Pharmacokinetic Study to Compare the Systemic Exposure of Differin® Gel, 0.3% or Differin® Gel, 0.1%

Galderma

Status and phase

Completed

Phase 4

Conditions

Acne Vulgaris

Treatments

Drug: Adapalene

Study type

Interventional

Funder types

Industry

Identifiers

NCT00660985

RD.06.SPR.18115

Details and patient eligibility

About

Phase 4 commitment pharmacokinetic study to determine systemic exposure to adapalene.

Full description

Multi-center, double-blind, randomized, parallel group study enrolling male or female subjects with acne vulgaris.

Screening will take place within 14 days prior to Baseline. At the Baseline visit, and at each study day up to Day 30, a trained nurse or technician will apply 2 grams of study medication (either Differin® Gel, 0.3% or Differin® Gel, 0.1%) to the face, upper part of chest, and upper part of back of the subjects. To ensure maximal usage conditions, 2 grams study medication will be applied once daily to a total body surface area of approximately 1000 cm², which is equivalent to 2 mg/cm2.

Subjects will arrive at the clinic the night before on visit days (Day 1, Day 15 and Day 30) when PK blood samples will be drawn. Subjects will be discharged from the clinic on Day 2 and Day 16 following the 24-hour post-dose blood sample, and on Day 31 after the 36-hour post-dose blood samples.

Cutaneous safety (local tolerability assessments) will be assessed, by recording erythema, scaling, dryness, and stinging/burning sensation as separate scores on the face, upper part of the chest, and upper part of the back using a 4-point scale (0 = None to 3 = Severe). Local tolerability assessments will be performed weekly on Day 1, 8, 15, 22 and Day 30, prior application of study medication.

Efficacy will be evaluated by Inflammatory and Non-inflammatory lesion counts on the face performed at Screening, Baseline (Day 1), and on Day 30.

Subjects will have routine laboratory tests (fasting hematology, blood chemistry) performed at Screening and at Day 30 visits.

Blood samples for determination of adapalene plasma concentrations will be drawn on Day 1, Day 15, and Day 30 before the morning study medication application (pre-dose) and 1, 2, 4, 6, 8, 10, 12, 16 and 24 hours after application of study medication; and additionally after the last study medication application (Day 31, 32, 33) at 32, 36, 48 and 72 hours post-dose.

The adapalene plasma concentrations will be determined by a high performance liquid chromatography (HPLC) and fluorescence detection method.

Enrollment

51 patients

Sex

All

Ages

18 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male or female 18 to 35 years of age
Clinical diagnosis of acne vulgaris
Minimum of 20 Inflammatory
Minimum of 20 Non-inflammatory lesions
The subject has a body weight between 45 and 100 kg, and a Body Mass Index (BMI) between 18 and 30Kg/m2

Exclusion criteria

More than 1 nodule or any cyst on the face (excluding the nose)
Acne conglobata, acne fulminans, secondary acne or severe acne
Underlying diseases or other dermatological conditions that require the use of interfering topical or systemic therapy
Pregnant or nursing or planning a pregnancy
Surgical or medical condition which might interfere with the absorption, distribution, metabolism, or excretion of the drug
Known allergies to any of the ingredients of the study medication
History of alcohol or drug abuse or positive test results for any drug abuse
Positive test results for hepatitis B surface antigen (HBs-Ag), hepatitis C virus (HCV) or human immunodeficiency virus antibodies (HIV Ab)
Use of prohibited medications prior to the study unless appropriate washout period is documented