A Phase 1, Open-Label, Dose-Escalation, Safety and Tolerability Study of INCB047986 in Subjects With Advanced Malignancies
试验速览
- 阶段
- 1 期
- 状态
- 终止
- 入组人数
- 5
- 主要终点
- Adverse events that are defined as dose limiting toxicities occurring in the first 21 days of treatment in Group 1 and the first 28 days of treatment in Group 2.
研究概览
简要总结
This is an open-label study of INCB047986 given to two distinct groups of patients (Group 1 and Group 2) with advanced malignancies. The purpose of the study is to evaluate the safety, tolerability and pharmacokinetics of INCB047986 and to determine the maximum tolerated dose of INCB047986 in combination with gemcitabine and nab paclitaxel in a select group of patients with solid tumors. Each patient group will participate in a phase of the study which is divided into two parts. The patient groups will be enrolled in a sequential manner starting with Patient Group 1.
Patient Group 1
Group 1 will be comprised of patients with advanced malignancies who will receive INCB047986 as monotherapy.
Part 1: Dose Escalation Phase - This phase will evaluate the safety, tolerability and pharmacokinetics (PK) of INCB047986 when given as described to patients with advanced malignancies. A goal of Part 1 will be to identify the maximally tolerated dose (MTD) of INCB047986 and/or other dose(s) that are tolerated doses and produce a substantial pharmacologic effect. These doses will be used in Part 2 of the study.
Part 2: Expansion Phase - This phase will further explore the safety, tolerability, PK, and preliminary clinical activity of INCB047986 using the doses identified in Part 1.
Group 2
Group 2 will be in subjects with advanced or metastatic pancreatic cancer, breast cancer or urothelial cancer.
Part 1: Dose Optimization Phase - This phase will identify the MTD of INCB047986 in combination with gemcitabine and nab-paclitaxel in patients with advanced or metastatic solid tumors. Specifically, these will be patients with pancreatic adenocarcinoma (first or second line), triple-negative breast cancer (second line) or urothelial cancer (second line).
Part 2: Expansion Phase - This phase will explore the safety, tolerability, PK, biomarkers, and preliminary clinical activity of the dose regimen(s) identified in Part 1. Patients enrolled in this phase will be limited to those with advanced or metastatic pancreatic cancer.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 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
- •Aged 18 years or older, with histologically or cytologically confirmed solid tumor, Hodgkin's lymphoma, aggressive or indolent non-Hodgkin's lymphoma. (NOTE: Patients with acute and chronic leukemia, Burkitt's lymphoma, precursor B lymphoblastic leukemia/lymphoma, and myeloma are excluded)
- •Life expectancy of 12 weeks or longer.
- •Subject must have received ≥ 1 prior treatment regimen.
- •The subject must not be a candidate for potentially curative therapy, including transplant.
- •Aged 18 years or older
- •Part 1 - Histologically or cytologically confirmed pancreatic adenocarcinoma (first or second line), triple-negative breast cancer (second line), or urothelial cancer (second line)
- •Part 2 - Histologically or cytologically confirmed pancreatic adenocarcinoma
- •No more than 1 prior chemotherapy regimen for advanced or metastatic disease (not including neoadjuvant and/or adjuvant therapy).
- •There is no restriction on the number of prior non-myelosuppressive targeted therapies or hormonal agents (e.g., epidermal growth factor receptor-targeted therapy for lung cancer and hormonal therapy for breast cancer or ovarian cancer); NOTE: Targeted and/or hormonal therapy alone will not be considered chemotherapy for the purposes of this study.
排除标准
- •Group 1 and 2
- •Received an investigational study drug within 28 days or 5 half-lives (whichever is longer) prior to receiving their first dose of study drug.
- •Received any approved anticancer medications within 21 days or 5 half-lives (whichever is longer) prior to receiving the first dose of study drug (42 days for nitrosoureas) EXCEPT steroids at ≤ 10 mg prednisone daily (or equivalent).
- •Has any unresolved toxicity ≥ Grade 2 from previous anticancer therapy without medical monitor approval.
- •o Subjects with ongoing chronic toxicities such as fatigue or neuropathy may be allowed after approval from the sponsor's medical monitor
- •Evidence of uncontrolled brain metastases or history of spinal cord compression, or primary central nervous system (CNS) tumors.
- •Has an Eastern Cooperative Oncology Group (ECOG) performance status of ≥
- •Received allogeneic hematopoietic stem cell transplant within the last 6 months, or has active graft versus host disease (GVHD) following allogeneic transplant, or is currently receiving immunosuppressive therapy following allogeneic transplant.
- •Received autologous hematopoietic stem cell transplant within the last 3 months.
- •Radiation treatment within the previous 4 weeks.
- •History of active hepatitis or positive serology for hepatitis B (unless due to vaccination) or C
研究组 & 干预措施
Group 1 INCB047986
干预措施: INCB047986 (Drug)
Group 2 Experimental: INCB047986, gemcitabine, nab-paclitaxel
干预措施: INCB047986 (Drug)
Group 2 Experimental: INCB047986, gemcitabine, nab-paclitaxel
干预措施: Gemcitabine (Drug)
Group 2 Experimental: INCB047986, gemcitabine, nab-paclitaxel
干预措施: nab-paclitaxel (Drug)
结局指标
主要结局
Adverse events that are defined as dose limiting toxicities occurring in the first 21 days of treatment in Group 1 and the first 28 days of treatment in Group 2.
时间窗: Approximately 21 days (Group 1); Approximately 28 days (Group 2)
Safety and tolerability of INCB047986 monotherapy and in combination with gemcitabine and nab-paclitaxel as assessed by summary of clinical laboratory assessments, Electrocardiogram (ECG), and Adverse Events (AEs).
时间窗: Group 1 and Group 2: up to 6 months
Group 1: Baseline and weekly for Cycle 1 and then Day 1 for all subsequent cycles until the End of Treatment visit. Group 2: Baseline and weekly for Cycle 1 and then Day 1, Week 8 and Week 15 for all subsequent cycles until the End of Treatment visit.
次要结局
- Plasma concentrations will be used to estimate peak plasma concentration (cmax) and area under the plasma concentration curve (AUC)(Day 15 of treatment at a given dose)
- Change in Eastern Cooperative Oncology Group (ECOG) status from baseline to each visit where the variable is measured(Approximately 6 months)
- Tumor response rates will be derived from investigator assessment of response in subjects with measurable disease(Approximately 6 months)
- Duration of Response (DOR) and Progression Free Survival (PFS) in subjects with measureable disease(Approximately 6 months)
- Plasma concentration of biomarkers and cytokines before and during treatment(Approximately 6 months)
- Change in body weight(Approximately 6 months)