Michael Fleming, MBA
Michael has 35+ years of experience in business development and commercialization within the biotech industry. Prior to joining Neutrolis, Michael held leadership roles at GSK, Genentech, Elan, Anacor, and Coherus BioSciences. At Neutrolis, he drives the company's growth and strategic direction, focusing on market analysis, strategic partnerships, and fundraising efforts. Michael leads cross-functional teams, ensures regulatory compliance, and fosters a culture of innovation, ensuring Neutrolis’ products align with market needs and achieve successful market entry.
Andreas Reiff, MD
Andreas has extensive experience in medical leadership, with a focus on advancing treatments for autoimmune and inflammatory diseases. Prior to joining Neutrolis, Andreas served as Rheumatology Division Head at Children's Hospital Los Angeles (CHLA), University of Southern California; as Senior VP (Immunology & Inflammation) at Parexel, and founded TheraKine Ltd. At Neutrolis, he oversees clinical development and medical strategy, to ensure the highest standards of medical ethics, safety and efficacy. Andreas guides the company through clinical trials, regulatory submissions, and medical affairs, dedicated to bringing transformative treatments to market.
Ralph Lambalot, PhD
Ralph has 25+ years of experience developing manufacturing processes and analytical methods in support of commercial, clinical and preclinical biotherapeutic products. Prior to joining Neutrolis, Ralph was VP of Biologics Operations Science & Technology at AbbVie overseeing development and commercial manufacturing of Humira® and previously held senior scientist roles at Pfizer and BASF. Ralph is a bioorganic chemist and trained at Brown University and Harvard Medical School. At Neutrolis, Ralph leads chemistry manufacturing and controls (CMC).
Ken Olivier Jr., PhD
Ken has 22+ years of experience in drug development and regulatory strategy and is skilled in toxicology, regulatory affairs, and quality assurance. Ken is an experienced drug development veteran with a history of developing therapies in the biotechnology and pharmaceutical industry. Ken previously held positions in Regeneron, Biogen, GSK, and Merimak Pharmaceuticals. Ken received his Bachelors in Toxicology from the University of Louisiana at Monroe and PhD in Veterinary Biomedical and Clinical Sciences from Oklahoma State University. At Neutrolis, Ken oversees product development and assists with non-clinical and regulatory strategies.
Ghazaleh Gouya Lechner, MD
Ghazaleh has 20+ years of clinical research experience and is an Associate Professor in Internal Medicine and board certified in internal medicine, cardiology, and clinical pharmacology. Previously, Ghazaleh lead a research group at the phase I Unite of the Medical University Vienna and was Medical Director at a global CRO. She has been involved in the development and approval of numerous products and has led product strategy and protocol development by identifying and documenting the best ways to help patients. Ghazaleh and her clinical team at Gouya Insights lead Neutrolis’ clinical strategy and operations.