A Phase 2, Single Dose, Open-Label Study to Investigate the Safety and Efficacy of OTL38 Injection (OTL38) for Intra-operative Imaging of Folate Receptor-alpha Positive Ovarian Cancer
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 48
- 试验地点
- 4
- 主要终点
- Positive Predictive Value (PPV) of OTL38 in Detecting Folate Receptor-alpha Positive Ovarian Cancer During Surgery.
研究概览
简要总结
This study is being done to:
- test the safety of OTL38
- see if OTL38 helps light up the cancer when viewed with the special camera system
- test the safety of the special camera system for use along with OTL38 during surgery
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Female patients 18 years of age and older
- •Have a primary diagnosis, or at high clinical suspicion, of primary ovarian cancer (of epithelial type), planned for primary debulking or interval debulking surgery, and:
- •Who are scheduled to undergo laparotomy for the debulking surgery OR
- •Who are scheduled to undergo laparoscopy and pre-authorized to undergo laparotomy for the debulking surgery, if cancer is detected on the laparoscopy
- •A negative serum pregnancy test at Screening followed by a negative urine pregnancy test on the day of surgery or day of admission for female patients of childbearing potential
- •Female patients of childbearing potential or less than 2 years postmenopausal agree to use an acceptable form of contraception from the time of signing informed consent until 30 days after study completion
- •Ability to understand the requirements of the study, provide written informed consent and authorization of use and disclosure of protected health information, and agree to abide by the study restrictions and to return for the required assessments
排除标准
- •Previous exposure to OTL38
- •Known FR alpha-negative ovarian cancer
- •Planned surgical approach via laparoscopy or robotic surgery
- •Any medical condition that in the opinion of the investigators could potentially jeopardize the safety of the patient
- •History of anaphylactic reactions or severe allergies
- •History of allergy to any of the components of OTL38, including folic acid
- •Pregnancy, or positive pregnancy test
- •Clinically significant abnormalities on electrocardiogram (ECG)
- •Presence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule
- •Impaired renal function defined as eGFR< 50 mL/min/1.73m2
- •Impaired liver function defined as values > 3x the upper limit of normal (ULN) for alanine aminotransferase (ALT) or aspartate aminotransferase (AST), alkaline phosphatase (ALP), or total bilirubin.
- •Known Stage IV ovarian cancer with Brain Metastases
- •Received an investigational agent in another investigational drug or vaccine trial within 30 days prior to surgery
- •Known sensitivity to fluorescent light
研究组 & 干预措施
Patients Receiving OTL38
All patients in this arm will receive OTL38 for injection and undergo intraoperative imaging.
干预措施: OTL38 (Drug)
Patients Receiving OTL38
All patients in this arm will receive OTL38 for injection and undergo intraoperative imaging.
干预措施: Near infrared camera imaging system (Device)
Patients Receiving OTL38
All patients in this arm will receive OTL38 for injection and undergo intraoperative imaging.
干预措施: Laparotomy (Procedure)
结局指标
主要结局
Positive Predictive Value (PPV) of OTL38 in Detecting Folate Receptor-alpha Positive Ovarian Cancer During Surgery.
时间窗: Day of Surgery (Day 1)
PPV for the detection of FRAP ovarian cancer lesions is defined as the ratio (multiplied by 100) of the number of FRAP ovarian cancer lesions confirmed by both fluorescent light and the pathology/ and immunohistochemistry lab (TP) over the number of FRAP ovarian cancer lesions confirmed by fluorescent light (TP + FP). 95% lower one-sided confidence interval was used.
Sensitivity of OTL38 in Detecting Folate Receptor-alpha Positive Ovarian Cancer During Surgery.
时间窗: Day of Surgery (Day 1)
Sensitivity for the detection of folate receptor-alpha positive (FRAP) ovarian cancer lesions is defined as the ratio (multiplied by 100) of the number of FRAO ovarian cancer lesions confirmed by both fluorescent light and the pathology/ and immunohistochemistry lab (TP) over the number of FRAP ovarian cancer lesions confirmed by the pathology/ and immunohistochemistry lab (TP+FN). 95% lower one-sided confidence interval was used.
次要结局
未报告次要终点