A Study to Evaluate the Safety and Tolerability of MEDI-565 in Adults With Gastrointestinal Adenocarcinomas

Completed · Phase 1

Conditions studied: Gastrointestinal Adenocarcinomas

In brief

To determine the maximum tolerated dose and/or optimum biologic dose of MEDI-565 in adult subjects and evaluate the safety profile in adult subjects with advanced gastrointestinal adenocarcinomas who have no available standard or curative treatments.

Key facts

Study ID

NCT01284231

Run by

MedImmune LLC

People needed

78

Starts

2010-12-01

Expected to finish

2015-01-01

Last updated by the study team

2015-03-03

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age ≥ 18 years of age at the time of screening
• Adequate contraception from screening through end of trial
• For the dose-escalation phase, subjects with GI adenocarcinomas with no available standard or curative treatments
• Adequate hematological function
• Adequate organ function
• For subjects who had prior treatment with chemotherapy, biological therapy, radiotherapy, or had prior surgery: eligible for study entry if at least 30 days have passed since their treatment/surgery
• Life expectancy of at least 3 months
• Karnofsky performance status ≥ 70%
• Body weight ≥ 45 kg

You may not qualify if…

• Concurrent enrollment in another clinical study
• Employees of the clinical study site or any other individuals involved with the conduct of the study, or immediate family members of such individuals
• Prior treatment with MEDI-565
• History of allergy or reaction to any component of the MEDI-565 formulation
• History of malignancy other than GI adenocarcinoma, within 5 years prior to study entry, with the exception of ductal carcinoma in situ of the breast, basal cell carcinoma of the skin or carcinoma in situ of the cervix successfully treated with curative therapy
• Diagnosis of hepatocellular carcinoma
• Clinical history of significant CNS pathology
• Active bacterial infection or known bacteremia.
• Vaccination within 2 weeks prior to initiation of MEDI-565
• Infection with HIV-1 or HIV-2; chronic infection with hepatitis B or C
• History of primary immunodeficiency
• History of chronic autoimmune disease
• Elective surgery planned during the study period through 30 days after discontinuation of MEDI-565.
• Treatment with any chemotherapy, radiotherapy, immunotherapy, biologic, or hormonal therapy for cancer treatment within 30 days prior to study entry and not recovered from treatment
• Treatment with any investigational agent within 30 days prior to initiation of MEDI-565
• Regular dose of systemic corticosteroids during the 30 days prior to initiation of MEDI-565 or anticipated need of corticosteroids exceeding prednisone 40 mg/day of prednisone or equivalent during the trial, or any other systemic immunosuppressive therapy within 30 days prior to study entry (some maintenance doses allowed)
• Contraindication to any protocol-specified concomitant medications administered during this study
• Pregnancy or lactation
• Evidence of any uncontrolled systemic disease (other than GI adenocarcinoma)
• Recent history of cardiac disease, including myocardial infarction, unstable angina pectoris or uncontrolled arrhythmia within 6 months, or evidence of severe congestive heart failure
• A marked baseline prolongation of corrected QT interval interval

Where it is running

• Research Site — Washington D.C., District of Columbia, United States
• Research Site — Augusta, Georgia, United States
• Research Site — Durham, North Carolina, United States
• Research Site — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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