Phase I - Escalating Dose Study of siG12D LODER (Local Drug EluteR) in Patients With Locally Advanced Adenocarcinoma of the Pancreas, and a Single Dose Study of siG12D LODER (Local Drug EluteR) in Patients With Non-operable Adenocarcinoma of the Pancreas
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 15
- 试验地点
- 3
- 主要终点
- Number of Participants with Adverse Events
研究概览
简要总结
Phase 0 - Open label, Single dose study of siG12D LODER in Patients with operable adenocarcinoma of the pancreas.
The primary endpoint:
To assess efficacy and local distribution of siRNA out of eight high dose siG12D LODERs in patients diagnosed with operable adenocarcinoma of the pancreas.
The Secondary endpoint:
Short term tolerability and safety assessment
Phase I - This study is designed to investigate the safety of siG12D LODER (Local Drug EluteR) in patients diagnosed with adenocarcinoma of the pancreas.
The primary endpoint:
To asses efficacy of siG12D LODER and local distribution in non-operable patients by histopathology measurements, local distribution by RNA analysis.
To define the dose-limiting toxicities (DLT)
The Secondary endpoint
- To determine the recommended Phase II dose (RP2D)
- To define and maximum tolerated dose (MTD)
- In the event of surgery, assessment of siG12D LODER local distribution and efficacy will be based on histopathology measurements and RNA analysis.
- Progression free survival - only by long term follow-up
详细描述
The investigational agent siG12D LODER (Local Drug EluteR) is a miniature biodegradable polymeric matrix that encompasses anti KRASG12D siRNA (siG12D) drug, designed to release the drug regionally within a pancreatic tumor, at a prolonged rate of 12-16 weeks.
The majority of pancreatic ductal adenocarcinomas involve mutations in the KRAS oncogene (the most common is G12D), therefore stable administration of KRASG12D siRNA has the potential to silence and lead to apoptosis of such cancer cells and thereby slow and even halt the tumor growth.
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
- •Provide written informed consent and be between the ages of 18 and up, inclusive.
- •Patient that is diagnosed as respectable locally pancreatic tumor
- •Have a target tumor accessible for intratumoral administration by EUS (Endoscopic Ultrasound) guidance as determined by the physician performing the EUS guided LODER insertion.
- •Have a Karnofsky performance status of ≥ 70%.
- •Have a life expectancy of >= 3 months.
- •If female and of child-bearing potential, have a negative serum pregnancy test during screening.
- •Agree to use of a barrier method of contraception if sexually active (both men and women) from the time of administration of the first treatment and for at least 8 weeks after treatment.
- •Have serum creatinine < 2.0 mg/dL, , PT, - INR < 1.5 absolute neutrophil count (ANC) > 1,000 x 103 cells/mL, platelets ≥ 75,000/mL, and hemoglobin >= 10 mg/dL.
- •Have screening procedures completed within 2 weeks of starting treatment.
- •No other malignancy present that would interfere with the current intervention.
- •Have measurable disease.
- •Provide written informed consent and be between the ages of 18 and up.
- •Have an unresectable, locally advanced diagnosed or highly suspected adenocarcinoma of the pancreas. Or patients with a tumor and are not planed to undergo surgery due to a high surgical risk (e.g. coagulopathy or severe congestive heart failure).
- •Allocated to receive standard of care chemo as first line treatment.
- •Have a target tumor that is accessible for intratumoral administration by PTA or EUS guidance as determined by the radiologist/gastroenterologist performing the PTA/EUS injection.
- •Have a Karnofsky performance status of ≥ 70%.
- •Have a life expectancy of >= 3 months.
- •If female and of child-bearing potential, have a negative serum pregnancy test during screening.
- •Agree to use of a barrier method of contraception if sexually active (both men and women) from the time of administration of the first treatment and for at least 8 weeks after treatment.
- •Have serum creatinine < 2.0 mg/dL, PT - INR < 1.5, absolute neutrophil count (ANC) > 1,000 x 103 cells/mL, platelets ≥ 75,000/mL, and hemoglobin >= 10 mg/dL.
- •Have screening procedures completed within 4 weeks of starting treatment.
- •No other malignancy present that would interfere with the current intervention.
- •Have measurable disease.
排除标准
- •Have distant metastasis spread (such as liver or lung, or lymph nodes metastases), peritoneal spread or malignant sites.
- •Have clinically significant pancreatitis within 12 weeks of treatment.
- •If female, be breast feeding.
- •Have a medical condition contraindicated for both percutaneous- and endoscopic- guided delivery or any intercurrent medical illness or other medical condition that would in the judgment of the investigator compromise patient safety or the objectives of the study.
- •Have a history of bleeding coagulopathy.
- •Have participated in any therapeutic research study within the last 4 weeks.
- •Have distant metastatic spread (such as liver, lung, or lymph nodes metastases), peritoneal spread or malignant sites.
- •Have clinically significant pancreatitis within 12 weeks of treatment.
- •If female, be breast feeding.
- •Have a medical condition contraindicated for both percutaneous- and endoscopic- guided delivery or any intercurrent medical illness or other medical condition that would in the judgment of the investigator compromise patient safety or the objectives of the study.
- •Have a history of bleeding coagulopathy.
- •Have participated in any therapeutic research study within the last 4 weeks.
研究组 & 干预措施
1 arm
SOC + siG12D LODER
干预措施: siG12D LODER (Drug)
结局指标
主要结局
Number of Participants with Adverse Events
时间窗: Phase 0 - 6 weeks, Phase I - 2 months
次要结局
未报告次要终点