Non-Hodgkin's Lymphoma
Conditions
Brief summary
This is a Phase I/II, multicenter, open-label, dose-escalation study designed to evaluate the efficacy, safety, tolerability and pharmacokinetics (PK) of a novel T-Cell bispecific (TCB), glofitamab, administered by intravenous (IV) infusion as a single agent and in combination with obinutuzumab, following pre-treatment with a one-time, fixed dose of obinutuzumab. This entry-into-human (EIH) study is divided in 3 parts: dose escalation (Parts I and II) and dose expansion (Part III). Single-participant dose-escalation cohorts will be used in Part I, followed by conversion to multiple participant dose-escalation cohorts (Part II), in order to define a tentative maximum tolerated dose (MTD) or optimal biological dose (OBD). The expansion cohorts (Part III) will be initiated when the tentative MTD/OBD is defined, to further evaluate the safety, PK and therapeutic activity of glofitamab.
Interventions
DRUGGlofitamab
Glofitamab will be administered at a dose and as per the schedule specified in the respective arms.
DRUGObinutuzumab
Obinutuzumab 1000 mg single dose IV infusion on Day -7; or 2000 mg single dose administered on Day -7, or split into two 1000 mg doses administered on Days -1 and -7, and per the schedule specified in the respective arms.
DRUGTocilizumab
Tocilizumab will be administered as an IV infusion, if required, for the management of severe Cytokine Release Syndrome (CRS) occurring during or after any infusion of glofitamab, as per the methods described in the Summary of Product Characteristics (SmPC) or other similar local prescribing documents.
Sponsors
Hoffmann-La Roche
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Depending upon study part, a history or status of: 1) a histologically-confirmed hematological malignancy that is expected to express cluster of differentiation (CD)20; 2) relapse after or failure to respond to at least one prior treatment regimen; and 3) no available treatment options that are expected to prolong survival (e.g., standard chemotherapy or autologous stem cell transplant \[ASCT\]) * Measurable disease, defined as at least one bi-dimensionally measurable nodal lesion, defined as \> 1.5 cm in its longest dimension, or at least one bi-dimensionally measurable extranodal lesion, defined as \> 1.0 cm in its longest dimension * Able to provide a tumor tissue pretreatment biopsy at last relapse or during screening from a safely accessible site, per investigator determination, providing the patient has more than one measurable target lesion * Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 * Life expectancy of \>/=12 weeks * AEs from prior anti-cancer therapy must have resolved to Grade less than or equal to (\</=) 1 * Adequate liver, hematological and renal function * Negative serologic or polymerase chain reaction (PCR) test results for acute or chronic Hepatitis B virus (HBV) infection * Negative test results for Hepatitis C virus (HCV) and human immunodeficiency virus (HIV) * Negative serum pregnancy test within 7 days prior to study treatment in women of childbearing potential. Women who are not of childbearing potential who are considered to be post-menopausal (at least 12 months of non-therapy amenorrhea) or surgically sterile (absence of ovaries and/or uterus) are not required to have a pregnancy test
Exclusion criteria
* Inability to comply with protocol mandated hospitalizations and restrictions * Participants with chronic lymphocytic leukemia (CLL), Burkitt lymphoma and lymphoplasmacytic lymphoma * Participants with a known or suspected history of hemophagocytic lymphohistiocytosis (HLH) * Participants with acute bacterial, viral, or fungal infection at baseline, confirmed by a positive blood culture within 72 hours prior to obinutuzumab infusion or by clinical judgment in the absence of a positive blood culture * Participants with known active infection, or reactivation of a latent infection, whether bacterial, viral, fungal, mycobacterial, or other pathogens or any major episode of infection requiring hospitalization or treatment with IV antibiotics within 4 weeks of dosing * Prior treatment with systemic immunotherapeutic agents, including, but not limited to, radio-immunoconjugates, antibody-drug conjugates, immune/cytokines and monoclonal antibodies (e.g., anti-cytotoxic T-lymphocyte-associated protein 4 \[anti-CTLA4\], anti-programmed death 1 \[anti-PD1\] and anti-programmed death ligand 1 \[anti-PDL1\]) within 4 weeks or five half-lives of the drug, whichever is shorter, before obinutuzumab infusion on Cycle 1 Day -7 * History of treatment-emergent immune-related AEs associated with prior immunotherapeutic agents * Documented refractoriness to an obinutuzumab-containing regimen * Treatment with standard radiotherapy, any chemotherapeutic agent, or treatment with any other investigational anti-cancer agent, including chimeric antigen receptor therapy (CAR-T) within 4 weeks prior to obinutuzumab infusion * Prior solid organ transplantation * Prior allogeneic stem cell transplantation (SCT) * Autologous SCT within 100 days prior to obinutuzumab infusion * Participant with history of confirmed progressive multifocal leukoencephalopathy (PML) * Current or past history of central nervous system (CNS) lymphoma * Current or past history of CNS disease, such as stroke, epilepsy, CNS vasculitis, or neurodegenerative disease. Participants with a past history of stroke that have not experienced a stroke or transient ischemic attack in the past 2 years and have no residual neurologic deficits are allowed * Evidence of significant, uncontrolled concomitant diseases that could affect compliance with the protocol or interpretation of results, including diabetes mellitus, history