Phase Ib / II Open-Label Stduy of APG-2575 Monotherapy or in Combination With Lenalidomide / Dexamethasone in Subjects With Relapsed or Refractory Multiple Myeloma
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 入组人数
- 48
- 试验地点
- 12
- 主要终点
- Dose Limiting Toxicity
研究概览
简要总结
This is a Phase Ib/II, open-label, multi-center study evaluating the safety, tolerability, efficacy, and PK/ Pharmacodynamics of APG2575 monotherapy or in combination with lenalidomide (R) and dexamethasone (d) in patients with relapsed/refractory (R/R) multiple myeloma (MM). The primary objective is to evaluate the safety and tolerability, identify dose-limiting toxicities (DLT), the maximum tolerated dose (MTD) and the recommended dose (RP2D) of APG-2575 monotherapy or in combination with Rd in Chinese R/R MM patients.
详细描述
This is a Phase Ib/II, open-label, multi-center study evaluating the safety, tolerability, efficacy, and PK/ Pharmacodynamics of APG2575 monotherapy or in combination with lenalidomide (R) and dexamethasone (d) in patients with relapsed/refractory (R/R) multiple myeloma (MM). The primary objective is to evaluate the safety and tolerability, identify dose-limiting toxicities (DLT), the maximum tolerated dose (MTD) and the recommended dose (RP2D) of APG-2575 monotherapy or in combination with Rd in Chinese R/R MM patients.
This study consists of two arms of APG-2575 single agent (arm A) and APG-2575 in combination with Rd (arm B). All subjects will receive consecutive treatment in 28-day cycles.
All subjects will continue to receive treatment until disease progression, unacceptable toxicities, or other treatment discontinuation criteria fdefined by the protocol. All subjects will complete survival follow up after treatment discontinuation until end of the study, withdrawal of informed consent, loss of follow-up, or death.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Sequential
- 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
- •≥ 18 years of age;
- •Life expectancy ≥ 6 months;
- •Eastern Cooperative Oncology Group (ECOG) ≤ 2;
- •Corrected QT interval (QTc) based on Frederica or Bazett formula ≤ ≤450ms (male)，or ≤ 470ms (female);
- •Patients with Relapsed/Refractory MM, previously treated with at least 1 prior line of therapy for MM;
- •Symptomatic MM patients with measurable disease (IMWG 2016);
- •Patients with a history of autologous HSCT must have an adequate bone marrow function and have recovered from any transplant-related toxicity, and meet a minimum of 6 months post-autologous transplant (prior to first dose).
- •Adequate hematologic function without growth factor support
- •Adequate hepatic, renal and coagulation function
- •Male and female subjects of childbearing potential who agree to use highly effective methods of birth control during the period of therapy and for 90 days after the last dose of study drug.
- •Ability to understand and voluntarily sign a written informed consent form before performing any study procedures.
- •Compliance to study procedures.
排除标准
- •monoclonal antibody therapy within 4 weeks prior to first dose; CAR-T therapy within 3 months prior to first dose; or other anti-myeloma therapy within 2 weeks prior to first dose.
- •Only Arm B:intolerance to lenalidomide.
- •Plasma cell leukemia, non-secretory multiple myeloma, Fahrenheit macroglobulinemia, primary amyloidosis, POEMS syndrome.
- •Subjects planning to undergo a stem cell transplant prior to progression of disease on this study, i.e., these subjects should not be enrolled in order to reduce disease burden prior to transplant.
- •Subject has previously received an allogenic stem cell transplant (regardless of timing).
- •Participated in other clinical trial treatments within 14 days before the first dose (calculated from the time of withdrawal from the study treatment).
- •Unable to swallow tablets or malabsorption syndrome, disease significantly affecting gastrointestinal function.
- •Known central nervous system involvement.
- •Failure to have fully recovered (i.e., ≤ Grade 1 toxicity) from the reversible effects of prior treatment.
- •Not recovered from recent surgical procedures based on investigator's discretion. Major surgical procedure within ≤28 days or minor surgical procedure within ≤14 days prior to initiating study treatment, or anticipation of the need for major surgery during the course of the study treatment and 14 days post last treatment, radiotherapy ≤14 days.
- •Unstable angina, myocardial infarction, or coronary revascularization within 180 days prior to the first dose.
- •Active rheumatoid arthritis, active inflammatory bowel disease, or other chronic inflammatory diseases.
- •Active infection need systemic treatment, including HIV antibody positive, HCV Ab or RNA more than ULN, or HBV-DNA more than ULN.
- •Severe uncontrollable medical condition, including, but not limited to, symptomatic congestive heart failure, severe arrhythmias, unstable angina, or a psychiatric disorder that may affect study adherence;
- •Subject has any concurrent or recent malignancy ≤ 5 year prior to registration with the exception of: basal or squamous cell skin cancer and any carcinoma in situ with adequate therapy, or other cancers successfully cured with surgical procedures or drugs ≥ 2 years.
- •Any other condition or circumstance that would, in the opinion of the investigator, make the patient unsuitable for participation in the study.
- •Female patients who are pregnant or breastfeeding.
- •Requires treatment with a strong cytochrome P450 (CYP) 3A4 inhibitor or inducer、strong CYP2C8 inhibitor (except study treatment).
研究组 & 干预措施
Arm A (Single agent)
Dose escalation APG-2575 at 3 dose levels 3+3 design.
干预措施: APG-2575 (Drug)
Arm B (combo)
Dose escalation APG-2575 at 3 dose levels in combination with Rd, 3+3 design.
干预措施: APG-2575 (Drug)
Arm B (combo)
Dose escalation APG-2575 at 3 dose levels in combination with Rd, 3+3 design.
干预措施: Rd (Drug)
结局指标
主要结局
Dose Limiting Toxicity
时间窗: 28 days
DLT will be defined based on the rate of drug-related grade 3-5 adverse events experienced within the first 28 days of study treatment. These will be assessed via CTCAE version 5.0.
次要结局
未报告次要终点