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Sana Biotechnology Inc

Sana Biotechnology, Inc., a biotechnology company, focuses on utilizing engineered cells as medicines in the United States. It develops ex vivo and in vivo cell engineering platforms for various therapeutic areas with unmet treatment needs, including type 1 diabetes, B cell mediated autoimmune diseases, and oncology. The company's product pipeline includes UP421, a HIP-modified allogeneic primary islet cell product, which is in phase 1 clinical trial to treat type 1 diabetes; SC451, a HIP-modified, stem cell derived pancreatic islet cell therapy, which is in preclinical trial for the treatment of type 1 diabetes; SG293 and SG299, a CD8-targeted fusosome for the treatment of B cell hematologic malignancies and B cell mediated autoimmune diseases. The company has an option and license agreement with Beam Therapeutics Inc. for use of Beam's proprietary CRISPR Cas12b nuclease editing technology to research, develop, and commercialize engineered cell therapy products; and a license agreement with Harvard College to access certain intellectual property for the development of hypoimmune-modified cells. The company has a strategic collaboration with Mayo Clinic for the development of SC451, a hypoimmune-modified pancreatic islet cell therapy for type 1 diabetes. The company was formerly known as FD Therapeutics, Inc. and changed its name to Sana Biotechnology, Inc. in September 2018. Sana Biotechnology, Inc. was incorporated in 2018 and is headquartered in Seattle, Washington.

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Biotech & Genomic Medicine

mRNA Cancer Vaccine Market to Surpass $1.20 Billion in 2026, Report Finds

The global mRNA cancer vaccine market is projected to exceed US$1.20 billion by 2026, according to a new report from ResearchAndMarkets.com. The market is expected to see continued robust growth through 2036, driven by advances in precision oncology, sequencing technologies, and an expanding pipeline of clinical candidates. Key players such as BioNTech, Moderna, Arcturus Therapeutics, and Sana Biotechnology are advancing platform and clinical innovations, while innovations like self-amplifying mRNA constructs and improved lipid nanoparticle delivery systems are enhancing scalability. The report also highlights that production relies on globally sourced inputs like lipid nanoparticles and nucleotides, making supply chains vulnerable to tariffs and disruptions, which could impact costs and development timelines. The analysis covers market segmentation by vaccine type, therapeutic approach, clinical phase, indication, and end-user across regions including North America, Europe, Asia Pacific, Latin America, and the Middle East and Africa.
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