A dermal inflammatory challenge study to evaluate complement activation in healthy volunteers

CHDR0 sites15 target enrollmentTBD

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Not specified
Sponsor: CHDR
Enrollment: 15
Status: Not yet recruiting
Last Updated: last year

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

.A.

Registry

who.int

Start Date

TBD

End Date

TBD

Last Updated

last year

Study Type

Interventional

Investigators

Sponsor

CHDR

Eligibility Criteria

Inclusion Criteria

•1\. Healthy male subjects, 18 to 65 years of age, inclusive. Healthy status is defined by absence of evidence of any active or chronic disease following a detailed medical and surgical history, a complete physical examination
•including vital signs, 12\-lead ECG, hematology, coagulation, blood chemistry, blood serology and urinalysis. In the case of uncertain or questionable results, tests performed during screening may be repeated before randomization to confirm eligibility or judged to be clinically irrelevant for healthy subjects;
•2\. Body mass index (BMI) between 18 and 30 kg/m2 and a minimum weight of 50 kg, inclusive;
•3\. Fitzpatrick skin type I\-III (Caucasian);
•4\. Subjects and their partners of childbearing potential must use effective contraception for the duration of the study;
•5\. Able and willing to give written informed consent and to comply with the study restrictions.

Exclusion Criteria

•1\. History of pathological scar formation (keloid, hypertrophic scar) or keloids or surgical scars in the target treatment area that in the opinion of the investigator, would limit or interfere with dosing and/or measurement in the trial;
•2\. History of skin cancer (basal cell carcinoma, squamous cell carcinoma, melanoma);
•3\. Have any current and / or recurrent clinically significant skin condition at the treatment area (i.e. atopic dermatitis); including tattoos;
•4\. History or presence of post\-inflammatory hyperpigmentation.
•5\. Using immunosuppressive or immunomodulatory medication within 30 days prior to enrolment or planned to use during the course of the study;
•6\. Use of topical medication (prescription or over\-the\-counter \[OTC]) within 30 days of study drug administration, or less than 5 half\-lives (whichever is longer) in local treatment area;
•7\. Participation in an investigational drug or device study within 3 months prior to screening or more than 4 times a year;
•8\. Loss or donation of blood over 500 mL within three months prior to screening or donation of plasma within 14 days of screening;
•9\. Any (medical) condition that would, in the opinion of the investigator, potentially compromise the safety or compliance of the patient or may preclude the patient’s successful completion of the clinical trial;
•10\. Chronic infection with HIV, hepatitis B (HBV) or hepatitis C (HCV). A positive HBV surface antigen (HBsAg) test at screening excludes a subject;