We believe in connecting rigorous science with our innate sense of urgency to rapidly generate breakthrough therapies for patients in need of a better quality of life.
Our company
At our core, we are an experienced team of drug developers and biotech entrepreneurs with a proven track record of advancing complex biologics from early discovery through clinical validation.
Ilia is a serial biotech entrepreneur and executive who has successfully raised over $300M in funding and achieved multiple exits.
Prior to 35Pharma, he founded Forbius and served as CEO and President until its acquisition by Bristol Myers Squibb in Sep 2020.
Previously, Ilia held various roles at YM Biosciences until its acquisition by Gilead.
Ilia holds an MBA and a Masters of Biotechnology degree from the University of Toronto.
George is a physician specializing in internal medicine, pulmonary diseases, and critical care medicine with over 25 years of experience in the pharmaceutical industry dedicated to developing and introducing novel and impactful therapeutics to benefit patients and healthcare providers.
Throughout his career, George has extensively contributed to the development, execution and/or reporting of more than 45 phase I-IV clinical trials, numerous original peer-reviewed manuscripts and scientific abstracts, as well as the medical evaluation of dozens of business development and in-licensing opportunities in the areas of IPF, PAH, COPD, Asthma & anaphylaxis.
In his most recent role at a specialty pharmaceutical company, George oversaw the company's entire respiratory pipeline across phase I-IV for Asthma, COPD, bronchiectasis, refractory chronic cough, IPF and PAH, as well as the clinical evaluation of external opportunities in these disease areas.
He holds an Medical Doctorate from the American University of Beirut (Beirut, Lebanon), and completed his residency in Internal Medicine at the University Hospitals of Cleveland (Cleveland, Ohio), and completed his fellowship in Pulmonary and Critical Care Medicine at the University of Colorado Health Sciences Center (Denver, Colorado).
Maureen is a recognized leader in TGF-beta biology who trained with Professor Michael Sporn in the 1980’s, shortly after his discovery of TGF-beta. Over the following 4 decades, she refined her expertise in TGF-beta ligand-receptor structure-activity relationships, authored over 50 publications in the TGF-beta field alone and built an extensive network with the leading scientists in the field.
Her 35+ year successful track record in protein engineering and R&D of biological therapies led to over 100 scientific publications overall, 14 patents granted and numerous transactions with pharmaceutical companies including most recently the sale of Forbius to Bristol Myers Squibb (BMS).
In her former role as CSO of Forbius (2015 – 2020), Maureen drove the development of AVID200, a best-in-class biologic specifically targeting TGF-beta 1 and 3. AVID200 was successfully advanced from discovery stage into 3 Phase 1 clinical trials ultimately resulting in the sale of Forbius to BMS who are now developing AVID200 in oncology.
Prior to Forbius, she served as Scientific Leader of the National Research Council of Canada’s (NRCC) Biologics Program and spearheaded the development of innovative protein therapeutics in collaboration with the private sector resulting in five clinical and numerous pre-clinical stage programs.
Maureen received her PhD in Biochemistry from the University of Alberta.
Dmitry has over 25 years of experience in finance, accounting, SCM, HR and complex project management combined with strong operational expertise in finance, contracting and vendor management from global public companies. Previously, he served as VP of Finance and Operations for Forbius.
Monique brings more than 30 years of experience in the pharmaceutical, biotechnology, contractual and medical device industries and extended knowledge of the regulatory landscape and regulations for global product development, including biologics and medical devices. She has amassed hands-on experience and expertise in Phases 1 through 3 of clinical development, clinical operations and operations improvement, global project management, regulatory affairs, process development and integration, as well as alliance management.
In Monique's most recent role at a late-stage specialty pharma company, she built and led the clinical operations team, overseeing the clinical research strategy, clinical trial operations and development and clinical data. Prior to that, she had provided her project management expertise to a Dermatology CRO in Montréal and expertise in Clinical and Regulatory Affairs knowledge to several biotechnology companies targeting cancer, as well as certain immune, neurocognitive and orphan diseases.
Monique holds a Master of Science degree in Pharmaceutical Sciences and a Bachelor of Pharmacy, both from the Université de Montréal.
