DelveInsight’s, “Sanfilippo Syndrome Pipeline Insight 2025” report provides comprehensive insights about 8+ companies and 10+ pipeline drugs in Sanfilippo Syndrome pipeline landscape. It covers the pipeline drug profiles, including clinical and nonclinical stage products. It also covers the Sanfilippo Syndrome pipeline therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.
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Key Takeaways from the Sanfilippo Syndrome Pipeline Report
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Sanfilippo Syndrome Emerging Drugs Profile
UX111 (rebisufligene etisparvovec) is an investigational novel in vivo gene therapy under evaluation for Sanfilippo syndrome type A (MPS IIIA). UX111 is designed to be dosed in a one-time intravenous infusion using a self-complementary AAV9 vector to deliver a functional copy of the SGSH gene to cells. The therapy is designed to address the underlying sulfamidase enzyme deficiency responsible for abnormal accumulation of heparan sulfate, a glycosaminoglycan, in the brain that results in progressive cell damage and neurodegeneration. The UX111 program has received Regenerative Medicine Advanced Therapy, Fast Track, Rare Pediatric Disease, and Orphan Drug designations in the U.S., and PRIME and Orphan Drug designations in the EU. In December 2024, Ultragenyx Pharmaceutical announced the submission of a Biologics License Application to the US Food and Drug Administration seeking accelerated approval for UX111 (ABO-102) AAV gene therapy as a treatment for patients with Sanfilippo syndrome type A.
OTL-201 is an ex vivo autologous gene therapy being developed for the treatment of Sanfilippo syndrome. It uses a modified virus to insert a functional copy of the SGSH gene into a patient’s cells. OTL-201 has received rare pediatric disease designation from the FDA and is currently being evaluated in an ongoing proof-of-concept clinical trial. OTL-201 is an investigational therapy and has not been approved by any regulatory agency or health authority.
DNL126 is an investigational enzyme replacement therapy developed for the treatment of Sanfilippo Syndrome type A (MPS IIIA). Utilizing Denali’s proprietary Enzyme Transport Vehicle (ETV) technology, DNL126 is designed to effectively cross the blood-brain barrier through receptor-mediated transcytosis, allowing for targeted delivery of SGSH to the central nervous system. By replenishing the deficient enzyme, DNL126 aims to reduce the toxic buildup of heparan sulfate in brain tissues, potentially alleviating neurological symptoms and improving overall outcomes for patients. DNL126 is a recombinant SGSH enzyme engineered to cross the blood-brain barrier, replace the SGSH enzyme and treat neuropathic and systemic forms of the Sanfilippo syndrome A. Currently, the drug is in Phase I/II stage of its clinical trial for the treatment of Sanfilippo Syndrome.
The Sanfilippo Syndrome Pipeline Report Provides Insights into
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Sanfilippo Syndrome Companies
Ultragenyx Pharmaceutical Inc, JCR Pharmaceuticals Co., Ltd., GC Biopharma Corp, Denali Therapeutics Inc., Orchard Therapeutics plc, Seelos Therapeutics and others.
Sanfilippo Syndrome pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as
Sanfilippo Syndrome Products have been categorized under various Molecule types such as
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Scope of the Sanfilippo Syndrome Pipeline Report
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