Esophageal Cancer Clinical Trial

Combination Margetuximab and Pembrolizumab for Advanced, Metastatic HER2(+) Gastric or Gastroesophageal Junction Cancer

Summary

This main purpose of this clinical study is to learn about the safety and activity of margetuximab and pembrolizumab combination treatment in patients with HER2+ gastric and gastroesophageal junction cancer.

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Full Description

Detailed Description: Both margetuximab and pembrolizumab are monoclonal antibodies used in combination to treat HER2+ gastric and gastroesophageal junction cancer. This study has two parts: Dose Escalation and Dose Expansion. The Dose Escalation phase of the study will evaluate safety of escalating doses of the combination treatment. The Dose Expansion phase will evaluate safety and activity of the combination in patients with gastric or gastroesophageal cancer once the final dose and schedule are defined. In addition, a cohort of patients with HER2+ 3+ gastric cancer patients will be enrolled in the Dose Expansion Phase.

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Eligibility Criteria

Inclusion Criteria:

Signed written informed consent.
Age ≥ 18 years old (or minimum age based upon local regulations)
Unresectable locally advanced or metastatic histologically proven HER2+ gastroesophageal junction (GEJ) or gastric cancer. Gastric Cancer Expansion Phase will include only gastric cancer patients with 3+ HER2 positivity.
HER2+ as 3+ (as defined in AJCC staging manual 8th edition) by IHC or in-situ hybridation (ISH) amplified.
Have received prior treatment with trastuzumab.
Have received treatment with at least one or more lines of cytotoxic chemotherapy in the metastatic setting.
Resolution of chemotherapy, immunotherapy or radiation-related toxicities.
Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
Life expectancy ≥ 12 weeks.
Measurable disease as per RECIST 1.1 criteria.

Exclusion Criteria:

Patients with symptomatic central nervous system (CNS) metastases.
Patients with any history of known or suspected autoimmune disease with the specific exceptions of vitiligo, atopic dermatitis, or psoriasis not requiring systemic treatment.
History of prior allogeneic bone marrow, stem-cell or solid organ transplantation.
Treatment with any systemic anti-neoplastic therapy, or investigational therapy within the 3 weeks prior to the initiation of study drug.
Treatment with radiation therapy within 3 weeks prior to the initiation of study drug administration.
Treatment with corticosteroids (≥10 mg per day prednisone or equivalent) or other immune suppressive drugs within the 14 days prior to the initiation of study drug administration.
History of clinically-significant cardiovascular disease.
Clinically-significant pulmonary compromise, including a requirement for supplemental oxygen use to maintain adequate oxygenation.
History of (non-infectious) pneumonitis that required steroids or presence of active pneumonitis
Clinically-significant gastrointestinal disorders, such as perforation, gastrointestinal bleeding, or diverticulitis.
Evidence of active viral, bacterial, or systemic fungal infection.

Study is for people with:

Esophageal Cancer

Phase:

Phase 1

Estimated Enrollment:

95

Study ID:

NCT02689284

Recruitment Status:

Completed

Sponsor:

MacroGenics

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There are 16 Locations for this study

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Yale School of Medicine
New Haven Connecticut, 06520, United States
Georgetown University-Lombardi Comprehensive Cancer Center
Washington District of Columbia, 20007, United States
University of Chicago
Chicago Illinois, 60637, United States
Johns Hopkins University Medical Center
Baltimore Maryland, 21231, United States
Dana-Farber Cancer Institute/Harvard University Medical Center
Boston Massachusetts, 02215, United States
Karmanos Cancer Institute
Detroit Michigan, 48201, United States
Washington University School of Medicine
Saint Louis Missouri, 63110, United States
Duke University Medical Center
Durham North Carolina, 27710, United States
Fox Chase Cancer Center
Philadelphia Pennsylvania, 19107, United States
Sarah Cannon Research Institute
Nashville Tennessee, 37203, United States
Swedish Cancer Institute
Seattle Washington, 98104, United States
Juravinski Cancer Centre - McMaster University
Hamilton Ontario, L8V5C, Canada
McGill University Health Centre
Montreal Quebec, H4A3J, Canada
Kyungbuk National University Hospital
Daegu , 41404, Korea, Republic of
Gachon University Gil Medical Center
Incheon , 21565, Korea, Republic of
Chonbuk National University Hospital
Seoul , 54907, Korea, Republic of
Asan Medical Center
Seoul , , Korea, Republic of
Korea University Anam Hospital
Seoul , , Korea, Republic of
Korea University Guro Hospital
Seoul , , Korea, Republic of
Samsung Medical Center
Seoul , , Korea, Republic of
Seoul National University Bundang Hospital
Seoul , , Korea, Republic of
Seoul National University Hospital
Seoul , , Korea, Republic of
National Cancer Centre
Singapore , , Singapore
National University Hospital
Singapore , , Singapore
Raffles Hospital
Singapore , , Singapore
National Taiwan University Hospital
Taipei , , Taiwan
Taipei Veterans General Hospital
Taipei , , Taiwan
Tri-Service General Hospital
Taipei , , Taiwan

How clear is this clinincal trial information?

Study is for people with:

Esophageal Cancer

Phase:

Phase 1

Estimated Enrollment:

95

Study ID:

NCT02689284

Recruitment Status:

Completed

Sponsor:


MacroGenics

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