ReCode Therapeutics Expands Scientific Team for mRNA Advances
ReCode Therapeutics Strengthens Scientific Advisory Board
ReCode Therapeutics, a pioneering clinical-stage genetic medicines company, has announced two significant appointments to its scientific advisory board (SAB) as it continues to innovate in the realms of mRNA and gene correction therapeutics.
Key Additions to the Advisory Team
The newly appointed members bringing their exceptional expertise include:
Andrew Bellinger, M.D., Ph.D.
Dr. Andrew Bellinger offers extensive knowledge in gene correction, genetic payload exploration, and rare disease drug development. His previous role as chief scientific officer at Verve Therapeutics equipped him with valuable insights. He also co-founded Lyndra Therapeutics, where he played a crucial role in advancing the company’s research and establishing external collaborations.
Katalin Karikó, Ph.D.
Dr. Katalin Karikó is celebrated globally for her groundbreaking contributions to biochemistry. She, along with Drew Weissman, earned a Nobel Prize for advancements crucial to developing COVID-19 vaccines through modified mRNA. Her continued dedication includes developing therapies for cystic fibrosis and various genetic disorders.
Strategic Importance of These Appointments
Shehnaaz Suliman, M.D., MBA, M.Phil., the CEO of ReCode Therapeutics, expressed her enthusiasm regarding the invaluable knowledge these esteemed professionals will bring. She noted, “Their unparalleled expertise in mRNA and gene correction drug discovery and development brings a wealth of knowledge and experience that will significantly enhance our ability to advance new therapies for rare genetic diseases.”
Current Scientific Advisory Board Members
Joining these new experts are existing members of the advisory board:
Dan Siegwart, Ph.D.
As the chair of ReCode’s SAB and a co-founder, Dr. Dan Siegwart leads with a strong background in molecular oncology research at the University of Texas Southwestern Medical Center. His pioneering work in delivery technologies has led to the development of the Selective Organ Targeting (SORT) lipid nanoparticle (LNP) platform.
Justin Hanes, Ph.D.
Dr. Justin Hanes is recognized as the Lewis J. Ort professor of ophthalmology at Johns Hopkins University. His multidisciplinary expertise spans delivering genetic medicines and studying nanoparticles capable of penetrating mucus barriers.
Eric Olson, Ph.D.
As the founding chair of the Department of Molecular Biology at the University of Texas Southwestern Medical Center, Dr. Eric Olson is renowned for his groundbreaking discoveries related to genes that influence heart and muscle development, including new CRISPR strategies aimed at correcting muscular dystrophy mutations.
Senior Advisors Enhancing Research Strategies
The company also benefits from the insights of two senior scientific advisors, who provide strategic guidance:
John Englehardt, Ph.D.
Dr. Englehardt is the director for Gene Therapy and chair at the University of Iowa Carver College of Medicine. His research is directed toward understanding cystic fibrosis disease mechanisms and advancing gene therapy applications.
Elliott Sigal, M.D., Ph.D.
Dr. Elliott Sigal serves as co-chair of Amgen’s scientific advisory board and is a prominent figure on several boards, including Adaptimmune Therapeutics and Vir Biotechnology. His leadership experience includes roles such as executive vice president at Bristol Myers Squibb.
Looking Ahead: ReCode’s Vision
David Lockhart, Ph.D., the chief scientific officer of ReCode Therapeutics, highlighted the excitement surrounding the company’s trajectory. “This is an exciting time for ReCode, particularly as we move our home-grown therapeutic programs into the clinic and begin treating patients,” he stated. The company envisions leveraging the advisory expertise to refine their research strategies and accelerate the development of medicines for conditions like cystic fibrosis.
About ReCode Therapeutics
ReCode Therapeutics is at the forefront of genetic medicines, employing precision delivery methods to develop innovative mRNA and gene correction therapies. The proprietary SORT LNP platform facilitates precise and targeted delivery, enhancing treatment efficacy for genetic disorders. Current lead programs include RCT1100 and RCT2100, focusing on conditions stemming from specific genetic mutations resistant to existing treatments. The company continues to broaden its pipeline into more genetic diseases while nurturing a supportive workplace.
Frequently Asked Questions
What is the significance of ReCode's new advisory board members?
Their expertise will significantly enhance ReCode's capacity in advancing new therapies for rare genetic diseases.
What are the specific areas of research that ReCode focuses on?
ReCode is dedicated to mRNA and gene correction therapeutics, with an emphasis on conditions like cystic fibrosis and primary ciliary dyskinesia.
Who is leading the scientific advisory board?
Dan Siegwart, Ph.D., serves as the chair of the advisory board.
How does ReCode ensure effective delivery of genetic medicines?
The company utilizes its proprietary Selective Organ Targeting (SORT) lipid nanoparticle platform to achieve precise delivery.
What is the company's vision for the future?
ReCode aims to develop tailored genetic medicines for genetic disorders while expanding its research pipeline.
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