About Us

About Us - Kinevant

Kinevant Sciences (kine-a-vant) is a clinical-stage biopharmaceutical company dedicated to treating rare inflammatory and autoimmune diseases with significant unmet need. Our lead candidate namilumab is a novel monoclonal antibody being developed for the treatment of pulmonary sarcoidosis. Namilumab targets GM-CSF, a key pro-inflammatory cytokine involved in the pathogenesis of sarcoidosis and other inflammatory disorders.

Kine

(from the Ancient Greek: kīnéō, “to move” or “set in motion”)

Diseases shouldn’t define us. We are dedicated to improving patients’ quality of life, so they spend less time on the sidelines and more time on the move.

Management Team

Our leadership team has significant experience developing new therapies for inflammatory and immunological disorders.

Our executive team is supported by an accomplished board of directors and expert panel of scientific advisors.

Kinevant Management Team
Bill Gerhart
Bill Gerhart
Chief Executive Officer

Bill Gerhart has more than 20 years of experience building high-performance execution teams to develop new therapeutics for serious diseases. Prior to joining Kinevant in 2021, he was the CEO of Respivant/Patara Pharma, Elevation Pharma, and Mpex Pharma which focused on developing new medicines for pulmonary fibrosis, chronic obstructive pulmonary disease, and cystic fibrosis, respectively. In addition to his biotech activities, Bill serves as the Vice Chair of Sanford Burnham Prebys Institute’s Board of Trustees, a non-profit medical research institute focused on basic and translational research in cancer, neurodegeneration, infectious, and inflammatory diseases.

Bill earned a BA from Baylor University and an MBA from Harvard Business School.

Tuan Nguyen
Tuan Nguyen
Chief Financial Officer

Tuan Nguyen has more than 15 years of experience in biopharma working on small molecules and AAV gene therapies. Most recently, he was VP of Finance at Adverum Biotechnologies. Prior to that he held various senior Finance leadership roles at Intarcia Therapeutics, Fibrogen, and UCB. He has helped raise over $1 billion in dilutive and non dilutive capital. Tuan earned his MBA with dual concentration in Finance and Entrepreneurship, Innovation, & Change from Emory University.

Gary Barrera
Gary Barrera
Senior Vice President, Regulatory, Quality, and Drug Safety

Gary has more than 25 years of experience in Clinical and Commercial biologics and small molecules with increasing levels of leadership. Most recently, Gary was Senior Vice President of Quality at Allakos Inc. Prior to that, his leadership spanned Quality, Regulatory, Drug Safety and Operational Excellence at Theravance Biopharma. Gary also was the Site Head of Quality at Boehringer Ingelheim’s Fremont, California facility and he worked at Genentech for 16 years in roles of increasing responsibility.

Gary graduated from UC Berkeley with a Degree in Integrative Biology and Environmental Science in 1996 and a Masters of Business Administration from St. Mary’s College in 2011. Gary serves as an adjunct professor for the Keck Institute, teaching a Master’s Level course called Pharmaceutical Quality.

Chantal Petit
Chantal Petit
Vice President, Program Management

Chantal brings more than two decades of experience in biopharma working on small molecules, biologics, and AAV gene therapies from discovery through commercialization. She most recently was Chief of Staff to the Chief Scientific Officer and the Research division at PTC Therapeutics Inc. Prior to that she was the program/alliance management lead at Provention Bio; product development lead at Regenxbio; project leader at Shire and GlaxoSmithKline; and senior investigator at Smithkline Beecham, leading research in the antimicrobial field.

Chantal earned a Ph.D. in microbiology and biochemistry from the University of Nancy, France. She completed post-doctoral training in Canada and the UK, as well as a Certificate in Clinical Trial Management from Temple University.

