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A Trial to Evaluate the Safety and Efficacy of DBI-001 Gel, DBI-002 Gel, and Aqueous Gel in Subjects With Onychomycosis

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DermBiont

Status and phase

Suspended
Phase 2

Conditions

Onychomycosis

Treatments

Biological: DBI-002
Biological: Aqueous Gel
Biological: DBI-001

Study type

Interventional

Funder types

Industry

Identifiers

Details and patient eligibility

About

This is a randomized, observer-blinded, Aqueous Gel-controlled trial examining the safety and efficacy of daily application of DBI-001 Gel vs. DBI-002 Gel vs. Aqueous Gel for 24 consecutive weeks in subjects with onychomycosis.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 to 50 years of age, inclusive, at Screening
  • Willing to abstain from all cosmetic activities involving the toenails during the entire course of the study
  • Distal subungual onychomycosis defined as a great toenail with onycholysis and thickening of the nail bed with keratinous material
  • Willing to have his/her treatment-targeted great toenail(s) clipped to remove onycholytic nail plate at each visit
  • At least one treatment-targeted great toenail must have at least 6 mm of clear nail from the proximal nail fold to the proximal limit of disease and, after trimming to within 1mm distal nail groove, have at least 3mm of involved nail from distal nail groove to proximal limit of disease
  • Confirmed presence of microorganisms of interest by KOH and qPCR at Screening
  • The affected treatment-targeted great toenail(s) is capable of re-growth as documented by subject self-reported history of clipping nails at least monthly

Exclusion criteria

  • Positive urine pregnancy test, pregnant, lactating, or female of childbearing potential who does not agree to use an active method of birth control for the duration of the study
  • Any dermatological conditions that could interfere with clinical evaluations
  • Great toenails with only superficial white onychomycosis, any evidence of subungual mycetoma as evidenced by yellow or white spikes, or any evidence of proximal onychomycosis
  • Any underlying disease(s) or other dermatological condition(s) that requires the use of interfering topical or systemic therapy, with the exception of certain protocol-specified that require a defined washout period for eligibility
  • Treatment of any type of cancer within the last 6 months, with the exception of superficial skin cancers such as basal cell carcinoma and squamous cell carcinoma
  • History of any significant internal disease which contraindicates the use of live microbiome
  • History of failing oral or prescription topical treatment for onychomycosis
  • A history of current episode of onychomycosis present for more than 3 years
  • Nail or anatomic abnormalities of the target great toenail(s)
  • AIDS or AIDS-related complex by medical history
  • History of current street drug or alcohol abuse, or street drug or alcohol abuse within the past year
  • Subjects known or suspected to be taking immune suppressive medications or subjects who are immunosuppressed
  • Subjects with poorly controlled diabetes mellitus requiring medical intervention/treatment
  • Subjects with peripheral vascular disease based on medical history
  • Subjects who have participated in any other trial of an investigational drug or device within 60 days prior to enrollment or participation in a research study concurrent with this study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

60 participants in 3 patient groups, including a placebo group

DBI-001 Gel
Experimental group
Description:
Topical application of DBI-001 gel on foot/feet affected with onychomycosis.
Treatment:
Biological: DBI-001
DBI-002 Gel
Experimental group
Description:
Topical application of DBI-002 gel on foot/feet affected with onychomycosis.
Treatment:
Biological: DBI-002
Aqueous Gel
Placebo Comparator group
Description:
Topical application of aqueous gel on foot/feet affected with onychomycosis.
Treatment:
Biological: Aqueous Gel

Trial contacts and locations

5

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Data sourced from clinicaltrials.gov

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