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A Study of CN1 in Combination With CN401 in Adult Patients With Relapsed/Refractory Lymphoid Malignancies

An Open-label, Multi-centre, Phase I/II Study to Investigate the Safety, Tolerability, and Preliminary Efficacy of CN1 in Combination With CN401 in Adult Patients With Relapsed/Refractory Lymphoid Malignancies

The study is designed to investigate the safety, tolerability and preliminary efficacy in combination with CN1 and CN401 in adult patients with relapsed/refractory lymphoid malignancies.

研究概览

详细说明

This is an open-label, multi-center, phase I/II study. The study includes two study drugs CN1 and CN401 and will be conducted in two parts: phase 1 and phase 2.

Phase I: Dose-finding study for the assessment of dose limiting toxicities (DLTs) at 3 or more dose levels in patients with advanced lymphoid malignancies.

Phase II: Expansion study to evaluate the preliminary efficacy of CN1 in combination with CN401 at the RP2D in parallel patient cohorts grouped by non-Hodgkin's Lymphoma (NHL) subtype.

There will 9-18 patients enrolled in the Phase 1 portion of the study and 15- 60 patients will be enrolled in Phase 2 - dosing determined by Phase 1.

研究类型

介入性

注册 (实际的)

7

阶段

  • 阶段2
  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Victoria
      • Bentleigh、Victoria、澳大利亚、3168
        • Monash Health - Monash Medical Centre

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Age ≥ 18 years on the day of signing informed consent.
  2. Based on pathology review at the local institution, using the most recent edition of the World Health Organization (WHO) Classification of Tumors of Hematopoietic and Lymphoid Tissues as guidance, leading to the diagnosis of one of the following diseases and their histological subtypes: PTCL, CTCL, and B-cell NHL.
  3. Patients must have relapsed or refractory disease after at least one prior systemic anti-tumor treatment.
  4. The patients enrolled in Phase II of the study should have received NOT more than five lines of prior systemic therapies.
  5. Patients must have at least one evaluable lesion per Lugano 2014 Criteria. Measurable lesions are defined as those that can be accurately measured in at least two dimensions with conventional techniques (positron emission tomography/Computed tomography [PET/CT], magnetic resonance imaging [MRI]) or as > 1.5 cm with spiral CT scan. Patients with non-measurable lesions but assessable diseases (e.g., marrow disease without other radiographically measurable diseases) may be enrolled on a case-by-case basis in discussion with the Sponsor.
  6. ECOG performance status 0 to 2.
  7. At least 3 months of expected survival.
  8. Adequate organ functions, further defined as:

    • Hemoglobin ≥ 9 g/dL.
    • Absolute neutrophil count (ANC) ≥ 1 × 10E+09/L.
    • Platelets ≥ 50 × 10E+09/L (patient without bone marrow [BM] involvement) and ≥ 30 × 10E+09/L (patient with BM involvement).
    • Total bilirubin ≤ 1.5 times the upper limit of normal (ULN).
    • Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5 × ULN if known liver involvement. The ALT and AST should be ≤ 1.5 × ULN in absence of liver involvement/metastasis.
    • Serum creatinine ≤ 2.0 mg/dL or calculated creatinine clearance ≥ 50 mL/min (as calculated by the Cockcroft-Gault method).
    • Activated partial thromboplastin time (APTT) or international normalized ratio (INR) ≤ 1.5 × ULN (unless patient is receiving anticoagulants).

Exclusion Criteria:

  1. Received any anti-tumour treatment (i.e., chemotherapy, radiotherapy, immunotherapy, biologic therapy, endocrine therapy, etc.,) within four weeks (or five half-lives of the agent, whichever is shorter) prior to the first dose of study drugs, with the following exceptions:

