EUCTR2021-001700-15-ES进行中（未招募）1 期
A Phase 2, Open-label Study to Evaluate the Safety and Efficacy of MK-7684A (MK-7684 [Vibostolimab] with MK-3475 [Pembrolizumab] Coformulation) in Participants with Relapsed or Refractory Hematological Malignancies - A Phase 2 Study of MK-7684A in Relapsed/Refractory Hematological Malignancies
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 180
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1. Cohort A
- •a) Diagnosis of cHL, according to the WHO classification
- •b) Relapsed or refractory cHL to at least 1 prior line of therapy
- •c) Not been previously treated with an anti-PD-1 or anti-PD-L1 therapy
- •d) Diagnosis of PMBCL, according to the WHO classification
- •e) Relapsed or refractory PMBCL to at least 2 prior lines of therapies
- •f) Mus have previously received rituximab as part of prior treatment
- •g) Not been previously treated with an anti-PD-1 or anti-PD-L1 therapy
- •2. Cohort B
- •a) Diagnosis of cHL, according to the WHO classification
- •b) Relapsed or refractory cHL to at least 2 prior lines of therapies
- •c) Have progressed on treatment with an anti-PD-1/L1 mAb administered as monotherapy or with other checkpoint inhibitors or other therapies
- •d) Diagnosis of PMBCL, according to the WHO classification
- •e) Relapsed or refractory PMBCL to at least 3 prior lines of therapies
- •f) Must have previously received rituximab as part of prior treatment
- •g) Have progressed on treatment with an anti-PD-1/L1 mAb administered as monotherapy or with other checkpoint inhibitors or other therapies
- •3. Cohort C
- •a) Diagnosis of FL (all grades permitted; 1 to 3b), according to the WHO classification
- •b) Relapsed or refractory to at least 2 prior lines of therapy, chemoimmunotherapy and immunomodulatory agents
- •4. Cohort D
- •a) Diagnosis of DLBCL, according to the WHO classification. Cell of Origin is known for DLBCL, NOS, germinal center B-cell type or activated B-cell type.
- •b) Must have progressed after at least 2 lines of previous therapy, including progression after an auto-SCT, or are not a candidate for an auto-SCT
- •5. Cohort E
- •a) Histologically or cytologically confirmed diagnosis of active MM as per IMWG criteria
- •b) Measurable disease defined as meeting at least 1 of the following criteria:
- •i. Serum monoclonal protein (M-protein) levels =0.5 g/dL (=5 g/L), OR
- •ii. Urine monoclonal protein (M-protein) levels =200 mg/24 h, OR
- •iii. Abnormal serum-free light chain ratio (FLC k/l <0.26 or >1.65) with involved FLC level =100 mg/L (normal serum FLC k/l value: 0.26-1.65)
- •c) Must have undergone stem cell transplant and have relapsed after auto-SCT or have failed to achieve a CR or PR following auto-SCT, or is considered ineligible for auto-SCT
- •d) Participants must have received all regionally approved antimyeloma therapy including IMiD (pomalidomide, lenalidomide, or thalidomide), proteasome inhibitor (bortezomib, carfilzomib, or ixazomib), anti-CD38 monoclonal antibody, selenixor, and anti BCMA therapies alone or in combination.
- •e) Participants must have failed their last line of therapy
- •6. Cohort F
- •a) Have histologically confirmed diagnosis of B-cell lymphoma other than cHL, PMBCL, DLBCL, or FL, according to the WHO classification
- •b) Participants must have progressed after at least 2 lines of previous therapy
- •7. Cohorts A, B, C, D, and F (non-FDG-avid lymphoma participants):
- •a) Have measurable disease, defined as at least 1 lesion that can be accurately measured in at least 2 dimensions with spiral CT scan
- •b) Be able to provide newly obtained bone marrow biopsy material for tumor response assessment by local investigator sites
- •8. Cohort E (MM participants): Be able to provide newly obtained (within 3 months) bone marrow biopsy or aspirate material for disease assessment and submit biomarker analysis
- •9. Participants who have received CAR T-cell therapy at least 3 months before study entry and have experienced disease progression post
排除标准
- •1. For Cohort D and F (DLBCL and NHL): Has lymphoplasmacytic lymphomas, Waldenstrom’s macroglobulinema, chronic lymphocytic leukemia (not associated with small lymphocytic lymphoma), Burkitt (-like) lymphoma, mature T cell and NK cell neoplasms, immunodeficiency associated lymphoproliferative neoplasms, or histiocytic and dendritic cell neoplasms.
- •2. For Cohort E (MM):
- •a) Has oligo-secretory myeloma, plasma cell leukemia, smoldering multiple myeloma, monoclonal gammopathy of undetermined significance.
- •b) History of primary amyloidosis, hyperviscosity or POEMS syndrome (plasma cell dyscrasia with polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes).
- •3. Has known prior or current CNS involvement.
- •4. A WOCBP who has a positive urine pregnancy test within 72 hours before study intervention allocation. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.
- •5. Has clinically significant cardiovascular disease within 12 months from first dose of study intervention, including New York Heart Association Class III or IV congestive heart failure, unstable angina, myocardial infarction, cerebral vascular accident, or cardiac arrhythmia associated with hemodynamic instability.
- •6. Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the study, interfere with the participant's participation for the full duration of the study, or is not in the best interest of the participant to participate, in the opinion of the treating investigator.
- •7. Has a history of a second malignancy, unless potentially curative treatment has been completed with no evidence of malignancy for 3 years.
- •8. Has received prior therapy with an mAb blocking TIGIT or its coreceptors, or an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent or with an agent directed to another stimulatory or coinhibitory T-cell receptor (eg, CTLA-4, OX-40, CD137).
- •9. Has received prior therapy with an anti-TIGIT agent.
- •10. Any PMBCL participants in Cohort A and B that require the use of urgent cytoreductive therapy.
- •11. Has received prior systemic anticancer therapy, including investigational agents, within 2 weeks (small molecules like kinase inhibitors) or 4 weeks (chemotherapies and monoclonal antibodies) before cohort allocation.
- •12. If the participant had major surgery, the participant must have recovered adequately from the procedure and/or any complications from the surgery before starting study intervention.
- •13. Has received prior radiotherapy within 2 weeks of start of study intervention.
- •14. Has received a live or live-attenuated vaccine within 30 days before the first dose of study intervention. Administration of killed vaccines are allowed.
- •15. Is currently participating in or has participated in a study of an investigational agent or has used an investigational device within 4 weeks before the first dose of study intervention.
- •16. Known severe hypersensitivity to MK-7684A, vibostolimab or pembrolizumab and/or any of its excipients.
- •17. Has a known history of HIV infection. No HIV testing is required unless mandated by local health authority.
- •18. Has an active autoimmune disease that has required systemic treatment in past 2 years (ie, with use of disease modifying agents, corticosteroids or immunosuppressive drugs).
- •19. Has a history of (noninfectious) pneumonitis/interstitial lung disease that required steroids or has current pneumonitis/interst
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