Continuation Study of Lapatinib Monotherapy or Lapatinib in Combination With Other Anti-cancer Agents



Status:Completed
Conditions:Breast Cancer, Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:3/2/2017
Start Date:October 2008
End Date:August 19, 2016

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An Open-Label Phase Ib Continuation Study of Lapatinib Monotherapy or Lapatinib in Combination With Other Anti-Cancer Treatment in Patients With Solid Tumors

This study is designed to provide continued access to lapatinib as monotherapy or as part of
a combination regimen to cancer subjects who are currently participating in a phase I trial
that has met its study objectives.


Inclusion Criteria:

- Participation in a Phase I lapatinib trial that has met its study objectives.

- Ability to understand and provide written informed consent to participate in this
study.

- Male or female greater than or equal to 18 years of age.

- A female subject is eligible to participate if she is of:

- Non-childbearing potential defined as pre-menopausal females with a documented tubal
ligation or hysterectomy; or post-menopausal defined as 12 months of spontaneous
amenorrhea. Females on hormone replacement therapy (HRT) and whose menopausal status
is in doubt will be required to use one of the contraception methods stated in the
protocol if they wish to continue their HRT during the study. Otherwise, they must
discontinue HRT to allow confirmation of post-menopausal status prior to study
enrollment. For most forms of HRT, at least two to four weeks will elapse between the
cessation of therapy and the blood draw; this interval depends on the type and dosage
of HRT. Following confirmation of their post-menopausal status, they can resume use
of HRT during the study without use of a contraceptive method.

- Child-bearing potential, has a negative serum pregnancy test at baseline, and agrees
to use one of the contraception methods listed in the protocol for an appropriate
period of time (as determined by the product label or investigator) prior to the
start of dosing to sufficiently minimize the risk of pregnancy at that point. Female
subjects must agree to use contraception from two weeks prior to the administration
of study drug and throughout the entire active study treatment period until four
weeks after the last dose of study medication.

Exclusion Criteria:

- Permanent discontinuation of lapatinib in the previous study due to intolerance or
treatment failure.

- Is a pregnant or lactating female.

- Is considered medically unfit for the study by the investigator as a result of the
medical interview, physical exam, or baseline investigations.

- Currently receiving treatment with any medications listed on the prohibited
medication listed in the protocol

- Has Class III or IV heart failure as defined by the New York Heart Association (NYHA)
functional classification system.

- Have current active hepatic or biliary disease (with exception of subjects with
Gilbert's syndrome, asymptomatic gallstones, liver metastases or stable chronic liver
disease per investigator assessment).
We found this trial at
16
sites
Detroit, Michigan 48202
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Detroit, MI
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Atlanta, Georgia 30322
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Atlanta, GA
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Buffalo, New York 14215
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Buffalo, NY
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Cleveland, Ohio 44109
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Cleveland, OH
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Durham, North Carolina 27710
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Durham, NC
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Edmonton, Alberta
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Edmonton,
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Fort Myers, Florida 33912
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Fort Myers, FL
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Greenville, South Carolina 29605
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Greenville, SC
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Lebanon, New Hampshire 03756
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Lebanon, NH
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Memphis, Tennessee 38120
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Memphis, TN
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Nashville, Tennessee 37205
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Nashville, TN
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Salt Lake City, Utah 84103
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Salt Lake City, UT
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Santa Monica, California 90404
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Santa Monica, CA
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Scottsdale, Arizona 85251
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Scottsdale, AZ
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Tucson, Arizona 85745
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Tucson, AZ
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Washington, District of Columbia 20007
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Washington,
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