Potential Effect of Topical Imiquimod on Atrial Ectopy in Patients With Actinic Keratosis

Medicis Global Service

Status and phase

Unknown

Phase 4

Conditions

Actinic Keratosis

Treatments

Drug: Imiquimod cream 3.75%

Drug: Placebo cream

Study type

Interventional

Funder types

Industry

Identifiers

NCT01413763

GW01-1001

Details and patient eligibility

About

The purpose of this study is to determine the potential effect of topically applied 3.75% imiquimod cream on atrial ectopy in actinic keratosis (AK) patients. The primary endpoint is the change in the 24-hour supraventricular premature beat count. The secondary endpoint is the change in 24-hour supraventricular premature couplet and run counts and atrial fibrillation (% time); change in 24-hour mean heart rate; change in 24-hour ventricular premature beat count, ventricular premature couplet and run counts.

Full description

This study is a double-blind, randomized, placebo-controlled, 2-way crossover study designed to assess the potential effect of topically applied 3.75% imiquimod cream on atrial ectopy in actinic keratosis (AK) patients. Candidates for study participation will begin screening procedures up to 28 days prior to enrollment. Qualified subjects shall be admitted to the CRU on Day -1 for baseline evaluations and will be randomized to one of two possible treatment sequences. Each subject will receive both the active 3.75% imiquimod cream and the matching placebo in a randomized crossover fashion with a 2-week washout in between each treatment. The application area is the entire face (exclusive of nares, vermilion, periocular areas and ears) or balding scalp. Atrial ectopy will be monitored for 24 hours at Baseline (Day -1; prior to the first dose of study medication), and at the conclusion of each 14-day treatment period using a continuous 12-lead digital Holter recorder.

Adverse events, concomitant medication use, study medication accountability, and subject compliance will be reviewed at each visit.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male and female AK patients with at least 5 typical visible or palpable AK lesions on face or balding scalp
AK patients in otherwise good general health age 18 years and above
Female subjects of childbearing potential must be non-pregnant and non-lactating

Exclusion criteria

Previous clinical study participation within 30 days (drug or device)
Evidence of clinically significant diseases
History of drug or alcohol abuse
Subjects with uncontrolled systemic hypertension, NYHA heart failure classification Class > II, or a history of atrial fibrillation or atrial flutter
Subjects using imiquimod or interferon within 30 days prior to the first dose of study medication
Have known allergies to any excipient in the study cream
Have melanoma anywhere on the body