Clinical Pilot Study in Healthy Men to Characterize the Uptake of Buprenorphine Into and Its Elimination From the Body After Topical Application of Two New Forms of a Skin Patch in Comparison to a Reference Patch

NCT ID: NCT03785613

Last Updated: 2018-12-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 47 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2005-11-07
• Study Completion Date: 2006-03-14

Brief Summary

This study is intended to produce information on the pharmacokinetic characteristics (uptake into and elimination from the body) of two new patch formulations of the analgesic buprenorphine as compared to the reference patch Transtec (Registered Trademark) 35 micrograms per hour (μg/h) in order to assess the suitability of the test formulations for a later confirmatory bioequivalence study.

In addition to a reduced buprenorphine load, the new patch formulations may potentially provide improved wearing properties. A placebo patch formulation of the respective test or reference patch will be applied simultaneously to explore the skin tolerability and skin adhesiveness of the patch formulations. Furthermore, the safety and tolerability of the treatments will be assessed.

Conditions

Pain

Study Design

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

Study Groups

Test Product T1: Buprenorphine patch (9 mg)

Buprenorphine transdermal patch formulation, containing 9 milligrams buprenorphine in an active surface area of 25 square centimeters. Single application of transdermal patch during 96 hours, on skin in the midclavicular line directly under the clavicle.

Matching placebo patch to T1: simultaneous application for 96 hours on the upper back.

Group Type: EXPERIMENTAL

Test Product T1: Buprenorphine patch (9 mg)

Intervention Type: DRUG

Buprenorphine transdermal patch formulation, containing 9 milligrams buprenorphine in an active surface area of 25 square centimeters.

Matching placebo patch to T1

Intervention Type: DRUG

Placebo patch to T1.

Test Product T2: Buprenorphine patch (3.8 mg)

Buprenorphine transdermal patch formulation, containing 3.8 milligrams buprenorphine in an active surface area of 10 square centimeters. Single application of patch during 96 hours, on skin in the midclavicular line directly under the clavicle.

Matching placebo patch to T2: simultaneous application for 96 hours on the upper back.

Group Type: EXPERIMENTAL

Test Product T2: Buprenorphine patch (3.8 mg)

Intervention Type: DRUG

Buprenorphine transdermal patch formulation, containing 3.8 milligrams buprenorphine in an active surface area of 10 square centimeters.

Matching placebo patch to T2

Intervention Type: DRUG

Placebo patch to T2.

Reference Product R: Transtec patch (20 mg)

Transtec (Registered Trademark) transdermal patch containing 20 milligrams buprenorphine in an active surface area of 25 square centimeters. Single application of transdermal patch during 96 hours, on skin in the midclavicular line directly under the clavicle.

Matching placebo patch to R: simultaneous application for 96 hours on the upper back.

Group Type: ACTIVE_COMPARATOR

Reference Product R: Transtec patch (20 mg)

Intervention Type: DRUG

Transtec (Registered Trademark) transdermal patch containing 20 milligrams buprenorphine in an active surface area of 25 square centimeters, release rate 35 micrograms per hour.

Matching placebo patch to R

Intervention Type: DRUG

Placebo patch to R.

Interventions

Test Product T1: Buprenorphine patch (9 mg)

Buprenorphine transdermal patch formulation, containing 9 milligrams buprenorphine in an active surface area of 25 square centimeters.

Intervention Type: DRUG

Test Product T2: Buprenorphine patch (3.8 mg)

Buprenorphine transdermal patch formulation, containing 3.8 milligrams buprenorphine in an active surface area of 10 square centimeters.

Intervention Type: DRUG

Reference Product R: Transtec patch (20 mg)

Transtec (Registered Trademark) transdermal patch containing 20 milligrams buprenorphine in an active surface area of 25 square centimeters, release rate 35 micrograms per hour.

Intervention Type: DRUG

Matching placebo patch to T1

Placebo patch to T1.

Intervention Type: DRUG

Matching placebo patch to T2

Placebo patch to T2.

Intervention Type: DRUG

Matching placebo patch to R

Placebo patch to R.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Male Caucasian participants aged 18-55 years.
• Body mass index (BMI) between 18 and 30 kilograms per square meter inclusive.
• Participants must be in good health as determined by medical history, physical examination, 12-lead electrocardiogram, vital signs, and clinical laboratory parameters.
• Participants giving written informed consent to participate within this trial.

Exclusion Criteria

• Resting pulse rate less than or equal to 45 or greater than or equal to 95 beats per minute (participant has rested in the sitting position for at least 3 minutes).
• Resting blood pressure (participant has rested in the sitting position for at least 3 minutes) systolic blood pressure less than or equal to 100 and greater than or equal to 140 millimeters mercury (mmHg), diastolic blood pressure less than or equal to 50 and greater than or equal to 95 mmHg.
• Positive human immunodeficiency virus (HIV) type 1/2 antibodies, hepatitis B surface (HBs) antigen, hepatitis B core (HBc) antibodies, hepatitis C virus (HCV) antibodies.
• History or presence of orthostatic hypotension.
• Participation in another clinical study in the last three months before starting this study (exception: characterization of metabolizer status).
• Positive drug of abuse screening (amphetamines, tetrahydrocannabinol [THC], cocaine, morphines, or positive breath alcohol) at screening or baseline.
• Diseases or condition known to interfere with the absorption, distribution, metabolism or excretion of drugs.
• Marked repolarization abnormality (e.g., suspicious or definite congenital long QT syndrome) or co-medication that is known to influence cardiac repolarization substantially.
• Bronchial asthma.
• Definite or suspected history of drug allergy or hypersensitivity, especially known sensitivity to buprenorphine, naltrexone or naloxone.
• Patch allergy.
• Participants who have received any prescribed and non-prescribed systemic or topical medication two weeks before and during the study with the exception of short term medication, e.g. paracetamol for the treatment of headache.
• History or suspicion of alcohol or drug abuse, e.g., use of barbiturates, amphetamines, ecstasy, meta-chlorophenylpiperazine (mCPP), cannabis, or narcotics.
• Not able to abstain from drinking of caffeine containing beverages (tea, coffee, chocolate, or cola).
• Consumption of any quinine containing beverages (bitter lemon, tonic water) or food within two weeks before and during the study.
• Drinking of alcohol containing beverages within 48 hours before administration of investigational product(s).
• Blood donation or comparable blood loss (more than 100 milliliters) during the last 3 months.
• History of seizures or at risk (i.e., head trauma, epilepsy in family anamnesis, unclear loss of consciousness).
• Known or suspected of not being able to comply with the study protocol.
• Not able to communicate meaningfully with the investigator and staff.
• Smoking of more than 20 cigarettes per day or equivalent.
• History of any disorder of the respiratory center.
• Unhealthy skin according to examination by the study physician, not allowing proper patch administration.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

Grünenthal GmbH

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Grünenthal Study Director

Role: STUDY_DIRECTOR

Grünenthal GmbH

Locations

Swiss Pharma Contract

Allschwil, , Switzerland

Countries

Switzerland

Other Identifiers

HP5303/05

Identifier Type: -

Identifier Source: org_study_id