Hunter Syndrome Pipeline 2024: Clinical Trials Assessment, FDA Approvals, Therapies, and Key Companies Involved by DelveInsight | REGENXBIO, Takeda, Triley Bidco, JCR Pharma, Sangamo Therapeutics

(Las Vegas, Nevada, United States) As per DelveInsight's assessment, globally, Hunter Syndrome pipeline constitutes 10+ key companies continuously working towards developing 10+ Hunter Syndrome treatment therapies, analysis of Clinical Trials, Therapies, Mechanism of Action, Route of Administration, and Developments analyzes DelveInsight.
The Hunter Syndrome Pipeline report embraces in-depth commercial and clinical assessment of the pipeline products from the pre-clinical developmental phase to the marketed phase. The report also covers a detailed description of the drug, including the mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, collaborations, mergers acquisition, funding, designations, and other product-related details.

"Hunter Syndrome Pipeline Insight, 2024 [https://www.delveinsight.com/sample-request/hunter-syndrome-pipeline-insight?utm_source=abnewswire&utm_medium=pressrelease&utm_campaign=gpr]" report by DelveInsight outlines comprehensive insights into the present clinical development scenario and growth prospects across the Hunter Syndrome Market.

Some of the key takeaways from the Hunter Syndrome Pipeline Report:

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Companies across the globe are diligently working toward developing novel Hunter Syndrome treatment therapies with a considerable amount of success over the years.

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Hunter Syndrome companies working in the treatment market are Capsida Biotherapeutics, JCR Pharmaceuticals, Takeda, Green Cross Corporation/GC Pharma, Denali Therapeutics, Regenxbio, Sangamo Therapeutics, AVROBIO, and others, are developing therapies for the Hunter Syndrome treatment

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Emerging Hunter Syndrome therapies in the different phases of clinical trials are- CAP 001, JR-141, TAK-609/SHP609/HGT-2310, GC1111 (Hunterase), DNL310, RGX-121, SB-913, AVR-RD-05, and others are expected to have a significant impact on the Hunter Syndrome market in the coming years.

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In February 2024, GC Biopharma, a South Korean biopharmaceutical company led by CEO Eun-Chul Huh, announced on February 14th that it has shared updates on its lysosomal storage disease (LSD) treatments at the WORLDSymposium 2024. During the symposium, GC Biopharma delivered an oral presentation on the Phase III clinical trial results of "Hunterase," its treatment for Hunter syndrome, and presented posters on the non-clinical results of "GC1130A," a treatment for Sanfilippo syndrome type A (MPS IIIA), and "GC1134A/HM15421," a treatment for Fabry disease.

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In November 2023, JCR Pharmaceuticals administered the initial dose to a patient in its Phase I/II clinical trial of JR-441, targeting Mucopolysaccharidosis Type IIIA (MPS IIIA; Sanfilippo Syndrome Type A). This trial is being conducted at the International Center for Lysosomal Disorders (ICLD) at the University Hospital of Hamburg Eppendorf (UKE) in Germany. The study, based at a single center, aims to enroll 12 patients between the ages of one and 18, who are at various stages of the disease.

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In June 2023, Denali Therapeutics Inc. (NASDAQ: DNLI) has reported new interim findings from the ongoing open-label, single-arm Phase 1/2 trial of DNL310 (ETV:IDS) in children diagnosed with MPS II (Hunter syndrome). At the time of the interim analysis, 13 participants who completed two years of treatment showed a significant mean reduction of 64% (p



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