A Study to Evaluate the Effect of Heat Application on the Delivery Profile of Corplex™ Donepezil Transdermal Delivery System (TDS)

NCT ID: NCT03438604

Last Updated: 2018-09-14

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-02-13
• Study Completion Date: 2018-06-30

Brief Summary

A study to assess the effect of heat application on the delivery profile of Corplex™ Donepezil Transdermal Delivery System (TDS)

Detailed Description

2-Way Crossover study

Approximately 24 healthy, adult male and female subjects will be enrolled.

Subjects will be randomized to 1 of 2 treatment sequences prior to the first TDS application in treatment period 1.

For each treatment period, subjects will have one 7-day TDS applied on their back. Depending on which sequence a subject is randomized to, the healthy subject will either be exposed to heat or not during the TDS wear time.

Blood samples for Donepezil PK will be collected pre-dose until the end of each treatment period.

Adhesion will be monitored throughout the TDS wear time, and skin irritation will be monitored after TDS removal.

Subjects who complete the 2-way crossover study may be eligible to participate in the optional Study Extension Period. In the Study Extension Period, subjects will have their skin surface temperature monitored under the patch and adjacent to the TDS.

Blood samples for Donepezil PK will not be collected, and adhesion will not be monitored for the Study Extension TDS wear period.

Safety will be monitored throughout the study by adverse event reporting and repeated clinical and laboratory evaluations.

Conditions

Alzheimer's Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Donepezil TDS with Heat Applied

Corplex Donepezil TDS 5 mg/day with heat applied

Group Type: OTHER

Donepezil TDS

Intervention Type: DRUG

Donepezil Hydrochloride Transdermal Delivery System

Donepezil TDS without Heat

Corplex Donepezil TDS 5 mg/day with no heat applied

Group Type: OTHER

Donepezil TDS

Intervention Type: DRUG

Donepezil Hydrochloride Transdermal Delivery System

Donepezil TDS Extension Study with Heat

Corplex Donepezil TDS 5 mg/day with heat. Two skin sensors will be placed underneath the TDS and adjacent to the TDS.

Group Type: OTHER

Donepezil TDS

Intervention Type: DRUG

Donepezil Hydrochloride Transdermal Delivery System

Interventions

Donepezil TDS

Donepezil Hydrochloride Transdermal Delivery System

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Healthy, adult, male or female ≥ 30 years of age

Exclusion Criteria

• History of any illness that, in the opinion of the investigator, might confound the results of the study or poses an additional risk to the subject by participation in the study
• History or presence of alcoholism or drug abuse within the past 2 years prior to the first study product treatment
• History or presence of hypersensitivity or idiosyncratic reaction to the study products or related compounds
• History of significant multiple and/or severe allergies, or has had an anaphylactic reaction or significant intolerability to prescription or nonprescription drugs
• History or presence of excessive sweating
• History or presence of hairy skin on application sites
• History or presence of significant skin damage or disease at application sites
• Any medical or surgical procedure or trauma within 28 days prior to the first study product treatment

• Minimum Eligible Age: 30 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Corium, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Danielle Armas, MD

Role: PRINCIPAL_INVESTIGATOR

Celerion

Locations

Celerion

Phoenix, Arizona, United States

Countries

United States

Other Identifiers

P-16039

Identifier Type: -

Identifier Source: org_study_id