Julia's experience is rooted in early-stage biotech business development, investor relations and strategy gained in North America and Europe. She has supported both private and public fundraises, including IPO as well as PIPEs, and has built a strong network of generalist and specialist investors.
In Julia’s business development and strategic alliance roles, she has worked with prominent pharma companies, including Bristol Myers Squibb and Merck & Co., as well as physicians and KOLs at leading hospitals worldwide.
Most recently, she was Director of Business Development and Investor Relations at Forbius where she acted as business development lead for its subsequent acquisition by BMS in 2020. Previously, Julia led Business Development and Strategic Communications at BerGenBio, having supported the company through its IPO and multi-year immuno-oncology clinical trial collaboration with Merck & Co.
Julia holds a PhD in Biomedicine from University of Bergen, Norway, a dual degree MBA with distinction from IE Business School and Brown University and an MSc in Biotechnology & Biophysical Chemistry from Heidelberg University.
Gilles specializes in biologics-based drug development from discovery and preclinical operations to non-clinical IND-enabling studies.
Most recently, he was the Director of Preclinical Development at Forbius where his responsibilities included the completion of GLP toxicology studies and Phase 1 PK/PD assessments of AVID200 which supported its acquisition by BMS in September 2020.
Previously, Gilles acted as VP of Research at Alethia Biotherapeutics. He holds a PhD in Molecular Biology from McGill University and was an MRC of Canada post-doctoral fellow at the Molecular Oncology Group of the MUHC.
Thomas is an expert in CMC of complex biologics from early stage to commercial readiness.
He is a co-inventor and was CMC lead for asfotase alfa, an approved Enzyme Replacement Therapy against hypophosphatasia, which was developed by Enobia and eventually acquired by Alexion and, now marketed as Strensiq.
Most recently, Thomas was Director of Manufacturing at Forbius, where he was responsible for AVID100, a Phase 2 Antibody-Drug-Conjugate and AVID200, a Phase 1 receptor ecto-domain trap which was acquired by BMS in September 2020.
Previously, he led the manufacturing operations at ProMetic (now Liminal BioSciences) contributing towards the development Ryplazim (plasminogen), now FDA approved,
Thomas holds a PhD in Biochemistry from the Université de Montréal and completed a post-doctoral fellowship at Centre national de la recherche scientifique (CNRS) in France, identifying an actin-based mechanism of cell motility.
Caroline has over 25 years of experience as a legal leader and advisor to management teams within public and private multinational enterprises. Her expertise and involvement includes international expansion, structuring, governance, compliance, financing, as well as closing multi-million-dollar value transactions around the world in the pharmaceutical, biotechnology and other manufacturing industries.
Caroline holds an MBA with Honors from Strayer University (USA), a Master of International Business Laws from the University of Ottawa (Canada), and a Bachelor of Laws from the Laval University (Canada). She is a member of the Québec Bar.
Walter has broad and deep experience in the discovery and development of complex biologics paired with a highly successful industry track record as a senior biotech executive and board member.
He was the scientific founder of ImmunoGen, served as its EVP of Science and Technology and was an inventor of Kadcyla™. He co-founded Costim, acquired by Novartis, and served as its VP of Development. Walter also co-founded Semma Therapeutics, acquired by Vertex. He was a member of the Supervisory Board of Morphosys chairing the Science and Technology Committee (2007 - 2015) and was Chairman of Forbius (acquired by Bristol Myers Squibb in 2020).
Guy is a trained pulmonologist and was a member of the Executive Committee and Head of Global Clinical Development at Actelion up until its $30 billion acquisition by Janssen. While at Actelion, he led the development and ultimate approval of several branded drugs for the treatment of Pulmonary Hypertension, establishing Actelion as the PAH market leader.
Guy’s background also includes the CMO position at Merck Serono, CMO International at Serono, as well as medical executive positions at Astra, Fisons, Rhône-Poulenc Rorer, Glaxo Wellcome, GSK and Chiron. Most recently, he served as Executive VP and Chief Medical Officer at Idorsia Ltd, where he had been integral to rapidly advancing the company’s broad clinical pipeline, achieving the first registration less than five years after the company’s inception. Over his more than three-decades long industry career, Guy has led numerous medicines to approval and has led line extensions across a diverse group of therapeutic areas.
