A Single-center, Open-label, Single-arm Phase Ib Clinical Study to Evaluate the Pharmacokinetics and Pharmacodynamic Characteristics of SHR-2017 Injection in Patients With Bone Metastases
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 25
- 试验地点
- 1
- 主要终点
- The pharmacodynamic parameter of SHR-2017 after administration include BALP [Time
研究概览
简要总结
To evaluate the pharmacokinetic characteristics, pharmacodynamic characteristics, safety, tolerability and immunogenicity of SHR-2017 injection in patients with bone metastases, and to evaluate the efficacy of SHR-2017 injection in the treatment of skeletal-related event and cancer pain.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Able and willing to provide a written informed consent
- •Male or female, age ≥ 18 years;
- •Solid tumors confirmed by histological or cytological examination;
- •At least 1 bone metastasis from a documented tertiary A hospital during the screening period;
- •Worst pain score NRS ≥5 points when treated with a stable analgesic regimen during the baseline assessment period;
- •Received a stable anti-tumor regimen within 28 days prior to the baseline assessment period
- •During the screening period, the physical status score of the Eastern Cooperative Oncology Group (ECOG) was 0-2 points;
- •Life expectancy judged by the investigator to be at least 6 months
- •Good organ function during the screening period (repeated testing can be confirmed if necessary);
- •Female subjects of childbearing potential with negative blood pregnancy test results within 7 days prior to the first dose of study drug and not lactating.
排除标准
- •Previous occurrence or concomitant osteomyelitis of the jaw or osteonecrosis of the jaw, dental disease or jaw disease that is active, requiring oral surgery, dental surgery or oral surgery wound that has not fully healed, or has planned invasive dental procedures during the study;
- •History of major joint trauma or surgery within 1 year prior to enrollment
- •Cardiac dysfunction Within 6 months before enrollment;
- •Resting tachycardia or resting bradycardia on ECG at screening；
- •Subjects who have evidence of orthostatic hypotension at screening；
- •Hepatitis B surface antigen (HBSAG), hepatitis C antibody (HCVAB), human immune defect antivirus (HIV) antibody, syphilis antibody;
- •The pain of the subjects not predominantly related to a bone metastasis;
- •The subject with neurological diseases and/or mental illness and/or cognitive dysfunction ；
- •Receipt of radiopharmaceutical treatment or radiotherapy for treatment of bone metastasis within 1 month of the treatment period, and the subject who received the radiotherapy within one month before the first research drug administration
- •Subject has a history of allergic or anaphylactic reaction to mammalian -based drugs, or allergies to supplements (calcium or vitamin D supplements), or have a history of allergens of opioids, or past history of treatment or diagnostic monoclonal antibody, Or other allergies;
- •The subject participated in the treatment of other clinical trials within one month before receiving the experimental drug (except for participating in other clinical trial screening losers);
- •In the judgment of the investigator, would make the subject inappropriate for entry into this study;
研究组 & 干预措施
SHR-2017
干预措施: SHR-2017 (Drug)
结局指标
主要结局
The pharmacodynamic parameter of SHR-2017 after administration include BALP [Time
时间窗: First dose up to 169 days post-dose
The pharmacodynamic parameter of SHR-2017 after administration include uNTX/uCr
时间窗: First dose up to 169 days post-dose
The Pharmacokinetic parameters of SHR-2017 after administration, including CL/F
时间窗: First dose up to 169 days post-dose
The pharmacodynamic parameter of SHR-2017 after administration include β-CTX
时间窗: First dose up to 169 days post-dose
The Pharmacokinetic parameters of SHR-2017 after administration, including Cmax
时间窗: First dose up to 169 days post-dose
The Pharmacokinetic parameters of SHR-2017 after administration, including Tmax
时间窗: First dose up to 169 days post-dose
The Pharmacokinetic parameters of SHR-2017 after administration, including t1/2
时间窗: First dose up to 169 days post-dose
The Pharmacokinetic parameters of SHR-2017 after administration, including AUC0-t
时间窗: First dose up to 169 days post-dose
The Pharmacokinetic parameters of SHR-2017 after administration, including AUC0-∞
时间窗: First dose up to 169 days post-dose
次要结局
- Average daily total opioids consumption(First dose up to 169 days post-dose])
- Change from baseline in worst pain/average pain at the designated bone metastasis pain site after dosing(First dose up to 169 days post-dose)
- Incidence of skeletal-related event(First dose up to 169 days post-dose)