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Spots Global Cancer Trial Database for Phase 1 Study of MGD007 in Relapsed/Refractory Metastatic Colorectal Carcinoma

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Trial Identification

Brief Title: Phase 1 Study of MGD007 in Relapsed/Refractory Metastatic Colorectal Carcinoma

Official Title: A Phase 1, First-in-Human, Open Label, Dose Escalation Study of MGD007, A Humanized gpA33 x CD3 DART® Protein in Patients With Relapsed/Refractory Metastatic Colorectal Carcinoma

Study ID: NCT02248805

Interventions

MGD007

Study Description

Brief Summary: The primary goal of this Phase 1 study is to characterize the safety and tolerability of MGD007 and establish the maximum tolerated dose (MTD) and schedule of MGD007 administered to patients with metastatic colorectal carcinoma. Pharmacokinetics, pharmacodynamics, and the anti-tumor activity of MGD007 will also be assessed.

Detailed Description: This is an open-label, multi-center, Phase 1 dose-escalation study to define a MTD, describe preliminarily safety, and to assess PK, immunogenicity, and potential anti-tumor activity of MGD007 in patients with relapsed or refractory metastatic colorectal cancer. In the initial phase of the study, two dose schedules will be assessed in dose escalation, once weekly and once every three weeks administration of single agent MGD007. Following the establishment of an MTD, additional patients will enroll in four separate dose expansion cohorts to further optimize the dose and schedule of MGD007 administration. In all segments of the study, patients who benefit from MGD007 treatment and continue to meet eligibility may continue treatment in Cycles 2 and beyond.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Yale University, Yale Cancer Center, New Haven, Connecticut, United States

H. Lee Moffitt Cancer Center & Research Institute, Inc, Tampa, Florida, United States

Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, United States

Massachusetts General Hospital, Boston, Massachusetts, United States

Dana Farber Cancer Institute, Boston, Massachusetts, United States

Duke University Medical Center, Durham, North Carolina, United States

Carolina Biooncology Institute, Huntersville, North Carolina, United States

Providence Portland Medical Center, Portland, Oregon, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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