The purpose of this study is to determine the dosing strategy for adolescents aged 13 to 17
Drug: granisetron transdermal system
Drug: Granisetron IV
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Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT01596400
Ages eligible for Study
13 Years to 17 Years
Genders eligible for Study
Accepts Healthy Volunteers
13 to 17 years of age inclusive at screening.
Written patient or parental (or appropriate legal representative) IRB approved informed consent as appropriate.
Written patient assent (as appropriate).
Scheduled to receive 2 or more cycles* of emetogenic chemotherapy requiring 5-HT3 antagonist treatment.
Scheduled to receive one or more consecutive days of 5-HT3 antagonist treatment, per cycle, as CINV prophylaxis.
The cycles of chemotherapy must be consecutive (i.e. one followed by the other) but do not have to be the first and second cycle of a line of treatment.
Hypersensitivities, allergies or contraindications to study medications; intolerance of medical tape or sticking plaster.
Clinical or laboratory signs and symptoms of significant cerebral, cardiovascular, respiratory, renal, hepatobiliary, pancreatic or infectious disease, which in the Investigator's judgment may interfere with the study assessment or completion of the study.
Patients with a known history or predisposition to cardiac conduction interval abnormalities, including QT Syndrome, or known family history of long QT Syndrome or taking medications that are known to prolong the QT interval.
Patients scheduled to have routine surgery during the study duration.
Patients with a life expectancy of < 6 months.
Scarring or significant skin disease on both upper arms.
Female patients who are pregnant or breast-feeding. All post menarche female patients must have a pregnancy test at screening.
Patients who are known or thought to be sexually active must use effective birth control.**
Administration of other investigational drugs within 30 days preceding the screening visit, except for anticancer treatments.
Any conditions associated with non-compliance.
Effective birth control includes absolute abstinence, or double barrier birth control methods, i.e. condom and one of the following: combined oral contraceptive, diaphragm, depot contraceptive injection.
All locations for NCT01596400
United States (12)
David Geffen School of Medicine at UCLA
Los Angeles, California, United States, 90095-1690
Children's Hospital of Orange County
Orange, California, United States, 92868
Children's Hospital Colorado, Center for Cancer and Blood Disorders
Aurora, Colorado, United States, 80045
University of Florida
Gainesville, Florida, United States, 32610-0296
Nemours Children's Clinic
Jacksonville, Florida, United States, 32207
University of South Florida
Tampa, Florida, United States, 33606
University of Mississippi Medical Center
Jackson, Mississippi, United States, 39216
Penn State Milton S. Hershey Medical Center
Hershey, Pennsylvania, United States, 17033-0850
UTSW/Childrens Medical Center
Dallas, Texas, United States, 75390-9063
UT Southwestern Medical Center
Dallas, Texas, United States, 75390
Providence Sacred Heart Medical Center and Children's Hospital
Spokane, Washington, United States, 99201
Madigan Army Medical Center
Tacoma, Washington, United States, 98431
View full eligibility
Tris trial is registered with FDA with number: NCT01596400. The sponsor of the trial is Kyowa Kirin Pharmaceutical Development Ltd and it is looking for 19 volunteers for the current phase.
Official trial title: An Open-label, Cross-over, Pharmacokinetic Study to Assess the Safety and Pharmacokinetics of Transdermal Granisetron (Sancuso® Patch) and IV Granisetron in a Pediatric Oncology Population (Aged 13 to 17 Years)
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