Study in Elderly Alzheimer's Patients to Assess Skin Tolerability, Irritation With 3, 7-Day Applications of DTP-System

Teikoku Pharma

Status and phase: Completed; Phase 2

Conditions: Irritation/Irritant

Treatments: Drug: 350 mg Donepezil Transdermal Patch; Drug: Placebo Patch

Study type: Interventional

Funder types: Industry

Identifiers

NCT00916383

TPU-TAD-US02-0810

Details and patient eligibility

About

This study is designed to assess skin tolerability, skin irritation, and adhesion of the 350 mg Donepezil Transdermal Patch (DTP-system), following 3, 7-day applications to 3 specific areas of the body (upper back, upper middle arm, side of torso) of elderly Alzheimer's patients. The total application time for the DTP-system is 21 days.

Full description

This is a randomized, placebo-controlled study designed to evaluate skin irritation, skin tolerability, and adhesion of the 350 mg DTP-system following 3 consecutive 7-day applications to 3 specific areas of the body (upper back, upper arm, side of torso) of elderly Alzheimer's patients. The total exposure time for the DTP-system is 21 days.

All patients receive 1 Donepezil Transdermal Patch (DTP-system) and 1 placebo patch, each applied to opposite sides of the body (e.g., placebo patch to the left side of the upper back, and DTP-system to the right side of the upper back). Patients are randomized to receive the active patch to either the left or the right side of the body according to 1 of 6 treatment sequences listed below. The treatment sequence is repeated for the opposite side of the body for a total of 12 treatment sequences (4 patients in each treatment sequence). The patches are applied to one of 3 body locations for 7 days, for a total exposure period of 21 days, according to one of the following sequences:

1. Upper Back, Upper Arm, Side of Torso (Right)
2. Upper Arm, Side of Torso, Upper Back (Right)
3. Side of Torso, Upper Back, Upper Arm (Right)
4. Upper Back, Side of Torso, Upper Arm (Right)
5. Upper Arm, Upper Back, Side of Torso (Right)
6. Side of Torso, Upper Arm, Upper Back (Right)
7. Upper Back, Upper Arm, Side of Torso (Left)
8. Upper Arm, Side of Torso, Upper Back (Left)
9. Side of Torso, Upper Back, Upper Arm (Left)
10. Upper Back, Side of Torso, Upper Arm (Left)
11. Upper Arm, Upper Back, Side of Torso (Left)
12. Side of Torso, Upper Arm, Upper Back (Left)

Patches are applied on Days 1, 8, and 15 according to the randomization schedule. Oral Aricept is taken daily through Day -1, and is re-started on Day 22 or at the time of early termination if before Day 22. Patients are seen in the clinic at Screening and on Days 1, 8, 15, 22, and at the End of Study Visit; for all other daily visits, the patients may be seen either at the clinic or in their residence, provided the assessments are completed as described in the protocol. Skin irritation is assessed immediately upon patch removal and at 1, 24, and 48 hours after removal.

Enrollment: 49 patients

Sex: All

Ages: 65+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Male or female at least 65 years of age.
• Established dose of Aricept 10 mg at least 2 months prior to enrollment.
• Established diagnosis of stable Alzheimer's disease treated with oral Aricept
• Must be willing to change from oral Aricept to DTP (and placebo patch).
• Body mass index of at least 18 and a minimum weight of at least 45 kg.
• Blood pressure (sitting) must be diastolic <95mmHg, and systolic <145, stable for at least 3 months. Patients with well-controlled hypertension (with medication) may enroll as long as 3-month stability criterion is met.
• Those with stable cardiac disease may be enrolled provided the patient has been on appropriate medication for 3 months prior to screening. Those with a pacemaker may be enrolled.
• Pulse rate between 45 - 100 bpm; respirations between 8 - 20 per minute.
• Those with thyroid disease may enroll if stable on treatment for at least 3 months prior to screening, and maintain the same dose of thyroid medication throughout the study.
• Must have a caregiver who is either living with the patient or is in daily contact with the patient, agrees to be present at all visits, provide information as required, and ensure compliance with the medication schedule.
• Free from any abnormality at Screening which may compromise the patient's ability to participate.
• Free of any dermatologic conditions, excessive hair or skin allergies and sensitivities.
• Male patients who have female partners of childbearing potential must use a condom.
• Must understand and provide written informed consent (or have a Legally Authorized Representative who is able), prior to the initiation of any protocol-specific procedures.
• Must be willing and able to abide by all study requirements and restrictions.
• Must be on stable medications for at least 30 days prior to enrollment into the study.

Exclusion criteria

• Use of systemic or topical antihistamines within 72 hours prior to enrollment, or systemic or topical corticosteroids within 3 weeks of study enrollment or foreseen use during the study.
• History of allergy to Donepezil hydrochloride or to piperidine derivatives, related drugs, or any of the drug excipients or other drug product components.
• Those with a recent (< 2 years) cancer (except for non-melanoma skin cancers, females with in-situ cancer of the cervix or males with localized prostate cancer requiring no treatment).
• Presence of history of a psychiatric disorder, or other seizure disorder deemed clinically significant.
• Those with a known plan for elective surgery during the study period.
• Those taking antidepressant medication.
• Abnormality (e.g., scar, tattoo) or unhealthy skin (e.g., burns, wounds) at the application site; or an existing chronic skin disease or history of skin disease at the application site(s) within the 30 days prior to enrollment.
• Treatment with any investigational drug within 30 days prior to enrollment in the study.
• Any condition which would make the patient or caregiver, in the opinion of the investigator or designee, not suitable for the study for any reason.
• Current or pending legal charges that may affect patient or caregiver compliance.
• Treatment with medications contraindicated for use with Aricept

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Triple Blind

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49 participants in 3 patient groups

Upper Back

Experimental group

Description:

350 mg Donepezil Transdermal Patch (active) and placebo patch, each applied to opposite sides of the upper back.

Treatment:

Drug: 350 mg Donepezil Transdermal Patch

Drug: Placebo Patch

Upper Arm

Experimental group

Description:

350 mg Donepezil Transdermal Patch (active) and placebo patch, each applied to opposite arms.

Treatment:

Drug: 350 mg Donepezil Transdermal Patch

Drug: Placebo Patch

Side of Torso

Experimental group

Description:

350 mg Donepezil Transdermal Patch (active) and placebo patch, each applied to opposite sides of torso.

Treatment:

Drug: 350 mg Donepezil Transdermal Patch

Drug: Placebo Patch