A Phase 1b Study to Assess the Safety and Efficacy of YY-20394 in Subjects With Recurrent and/or Refractory B-cell Hematologic Malignancies
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 43
- 试验地点
- 1
- 主要终点
- disease control rate
研究概览
简要总结
Protocol YY-20394-007 is a phase1 open-label, single-arm, multi-centre study to assess the safety and efficacy of YY-20394 in participants with relapse and/or refractory B cell malignant hematological tumor. eligible participants will initiate oral therapy with YY-20394 at a starting dose of 80mg taken once per day. treatment with YY-20394 can continue in compliant participants as long as the study is still ongoing and the participants appear to benefiting from treatment with acceptable safety.
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
- •histologically or cytologically confirmed relapse and/or refractory B cell hematologic malignancies(Excluding follicular lymphoma)
- •prior treatment with ≥1 prior standard anti-tumor regimens and 2 courses of treatments at least
- •eastern cooperative oncology group performance status of 0 to 2
- •life expectancy of at least 3 months
- •presence of >1.5cm radiographically measurable lymphadenopathy or extranodal lymphoid malignancy, and legibility in two vertical directions
- •acceptable organ functions
- •discontinuation of all other antitumor therapies before the first drug dose administration
- •for men and women of childbearing potential, willingness to abstain from sexual intercourse or employ an effective method of contraception during the study drug administration and follow-up six periods
- •willingness and ability to provide written informed consent and to comply with the protocol requirements
排除标准
- •prior therapy with PI3K-delta inhibitors（except the intolerable subjects）
- •the dosage of steroid hormone(predisone equivalent) was greater than 20mg/d, and lasted for more than 14 days
- •medical condition of difficulty in swallowing, malabsorption, or other chronic gastrointestinal disease, or conditional that may hamper compliance and/or absorption of the investigational product
- •concurrent drugs which maybe prolong the QT during the study period
- •subjects with central nervous system metastasis
- •Prior or current medical condition of pulmonary fibrosis, interstitial pneumonia, pneumoconiosis, radiation pneumonia, drug-related pneumonia, severe impairment of lung function, etc
- •active, uncontrolled bacterial, viral, or fungal infections, requiring systemic therapy
- •known history of chronic active hepatitis B infection, chronic active hepatitis C
- •known history of immunodeficiency, including HIV positive test, other acquired or congenital immunodeficiency disorders, organ transplantation or allogeneic bone marrow transplantation
- •autologous hematopoietic stem cell transplantation was received within 90 days before the first dose administration
- •prior or ongoing heart disease, including: angina pectoris, clinically significant arrhythmia, myocardial infarction, heart failure, and any other heart disease judged by the researchers not eligible to the study
- •pregnancy or breastfeeding
- •prior or ongoing clinically significant illness, medical condition, surgical history, physical finding, or laboratory abnormality that, in the investigator's opinion, could affect the safety of the participant or impair the assessment of study results
- •receiving granulocyte colony-stimulating factor(GCSF) or blood transfusion within seven days before screening
- •history of a non-lymphoma malignancy except for adequately treated local basal cell carcinoma of the skin and cervical carcinoma in situ
- •subjects, in the opinion of the the Investigator, who are unsuitable to participate in the study for any other reason.
研究组 & 干预措施
YY-20394
treatment with YY-20394 will be continued until tumor progression or development of unacceptable toxicity.
干预措施: YY-20394 (Drug)
结局指标
主要结局
disease control rate
时间窗: Throughout the study for approximately 2 years
the percentage of participants achieving a complete response or partial response or stable disease
Adverse events evaluated by NCI CTCAE V5.0
时间窗: Throughout the study for approximately 2 years
incidence of adverse events and associated dose of YY-20394
Overall response rate
时间窗: Throughout the study for approximately 2 years
the percentage of participants achieving a complete response or partial response
次要结局
未报告次要终点