Lisa Sherman
Lisa Sherman
Director of Clinical Operations

Lisa Sherman has more than 17 years of experience in Clinical Research. Prior to joining Kinevant, Lisa was the Director of Clinical Operations at Roivant, and prior to Roivant, she was a Sr. Project Manager, Clinical Operations at Lexicon Pharmaceuticals. During her time at Lexicon, she led a large phase 3 program in diabetes which ultimately resulted in a successful NDA filing and inspections, as well as EMA approval in Europe.

Lisa earned a BS in Kinesiology from the University of Houston and an MBA from the University of Phoenix.

Cynthia Scott
Cynthia Scott
Director of Regulatory Affairs

Cynthia Scott has more than 15 years of regulatory experience working on biologics and small molecules, in the areas of diabetes, oncology, infectious diseases, and rare diseases. Prior to joining Kinevant, Cynthia served as a regulatory consultant for over 10 years where she led cross-functional teams toward global product development goals, providing regulatory strategy and team leadership, ranging from early to late phase development.

Cynthia earned a BS from Eastern Nazarene College and an MS in Drug Regulatory Affairs and Health Policy from Massachusetts College of Pharmacy and Health Sciences.

Rayne Rodgers
Rayne Rodgers
Director of Patient Advocacy

Rayne has over eleven years of experience in patient advocacy, clinical trial recruitment, data science innovation, and program management.  Prior to Kinevant, Rayne worked with the Muscular Dystrophy Association as the Vice President of MOVR – a unified, national patient data hub for neuromuscular diseases – facilitating research initiatives with pharmaceutical and academic partners.  Before MDA, Rayne led global patient recruitment and advocacy efforts at miRagen Therapeutics across multiple rare hematological malignancies as the Director of Medical and Patient Affairs.  Rayne was also a Program Manager at Takeda where she launched a novel, systematic study of exceptional drug responders to oncology treatments, in collaboration with Harvard Medical School.

Rayne earned a BS in Finance from the University of Florida and an MPH from Emory University.

Board of Directors

Frank Torti, MD
Roivant Vant Chair

Frank Torti serves as Vant Chair at Roivant Sciences and is responsible for the operating companies in the Roivant Pharma family. He previously served as Vant Investment Chair, where he oversaw a group of companies responsible for the development of thirty-five investigational drugs in eleven therapeutic areas and over fifty clinical trials, including four successful Phase 3 trials. Dr. Torti joined Roivant in 2018 from New Enterprise Associates (NEA), a leading venture capital firm where he served as partner. Prior to joining NEA in 2007, Dr. Torti was a researcher at the Duke University Center for Clinical & Genetic Economics.

Dr. Torti received his M.D. from the University of North Carolina School of Medicine and his M.B.A. from Harvard Business School.

Bill Gerhart
Chief Executive Officer

Bill Gerhart has more than 20 years of experience building high-performance execution teams to develop new therapeutics for serious diseases. Prior to joining Kinevant in 2021, he was the CEO of Respivant/Patara Pharma, Elevation Pharma, and Mpex Pharma which focused on developing new medicines for pulmonary fibrosis, chronic obstructive pulmonary disease, and cystic fibrosis, respectively. In addition to his biotech activities, Bill serves as the Vice Chair of Sanford Burnham Prebys Institute’s Board of Trustees, a non-profit medical research institute focused on basic and translational research in cancer, neurodegeneration, infectious, and inflammatory diseases.

Bill earned a BA from Baylor University and an MBA from Harvard Business School.

Eric Venker, MD, PharmD
Roivant President and Chief Operating Officer

Eric Venker serves as President and Chief Operating Officer of Roivant Sciences. Dr. Venker first joined Roivant in 2014 and has since served in various roles of increasing responsibility, including Chief of Staff to the CEO. Prior to joining Roivant, Dr. Venker was a physician at New York Presbyterian Hospital, Columbia University Medical Center, where he trained in internal medicine. Earlier in his career, Eric was a Clinical Pharmacist at Yale-New Haven Hospital.

Dr. Venker received his Pharm.D. from St. Louis College of Pharmacy and his M.D. from Yale School of Medicine.