A Dose-escalation Study to Evaluate the Safety, Tolerability, and Antitumor Activity of MEDI-573 in Subjects With Advanced Solid Tumors

Completed · Phase 1

Conditions studied: Cancer

In brief

Evaluate the safety and tolerability of MEDI-573 in adult subjects with advanced solid tumors refractory to standard therapy or for which no standard therapy exists.

Key facts

Study ID

NCT00816361

Run by

MedImmune LLC

People needed

43

Starts

2009-03-09

Expected to finish

2012-09-11

Last updated by the study team

2019-03-04

Who can join

Age: 18 and older, up to 99. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Histologically confirmed advanced solid tumor for which no curative or standard therapies exist.
• Karnofsky Performance Status ≥60.
• Adequate hematological function.
• Adequate organ function.
• Women of non-child-bearing potential (defined as being >1 year post-menopausal) or using effective contraception, e.g., use of oral contraceptives with an additional barrier method (since the investigational product may impair the effectiveness of oral contraceptives), double barrier methods (diaphragm with spermicidal gel or condoms with contraceptive foam), Depo-Provera, partner vasectomy, or total abstinence, from the time the informed consent is signed through 30 days after the last dose of MEDI-573. Male subjects with partners of child-bearing potential must be surgically sterile or use contraceptive method as described above from the time of the initiation of MEDI-573 through 30 days after the last dose of MEDI-573.

You may not qualify if…

• No prior treatment within 4 weeks of study drug administration.
• No concurrent therapy for treatment of cancer.
• No uncontrolled diabetes.
• New York Heart Association Grade ≥ 2 congestive heart failure.
• History of myocardial infarction, unstable angina, transient ischemic attack or stroke within the previous 6 months prior to study entry.
• Documented brain metastasis.
• Pregnancy or lactation or plans to become pregnant while on study.
• Clinically significant abnormality on ECG.

Where it is running

• Research Site — Scottsdale, Arizona, United States
• Research Site — Jacksonville, Florida, United States
• Research Site — Boston, Massachusetts, United States
• Research Site — Detroit, Michigan, United States
• Research Site — Rochester, Minnesota, United States
• Research Site — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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