Overview
Performance of SGM-101 for the Delineation of Primary and Recurrent Tumor and Metastases in Patients Undergoing Surgery for Colorectal Cancer
Status:
Recruiting
Recruiting
Trial end date:
2021-12-01
2021-12-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The performance of SGM-101, an intraoperative imaging agent, will be compared to that of standard "white light" visualization during surgical resections of colorectal cancer.Phase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
SurgimabTreatments:
Antibodies, Monoclonal
Criteria
Inclusion Criteria:- Patients should be scheduled for curative colorectal cancer surgery of primary cT4
colon cancer or primary cT3/4 rectal cancer, recurrent colorectal cancer or peritoneal
metastasized colorectal cancer.
- Female patients must be of non-child-bearing potential (i.e., women with functioning
ovaries who have a documented tubal ligation or hysterectomy, ovariectomy or women who
are post-menopausal). Women of child-bearing potential will be included provided that
they have a negative urine pregnancy test at the day of the injection and agree to
practice adequate contraception for 30 days prior to administration of investigational
product, and 30 days after completion of injection.
Exclusion Criteria:
1. Other malignancies, either currently active or diagnosed in the last 5 years, except
for adequately treated in situ carcinoma of the cervix and basal or squamous cell skin
carcinoma;
2. Primary appendiceal cancer;
3. Laboratory abnormalities defined as:
- Aspartate AminoTransferase, Alanine AminoTransferase, Gamma Glutamyl Transferase)
or Alkaline Phosphatase levels above 5 times the ULN or;
- Total bilirubin above 2 times the ULN or;
- Serum creatinine above 1.5 times the ULN or;
- Absolute neutrophils counts below 1.5 x 109/L or;
- Platelet count below 100 x 109/L or;
- Hemoglobin below 4 mmol/L (females) or below 5 mmol/l (males);
4. Known positive test for human immunodeficiency virus (HIV), hepatitis B surface
antigen (HBsAG) or hepatitis C virus (HCV) antibody or patients with untreated serious
infections;
5. Any condition that the investigator considers to be potentially jeopardizing the
patient's well-being or the study objectives.