Efficacy and Safety of SHR0302 in Patients With Relapsed/Refractory Peripheral T/NK Cell Lymphoma
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Incidence and severity of AEs and SAEs
研究概览
简要总结
This is a non-randomized, open-label, Phase 1b clinical study to evaluate the safety, tolerability and anti-tumor efficacy of SHR0302 as monotherapy in patients with relapsed/refractory peripheral T/NK cell lymphoma. Around 7-18 patients will be subsequently enrolled into 3 different dose ascending cohorts. Additional 12-18 patients may be enrolled to further explore a selected dose defined by dose escalation cohorts.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 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
- •Pathologically confirmed T or NK cell lymphoma at the enrolling institution;
- •Measurable disease;
- •Relapse or refractory disease after at least 1 systemic therapy;
- •Eastern Cooperative Oncology Group (ECOG) Performance Status of 0, 1, or 2 ；
- •With a life expectancy of ≥12 weeks;
- •Adequate bone marrow reserve and organ system functions;
- •Women of Childbearing Potential (WOBCP) must undergo a serum pregnancy test within seven days before the first medication and the results are negative. WOBCP or men and their WOBCP partners should agree to take effective contraceptive measures from the signing of ICF until 180 days after the last dose of the study drug is used;
- •Willing to provide written informed consent.
排除标准
- •Patient has undergone an allogeneic stem cell transplant. Or patient had autologous stem cell transplant within 6 months;
- •Any unsolved toxicity > Common Terminology Criteria for Adverse Events (CTCAE) grade 1 from previous anti-cancer therapy (except alopecia);
- •Central nervous system (CNS) or leptomeningeal lymphoma;
- •received any antitumor therapy within 28 days prior to the first drug use, or the first dose was given within five half-lives of the previous antitumor drug, whichever is shorter;
- •Major surgical procedures were performed within 28 days before the first dose of study treatment, or surgery was planned during the study period;
- •Diagnosed with any other malignancies ≤5 years prior to the first dose, early tumors cured after radical treatment were evaluated by PI and considered for exclusion or not;
- •History of psychotropic substance abuse or drug use;
- •Previous history of allergy to the investigational drug or its excipients;
- •Severe cardiovascular disease;
- •Significant impairment of lung function;
- •Active infections;
- •Pregnant or lactation;
- •Known GI disease or GI procedure that could interfere with the oral absorption of oral medications, including not well controlled refractory nausea, vomiting, chronic gastrointestinal disorders, or capsule swallowing difficulties, or prior surgical resection of intestinal segments;
- •Concomitant disease or condition that could interfere with the conduct of the study, or that would, in the opinion of the investigator, pose an unacceptable risk to the subject in this study.
研究组 & 干预措施
SHR0302 Group A
干预措施: SHR0302 (Drug)
SHR0302 Group B
干预措施: SHR0302 (Drug)
SHR0302 Group C
干预措施: SHR0302 (Drug)
结局指标
主要结局
Incidence and severity of AEs and SAEs
时间窗: The first dose until 30 days after last dose
To evaluate the safety and tolerability of SHR0302 in patients with PTCL in terms of AEs and SAEs as Assessed by CTCAE v5.0
RP2D
时间窗: Up to 30 days after the first dose
The RP2D is defined as the dose level chosen for phase II study, based on safety, tolerability, efficacy, collected during the dose escalation study of SHR0302.
次要结局
未报告次要终点