Study of Mycamine® in Children With Fungal Infections to Evaluate Safety and Blood Levels of the Drug

This is a prospective, multicenter, open-label, repeat-dose study conducted in two groups. Subjects in Group 1 and Group 2 will receive treatment for 10 to 14 days (per investigator clinical judgment); dose level (3.0 mg/kg or 4.5 mg/kg) will be determined by the subject's weight at baseline. Study procedures in both groups will be similar except that serial blood samples for assessment of pharmacokinetics will be collected in Group 1. Subjects may only participate in one group of the study.

At least 24 subjects, with at least 8 in each of three age ranges, will be enrolled in Group 1 (PK + safety). At least 36 subjects will be enrolled in Group 2 (safety), with at least 12 in each of the three age ranges.

Inclusion criteria

• Subject is 2 to 16 years inclusive
• Subject has suspected, proven or probable candidiasis, candidemia or other invasive candidiasis
• Subject has sufficient venous access to permit administration of study medication, collection of pharmacokinetic samples, and monitoring of laboratory safety variables

Exclusion criteria

• Subject has evidence of significant liver disease, as defined by aspartate transaminase (AST), alanine transaminase (ALT), bilirubin or alkaline phosphatase > 5 times the upper limit of normal (ULN)
• Subject has a concomitant medical condition that in the opinion of the investigator and/or medical monitor precludes enrollment into the study
• Subject has a history of anaphylaxis, hypersensitivity, or any serious reaction to the echinocandin class of antifungals
• Subject has received treatment with an echinocandin within one week prior to first dosing
• Subject status is unstable and subject is unlikely to complete all study required procedures