Title

A Study to Evaluate TMI-358 in the Treatment of Distal Subungual Onychomycosis
A Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of TMI-358 in the Treatment of Distal Subungual Onychomycosis of the Toenail
  • Phase

    Phase 2
  • Study Type

    Interventional
  • Status

    Terminated
  • Study Participants

    120
The purpose of this study is to determine if a local treatment is effective for the treatment of toenail fungus (distal subungual onychomycosis).
Study Started
Sep 30
2009
Primary Completion
Apr 30
2011
Anticipated
Last Update
Jan 17
2011
Estimate

Drug TMI-358

Micro implant monthly x 3

Drug MMI-467

Micro implant monthly x 3

TMI-358 Experimental

Active treatment

MMI-467 Placebo Comparator

Criteria

Inclusion Criteria:

Male or female, 18 to 75 years of age, inclusive
Diagnosed with distal subungual onychomycosis (DSO) of the toenails
Great toe(s) with intact skin and intact neurologic functions
Great toenail(s) free of nail polish

At least one target great toe which has:

25 to 75% involvement of the area of the nail unit (including destroyed or missing parts of the nail plate)
at least 2 mm of uninvolved nail growth as measured from the proximal nail fold to the most proximal point to the disease process and with no lunular involvement
nail unit hyperkeratosis at the most distal edge which measures no greater than 3 mm
a positive KOH and culture

Exclusion Criteria:

Any significant disease of the hepatic, renal, endocrine (including diabetes mellitus), immune systems, or other health conditions which could interfere with or confound the results of study assessments
Pre-existing chronic foot pain, neurologic deficit or skin disease/injury in treated foot
In the case of female subjects, are pregnant, nursing, or planning to become pregnant within the study period
History of clinically significant abnormal laboratory values, including liver function test results equal to or greater than 2 x the upper limit of normal
Disease-like psoriatic toenails, significant toenail abnormalities/dystrophies, toenail injuries or any other condition in the toenail which could interfere with study evaluations (e.g., prevent obtaining normal appearing nail, after clearing of onychomycosis, due to chemical damage, genetic or pigmentary disorders, etc.)
Have white superficial onychomycosis, proximal subungual onychomycosis, yellow spikes, or dermatophytoma
Have paronychia
Have a history of chronic alcohol or drug abuse
No Results Posted