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Spots Global Cancer Trial Database for A Safety Study of SGN-CD47M in Patients With Solid Tumors

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Trial Identification

Brief Title: A Safety Study of SGN-CD47M in Patients With Solid Tumors

Official Title: A Phase 1 Study of SGN-CD47M in Patients With Advanced Solid Tumors

Study ID: NCT03957096

Interventions

SGN-CD47M

Study Description

Brief Summary: 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.

Detailed Description: 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.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Case Western Reserve University / University Hospitals Cleveland Medical Center, Cleveland, Ohio, United States

Providence Portland Medical Center, Portland, Oregon, United States

Tennessee Oncology-Nashvilee/Sarah Cannon Research Institute, Nashville, Tennessee, United States

MD Anderson Cancer Center / University of Texas, Houston, Texas, United States

NEXT Oncology, San Antonio, Texas, United States

Contact Details

Name: Michael Schmitt, MD, PhD

Affiliation: Seagen Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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