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 |
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.
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.
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
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University of Chicago One of the world's premier academic and research institutions, the University of...
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Seattle Cancer Care Alliance Seattle Cancer Care Alliance (SCCA) is a cancer treatment center that...
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Dana-Farber Cancer Institute Since it’s founding in 1947, Dana-Farber has been committed to providing adults...
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Duke Univ Med Ctr As a world-class academic and health care system, Duke Medicine strives...
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1515 Holcombe Blvd
Houston, Texas 77030
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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4921 Parkview Place
Saint Louis, Missouri 63110
Saint Louis, Missouri 63110
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