Skin Inflammation and PK of Azithromycin

Skin Infection Clinical Trial

— AZI_IMQ_LPS  

Official title:

Validation of Imiquimod- and LPS-induced Skin Inflammation Models and Their Application in the Investigation of Azithromycin Concentration in Inflamed, Infected, and Healthy Subcutaneous Tissue

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06170983
• Other study ID #: Pro_AZI_IMQ_LPS
• Status: Not yet recruiting
• Phase: N/A
• Start date: January 1, 2024
• Est. completion date: July 1, 2026

Study information

• Verified date: December 2023
• Source: Medical University of Vienna
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will investigate the tissue distribution of azithromycin in healthy, artificially inflamed and actually infected tissue of humans.

Description:

This single-center, prospective, open-label, adaptive, pharmacokinetic study will comprise three parts: Part 0a-c, Part A, and Part B.

Objectives: This study primarily aims to characterize and establish a new skin inflammation model using topically applied LPS. The secondary aim of this research is to deepen our understanding of the role of leukocytes as potential transport vehicles for macrolides and other antibiotics in humans.

Intervention: Part 0 will serve as a pilot experiment in healthy volunteers to validate the imiquimod and LPS challenge in a controlled design. The investigators will clinically assess the tolerability of increasing LPS doses and the already published design of the imiquimod challenge. In general, the investigators will perform the different designs of skin inflammation models using tape stripping and an occlusive 18-mm Finn chamber.

The inflammation will not only be clinically assessed but also objectively quantified using the imaging-based mobile phone application Scarletred®Vision. Considering these results, the investigators will again carry out the LPS and imiquimod challenge in healthy volunteers and additionally perform biopsies in Part 0c to collect specimens for flow cytometry. Thus, the investigators will be able to characterize the skin inflammation models at a cellular level. Using NGS, the investigators will also explore transcriptional changes within cell subset that are affected by the inflammation.

In Part 0c, the investigators will include 12 healthy volunteers and will perform in each subject three skin punch biopsies, including a negative control, IMQ-challenged skin and LPS-challenged skin. Using flow cytometry, the investigators will measure the infiltration of leukocytes subsets.

Part A will employ a skin inflammation challenge based on either LPS or the imiquimod according to the results of Part 0 (i.e., the one showing the greater leucocyte infiltration). Azithromycin will be given in parallel once daily for 3 consecutive days. After the last application (i.e. day 3), two microdialysis probes will be placed in the inflamed subcutaneous tissue and one will be placed in the unmanipulated healthy subcutaneous fat. Hereafter, PK sampling and microdialysis of two thighs will be performed for two consecutive days. The investigators will isolate leukocytes from blood samples on day 3 to determine the average concentration of azithromycin in them. Biopsies from the unmanipulated and the challenged skin will be obtained on day 4.

Part B will involve patients with skin infections including erysipelas and cellulitis at their lower extremities. In contrast to Part A, only one microdialysis probe will be placed into the infected subcutaneous tissue and one into healthy, unaffected tissue. After three doses of azithromycin, pharmacokinetic sampling, leukocyte isolation, and microdialysis of the healthy thigh and the respective area of infection will be performed.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 36
• Est. completion date: July 1, 2026
• Est. primary completion date: January 1, 2026
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• • Men and women aged =18 and <55 years

• BMI =18 and =30 kg/m2

• Normal (or clinically irrelevant abnormal) findings in medical history and physical examination

• Women with child-bearing potential: use of effective contraception

• Laboratory parameters within the given reference range (or abnormal findings which are irrelevant for study purposes in the Investigator's opinion)

Exclusion Criteria:

• Known or suspected allergy to lipopolysaccharide, imiquimod, or sticking plasters

• Only Part 0c: Known or suspected allergy to local anesthetics

• History of severe allergic or anaphylactic reactions to any medication • Blood donation within the last 4 weeks before the study

• Treatment with an investigational drug within three weeks before the study

• Smoking of more than 5 cigarettes per day

• Regular use of medication or abuse of alcohol

• Use of any medication within one week before the study

• Symptoms of a clinically relevant illness in the 3 months before the study

• Liver or kidney dysfunction

• Pregnancy

• History of autoimmune diseases (especially psoriasis)

• Other objections to participating in the study in the opinion of the Investigator

Related Conditions & MeSH terms

• Cellulitis
• Dermatitis
• Inflammation
• Skin Diseases, Infectious
• Skin Infection

Intervention

Drug:
• Azithromycin
500 mg once daily for 3 days

Diagnostic Test:
• Biopsy
Skin punch biopsy

Other:
• Skin inflammation model
LPS- or imiquimod induced skin inflammation

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Medical University of Vienna

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Part 0: Area under the curve (AUC) of azithromycin in artificially inflamed tissue	The pharmacokinetic concentration-time profile in tissue will be assessed by microdialysis. Concentration-time profiles will be plotted. AUC and Cmax will be used as PK parameters.	Day 3
Primary	Part 0: Maximum concentration (Cmax) of azithromycin in artificially inflamed tissue	The pharmacokinetic concentration-time profile in tissue will be assessed by microdialysis. Concentration-time profiles will be plotted. AUC and Cmax will be used as PK parameters.	Day 3
Primary	Part A: Area under the curve (AUC) Azithromycin in healthy and inflamed tissue	The pharmacokinetic concentration-time profile in tissue will be assessed by microdialysis. Concentration-time profiles will be plotted. AUC and Cmax will be used as PK parameters.	Day 3
Primary	Part A: Maximum concentration (Cmax) Azithromycin in healthy and inflamed tissue	The pharmacokinetic concentration-time profile in tissue will be assessed by microdialysis. Concentration-time profiles will be plotted. AUC and Cmax will be used as PK parameters.	Day 3
Primary	Part B: Area under the curve (AUC) of Azithromycin in healthy and infected tissue	The pharmacokinetic concentration-time profile in tissue will be assessed by microdialysis. Concentration-time profiles will be plotted. AUC and Cmax will be used as PK parameters.	Day 3
Primary	Part B: Maximum concentration (Cmax) of Azithromycin in healthy and infected tissue	The pharmacokinetic concentration-time profile in tissue will be assessed by microdialysis. Concentration-time profiles will be plotted. AUC and Cmax will be used as PK parameters.	Day 3
Secondary	Part 0-A: Safety and tolerability of inflammation models	Data will be aggregated as: number of participants with treatment-related local adverse events due to the inflammation models; number of participants with treatment-related systemic adverse events due to the inflammation models	Day 0-3
Secondary	Part A-B: Safety and tolerability of azithromycin	Data will be presented as: number of participants with treatment-related systemic adverse events due to azithromycin; mean number of treatment-related systemic adverse events due to azithromycin per subject	Day 0-3