Ovarian Cancer Clinical Trial
OTL38 for Intra-operative Imaging of Folate Receptor Positive Ovarian Cancer
This is a phase 3, randomized, multi-center, single dose, open label, pivotal study in patients diagnosed with, or with high clinical suspicion of, ovarian cancer scheduled to undergo primary surgical cytoreduction, interval debulking, or recurrent ovarian cancer surgery.
The Phase 3 study is to confirm the efficacy of OTL38 in combination with fluorescent light to detect additional Folate Receptor-positive (FR+) ovarian cancer lesions not detected by palpation and visualization under normal light in patients with FR+ ovarian cancer scheduled to undergo primary surgical cytoreduction, interval debulking, or recurrent ovarian cancer surgery
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 surgical cytoreduction, interval debulking, or have recurrent ovarian cancer 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 for participation in the study 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
Previous exposure to OTL38
Known FR-negative ovarian cancer
Planned surgical debulking via laparoscopy or robotic surgery, with no intent of laparotomy.
Patients with known ovarian cancer miliary disease determined preoperatively to be inoperable.
Any medical condition that, in the opinion of the investigators, could potentially jeopardize the safety of the patient
History of anaphylactic reactions
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), aspartate aminotransferase (AST), alkaline phosphatase (ALP), or total bilirubin.
Known Stage IV ovarian cancer with brain metastases
Received an investigational agent in another clinical trial within 30 days prior to surgery
Known sensitivity to fluorescent light
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There are 11 Locations for this study
Phoenix Arizona, 85054, United States
Tucson Arizona, 85724, United States
Duarte California, 91010, United States
Orange California, 92868, United States
Tampa Florida, 33612, United States
Detroit Michigan, 48201, United States
Rochester Minnesota, 55905, United States
Saint Louis Missouri, 63108, United States
Kettering Ohio, 45427, United States
Philadelphia Pennsylvania, 19104, United States
Leiden South Holland, 2333 , Netherlands
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