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Kythera completes enrolment in REFINE-1, REFINE-2 trials of ATX-101

Kythera Biopharmaceuticals has completed enrolment in the Randomized Double-blind Evaluation of Submental Fat Reduction IN ATX-101 TrEated Patients (REFINE)-1 and REFINE-2 trials of ATX-101in the US and Canada.

ATX-101, a injectable facial aesthetic drug under clinical investigation for the reduction of submental fat, is a proprietary formulation of synthetic sodium deoxycholate, a well-characterised component of human bile that is naturally occurring in the body to promote the breakdown of dietary fat.

The trials initiated in March 2012 enrolled more than 1,000 patients, randomised to ATX-101 or placebo and the company anticipates releasing top-line results from the trials in mid-2013.

Kythera president and CEO Keith Leonard said, "We look forward to continued clinical development of ATX-101 as part of our corporate commitment to develop first-in-class, prescription products that address unmet needs for the aesthetic physician and patient communities."

The identical double-blind, placebo-controlled trials are designed to compare subcutaneous injections of ATX-101 dosed at 2mg/cm2 to similar injections of placebo, with the primary efficacy assessments at 12 weeks after final treatment.

The trials will use clinician-reported scale and a patient-reported scale as a composite to define a responder as a patient who simultaneously achieves a pre-defined threshold of improvement on both the scales.

Secondary endpoints will measure patients’ self-perception related to their submental fat in addition to the reduction in volume of submental fat using Magnetic Resonance Imaging in a subset of approximately 400 subjects at selected centres.