Anthera Pharmaceuticals, Inc. announced that the final patient has completed the last visit in the primary treatment phase of RESULT, a Phase 3 clinical study of Sollpura for exocrine pancreatic insufficiency ('EPI') due to cystic fibrosis. Although the data remains blinded, two successful interim futility analyses were conducted by the independent Data Monitoring Committee which is comprised of experts appointed by the Cystic Fibrosis Foundation’s Therapeutics Development Network. During these reviews, no safety concerns were reported, and it was recommended that the study continue as planned. The RESULT study enrolled 140 patients ages 7 to 58 years. Prior to randomization, the majority of patients were on Creon and 42% of patients were on gastric acid suppressants. Based on the outcome of the RESULT study, Sollpura has the potential to become the first oral, non-porcine PERT which may provide a reduction in the size and number of pills for patients with EPI.