BPX-01 Minocycline 1% Topical Gel for Reduction of Propionibacterium Acnes

BioPharmX

Status and phase

Completed

Phase 2

Conditions

Acne Vulgaris

Treatments

Drug: BPX-01 Vehicle Gel

Drug: BPX-01, 1% Topical Gel

Study type

Interventional

Funder types

Industry

Identifiers

NCT02709096

BPX-01-C02

Details and patient eligibility

About

This is a Phase 2a study which is being conducted in healthy volunteers in order to evaluate the comparative reduction of Propionibacterium acnes in-vivo following once daily topical administration of BPX-01 Minocycline 1% Topical Gel (BPX-01) or BPX-01 Vehicle control.

Full description

The objective of this study is to evaluate the comparative reduction of Propionibacterium acnes (P. acnes) in-vivo following once daily topical administration of BPX-01 Minocycline 1% Topical Gel or BPX-01 Vehicle control Gel.

A secondary objective is to assess the tolerance of the treatment regimen versus a vehicle control. Safety laboratory data (chemistry and hematology) and plasma levels of minocycline are also of significant interest to the sponsor.

This is a single center, randomized, double blind, two-cell, vehicle controlled P. acnes study. All subjects will be randomized 2:1 to 1% BPX-01 or vehicle control to be applied as a topical gel once daily for four (4) weeks.

This is a six (6) week study with a four (4) week treatment period and a two (2) week post treatment follow up visit. The clinical endpoint is in-vivo quantification of P.acnes. The safety/tolerance endpoints are; observer reported: erythema, scaling-peeling, edema, and subject reported: tightness, burning-stinging, and itching. Plasma levels of minocycline and basic hematology and chemistry laboratory values will be collected.

Enrollment

33 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Be a healthy, adult male and/or female volunteer 18 to 40 years of age with no past or present history of any significant disease based on PI discretion;
If female, must be post-menopausal, surgically sterile, or using effective birth control methods with a negative urine pregnancy test at the Screening and Baseline visits (female subjects of childbearing potential only);
Show a high degree of fluorescence of the face under a Wood's lamp at the screening visit.
Be willing to refrain from using antimicrobial topical products for the duration of study participation;
Be willing to return to the study center for all study visits;
Be willing to follow all study instructions and adhere to study restrictions;
Provide informed consent to the study procedures and restrictions

Exclusion criteria

Have a history of skin disease or presence of skin condition the PI believes would interfere with the study;
Females who report that they are pregnant, planning a pregnancy or breastfeeding or those females who are of child bearing potential, that test positive with a urine pregnancy test;
Have conditions or factors that the PI believes may affect the response of the skin or the interpretation of the results;
Participated in any clinical study within the previous 30 days, be concurrently participating in other studies, or be involved in any aspect of test administration;
Use of topical or systemic antibiotics or other products within the previous 4 weeks prior to baseline, that influence P. acnes counts;
Are known to be allergic to any of the test product(s) or any components in the test product(s);
Have a history of significant medical condition/disease that the PI believes may affect the response of the skin or the interpretation of the results;
Has any other condition that, in the opinion of the Investigator or his designee, could interfere with the subject's ability to use the treatment as instructed, alter their treatment response, or affect their ability to complete the study