Aaron Royston is a Managing Partner at venBio with a background in life science investing, healthcare strategy, and as an entrepreneur. He has been involved in launching and investing in a number of venBio companies including Apellis Pharmaceuticals (IPO 2017), Menlo Therapeutics (IPO 2018), Akero Therapeutics (IPO 2019), Harmony Biosciences (IPO 2020), Impel NeuroPharma (IPO 2021), Ventyx BioSciences (IPO 2021), RayzeBio, Ablaze Pharmaeuticals, HistoWiz and Swift Health Systems (DBA - Inbrace). Three of these companies have developed treatments that are now FDA approved drugs available to patients.
Earlier in his career, Dr. Royston coordinated clinical research at Mount Sinai Medical Center, where his research has been published and presented in multiple medical journals and conferences. He holds an MD and MBA both from the University of Pennsylvania and a BS in Biological Sciences from Duke University. In 2010, Aaron was recognized by the United States White House as a Champion of Change for his work in Technology and Innovation.
Gregg is the Co-founder and Managing Director of Danforth Advisors. He has extensive life science executive management experience specializing in finance and operations for both venture-backed start-ups and publicly held companies. Previously, he served as CFO of ImmunoGen and Archemix and was an investment banker with Adams, Harkness & Hill. Additionally, Gregg was a board member of Forbius until its acquisition. He holds a JD from the University of Pittsburgh School of Law, an MBA from Carnegie Mellon University and a BA from Middlebury College.
Rich is a Managing Partner at venBio with experience as a physician, entrepreneur, and life science investor. He currently serves on the board of Ventyx Biosciences, Acelyrin, Attralus, Aeovian Pharmaceuticals, Entact Bio, NorthSea Therapeutics and Arrakis Therapeutics and served as a board member or observer of Pharvaris, Akero Therapeutics and Harmony Biosciences.
Prior to joining venBio, Rich served as the head of translational medicine at Pliant Therapeutics. As a key member of the initial management team, he participated in the formation and launch of Pliant Therapeutics from Third Rock Ventures. During Rich's tenure at Third Rock Ventures, he was responsible for company creation to transform new areas of science into innovative drug discovery companies.
He began his career as a resident physician in Harvard’s Plastic and Reconstructive Surgery Program. Rich has published numerous articles in top-tier peer-reviewed journals including Nature Medicine and Nature Nanotechnology, holds more than a dozen patents, and was named one of Forbes “30 Under 30” in Science and Healthcare. Rich holds a BSE in Bioengineering from the University of Pennsylvania where he graduated summa cum laude. He received his MD and PhD in Bioengineering from Stanford University in the Medical Scientist Training Program.
Ilia is a serial biotech entrepreneur and executive who has successfully raised over $300M in funding and achieved multiple exits.
Prior to 35Pharma, he founded Forbius and served as CEO and President until its acquisition by Bristol Myers Squibb in Sep 2020.
Previously, Ilia held various roles at YM Biosciences until its acquisition by Gilead.
Ilia holds an MBA and a Masters of Biotechnology degree from the University of Toronto.
Maureen is a recognized leader in TGF-beta biology who trained with Professor Michael Sporn in the 1980’s, shortly after his discovery of TGF-beta. Over the following 4 decades, she refined her expertise in TGF-beta ligand-receptor structure-activity relationships, authored over 50 publications in the TGF-beta field alone and built an extensive network with the leading scientists in the field.
Her 35+ year successful track record in protein engineering and R&D of biological therapies led to over 100 scientific publications overall, 14 patents granted and numerous transactions with pharmaceutical companies including most recently the sale of Forbius to Bristol Myers Squibb (BMS).
In her former role as CSO of Forbius (2015 – 2020), Maureen drove the development of AVID200, a best-in-class biologic specifically targeting TGF-beta 1 and 3. AVID200 was successfully advanced from discovery stage into 3 Phase 1 clinical trials ultimately resulting in the sale of Forbius to BMS who are now developing AVID200 in oncology.
Prior to Forbius, she served as Scientific Leader of the National Research Council of Canada’s (NRCC) Biologics Program and spearheaded the development of innovative protein therapeutics in collaboration with the private sector resulting in five clinical and numerous pre-clinical stage programs.
Maureen received her PhD in Biochemistry from the University of Alberta.
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