Colorectal Cancer Clinical Trial
Official title:
A Phase 1 Study of SGN-CD47M in Patients With Advanced Solid Tumors
This trial will study SGN-CD47M to find out whether it is an effective treatment for different types of solid tumors and what side effects (unwanted effects) may occur. The study will have two parts. Part A of the study will find out how much SGN-CD47M should be given for treatment and how often. Part B of the study will use the dose found in Part A and look at how safe and effective the treatment is.
This is a dose-escalation study designed to evaluate the safety, tolerability,
pharmacokinetics (PK), and antitumor activity of SGN-CD47M in adults with advanced solid
tumors. The study will be conducted in 2 parts:
Part A - Dose escalation: Up to approximately 25 patients will be treated to evaluate the
safety, tolerability, and PK of SGN-CD47M, and to identify the maximum tolerated dose (MTD)
and/or optimal dose.
Part B - Dose expansion: Up to approximately 180 patients will be treated in expansion
cohorts at the MTD or optimal dose to further characterize the safety, PK, and antitumor
activity of SGN-CD47M.
In eligible patients, standard therapies must have failed, been intolerable, or been
considered medically inappropriate by the investigator. If the MTD is not reached in Part A,
safety, PK, pharmacodynamic, and biomarker analyses, as well as preliminary antitumor
activity, will be used to determine the optimal dose. Patients in Part A may continue on
treatment until confirmed progressive disease (PD) or unacceptable toxicity, whichever occurs
first. The dose(s) to be examined in Part B will be at or below the MTD and/or the optimal
dose determined in Part A.
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