Safety Study of Oral MGCD265 Administered Without Interruption to Subjects With Advanced Malignancies



Status:Completed
Conditions:Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:2/14/2019
Start Date:June 2008
End Date:January 2019

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Open-Label Dose-Escalation Trial to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Daily Oral MGCD265 Administered Without Interruption to Subjects With Advanced Malignancies

In this study, MGCD265, a new anticancer drug under investigation, is given daily to patients
with advanced malignancies to study its safety profile.

MGCD265 belongs to a new class of drugs with anticancer potential, known as tyrosine kinase
inhibitors. MGCD265 was shown to slow down the growth of human cancer cells in mice. Clinical
studies are being pursued to evaluate the safety of MGCD265 in cancer patients.

In this study, MGCD265 is orally administered on a daily basis to patients with advanced
malignancies.

Inclusion Criteria:

- Advanced metastatic or unresectable malignancy that is refractory to standard therapy
and/or existing therapies are not likely to achieve clinical benefit, and/or the
patient declines to receive standard treatment such as chemotherapy.

- Evaluable disease;

- Last dose of prior chemotherapy, radiation therapy, or investigational agents occurred
at least 4 weeks before the start of therapy;

- Recovery from the adverse effects ≤ grade 1;

- Acceptable ECOG status 0, 1, or 2;

- Life expectancy greater than 3 months following study entry;

- Adequate laboratory values;

- For patients enrolling in the four expansion cohorts:

- NSCLC patients must meet criteria for MET and/or Axl expression or,

- HNSCC patients must meet criteria for MET and/or Axl expression or,

- NSCLC patients must meet criteria for amplification of the MET gene locus,
defined MET mutations, or rearrangements involving the AXL or MET gene locus or;

- Patients with tumor types such as HNSCC, papillary renal carcinoma, gastric
adenocarcinoma, and other solid tumors must meet criteria for amplification of
the MET gene locus, defined MET mutations, or rearrangements involving the AXL or
MET gene locus

Exclusion Criteria:

- Uncontrolled concurrent illness;

- History of cardiovascular illness;

- QTc > 470 msec (including subjects on medication);

- Left ventricular ejection fraction (LVEF) < 50%;

- Immunocompromised subjects;

- History of bone marrow transplant;

- Lung tumor lesions with increased likelihood of bleeding;

- Symptomatic or uncontrolled brain metastases;

- Unable to swallow oral medications or with pre-existing gastrointestinal disorders.
We found this trial at
13
sites
2301 Erwin Rd
Durham, North Carolina 27710
919-684-8111
Duke Univ Med Ctr As a world-class academic and health care system, Duke Medicine strives...
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5801 South Ellis Avenue
Chicago, Illinois 60637
 773.702.1234
University of Chicago One of the world's premier academic and research institutions, the University of...
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Chicago, IL
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825 Eastlake Ave E
Seattle, Washington 98109
(206) 288-7222
Seattle Cancer Care Alliance Seattle Cancer Care Alliance (SCCA) is a cancer treatment center that...
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Seattle, WA
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450 Brookline Ave
Boston, Massachusetts 2215
617-632-3000
Dana-Farber Cancer Institute Since it’s founding in 1947, Dana-Farber has been committed to providing adults...
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Boston, MA
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Duarte, California 91010
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Duarte, CA
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Edmonton, Alberta
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Edmonton,
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1515 Holcombe Blvd
Houston, Texas 77030
 713-792-2121
University of Texas M.D. Anderson Cancer Center The mission of The University of Texas MD...
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Houston, TX
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New York, NY
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Orange, California 92868
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Philadelphia, Pennsylvania 19111
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4921 Parkview Place
Saint Louis, Missouri 63110
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Saint Louis, MO
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Salt Lake City, Utah 84112
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Salt Lake City, UT
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San Diego, California 92093
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San Diego, CA
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