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临床试验/NCT04021277
NCT04021277终止1 期

Phase I Trial of the Combination of PS101-Mediated Acoustic Cluster Therapy (ACT) With Chemotherapy for Treatment of Liver Metastasis In Patients With Solid Tumours With an Expansion Cohort in Metastatic Colorectal And Pancreatic Cancer

EXACT Therapeutics AS4 个研究点 分布在 2 个国家目标入组 11 人开始时间: 2019年9月17日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
终止
入组人数
11
试验地点
4
主要终点
Safety and tolerability: DLTs (Part 1a only)

研究概览

简要总结

Part 1: This clinical study will first test the safety and initial effect on the tumour of PS101-mediated ACT when given in combination with standard of care chemotherapy in patients with liver metastases (initially those with any solid tumors and then further in patients just with colorectal cancer [CRC]) in order to identify the recommended dose and schedule of PS101-mediated ACT that can be taken forward for further testing.

Part 2: Based on the Part 1 results, another part in patients with liver metastases from CRC and pancreatic cancer (if indicated) may take place following a substantial protocol amendment.

This record will focus on Part 1 of the study only and will be updated if Part 2 occurs.

详细描述

The suboptimal delivery of an anticancer agent to the target cancer cells represent a significant problem in many solid tumours, as it compromises the effectiveness of established therapeutics. If the amount of drug that reached any tumour could be increased without changing the amount administered systemically, it should be possible to increase the effectiveness of the treatment without adding to systemic toxicity.

PS101-mediated ACT involves the use of an experimental drug and an experimental device in patients with colon/rectal cancer that has spread to the liver and is given in combination with standard of care chemotherapy. The experimental drug, called PS101, is a liquid containing a mixture of positively and negatively charged microbubbles and microdroplets. It is injected into a vein (blood vessel) and from there follows the blood flow around the body to where the cancerous tumours are found. PS101 is given at the same time as a special type of ultrasound (performed using an ultrasound device) at the place in the liver where the cancerous tumour is found. The combination of PS101 and ultrasound is called Acoustic Cluster Therapy (ACT).

PS101-mediated ACT can potentially increase the uptake of an anticancer agent over the ultrasound targeted area. The preclinical development of PS101-mediated ACT suggests that this therapy may be of meaningful benefit while significant additional toxicity is not anticipated.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

盲法说明

The participant and radiologist are blinded to treatment dose

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Part 1a: ACT with chemotherapy in metastatic solid tumours

Experimental

20 uL/kg or 40 uL/kg PS101 administered together with standard of care chemotherapy (FOLFOX or FOLFIRI) and ultrasound insonation over the targeted liver metastasis in patients with solid tumours

干预措施: Ultrasound (Device)

Part 1a: ACT with chemotherapy in metastatic solid tumours

Experimental

20 uL/kg or 40 uL/kg PS101 administered together with standard of care chemotherapy (FOLFOX or FOLFIRI) and ultrasound insonation over the targeted liver metastasis in patients with solid tumours

干预措施: 20 uL/kg PS101 (Drug)

Part 1a: ACT with chemotherapy in metastatic solid tumours

Experimental

20 uL/kg or 40 uL/kg PS101 administered together with standard of care chemotherapy (FOLFOX or FOLFIRI) and ultrasound insonation over the targeted liver metastasis in patients with solid tumours

干预措施: 40 uL/kg PS101 (Drug)

Part 1b ACT with chemotherapy in metastatic CRC

Experimental

20 uL/kg or 40 uL/kg PS101 administered together with standard of care chemotherapy (FOLFIRI) and ultrasound insonation over the targeted liver metastasis in patients with metastatic colorectal cancer

干预措施: 20 uL/kg PS101 (Drug)

Part 1b ACT with chemotherapy in metastatic CRC

Experimental

20 uL/kg or 40 uL/kg PS101 administered together with standard of care chemotherapy (FOLFIRI) and ultrasound insonation over the targeted liver metastasis in patients with metastatic colorectal cancer

干预措施: 40 uL/kg PS101 (Drug)

Part 1b ACT with chemotherapy in metastatic CRC

Experimental

20 uL/kg or 40 uL/kg PS101 administered together with standard of care chemotherapy (FOLFIRI) and ultrasound insonation over the targeted liver metastasis in patients with metastatic colorectal cancer

干预措施: Ultrasound (Device)

结局指标

主要结局

Safety and tolerability: DLTs (Part 1a only)

时间窗: 4 weeks from the first ACT treatment in each patient

Proportion of patients with DLTs related to administration of PS101 IV bolus injection alone (without chemotherapy) or due to the addition of PS101 to FOLFOX or FOLFIRI

Number of patients with adverse events

时间窗: From informed consent to 12 weeks from study start

Adverse events are summarised in the adverse event section. An overall summary will be presented here

Number of patients with adverse device effects

时间窗: From the first PS101-mediated ACT procedure to 12 weeks from study start

Number of patients with any AE related to the use of an Investigational Medical Device.

次要结局

  • Preliminary anti-tumor activity at Week 8(Baseline to Week 8)
  • Best overall response (Part 1b only)(Baseline to 24 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (4)

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