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Effects of Aminocaproic Acid (ACA) on Rosacea-specific Inflammation

A Single Site Evaluation of the Effect of Topical Application of Aminocaproic Acid (ACA) to Inhibit Kallikrein 5 Serine Protease Activity and Production of LL-37 Cathelicidin Peptide, Biochemical Markers of Rosacea-specific Inflammation.

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01398280
Acronym
ACA
Enrollment
15
Registered
2011-07-20
Start date
2011-07-31
Completion date
2012-12-31
Last updated
2019-09-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rosacea

Keywords

Rosacea, Dermatology, UCSD, Skin disease

Brief summary

The purpose of this study is to determine the effect of topical aminocaproic acid on the immune system by assessing the levels of antimicrobial peptides in the skin of patients with rosacea. It is hypothesized that aminocaproic acid applied topically will alter the body's immune system in patients with rosacea by inhibiting activation of antimicrobial peptides.

Interventions

DRUGTopical aminocaproic acid (ACA) mixed with Vanicream

25% Aminocaproic acid cream twice daily for up to 12 weeks.

DRUGVehicle cream

Vehicle cream moisturizer twice daily for up to 12 weeks

Sponsors

University of California, San Diego
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Subject is male or non-pregnant female, 18 - 70 years of age. * Subjects willing and able to give informed consent. * Subjects willing and able to comply with the requirements of the study. * Subject has the clinical diagnosis of at least mild/moderate papulopustular rosacea (3-20 papulopustules) and at least mild erythema. * Subject has been on a stable dose for greater than 3 months of medications for treatment of concurrent medical condition (including oral contraceptive pills, vasodilators, adrenergic blocking agents) OR the investigator has determined that the medications are unlikely to affect the patient's rosacea and/or treatment during the study * Subject is in general good health in the opinion of the investigator. * Subject has a calculated creatinine clearance 100% of normal range. * Subject has normal baseline labs or in the opinion of the investigator are values are not clinically significant and would not inhibit the ability to monitor the patient for both safety and efficacy throughout the study.

Exclusion criteria

* Subject has a diagnosis of Steroid Rosacea or Pyoderma Faciale (rosacea fulminans) * Subject has a history of Carcinoid, Pheochromocytoma, Serotonin Syndrome or other systemic flushing causes. * Subject has used facial topical therapies (OTC drug products or prescription products) for any reason within the prior 28 days * Subject has used systemic corticosteroid or systemic antibiotics (especially doxycycline, minocycline, tetracycline, metronidazole) within the prior 28 days. * Subject has had laser or light-based treatment for rosacea within the prior 3 months. * Subject has had systemic retinoids and retinoid derivatives over the past 6 months * Subject has an active or recent history of any coagulation (hyper or hypo) disorder, genitourinary bleeding, myopathy, cardiomyopathy, rhabdomyolysis or evidence of clinically significant hepatic disease in the opinion of the investigator, * Subject is taking any medicines or supplements that interfere with blood clotting such as Coumadin, Plavix, or ASA (\>81mg/day). * Subject has a known hypersensitivity or allergy to aminocaproic acid or components of the vehicle. * Subject is pregnant or lactating or planning a pregnancy during the duration of the study * Subject has been treated with another investigational device or drug within 28 days prior to study enrollment or intends to participate in a clinical trial concurrent with this study * Subject has clinically significant findings, medical history or conditions (other than rosacea), which in the opinion of the Investigator may compromise the study, treatment protocol, or safety of the patient or treatment allocation.

Design outcomes

Primary

MeasureTime frameDescription
Kallikrein 5 (KLK5) Protease ActivityUp to 12 weeksSerine protease activity of KLK5 in adult skin from patients with rosacea is measured after treatment with vehicle or aminocaproic acid cream. Protease activity of facial skin surface is monitored using a synthetic fluorogenic trypsin-like proteinase substrate. Protease activity is monitored as an increase of fluorescence (RFU/uL) with SpectraMax GEMINI EM.

Countries

United States

Participant flow

Participants by arm

ArmCount
Aminocaproic Acid (ACA)
Subjects will treat their facial skin twice daily for up to 12 weeks with 5-6 visits and 2 telephone visits. Investigator and subject will be blinded. Tape strip samples will be collected from facial skin at each visit to assess KLK activity and LL-37 expression. Topical aminocaproic acid (ACA) mixed with Vanicream: 25% Aminocaproic acid cream twice daily for up to 12 weeks.
11
Vehicle Cream
Subjects will apply vehicle twice daily for up to 12 weeks with 5-6 visits and 2 telephone visits. Investigator and subject will be blinded. Tape strip samples will be collected from facial skin at each visit to assess KLK activity and LL-37 expression. Vehicle cream: Vehicle cream moisturizer twice daily for up to 12 weeks
4
Total15

Baseline characteristics

CharacteristicAminocaproic Acid (ACA)Vehicle CreamTotal
Age, Continuous53 years
STANDARD_DEVIATION 18.5
63 years
STANDARD_DEVIATION 5.6
55.7 years
STANDARD_DEVIATION 16.5
Ethnicity (NIH/OMB)
Hispanic or Latino
2 Participants1 Participants3 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
6 Participants2 Participants8 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
3 Participants1 Participants4 Participants
Sex: Female, Male
Female
7 Participants3 Participants10 Participants
Sex: Female, Male
Male
4 Participants1 Participants5 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 110 / 4
other
Total, other adverse events
0 / 110 / 4
serious
Total, serious adverse events
0 / 110 / 4

Outcome results

Primary

Kallikrein 5 (KLK5) Protease Activity

Serine protease activity of KLK5 in adult skin from patients with rosacea is measured after treatment with vehicle or aminocaproic acid cream. Protease activity of facial skin surface is monitored using a synthetic fluorogenic trypsin-like proteinase substrate. Protease activity is monitored as an increase of fluorescence (RFU/uL) with SpectraMax GEMINI EM.

Time frame: Up to 12 weeks

ArmMeasureValue (MEAN)Dispersion
Aminocaproic Acid (ACA)Kallikrein 5 (KLK5) Protease Activity581.1 RFU/uLStandard Deviation 261
Vehicle CreamKallikrein 5 (KLK5) Protease Activity816.5 RFU/uLStandard Deviation 422.4

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026