    1. Palliative radiation therapy within 2 weeks.
    2. Oral small molecule targeted therapies within 2 weeks prior to the first dose of study drugs or within 5 half-lives of the drug, whichever is shorter.
    3. Herbal medications within 7 days prior to the first dose.
  2. Received other investigational agents (not yet approved by any regulatory agency) within four weeks prior to the first dose of any study drugs.
  3. Immunosuppressive medication > 10 mg prednisolone per day or equivalent within 14 days prior to the first dose of the study drug. Note: Use of immunosuppressive medications as prophylaxis in subjects with contrast allergies are acceptable. In addition, temporary uses of corticosteroids considered non-clinically significant may be approved on a case-by-case basis in discussion with the Sponsor.
  4. Known clinically active central nervous system (CNS) or meningeal involvement. In the absence of symptoms, investigation into CNS involvement is not required. Patients are eligible if metastases have been treated, patients are neurologically returned to baseline or neurologically stable for at least four weeks and not requiring steroid therapy for at least one week prior to Cycle 1 Day 1.
  5. Active infection and in current need of, or likely to need, intravenous (IV) anti-infective therapy.
  6. History of immunodeficiency, including history of any positive test result for human immunodeficiency virus (HIV) antibody.
  7. Patients who are known to be hepatitis B or C positive (positive HBsAg and/or detectable level of HBV DNA or positive HCV antibody).
  8. Active Epstein Barr virus (EBV) unrelated to underlying lymphoma (positive serology for anti-EBV VCA IgM antibody and negative for anti-EBV EBNA IgG antibody, or clinical manifestations and positive EBV polymerase chain reaction [PCR] consistent with active EBV infection).
  9. Active CMV (positive serology for anti-CMV IgM antibody, negative for anti-CMV IgG antibody, and positive CMV PCR with clinical manifestations consistent with active CMV infection) and requiring therapy.
  10. Current history of a serious uncontrolled medical disorder, metabolic dysfunction, physical examination findings, or clinical laboratory findings giving reasonable suspicion of a disease or condition that contraindicates use of an investigational drug or render the patient at high risk from treatment complications.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:非随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:A (CN1 0.5mg/kg and CN401 400mg)

Patients were administered with CN1, 0.5mg/kg, once every three week in combination with 400mg CN401 twice a day, fasted.

Dosage/Route of admin: CN1- Intravenous Infusion(IV); CN401- Tablet, Oral

Three to six patients are expected to be enrolled in each arm.

CN1(0.5mg/kg) will be administered on Day 1 of each cycle (once every three weeks) for up to 12 months and CN401(400mg) will be administered orally twice daily.
实验性的:B (CN1 1mg/kg and CN401 600mg)

Patients were administered with CN1, 1mg/kg, once every three week in combination with 600mg CN401 twice a day, fasted.

Dosage/Route of admin: CN1- Intravenous Infusion(IV); CN401- Tablet, Oral

Three to six patients are expected to be enrolled in each arm

CN1(1mg/kg) will be administered on Day 1 of each cycle (once every three weeks) for up to 12 months and CN401(600mg) will be administered orally twice daily.
实验性的:C (CN1 1mg/kg and CN401 800mg)

Patients were administered with CN1, 1mg/kg, once every three week in combination with 800mg CN401 twice a day, fasted.

Dosage/Route of admin: CN1- Intravenous Infusion(IV); CN401- Tablet, Oral

Three to six patients are expected to be enrolled in each arm

CN1(1mg/kg) will be administered on Day 1 of each cycle (once every three weeks) for up to 12 months and CN401(800mg) will be administered orally twice daily.
实验性的:D (CN1 3mg/kg and CN401 800mg)

Patients were administered with CN1, 3mg/kg, once every three week in combination with 800mg CN401 twice a day, fasted.

Dosage/Route of admin: CN1- Intravenous Infusion(IV); CN401- Tablet, Oral

Three to six patients are expected to be enrolled in each arm

CN1(3mg/kg) will be administered on Day 1 of each cycle (once every three weeks) for up to 12 months and CN401(800mg) will be administered orally twice daily.
实验性的:E (CN1 10mg/kg and CN401 800mg)

Patients were administered with CN1, 10mg/kg, once every three week in combination with 800mg CN401 twice a day, fasted.

Dosage/Route of admin: CN1- Intravenous Infusion(IV); CN401- Tablet, Oral

Three to six patients are expected to be enrolled in each arm

CN1(10mg/kg) will be administered on Day 1 of each cycle (once every three weeks) for up to 12 months and CN401(800mg) will be administered orally twice daily.

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
To evaluate the safety and tolerability of CN1 in combination with CN401 in patients with relapsed/refractory lymphoid malignancies through Incidence of Treatment-Emergent Adverse Events as assessed by CTCAE v5.0
大体时间:Measurements at Baseline till completion of last safety visit (270 days)
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Measurements at Baseline till completion of last safety visit (270 days)
To determine maximum tolerated dose and/or Recommended Phase II Dose (RP2D) of CN1 in combination with CN401
大体时间:DLT assessed within 21 days after the first dose
Measured by Incidence of dose limiting toxicities (DLT) during the first cycle of treatment with CN1 in combination with CN401.
DLT assessed within 21 days after the first dose
To assess the change in anti-tumor activity of CN1 in combination with CN401 through Objective Response Rate analysis
大体时间:Baseline to End of the Treatment assessed up to an average of 1 year
Measured/determined by Objective Response Rate
Baseline to End of the Treatment assessed up to an average of 1 year

