Overview

Study of TF2 Carcinoembryonic Antigen (CEA) Antibody in Patients With Metastatic Colorectal Cancer

Status:
Withdrawn
Trial end date:
2018-08-01
Target enrollment:
Participant gender:
Summary
This study is being done to select an appropriate TF2 bsMAb dose suitable for pretargeting the 111In/90Y-labeled hapten-peptide (IMP-288). Eligible patients will receive a fixed dose of 90Y-IMP-288 4 days after the TF2 antibody injection. Two different dose levels of TF2 will be studied in the first part. Once an appropriate TF2 dose is selected based on information learned from the first 2 dose levels, patients will be enrolled onto several different increasing dose levels of 90Y-IMP-288.
Phase:
Phase 1
Details
Lead Sponsor:
Gilead Sciences
Immunomedics, Inc.
Collaborator:
National Cancer Institute (NCI)
Treatments:
Antibodies
Antibodies, Bispecific
Immunoglobulins