Pharmacokinetic and Safety Study of Lower Doses of Ceritinib Taken With a Low-fat Meal Versus 750 mg of Ceritinib in the Fasted State in Adult Patients With (ALK-positive) Metastatic Non-small Cell Lung Cancer (NSCLC)



Status:Active, not recruiting
Conditions:Lung Cancer, Lung Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:3/28/2019
Start Date:April 9, 2015
End Date:October 22, 2019

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A Multi-center, Randomized Open Label Study to Assess the Systemic Exposure, Effiacy, and Safety of 450 mg Ceritinib Taken With a Low-fat Meal and 600 mg Ceritinib Taken With a Low-fat Meal as Compared With That of 750 mg Ceritinib Taken in the Fasted State in Adult Patients With ALK Rearranged (ALK-positive) Metastatic Non-small Cell Lung Cancer (NSCLC)

A Phase I study to assess the systemic exposure, effiacy, and safety of 450 mg ceritinib
taken with a low-fat meal and 600 mg ceritinib taken with a low-fat meal as compared with
that of 750 mg ceritinib taken in the fasted state in adult patients with ALK rearranged
(ALK-positive) metastatic non-small cell lung cancer (NSCLC)


Inclusion:

1. Histologically or cytologically confirmed diagnosis of stage IIIB (and is not a
candidate for definitive multimodality therapy) or IV ALK-positive NSCLC.

2. Patients may have received one prior treatment regimen with crizotinib (all other ALK
inhibitors are excluded).

3. Patients may have received prior chemotherapy, biologic therapy, or other
investigational agents. ALK inhibitors other than crizotinib are excluded.

4. Patient has a World Health Organization (WHO) performance status 0-2.

Exclusion:

1. Prior treatment with an ALK inhibitor other than crizotinib.

2. History of carcinomatous meningitis.

3. Presence or history of a malignant disease other than an ALK-positive advanced tumor
that has been diagnosed and/or required therapy within the past 3 years.

5. Clinically significant, uncontrolled heart disease and/or recent cardiac event (within 6
months) 6. Patient has history of interstitial lung disease or interstitial pneumonitis,
including clinically significant radiation pneumonitis (i.e., affecting activities of daily
living or requiring therapeutic intervention).

7. Patient has other severe, acute, or chronic medical conditions 8. Patient is currently
receiving treatment with warfarin sodium (Coumadin®) or any other coumarin-derivative
anticoagulants.
We found this trial at
11
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Baltimore, Maryland 21201
Principal Investigator: Martin Edelman
Phone: 410-328-5009
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Belleville, New Jersey 07109
Principal Investigator: James Orsini
Phone: 973-751-8880
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Belleville, NJ
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Fayetteville, Arkansas 72703
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Greenville, South Carolina 29615
Principal Investigator: William Jeffery Edenfield
Phone: +1 864 455 3600
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Indianapolis, Indiana 46202
Principal Investigator: Ebenezer Kio
Phone: 574-364-2649
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Indianapolis, IN
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Loma Linda University
Loma Linda, California 92354
(909) 558-4000
Principal Investigator: Hamid R. Mirshahidi
Phone: 909-558-4050
Loma Linda University Loma Linda University (LLU) is a Seventh-day Adventist educational health-sciences institution with...
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Loma Linda, CA
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Long Beach, California 90813
Principal Investigator: Simon N. Tchekmedyian
Phone: 562-590-0345
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Long Beach, CA
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Rockville, Maryland 20850
Principal Investigator: Nicholas Farrell
Phone: 240-826-2120
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Rockville, MD
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Salt Lake City, Utah 84103
Principal Investigator: Justin D. Call
Phone: 801-281-6864
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Salt Lake City, UT
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Seattle, Washington 98101
Principal Investigator: Joseph Rosales
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Seattle, WA
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