Sangamo Therapeutics Announces Appointment of Lisa Rojkjaer, M.D., as Chief Medical Officer
“We are thrilled to welcome Dr. Rojkjaer, an experienced physician, drug developer, and regulatory expert, to the Sangamo team,” said Nathalie Dubois-Stringfellow, Chief Development Officer at Sangamo. “Her deep industry experience across all stages of clinical development will be pivotal for us as we advance our wholly owned Fabry program toward a potential Phase 3 trial, progress our industry-leading CAR-Treg program TX200 through Phase 1/2, and further develop our pre-clinical pipeline of epigenetic regulation for the central nervous system. Her leadership will be invaluable as we seek to create targeted potential genomic medicines for patients suffering from serious genetic diseases for which there are few or no available treatments today.”
Dr. Rojkjaer brings over 20 years of global and regional clinical development, regulatory, and medical affairs experience, as well as an international clinical practice background. She has held several senior leadership positions in both clinical development and medical affairs in biotech and global pharmaceutical companies, having most recently served as Chief Medical Officer at Viracta Therapeutics. She previously served in several senior positions focused on the development of small molecules and biologics for hematology and immunology indications, including Chief Medical Officer at Nordic Nanovector. Dr. Rojkjaer was the Global Clinical Program Head at Novartis Oncology, where she led development and supported the regulatory approval of Rydapt®. Other previous roles include Chief Medical Officer at Molecular Partners, and VP, Head of Clinical Development at MorphoSys AG. Earlier, at Novo Nordisk, she served as Director of Clinical Development, Hematology in the US and Head, Global Medical Affairs, Biopharmaceuticals while based in
Dr. Rojkjaer holds a Doctor of Medicine degree from the University of
About Sangamo Therapeutics
Sangamo Therapeutics is a clinical-stage biopharmaceutical company with a robust genomic medicines pipeline. Using ground-breaking science, including our proprietary zinc finger genome engineering technology and manufacturing expertise, Sangamo aims to create new genomic medicines for patients suffering from diseases for which existing treatment options are inadequate or currently don’t exist. To learn more, visit www.sangamo.com and connect with us on LinkedIn and Twitter.
Sangamo Forward Looking Statements
This press release contains forward-looking statements based on Sangamo's current expectations. These forward-looking statements include, without limitation, statements relating to the potential for Sangamo to create targeted genomic medicines, to advance its Fabry program toward a Phase 3 trial, to progress its CAR-Treg program TX200 through Phase 1/2, and to further develop its pre-clinical pipeline of epigenetic regulation for the central nervous system. These statements are not guarantees of future performance and are subject to certain risks and uncertainties that are difficult to predict. Factors that could cause actual results to differ include, but are not limited to, the research development process, including the results of clinical trials; the regulatory approval process for product candidates; and the potential for technological developments that obviate technologies used by Sangamo. Actual results may differ from those projected in forward-looking statements due to risks and uncertainties that exist in Sangamo's operations and business. These risks and uncertainties are described more fully in our Securities and Exchange Commission filings and reports, including in our Annual Report on Form 10-K for the year ended December 31, 2022 and our Quarterly Report on Form 10-Q for the quarter ended March 31, 2023. Forward-looking statements contained in this announcement are made as of this date, and Sangamo undertakes no duty to update such information except as required under applicable law.
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Source: Sangamo Therapeutics, Inc.
