, who have had a major surgery or significant traumatic injury within 4 weeks of start of study drug, patients who have not recovered from the side effects of any major surgery (defined as requiring general anesthesia).
• Patients with known HIV infection or hepatitis B or C infection. Testing for HIV is optional. Testing for hepatitis B and C is mandatory. Patients with hepatitis B core Ab positivity but negative surface antigen and negative viral load may be enrolled if they can be treated with a prophylactic agent (e.g., entecavir); patients with hepatitis C seropositivity who have a negative viral load can also be enrolled.
• Patients with a systemic fungal, bacterial, viral, or other infection not controlled (defined as exhibiting ongoing signs/symptoms related to the infection and without improvement, despite appropriate antibiotics or other treatment).
• Prior history of another malignancy (except for non-melanoma skin cancer or in situ cervical or breast cancer) unless disease free for at least 2 years. Patients with prostate cancer (Gleason score 6-7) are allowed if PSA is less than 1 ng/mL.
• Patients should not have received immunization with lives or live attenuated vaccine within one week of study entry or during study period.
• Patients who have any severe and/or uncontrolled medical conditions or other conditions that could affect their participation in the study or limit adherence to study requirements.
• Patients with any one of the following currently on or in the previous 6 months will be excluded: myocardial infarction, congenital long QT syndrome, torsade de pointes, unstable angina, coronary/peripheral artery bypass graft, or cerebrovascular accident.
• Patients with New York Heart Association Class III or IV heart failure.
• Inability to comply with protocol mandated hospitalizations and restrictions
• Patients who are pregnant, breast-feeding, or intending to become pregnant during the study.
• Prior solid organ or allogeneic stem cell transplantation
• History of known or suspected hemophagocytic lymphohistiocytosis (HLH).
• History of autoimmune disease, 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's granulomatosis, Sjögren's syndrome, Guillain-Barré syndrome, multiple sclerosis, vasculitis, or glomerulonephritis • Patients with a remote history of, or well controlled, autoimmune disease may be eligible to enroll after consultation with the study PI.

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

Sponsors

Genentech, Inc.

INDUSTRY

Sponsor Role: collaborator

Reid Merryman, MD

OTHER

Sponsor Role: lead

Responsible Party

Reid Merryman, MD

Principal Investigator

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Reid Merryman, MD

Role: PRINCIPAL_INVESTIGATOR

Dana-Farber Cancer Institute

Locations

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States

Dana-Farber Cancer Institute

Boston, Massachusetts, United States

Columbia University Irving Medical Center

New York, New York, United States

Mount Sinai Medical Center

New York, New York, United States

Countries

United States

Other Identifiers

22-632

Identifier Type: -

Identifier Source: org_study_id