Notice of Orphan Drug Designation for JR-446 for Mucopolysaccharidosis Type IIIB by the U.S. FDA
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MPS IIIB affects an estimated 500 to 1,000 individuals worldwide,1 causing severe central nervous system (CNS) symptoms. Despite the dire need, there are currently no approved treatments available for this condition. JR-446, developed using JCR’s proprietary J-Brain Cargo® technology, has shown promising non-clinical results in addressing the CNS symptoms of this challenging disorder, and is currently being studied in a Phase I/II trial that is being conducted in
“We are extremely pleased that JR-446 has received orphan drug designation from the
“This orphan drug designation is an important development step for the JR-446 clinical program,” said
In
With the ODD, JR-446 will be eligible for various incentives to encourage the development in the
About Orphan Drug Designation in the
The
About Mucopolysaccharidosis Type IIIB (Sanfilippo Syndrome Type B) Mucopolysaccharidosis type IIIB, or Sanfilippo syndrome type B, is an autosomal recessive disease caused by pathogenic mutations in the NAGLU gene, encoding a lysosomal enzyme involved in the degradation of heparan sulfate. With the accumulation of heparan sulfate in the central nervous system in the brain, individuals with this condition present rapid neurological decline, including sleep disorders, loss of speech, and behavioral changes, which may significantly affect the quality of life of patients and their families.
About the J-Brain Cargo® Platform Technology
About
About
JCR is a global specialty pharmaceuticals company dedicated to advancing treatments for rare and genetic diseases. With nearly 50 years of expertise in
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References
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Based on data from JCR’s own investigations, referring to the
Ministry of Health ,Labour and Welfare’s public research. -
Reference: Press release on the licensing agreement for JR-446 between
MEDIPAL and JCR (September 28, 2023 ).
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