A Study to Evaluate Efficacy and Safety of Four Posaconazole Regimens With Placebo and Terbinafine in the Treatment of Toenail Onychomycosis (Study P05082AM2)

Condition(s) targeted: Onychomycosis

Intervention: SCH 56592 (Drug); SCH 56592 (Drug); SCH 56592 (Drug); SCH 56592 (Drug); Terbinafine (Drug); Placebo (Drug)

Phase: Phase 2

Status: Active, not recruiting

Sponsored by: Schering-Plough

Official(s) and/or principal investigator(s):
Amir Tavakkol, PhD, Dip Bact, Study Director, Affiliation: Schering-Plough

The purpose of this study is to evaluate the efficacy, safety, and tolerability of oral administration of four dosing regimens of posaconazole relative to placebo and terbinafine, in the treatment of toenail onychomycosis.

Official title: An Investigator-Blinded Study Evaluating the Efficacy and Safety of Four Posaconazole Treatment Regimens With Placebo and Terbinafine in the Treatment of Onychomycosis of the Toenail

Study design: Treatment, Randomized, Single Blind (Investigator), Placebo Control, Parallel Assignment, Safety/Efficacy Study

Primary outcome: Complete cure of onychomycosis. Complete cure is defined as negative mycology (negative culture and KOH) and 0% nail involvement (defined as absence of onycholysis and subungual hyperkeratosis).

Secondary outcome:

Effective treatment of onychomycosis. Effective treatment is defined as negative mycology (negative culture and KOH) and either 0% nail involvement or >5 mm growth of unaffected nail.

Safety and pharmacokinetics

Minimum age: 18 Years. Maximum age: 75 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

- The subject must meet ALL the criteria listed below for entry:

- Subject must be between 18 and 75 years of age inclusive, of either sex, and of

any race;

- Subject must have distal subungual infection that affects approximately 25% to

75% of at least one great toenail, both clinically and mycologically diagnosed;

- Subject must have at least 2 mm of the proximal end of the target toenail free of

infection;

- Subject must have a target toenail that is assessed as capable of growing

approximately 1 mm/month, (eg, the subject needs to report cutting his or her toenails at least once per month);

- Subject must have liver function tests within 1. 5 x the upper limit of normal

(bilirubin and transaminases);

- Subject must have normal serum creatinine levels;

- Subject must be able to take study medication orally;

- Subject must have no history of current narcotic or alcohol addiction;

- Subject must be willing to give written informed consent and able to adhere to

dose, procedures, and visit schedules;

- Woman of childbearing potential who is currently sexually active must agree to

use a medically accepted method of contraception while receiving protocol-specified medication and for 30 days after stopping the medication. Methods include condoms (male or female) with or without a spermicidal agent, diaphragm or cervical cap with spermicide, medically prescribed intrauterine device, oral or systemic hormonal contraceptive (plus an additional reliable barrier method), and surgical sterilization (eg, hysterectomy or tubal ligation).

Woman of child-bearing potential who is not currently sexually active must agree to use a medically accepted method of contraception should she become sexually active while participating in the study.

- Woman of childbearing potential must have a negative serum pregnancy test within 72

hours prior to start of study drug.

Exclusion Criteria:

- The subject will be excluded from entry if ANY of the criteria listed below are met:

- Subject with one or more of the following conditions on the target toenail:

- proximal subungual onychomycosis,

- white superficial onychomycosis,

- dermatophytoma or "yellow spike/streak",

- exclusively lateral disease,

- inability to become normal in the opinion of the investigator.

- Subject with psoriasis, severe moccasin-type tinea pedis requiring treatment,

symptomatic interdigital tinea pedis, lichen planus, or other abnormalities that could result in a clinically abnormal nail;

- Subject with peripheral vascular disease or peripheral circulatory impairment;

- Subject with history of uncontrolled diabetes mellitus;

- Subject with known chronic or active liver disease;

- Subject with any known immunodeficiency;

- Subject with a family history of long QT syndrome;

- Subject with an electrocardiogram with QTc interval prolongation greater than 450

msec for males and 470 msec for females;

- Subject with potassium or magnesium lower than the lower limit of normal;

- Subject with any clinically significant condition or situation, other than the

condition being studied that, in the opinion of the investigator, would interfere with study evaluations or optimal participation in the study;

- Subject who has received systemic antifungal therapy within 3 months or topical

antifungal therapy applied to the foot or toenails within 1 month of study entry;

- Subject who has received radiation therapy, chemotherapy, and/or

immunosuppressive drugs within 6 months of Randomization, and/or oral corticosteroids for >1 month within the 6 months of Randomization (exception: inhaled steroids);

- Subject using medications known to interact with azoles such as terfenadine,

pimozide, quinidine, halofantrine, astemizole, alfentanil, cisapride, HMG-Co A (3-hydroxy-3-methylglutaryl coenzyme A) reductase inhibitors that are metabolized by CYP3A4, and ebastine, within 7 days prior to Randomization; and pravastatin within 14 days prior to Randomization;

- Subject using medications known to lower the serum concentration/efficacy of

azoles including rifampin, rifabutin, cimetidine, carbamazepine, phenytoin, barbiturates, and isoniazid, 3 doses or more within 7 days prior to Randomization;

- Subject with a known sensitivity to azoles, POS and/or its excipients,

terbinafine and/or its excipients;

- Subject who has been previously enrolled in this study or any other POS

investigational trial;

- Subject known to have received treatment with investigational drugs within 30

days prior to enrollment into this study;

- Woman who is breastfeeding, pregnant, or intends to become pregnant;

- Subject who is part of the staff personnel directly involved with this study;

- Subject who is a family member of the investigational study staff.

Investigational Site 9, Birmingham, Alabama 35233, United States

Investigational Site 21, San Diego, California 92123, United States

Investigational Site 22, Denver, Colorado 80210, United States

Investigational Site 12, Miami, Florida 33143, United States

Investigational Site 14, Newnan, Georgia 30263, United States

Investigational Site 13, Metairie, Louisiana 70006, United States

Investigational Site 25, Baltimore, Maryland 21214, United States

Investigational Site 11, St. Louis, Missouri 63104, United States

Investigational Site 20, Omaha, Nebraska 68144, United States

Investigational Site 17, Cary, North Carolina 27511, United States

Investigational Site 5, Lake Oswego, Oregon 97035, United States

Investigational Site 27, Altoona, Pennsylvania 16602, United States

Investigational Site 4, Dallas, Texas 75243, United States

Investigational Site 19, San Antonio, Texas 78229, United States

Investigational Site 28, Houston, Texas 77056, United States

Investigational Site 23, Salt Lake City, Utah 84124, United States

Investigational Site 2, Virginia Beach, Virginia 23464, United States

Investigational Site 18, NORFOLK, Virginia 23507, United States

Investigational Site 26, Harrisonburg, Virginia 22803, United States

Investigational Site 16, Milwaukee, Wisconsin 53209-0099, United States

Starting date: June 2007
Ending date: December 2008
Last updated: June 16, 2008