次要结果测量

结果测量
措施说明
大体时间
To further evaluate the safety and tolerability of CN1 in combination with CN401 in patients with relapsed/refractory lymphoid malignancies through Incidence of Treatment-Emergent Adverse Events as assessed by CTCAE v5.0
大体时间:Measurements at Baseline till completion of last safety visit (270 days)
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Measurements at Baseline till completion of last safety visit (270 days)
To evaluate safety and tolerability of CN1 and CN401 in patients with relapsed/refractory lymphoid malignancies through vital signs as assessed by heart rate
大体时间:Baseline to End of the Treatment assessed up to an average of 1 year
Measured by vital sign as assessed by heart rate
Baseline to End of the Treatment assessed up to an average of 1 year
To evaluate safety and tolerability of CN1 and CN401 in patients with relapsed/refractory lymphoid malignancies through vital signs as assessed by respiratory rate
大体时间:Baseline to End of the Treatment assessed up to an average of 1 year
Measured by vital sign as assessed by respiratory rate
Baseline to End of the Treatment assessed up to an average of 1 year
To evaluate safety and tolerability of CN1 and CN401 in patients with relapsed/refractory lymphoid malignancies through vital signs as assessed by body temperature
大体时间:Baseline to End of the Treatment assessed up to an average of 1 year
Measured by vital sign as assessed by body temperature
Baseline to End of the Treatment assessed up to an average of 1 year
To evaluate safety and tolerability of CN1 and CN401 in patients with relapsed/refractory lymphoid malignancies through vital signs as assessed by pulse, systolic blood pressure, and diastolic blood pressure
大体时间:Baseline to End of the Treatment assessed up to an average of 1 year
Measured by vital sign as assessed by pulse, systolic blood pressure, and diastolic blood pressure
Baseline to End of the Treatment assessed up to an average of 1 year
To characterize the pharmacokinetics of CN1 and CN401 when administered in combination through Area under the under the drug concentration-time curve.
大体时间:Baseline to End of the Treatment assessed up to an average of 1 year
The following parameter is used for evaluation during PK assessments: Area under the drug concentration-time curve (AUC(0-last), AUC0-inf, AUCtau)
Baseline to End of the Treatment assessed up to an average of 1 year
To characterize the pharmacokinetics of CN1 and CN401 when administered in combination through Cmax and Tmax.
大体时间:Baseline to End of the Treatment assessed up to an average of 1 year
The following parameter is used for evaluation during PK assessments: Maximum concentration (Cmax) and Time to maximum concentration (Tmax)
Baseline to End of the Treatment assessed up to an average of 1 year
To characterize the pharmacokinetics of CN1 and CN401 when administered in combination through Apparent terminal half-life (t½).
大体时间:Baseline to End of the Treatment assessed up to an average of 1 year
The following parameter is used for evaluation during PK assessments: Apparent terminal half-life (t½)
Baseline to End of the Treatment assessed up to an average of 1 year
To characterize the pharmacokinetics of CN1 and CN401 when administered in combination through Apparent terminal elimination rate constant (Kel).
大体时间:Baseline to End of the Treatment assessed up to an average of 1 year
The following parameter is used for evaluation during PK assessments: Apparent terminal elimination rate constant (Kel)
Baseline to End of the Treatment assessed up to an average of 1 year
To characterize the pharmacokinetics of CN1 and CN401 when administered in combination through Apparent clearance.
大体时间:Baseline to End of the Treatment assessed up to an average of 1 year
The following parameter is used for evaluation during PK assessments: Apparent clearance (CL/F and CL/Fss)
Baseline to End of the Treatment assessed up to an average of 1 year
To characterize the pharmacokinetics of CN1 and CN401 when administered in combination through Accumulation ration.
大体时间:Baseline to End of the Treatment assessed up to an average of 1 year
The following parameter is used for evaluation during PK assessments: Accumulation ration (RA)
Baseline to End of the Treatment assessed up to an average of 1 year
To characterize the pharmacokinetics of CN1 and CN401 when administered in combination through Apparent terminal volume of distribution.
大体时间:Baseline to End of the Treatment assessed up to an average of 1 year
The following parameter is used for evaluation during PK assessments: Apparent clearance (Vz/F and Vz/Fss)
Baseline to End of the Treatment assessed up to an average of 1 year
To further assess change in anti-tumor activity of CN1 in combination with CN401 through ORR
大体时间:Baseline to End of the treatment visit assessed up to an average of 1 year
Measured/determined by Objective Response Rate
Baseline to End of the treatment visit assessed up to an average of 1 year

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Jake Shortt、Monash Health

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2021年7月28日

初级完成 (实际的)

2022年8月29日

研究完成 (实际的)

2022年9月30日

研究注册日期

首次提交

2021年4月14日

首先提交符合 QC 标准的

2021年5月6日

首次发布 (实际的)

2021年5月10日

研究记录更新

最后更新发布 (实际的)

2022年10月24日

上次提交的符合 QC 标准的更新

2022年10月20日

最后验证

2022年10月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • CN1-201

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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