Moberg Pharma, a Swedish pharmaceutical company, has announced the completion of patient enrolment in the ongoing Phase II trial of MOB-015.
A topical formulation of terbinafine, MOB-015 has been developed for the treatment of onychomycosis (nail fungus) and has fungicidal and keratolytic properties to remove dead cells from the skin’s outermost layer.
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Moberg Pharma CEO Peter Wolpert said; "MOB-015 has the potential to become a valuable addition to our product portfolio and we look forward to the outcome of the study during next year."
The study is designed to confirm the product concept of MOB-015, as well as provide a basis for a Phase III study and out-licensing.
Patients will be treated for twelve months and later observed for a total of fifteen months, as per the normally accepted FDA and EMA endpoints for nail fungus.
The Phase II study is being conducted at Sahlgrenska University Hospital in Gothenburg, Sweden.
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