“Dune”-inspired Arrakis Therapeutics has tested its spice—an RNA-targeting small molecule—in a mouse model of myotonic dystrophy type 1 (DM1), with the drug reversing the prolonged muscle contraction that is characteristic of the disease.
Arrakis, based not on a desert planet but in Waltham, Massachusetts, presented the results at the Cell Symposia: Chemical biology in drugging the undrugged conference in San Francisco on Dec. 4, according to a release.
Patients with DM1 have copies of the DMPK gene that produce mRNA with repeated CUG nucleotide sequences; this errant mRNA disrupts the work of RNA-processing proteins, leading to symptoms such as muscle wasting, cardiac dysfunction, cognitive impairment and the characteristic myotonia, which is an inability for muscles to relax after contracting.
Arrakis’ small molecule binds to the repeated CUG sequences and neutralizes them, the company said in the release, and was able to restore normal RNA splicing in muscle cells derived from patients.
“While there have been serendipitous discoveries of small molecule drugs that bind to RNA, we believe this is one of the clearest examples of a rationally designed small molecule that has been purpose-built to address an RNA disease target” Arrakis CEO Michael Gilman, Ph.D., said in the release. “We believe that our DM1 program is the first of many potential RNA-targeted small molecule drug candidates that will emerge from our platform in coming years.”
DM1 is the most common form of myotonic dystrophy, estimated to affect about one in every 8,000 people. DM1 has no cure, with treatments instead focused on managing symptoms.
Much like its namesake fictional planet, Arrakis has attracted extensive attention for its drugs in its nine-year history, though the company has eschewed potential pharma suitors in the past. The firm teamed up with Roche for a $190 million upfront deal in 2020 after raising a $75 million series B the previous year.
Check out our mRNA service to expedite your vaccine research
PackGene Biotech is a world-leading CRO and CDMO, excelling in AAV vectors, mRNA, plasmid DNA, and lentiviral vector solutions. Our comprehensive offerings span from vector design and construction to AAV, lentivirus, and mRNA services. With a sharp focus on early-stage drug discovery, preclinical development, and cell and gene therapy trials, we deliver cost-effective, dependable, and scalable production solutions. Leveraging our groundbreaking π-alpha 293 AAV high-yield platform, we amplify AAV production by up to 10-fold, yielding up to 1e+17vg per batch to meet diverse commercial and clinical project needs. Moreover, our tailored mRNA and LNP products and services cater to every stage of drug and vaccine development, from research to GMP production, providing a seamless, end-to-end solution.
Related News
[2024/12/20] Gene and Cell Therapy- weekly digest from PackGene
FeaturedNewsArticlesPackGene's NewsletterReceive the latest news and insights to your inbox.About PackGenePackGene Biotech is a world-leading CRO and CDMO, excelling in AAV vectors, mRNA, plasmid DNA, and lentiviral vector solutions. Our comprehensive offerings span...
Sangamo and Astellas Collaborate to Advance Neurological Gene Therapies Using AAV Capsid Technology
Sangamo Therapeutics, Inc. (Nasdaq: SGMO), a leader in genomic medicine, and Astellas Pharma Inc. (TSE: 4503), a global innovator in life sciences, have partnered under a new license agreement. This collaboration centers around Sangamo’s cutting-edge neurotropic AAV...
Inceptor Bio and GRIT Bio Announce Strategic Partnership to Advance IB-T101, a Next-Generation Solid Tumor CAR-T Utilizing the OUTLAST™ Platform
SHANGHAI and MORRISVILLE, N.C., Dec. 18, 2024 /PRNewswire/ -- Inceptor Bio, a leading innovator in cell therapy, and GRIT Bio, a clinical-stage immunotherapy developer, today announced a strategic partnership to advance IB-T101, a potentially best-in-class CAR-T...
Proof-of-concept study bioengineers therapeutics for improved cancer treatment
Credit: Pixabay/CC0 Public DomainA team of Children's Medical Research Institute (CMRI) scientists has identified a new method for producing a therapeutic product that has the potential to improve the treatment of cancer. The work by Associate Professor Leszek...
Related Services
AAV Packaging Services
READ MORE
Off-the-Shelf AAV Products
READ MORE