Check out Jonathan D. Grinstein, PhD's take on growing momentum for cell and gene therapy based on his reporting from ARM’s recent Meeting on the Mesa for Inside Precision Medicine. He includes highlights of ARM’s ‘Reasons to Believe’ in CGT and promising medicines under development by ARM members Trogenix and Prime Medicine, Inc. https://lnkd.in/eCvhmmZ5 #CGMesa25 #cellandgenetherapy
Alliance for Regenerative Medicine
Biotechnology Research
Washington, District of Columbia 30,297 followers
We champion the benefits of engineered cell therapies & genetic medicines for patients, healthcare systems & society.
About us
The Alliance for Regenerative Medicine (ARM) is the leading international advocacy organization championing the benefits of engineered cell therapies and genetic medicines for patients, healthcare systems, and society. As a community, ARM builds the future of medicine by convening the sector, facilitating influential exchanges on policies and practices, and advancing the narrative with data and analysis. We actively engage key stakeholders to enable the development of advanced therapies and modernize healthcare systems so that patients benefit from durable, potentially curative treatments. As the global voice of the sector, we represent more than 400 members across 25 countries, including emerging and established biotechnology companies, academic and medical research institutions, and patient organizations. To learn more about ARM or to become a member, visit http://www.alliancerm.org.
- Website
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http://alliancerm.org
External link for Alliance for Regenerative Medicine
- Industry
- Biotechnology Research
- Company size
- 11-50 employees
- Headquarters
- Washington, District of Columbia
- Type
- Nonprofit
- Founded
- 2009
Locations
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Primary
1015 18th St NW
Suite 1102
Washington, District of Columbia 20006, US
Employees at Alliance for Regenerative Medicine
Updates
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A touching op-ed from the Co-Founder of the CureLGMD2i Foundation on how the dreams of her daughter and many other children with rare diseases depend on the reauthorization of the FDA's Rare Pediatric Disease Priority Review Voucher (PRV) Program. This vital program accelerates innovation in developing treatments, such as cell and gene therapies, to help treat and potentially cure rare diseases in children. However, its fate is currently stalled in Congress. We join Kelly in calling on Congress to swiftly reauthorize the PRV Program by passing the Give Kids a Chance Act before the end of the year.
Co-Founder/CEO at CureLGMD2i, Passionate Patient Advocate, Rare Mom, Public Speaker, Patient Advisory Board Member
The Pediatric Priority Review Voucher (#PPRV) is bipartisan legislation that creates a market based incentive for rare disease drug developers. It has spurred critical rare disease drug development, but sadly it was not reauthorized at the end of 2024. The #LGMDs are ultra rare muscle wasting diseases that have no approved therapy. Reauthorization of the PPRV would be the difference maker in the life Sammy and 25 million others who are living with rare diseases. See our story below... https://lnkd.in/eN73QESb Biotechnology Innovation Organization, PennLive.com, EveryLife Foundation for Rare Diseases, National Organization for Rare Disorders CureLGMD2i Foundation, Dion Foundation, Speak Foundation, LGMD2D Foundation, Coalition to Cure Calpain 3
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Solid tumors have been a challenge for modern medicine. However, the cell and gene therapy clinical pipeline is advancing potential breakthroughs. ARM's Stephen Majors sat down with Ken Macnamara, CEO of Trogenix, at ARM Studios during #CGMesa25 to highlight their precision genetic medicine, which is now entering the clinic and looking to be a transformative option for patients who face a terminal prognosis with glioblastoma.
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Looking to reshare your favorite moments from ARM's 2025 Cell & Gene Meeting on the Mesa? Conference photos can now be accessed through our Flickr account. 📸 ➡️ https://lnkd.in/efTSBYvE Attendees, speakers, and presenters are welcome to download photos of their favorite moments to share on social media. The photos are organized in albums by each day of the conference. #CGMesa25
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The regulatory picture for cell and gene therapy in 2026 continues to take form. Two more BLAs by the FDA were accepted, setting up new PDUFA dates in the spring of next year. 🧬 March 28, 2026 | Kresladi Rocket Pharmaceuticals' gene therapy to treat severe leukocyte adhesion deficiency type 1 https://lnkd.in/e_-2R7nm 🧪 April 6, 2026 | Orca-T Orca Bio's T-cell therapy to treat acute myeloid leukemia, acute lymphoblastic leukemia, and myelodysplastic syndromes https://lnkd.in/e2PcDsKW Four PDUFA dates are currently scheduled in 2026, with more therapies poised to advance in the pipeline. To learn more, look out for ARM's Q3 2025 Sector Snapshot this month.
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This year’s Cell & Gene Meeting on the Mesa brought together leading investors and analysts to discuss the evolving dynamics between the cell and gene therapy sector and capital markets. ARM CEO Tim Hunt had the opportunity to sit down with Samantha Semenkow, Ph.D., Vice President, SMid Biotech Equity Research Analyst at Citi, at ARM Studios to unpack some of the themes and trends highlighted at the conference. #CGMesa25
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And that’s a wrap for ARM's 2025 Cell and Gene Meeting on the Mesa. And what a week it was! Thanks to our sponsors, speakers, and partners for making this year’s Meeting on the Mesa possible, and to our amazing patient advocates for sharing their inspirational stories. Did you miss out on any panels or workshops you wanted to see? Attendees can rewatch any session through the online conference platform. Also, keep an eye out for more ARM Studios interviews with sector leaders in the coming weeks. 🎥 Safe travels, and see you next year! 🌵🧬 #CGMesa25
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2025 has also been a year of notable capital raises for cell and gene therapy companies, along with several announcements around large partnerships and acquisitions with big biopharma. During his opening remarks at this year’s Cell & Gene Meeting on the Mesa, ARM CEO Tim Hunt highlighted how these trends show promising momentum for sustainable growth in the sector. View the full #ReasonstoBelieve analysis and deck here: https://lnkd.in/ezeeyKrz #CGMesa25
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Scaling up cell and gene therapies is one of the sector’s toughest challenges. What approaches are being developed to help therapy developers reduce costs while maintaining quality and consistency? ARM's Adam Wolf sits down with Andreas Knaack, President and CEO of Invetech, at ARM Studios this week at the Meeting on the Mesa to unpack what's next in automation and how it's poised to transform #cellandgenetherapy. #CGMesa25 #Automation