Actinium Pharmaceuticals, Inc. announced that Dr. Jehan Rowlands has been appointed Vice-President, Head of Regulatory Affairs. Dr. Rowlands will be responsible for developing clinical regulatory strategies for Actinium’s antibody radio-conjugate (ARC) based drug candidates. This will include supporting the filing of a Biologics License Application (BLA) with the FDA for Iomab-B, Actinium’s lead myeloablation product that is currently in a pivotal Phase 3 trial. In addition, Dr. Rowlands will be responsible for supporting the development of a regulatory pathway for Actinium’s planned Actimab-MDS clinical trial, which is Actinium’s latest myeloablation initiative that leverages Actinium’s core competencies in bone marrow transplant (BMT). Finally, he will be responsible for developing and executing the clinical regulatory strategy for Actinium’s current and future clinical trials from its CD33 program and AWE technology platform.