Evaluating Ivonescimab in PD-1 Resistant Recurrent or Metastatic Nasopharyngeal Carcinoma (AK112)
Phase II Open-label Study Evaluating Ivonescimab in PD-1 Resistant Recurrent or Metastatic Nasopharyngeal Carcinoma
研究概览
详细说明
Participants will receive intravenous ivonescimab at a dose of 20 mg/kg administered every 3 weeks until disease progression, intolerable toxicities, or withdrawal from the study. All study treatments will be administered in an outpatient setting.
Participants will undergo clinical assessments every 3 weeks during the treatment period. Imaging assessments will be conducted every 6 weeks (±7 days) for the first 24 weeks of treatment, followed by every 9 weeks (±7 days) thereafter, continuing until treatment discontinuation.
研究类型
注册 (估计的)
阶段
- 阶段2
联系人和位置
学习联系方式
- 姓名:Wan Qin Chong
- 电话号码:+65 69082222
- 邮箱:wan_qin_chong@nuhs.edu.sg
学习地点
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Singapore、新加坡
- National University Cancer Institute, Singapore, National University Health System
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接触:
- Wan Qin Chong
- 电话号码:69082222
- 邮箱:wan_qin_chong@nuhs.edu.sg
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
Participant is eligible to be included in the study only if all the following criteria are met:
- The participant (or legally acceptable representative if applicable) provides written consent for the trial.
- Participant is at least 21 years of age on the day of signing informed consent
- Has a locally or centrally determined histologically or cytologically confirmed diagnosis of Epstein Barr Virus (EBV)-positive nasopharyngeal carcinoma Note: The EBV status is to be determined by the EBV-encoded small RNA in situ hybridization (EBER in situ hybridization [ISH]) assay. If EBV-positive status has been previously determined by EBER ISH assay, then no re-testing is required. If EBV status by EBER ISH assay has not been previously determined, tumour tissue from archival tissue may be submitted for EBV determination.
- Has recurrent or metastatic (R/M) disease not amenable to curative local therapy (surgery or radiation)
- Must have seen at least 1 prior line of systemic treatment and has progressed on prior platinum-based chemotherapy and anti-PD1 therapy in the R/M setting OR Progressed within 6 months of previous multimodal therapy containing platinum-based chemotherapy and anti-PD1 therapy in the locally advanced setting.
- Has measurable disease based on iRECIST.
- Has an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- Has an adequate organ function as defined in the following table (table 1). Specimens must be collected within 10 days prior to the start of study treatment
- Willing to provide blood and tumour tissue samples (newly obtained biopsy if clinically feasible or archival specimen) to support exploratory biomarker analysis.
Exclusion Criteria:
Participant is excluded from the study if ANY of the following criteria apply:
- Is currently participating in or has participated in a study of an investigational agent or has used an investigational device within 4 weeks prior to first dose of study treatment.
- Has prior anti-angiogenic therapy in the R/M setting or within 6 months as part of multimodality therapy in the locally advanced setting. [Applies to cohort A only]
- Has tumour that encases major arteries which in the opinion of the investigator carries high risk of vessel wall dehiscence.
Has a condition requiring systemic steroid therapy (> 10 mg daily prednisone equivalents) or any other form of immunosuppressive therapy within 14 days prior to the first dose of trial treatment.
Note: Inhaled or topical steroids and adrenal replacement doses <10 mg daily prednisone equivalents are permitted in the absence of active autoimmune disease. Patients are permitted to use topical, ocular, intra-articular, intranasal, and inhalational corticosteroids (with minimal systemic absorption). Physiologic replacement doses of systemic corticosteroids are permitted if < or = 10 mg/day prednisone equivalents. A brief course of corticosteroids for prophylaxis (e.g., contrast dye allergy) or for treatment of non-autoimmune conditions (e.g., delayed-type hypersensitivity reaction caused by contact allergen) is permitted.
Has active autoimmune disease that has required systemic treatment in the past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs).
Note: Replacement therapy (e.g. thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc) is not considered a form of systemic treatment.
- Has a history of (non-infectious) pneumonitis that required steroids or has current pneumonitis.
- Has hypersensitivity to ivonescimab or any of its components.
Has a known additional malignancy that is progressing or has required active treatment within the past 3 years.
Note: Participants with basal cell carcinoma of the skin, squamous cell carcinoma of the skin, transitional cell carcinoma of urothelial cancer, or carcinoma in situ (e.g. breast or cervical carcinoma in situ) that have undergone potentially curative therapy are not excluded.
- Has an active infection requiring systemic therapy, or serious non-healing wound, ulcer or bone fracture.
- Uncontrolled hypertension (failure of diastolic blood pressure to fall below 90 mmHg, despite the use of ≥ 3 anti-hypertensive drugs or systolic blood pressure greater than 150 mmHg).
