An Exploratory Study in Healthy Volunteers to Investigate the Cross-talk Between Local Drug Concentrations in the Skin and Systemic Concentrations During Topical Bioequivalence Studies Using Dermal Sampling Techniques

The clinical study is divided into a pilot and a pivotal study.

The pilot study will involve 6 healthy adult participants and in each participant the concentration of lidocaine/prilocaine will be assessed in the dermis and in the systemic circulation after topical application of lidocaine/prilocaine (dermal sampling visit). The pilot study aims to develop the optimal study design for the pivotal study. Thereby the effect of and removal of the topical dose will be tested as well as if this topical dose establishes well quantifiable systemic drug levels that allow an investigation of the cross-talk between skin and systemic circulation within the pivotal study. Further the feasibility of dermal microdialysis (dMD) will be tested and compared with dOFM.

The pivotal study will involve 20 healthy adult participants. It aims to investigate a potential cross-talk between skin and systemic circulation by comparing dermal lidocaine/prilocaine concentrations (assessed with dOFM and MD) and blood lidocaine/prilocaine concentrations in a dermal sampling visit. Furthermore, the systemic clearance of lidocaine will be investigated in each of the 20 participants in a separate clearance visit after intravenous infusion of lidocaine.

In the dermal sampling visits dOFM and microdialysis probes will be inserted into the dermis to monitor the dermal drug concentration up to 12 h post-dose in topically treated as well as untreated skin sites. Blood samples will be drawn to assess the systemic drug levels. All samples will be assayed for lidocaine and prilocaine concentrations. The blood samples in the clearance visit will be assayed for lidocaine only.

Inclusion criteria

• Healthy, adult volunteers of age 18 to 65 years (both inclusive).
• Males or non-pregnant, non-breast feeding females using adequate contraceptive methods or abstinence.
• Able to read, understand and sign the written informed consent form.
• Willing to follow the protocol requirements and comply with protocol restrictions.

Exclusion criteria

• Social Habits

• Smoker who is not willing to restrain from smoking during the in-house visits.
• History of drug and/or alcohol abuse within one year of start of study as judged by the investigator.
• Medications

• Current treatment with systemically effective corticosteroids, monoamine oxidase (MAO) inhibitors, systemic non-selective beta-blockers, warfarin or anticholinergic drugs, or use of any medications referred in the prescription information of the products.
• Hormonal contraceptive or hormone replacement therapy, routine vitamins or other prescribed medication are allowed if dose is stable.
• Diseases

• Congenital or idiopathic methemoglobinemia.
• History of deep vein thrombosis (DVT)/pulmonary emboly (PE)
• Inherited blood disorders (such as factor V Leiden) who are prone to hypercoagulable state
• Glucose-6-phosphate dehydrogenase deficiencies
• Presence of any acute or chronic diseases or malignancies unless deemed not clinically significant by the investigator.
• Any reason, which in the opinion of the investigator, would prevent the subject from safely participating in the study.
• Any abnormalities found at physical examination or vital signs, unless deemed not clinically significant by the investigator.
• Clinically significant abnormal laboratory evaluation results, as deemed by the investigator.
• Clinically significant abnormal 12-lead ECG at screening, as deemed by the investigator.
• Positive results to the test for hepatitis B antigen or hepatitis C antibodies.
• Positive HIV test.
• Positive alcohol breath test.
• Blood donation within 30 days or significant loss of blood or plasma (more than 550 ml) within 90 days prior to screening.
• Subject who have received an investigational drug within 30 days prior to the initial dose of study medication.
• Known or suspected allergy/hypersensitivity to lidocaine or prilocaine, known history of sensitivity to local anesthetics of the amide type or to any other component of the product, other related products, or any inactive ingredients.
• Tattoos or broken and/or damaged skin at the application areas.
• Active skin diseases like psoriasis or atopic dermatitis, as judged by the investigator.
• Scarring at the anterior part of the thighs.
• Subjects prone to keloid or hypertrophic scar formation or any known wound healing disorder.
• Recent and/or recurrent history of autonomic dysfunction (e.g., recurrent episodes of fainting, palpitations, etc.), as judged by the investigator.
• Not willing to avoid excessive sun exposure, steam baths, sauna, swimming and other strenuous activities for 14 days after Visit 2 to ensure good tissue regeneration.
• Not willing to refrain from shaving the planned application sites or using skin care products on the planned application sites for at least 5 days prior to start of Visit 2.
• Pronounced hairiness on the planned application sites that may negatively affect BE testing.
• Known allergy/hypersensitivity to any of the materials/supplies used during the study.
• Presence of needle phobia.