跳至主要内容
临床试验/NCT04950166
NCT04950166已完成2 期

A Phase 2, Open-Label Study to Evaluate the Performance and Safety of ONM100, an Intraoperative Fluor Imaging Agent for the Detection of Peritoneal Mets

OncoNano Medicine, Inc.5 个研究点 分布在 1 个国家目标入组 51 人开始时间: 2021年11月30日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
51
试验地点
5
主要终点
Percentage of Patients That Had at Least One Additional Lesion Detected Under Pegsitacianine Guidance Following CRS That Was Confirmed as Positive for Disease by Pathological Evaluation

研究概览

简要总结

Peritoneal carcinomatosis (PC) results from the metastasis of a primary cancer of the peritoneum (e.g., appendiceal, ovarian, uterine, colorectal, and gastric cancers) that then disseminates throughout the abdominal cavity. Historically progression to PC was considered terminal and resulted in survival times on the scale of a few months with palliative care being the best option for patients. More recently, cytoreductive surgery (CS) has emerged as a means to prolong and improve patient lives with a median increase in survival of up to ~5 years. It has been reported that for every 10% increase in cytoreduction there is a 5.5% increase in median survival time. In addition to surgical tumor debulking within the peritoneal space, it has also been shown that coupling surgical intervention with hyperthermic intraperitoneal chemotherapy (HIPEC) can have an even greater impact on patient outcomes. Pegsitacianine, a micellar fluorescence agent, exploits the ubiquitous pH differences observed between cancerous and normal tissues. This in turn, provides a highly sensitive and specific fluorescence response after localizing within the tumor microenvironment, thus allowing the detection of primary tumors, their margins, metastatic disease, and tumor-containing lymph nodes.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
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

入选标准

  • Imaging and biopsy confirmed metastatic disease of peritoneal origin

排除标准

  • Known hypersensitivity or allergy to any component of pegsitacianine
  • Tumor locations the surgeon deems unfeasible to image intraoperatively
  • Excessive and/or generalized metastatic disease deemed inoperative by the surgeon

研究组 & 干预措施

Fluorescence imaging with pegsitacianine

Experimental

1 mg/kg of pegsitacianine administered IV 24-72 hours prior to surgery.

干预措施: pegsitacianine (Drug)

结局指标

主要结局

Percentage of Patients That Had at Least One Additional Lesion Detected Under Pegsitacianine Guidance Following CRS That Was Confirmed as Positive for Disease by Pathological Evaluation

时间窗: 1 day

Percentage of patients that had at least one additional lesion detected under pegsitacianine guidance following standard of care cytoreductive surgery that would have been left behind had imaging not been performed and was confirmed to be positive for disease by pathological evaluation.

次要结局

  • Sensitivity of Pegsitacianine at Detecting Presence of Tumor Within the Tissue Specimen(7 days)
  • Specificity of Pegsitacianine at Detecting Presence of Tumor Within the Tissue Specimen(7 days)
  • Negative Predictive Value of Pegsitacianine(7 days)
  • Positive Predictive Value of Pegsitacianine(7 days)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (5)

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