Effect of External Heat on a Transdermal Granisetron Patc... | NCT01073696

NCT01073696

Protocol Section

Identification Module

Results Section

No data available

No data is available for this block.

Annotation Section

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No data is available for this block.

Document Section

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No data is available for this block.

Derived Section

Miscellaneous Info Module

ID	Type	Description	Link
2009-017036-40	EudraCT Number

Status Module

Oversight Module

Label	Type	Description	Intervention Names
granisetron IV	Active Comparator		Drug: granisetron IV
granisetron patch	Experimental		Drug: granisetron patch

Name	Type	Description	Arm Group Labels	Other Names
granisetron IV	Drug	IV	granisetron IV
granisetron patch

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Pharmacokinetic profile of the granisetron patch in healthy subjects when heat is applied	To assess the effect of locally applied heat on the pharmacokinetic profile of granisetron delivered from the patch. Subjects will be randomized to receive Treatment A Sancuso patch ONLY and Treatment B, Sancuso PLUS Cura-Heat pad. Sancuso will be worn by the subjects for 5 days continuously. The Cura-Heat pad will be applied over the patch for 4.5 hours on each of the 5 days. During these 5 days PK sampling is planned to measure the initial release of granisetron from the patch and cover the predicted maximum observed concentrations with or without the Cura-Heat pad in place.	0 - 196 hours post dose

Secondary Outcomes

Measure	Description	Time Frame
Safety and tolerability assessment	Safety and tolerability will be assessed by collection of adverse events, safety laboratory assessments, record of vital signs, conduct of physical examination and 12 lead ECG. In addition skin reaction at the patch and Cura-Heat pad application sites will be monitored.	Up to 23 days post dose

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Healthy male or female subjects aged ≥ 18 and ≤ 45 years at screening. Subjects must demonstrate understanding of the purposes and risks of the study and agree to follow the restrictions and schedule of study procedures, as evidenced by voluntary written informed consent (signed and dated) obtained before taking part in any trial-related activities.

Exclusion Criteria:

Any current or previous disease, disorder, allergy or condition (including recent unexplained weight loss) that could affect the study conduct or laboratory assessments, or that presents undue risk from the study medication or procedures. Hypersensitivity to adhesive plasters or surgical tape.
Any physical examination or screening investigation result that indicates the subject is unfit for the study.
Scarring on upper arms, including extensive tattoos making skin reactions unevaluable.
A positive virology test, urine test for drugs of abuse, or pregnancy test result (females of childbearing potential only).
Recent use of prescribed or over-the-counter medication that, in the opinion of the Investigator or the Sponsor, will interfere with the study procedures or compromise safety.
Received an investigational drug within 3 months (90 days) preceding patch application.
Loss of ≥ 400 mL of blood (e.g. been a blood donor) within the past 3 months.
Average weekly alcohol consumption of greater than 21 units (males) or 14 units (females), or habitually smokes ≥ 5 cigarettes or equivalent tobacco per day within the 6 months before patch application. Subjects may not smoke while confined to the study site. Subjects must not consume alcohol, or xanthine-containing foods or drinks within 48 hours prior to dosing until discharge.
Lactating female subjects, and female subjects of childbearing potential who are not willing to use an acceptable form of contraception from the screening visit, during the study and for 90 days after the study.
Employee of the Investigator or study centre, with direct involvement in the proposed study or other studies under the direction of that Investigator or study centre, as well as family members of the employees or the Investigator.