Recent cardiovascular thromboembolic event, such as the following:
- Cardiac chest pain, defined as moderate pain that limits instrumental activities of daily living, ≤ 4 weeks before enrolment
- Symptomatic pulmonary embolism ≤ 4 weeks before enrolment
- Any history of acute myocardial infarction ≤ 6 months before enrolment
- Any history of heart failure meeting New York Heart Association (NYHA) Classification III or IV (Appendix 4) ≤ 6 months before enrolment
- Any event of ventricular arrhythmia ≥ Grade 2 in severity ≤ 6 months before enrolment
- Any history of cerebrovascular accident ≤ 6 months before enrolment
- Persistent proteinuria of NCI-CTCAE Grade 3 or higher (> 3.5 g/24 hours, measured by urine protein/creatinine ratio on a random urine sample).
- Clinically significant bleeding (NCI-CTCAE Grade 3 or higher) within 30 days prior to start of study medication.
- Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator.
- Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
- Is pregnant, breastfeeding or expecting to conceive or father children within the projected duration of the trial, starting with the screening visit through 120 days after the last dose of trial treatment.
A woman of childbearing potential (WOCBP) who has a positive urine pregnancy test within 72 hours prior to randomization/allocation (see Appendix 3). If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.
Note: If 72 hours have elapsed between the screening pregnancy test and the first dose of study treatment, another pregnancy test (urine or serum) must be performed and must be negative for subject to start receiving study medication.
- Has a known history of Human Immunodeficiency Virus (HIV). Note: No HIV testing is required unless mandated by local health authority.
Known active Hepatitis B (defined as hepatitis B viral load detected) or Hepatitis C virus (defined as HCV RNA [qualitative] detected) infection. Patients on anti-virals but with undetectable Hepatitis B or C viral loads are not excluded.
Note: No testing for Hepatitis B and Hepatitis C is required unless mandated by local health authority.
- History of having received a live virus vaccination (e.g., yellow fever, MMR, nasal flu, chicken pox or Zostavax) within 4 weeks prior to the first dose of trial treatment. Note: Seasonal influenza vaccines for injection are generally killed virus vaccines and are allowed; however intranasal influenza vaccines (e.g., Flu-Mist®) are live attenuated vaccines and are not allowed.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的:Cohort A & B
We plan to enrol 32 patients with R/M NPC and who had failed prior platinum-based chemotherapy and anti-PD1 therapy in this study from (Cohort A) and we will have an additional cohort B consisting of 10 patients with R/M NPC and who had failed prior platinum-based chemotherapy, PD1-inhibitor and anti-angiogenic therapy.
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Subjects will receive intravenous ivonescimab at a dose of 20 mg/kg administered every 3 weeks until disease progression, intolerable toxicities, or withdrawal from the study.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Objective Response Rate (ORR)
大体时间:Best response at 1 year
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Objective Response Rate (ORR), defined as the proportion of patients with a confirmed complete response (CR) or partial response (PR) as assessed by investigator review using iRECIST
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Best response at 1 year
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
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Progression-Free Survival (PFS)
大体时间:3 years
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defined as time from first dose of ivonescimab to documented disease progression or death from any cause, whichever occurs first, as assessed by iRECIST.
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3 years
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Overall Survival (OS)
大体时间:3 years
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defined as time from first dose of ivonescimab to death from any cause.
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3 years
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Duration of Response (DoR)
大体时间:3 years
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defined as time from the first documentation of objective response (Complete response or Partial response) to disease progression or death.
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3 years
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Disease Control Rate (DCR)
大体时间:3 years
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defined as the proportion of patients achieving Complete Response (CR) + Partial Response (PR) + Stable disease for at least 12 weeks.
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3 years
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Incidence, nature, and severity of adverse events (AEs) and serious adverse events (SAEs)
大体时间:from enrolment till 3 months after end of treatment
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Incidence, nature, and severity of adverse events (AEs) and serious adverse events (SAEs) graded according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5.0.
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from enrolment till 3 months after end of treatment
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Frequency and proportion of treatment-related adverse events (TRAEs)
大体时间:from enrolment till 3 months after end of treatment
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Treatment-related adverse events (TRAEs) graded according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5.0.
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from enrolment till 3 months after end of treatment
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Incidence of immune-related adverse events (irAEs)
大体时间:from enrolment till 3 months after end of treatment
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Events will be identified based on clinical assessment and investigator attribution, summarized by type, frequency, and proportion of affected participants, and graded for severity according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE), version 5.0.
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from enrolment till 3 months after end of treatment
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Rates of dose delays, modifications, or treatment discontinuations due to adverse events.
大体时间:from enrolment till 3 months after end of treatment
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Measures how many participants had their treatment delayed, adjusted, or stopped completely because of treatment side effects.
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from enrolment till 3 months after end of treatment
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合作者和调查者
调查人员
- 首席研究员:Wan Qin Chong、National University Hospital, Singapore
出版物和有用的链接
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
关键字
其他研究编号
- 2025-1970
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
Individual patient data will be available, including data dictionaries and all clinical data collected in the conduct of the trial, in a deidentified format. These will be available beginning 3 months after Article publication with no end date. other researchers should submit requests for access to the patient-level data to the corresponding author, including a proposal outlining their reasons for required data.
Following a signed data access agreement, the data will be made available by a link sent from the corresponding author to the requester.
IPD 共享时间框架
IPD 共享访问标准
IPD 共享支持信息类型
- 研究方案
- 树液
- 国际碳纤维联合会
- 分析代码
- 企业社会责任
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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