Anthera Pharmaceuticals, Inc. announced that it has commenced screening in Europe in the result Phase 3 clinical study of Sollpura for exocrine pancreatic insufficiency (EPI) due to cystic fibrosis (CF). International enrollment is expected to provide topline data at the end of 2017 or early 2018. The RESULT clinical study design evolved from the data in the previous Sollpura trial (SOLUTION) and allows for more frequent and higher dose adjustments based upon clinical signs and symptoms. As with current practice with porcine enzymes, the RESULT study allows dose increases on an individualized basis to achieve maximum therapeutic benefit, while maintaining a potential reduction in daily pill burden due to Sollpura's significantly more compact formulation technology.