of relevant pulmonary disorders and known autoimmune diseases * Participants with another invasive malignancy in the last 2 years (with the exception of basal cell carcinoma and tumors deemed by the Investigator to be of low likelihood for recurrence) * Significant or extensive history of cardiovascular disease such as New York Heart Association Class III or IV or Objective Class C or D cardiac disease, myocardial infarction within the last 6 months, unstable arrhythmias, or unstable angina * Administration of a live, attenuated vaccine within 4 weeks before obinutuzumab infusion or anticipation that such a live attenuated vaccine will be required during the study * Received systemic immunosuppressive medications (including but not limited to cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-tumor necrosis factor agents) within two weeks prior to obinutuzumab infusion. Treatment with corticosteroid \</= 25 mg/day prednisone or equivalent is allowed. Inhaled and topical steroids are permitted * Any other diseases, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that would contraindicate the use of an investigational drug * 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. Participants with a remote history of, or well controlled autoimmune disease, may be eligible to enroll after consultation with the Medical Monitor * In Part III diffuse large B-cell lymphoma (DLBCL) dexamethasone cohort, participants with a history of hypersensitivity to dexamethasone or systemic corticosteroids will be excluded
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Part I and II: Percentage of Participants With Dose Limiting Toxicities (DLTs) | From Baseline up to 4 weeks |
| Part I, II and III: Percentage of Participants With Adverse Events (AEs) | From Baseline up to 90 days after last dose of study drug or until study completion or participant withdrawal (up to 5 years) |
| Part II: MTD or OBD of Glofitamab | From Baseline up to 4 weeks |
| Part II: Recommended Phase II Dose (RP2D) of Glofitamab | From Baseline up to 5 years |
| Part III: Complete Response (CR) Rate as Assessed by Independent Review Committee (IRC) According to Standard Non-hodgkin's Lymphoma (NHL) Response Criteria (Lugano Classification) | From treatment start up to 5 years |
| Part I, II and III: Area Under the Serum Concentration Versus Time Curve (AUC) of Glofitamab | At pre-defined intervals from Cycle 1 Day 1 to Day 71 |
| Part I, II and III: Maximum Serum Concentration (Cmax) of Glofitamab | At pre-defined intervals from Cycle 1 Day 1 to Day 198 |
| Part I, II and III: Minimum Serum Concentration (Cmin) of Glofitamab | At pre-defined intervals from Cycle 1 Day 1 up to Day 198 |
| Part I, II and III: Clearance (CL) of Glofitamab | At pre-defined intervals from Cycle 1 Day 1 to Day 71 |
| Part I, II and III: Volume of Distribution at Steady-state (Vss) of Glofitamab | At pre-defined intervals from Cycle 1 Day 1 to Day 71 |
| Part I, II and III: Half-life (t1/2) of Glofitamab | At pre-defined intervals from Cycle 1 Day 1 to Day 71 |
Secondary
| Measure | Time frame |
|---|---|
| Part I, II and III: Cmax of Obinutuzumab | Pre-dose of obinutuzumab on Day -7; pre-dose (Hr 0) of glofitamab on Day 1 of Cycle 1 |
| Part I, II and III: Cmin of Obinutuzumab | Pre-dose of obinutuzumab on Day -7; pre-dose (Hr 0) of glofitamab on Day 1 of Cycle 1 |
| Part I, II and III: Anti-drug Antibodies (ADA) to Glofitamab | Pre-dose of obinutuzumab on Day -7; pre-dose (Hr 0) of glofitamab on Day 1 of each cycle from Cycle 2 onwards for a maximum of 8-12 cycles, and at EOT/follow-up visit (up to 5 years) |
| Parts I and II: Percentage of Participants With Overall Response (Partial Response [PR] or Complete Response [CR]) as Determined by the Lugano Classification | From Baseline up to end of study or discontinuation due to disease progression (up to 5 years) |
| Part I, II and III: Percentage of Participants With PR or CR (Overall Response Rate [ORR]) as Determined by the Lugano Classifications | From Baseline up to end of study or discontinuation due to disease progression (up to 5 years) |
| Part I, II and III: Duration of Response (DOR) as Determined by the Lugano Classification | From first occurrence of documented objective response until disease progression, relapse or death due to any cause (up to 5 years) |
| Part I, II and III: Duration of Complete Response (DOCR) as Determined by the Lugano Classification | From the first occurrence of a documented, complete response, until the time of relapse or death from any cause (up to 5 years) |
| Part I, II and III: Progression-Free Survival (PFS) as Determined by the Lugano Classification | From first study treatment to the first occurrence of disease progression or death due to any cause (up to 5 years) |
| Overall Survival (OS) | From the time of first study treatment to death from any cause (up to 5 years) |
| Time to First Overall Response (TFOR) | From time of treatment start to first documented response (up to 5 years) |
| Time to First Complete Response (TFCR) | From treatment start to first documented complete response (up to 5 years) |
| Part III: Health Related Quality of Life (HRQoL) as Assessed by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-core 30 (EORTC QLQ-C30) | From baseline through follow-up or until disease progression (up to 5 years) |
| Part III: HRQoL as Assessed by the Functional Assessment of Cancer Therapy-lymphoma (FACT-lym) Scale | From baseline through follow-up or until disease progression (up to 5 years) |
Countries
Australia, Belgium, Canada, Czechia, Denmark, Finland, France, Italy, New Zealand, Poland, Spain, Taiwan, United States
Contacts
STUDY_DIRECTORClinical Trials
Hoffmann-La Roche
Outcome results
None listed