The Use of Onexton in Moderate Acne Vulgaris for Patients With Skin of Color
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ClinicalTrials.gov Identifier: NCT03402893 |
Recruitment Status :
Completed
First Posted : January 18, 2018
Results First Posted : February 19, 2019
Last Update Posted : April 2, 2019
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Acne Vulgaris Post Inflammatory Hyperpigmentation | Drug: ONEXTON Topical Gel | Phase 4 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 21 participants |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | The Use of Onexton in Moderate Acne Vulgaris for Patients With Skin of Color |
Actual Study Start Date : | July 28, 2017 |
Actual Primary Completion Date : | November 15, 2017 |
Actual Study Completion Date : | February 28, 2018 |

Arm | Intervention/treatment |
---|---|
Experimental: single arm Onexton gel application
Onexton gel will be supplied to all subjects and applied once daily to the face
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Drug: ONEXTON Topical Gel
Onexton gel applied once daily to face |
- Investigator Global Assessment Scale for Severity of Facial Acne [ Time Frame: Week 4, Week 8, Week 16 ]Percent of subjects achieving clear or almost clear on Investigator's Global Assessment (IGA) scale for facial acne; the IGA scale for acne reflects the Investigator's assessment of the severity of a subject's acne on a scale from 0 to 5 with 0 = Clear Skin, 1 = Almost Clear, 2 = Mild, 3 = Moderate severity, 4 = Severe, 5 = Very Severe Each of these gradations is based upon a lesion count by the Investigator.
- Investigator Global Assessment Scale for Severity of Post Inflammatory Hyperpigmentation [ Time Frame: Week 4, Week 8, Week 16 ]Percent of subjects achieving clear or almost clear on Investigator's Global Assessment (IGA) scale for severity of post inflammatory hyperpigmentation; the IGA scale of post-inflammatory hyperpigmentation reflects the Investigator's assessment of the severity of a subject's hyperpigmentation on a scale from 0 to 6 with 0 = None, 1 = Slight, 2 = Mild, 3 = Moderate, 4 = moderately Severe, 5 = Severe, 6 = Very severe Each of these gradations is based upon the investigator's impression
- Percent Change in Inflammatory Lesions [ Time Frame: Week 4, Week 8, Week 16 ]The Investigator will count the number of facial (from hairline to mandibular line) inflammatory acne lesions at each study visit. Inflammatory lesions include papules, pustules and nodules.
- Percent Change in Non-inflammatory Lesion Count [ Time Frame: Week 4, Week 8, Week 16 ]The Investigator will count the number of facial non-inflammatory acne lesions at each study visit. these include open and closed comedones.
- Percent Change in Total Lesion Count [ Time Frame: week 4, Week 8, Week 16 ]The Investigator will count the number of facial inflammatory and non-inflammatory acne lesions at each study visit. These include papules, pustules, nodules, and open and closed comedones.
- Post-Inflammatory Hyperpigmentation (PIH) Distribution [ Time Frame: baseline, Week 4, week 8, week 16 ]This measure as assessed by the Investigator seeks to quantify the extent to which post-inflammatory hyperpigmentation is distributed across the face, wherein 0= No PIH, 1=1-10% of the face affected, 2=11-20%, 3=21-30%, 4=31-40%, 5=41-50%, and 6=More than 50% of the face. Lower numbers reflect less severe disease.

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Ages Eligible for Study: | 12 Years and older (Child, Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
i. Outpatient, subjects of skin of color, age 12 or older. Female subjects of childbearing potential must have a negative urine pregnancy test result at Baseline and practice a reliable method of contraception throughout the study;
A female is considered of childbearing potential unless she is:
- postmenopausal for at least 12 months prior to study drug administration
- without a uterus and/or both ovaries; or
- has been surgically sterile for at least 6 months prior to study drug administration
Reliable methods of contraception are:
- intrauterine device in use ≥ 90 days prior to study drug administration;
- barrier methods plus spermicide in use at least 14 days prior to study drug administration; or
- vasectomized partner
[Exception: Female subjects of childbearing potential who are not sexually active will not be required to practice a reliable method of contraception. These subjects may be enrolled at the Investigator's discretion if they are counseled to remain sexually inactive during the study and understand the possible risks in getting pregnant during the study.]
ii. Facial acne vulgaris in patients with skin of color (Fitzpatrick Type V & VI Supplement VI) characterized by the following:
- IGA Score for acne vulgaris 3
- IGA Score for PIH 3
iii. Able to understand and comply with the requirements of the study and sign Informed Consent /HIPAA Authorization forms
Exclusion Criteria:
i. Female subjects who are pregnant (positive urine pregnancy test), breast-feeding, or who are of childbearing potential and not practicing a reliable method of birth control
ii. Allergy/sensitivity to any component of the test treatment
iii. IGA score for acne of 2 (mild) or 4 (severe)
iv. IGA score for Post Inflammatory Hyperpigmentation of 2 (mild) or 4 (severe)
v. Subjects who have not complied with the proper wash-out periods for prohibited medications (Supplement I).
vi. Medical condition that, in the opinion of the Investigator, contraindicates the subject's participation in the clinical study
vii. Skin disease/disorder that might interfere with the diagnosis or evaluation of acne vulgaris
viii. Evidence of recent alcohol or drug abuse
ix. History of poor cooperation, non-compliance with medical treatment, or unreliability
x. Exposure to an investigational study drug within 30 days of the Baseline Visit

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03402893
United States, Kentucky | |
DermResearch, PLLC | |
Louisville, Kentucky, United States, 40217 |
Documents provided by L.H. Kircik, M.D., Derm Research, PLLC:
Responsible Party: | L.H. Kircik, M.D., Medical Director, Derm Research, PLLC |
ClinicalTrials.gov Identifier: | NCT03402893 History of Changes |
Other Study ID Numbers: |
ONX-1701 |
First Posted: | January 18, 2018 Key Record Dates |
Results First Posted: | February 19, 2019 |
Last Update Posted: | April 2, 2019 |
Last Verified: | March 2019 |
Studies a U.S. FDA-regulated Drug Product: | Yes |
Studies a U.S. FDA-regulated Device Product: | No |
Product Manufactured in and Exported from the U.S.: | No |
Acne Vulgaris Hyperpigmentation Acneiform Eruptions Skin Diseases Sebaceous Gland Diseases Pigmentation Disorders Clindamycin |
Benzoyl Peroxide Dermatologic Agents Anti-Bacterial Agents Anti-Infective Agents Protein Synthesis Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action |