Patent ọgwụ ọhụrụ maka ọrịa Parkinson

Ntọhapụ n'efu | eTurboNews | eTN

BioArctic AB (publ) announced today that the US Patent and Trademark Office (USPTO) has granted a new drug substance patent for the antibody ABBV-0805, invented by BioArctic as a potential treatment of Parkinson’s disease. The patent will take effect on May 24, 2022, and expire in 2041, with the possibility of a patent term extension up until 2046.

The granted substance patent (US patent no. 11,339,212) focuses on the monoclonal antibody ABBV-0805, which selectively binds to and eliminates pathological aggregated forms called oligomers and protofibrils while sparing the physiological monomer form of alpha-synuclein. The aim is to develop a treatment that halts or slows the progression of Parkinson’s disease.

At the International Congress of Parkinson’s disease and movement disorders® (MDS) in September 2021, results presented from the Phase 1 study with ABBV-0805 supported continued development of the antibody in Phase 2 with once-monthly dosing.

“We are pleased that the US Patent and Trademark Office has granted this new drug substance patent for ABBV-0805, which secures a long period of patent protection. The decision is further confirmation of the innovative nature of BioArctic’s research and strengthens the protection for a potential future treatment of Parkinson’s disease in the US market,” says Gunilla Osswald, CEO, BioArctic.

IHE Ị GA-Ewepụ na edemede a:

  • The decision is further confirmation of the innovative nature of BioArctic’s research and strengthens the protection for a potential future treatment of Parkinson’s disease in the US market,”.
  • BioArctic AB (publ) announced today that the US Patent and Trademark Office (USPTO) has granted a new drug substance patent for the antibody ABBV-0805, invented by BioArctic as a potential treatment of Parkinson’s disease.
  • At the International Congress of Parkinson’s disease and movement disorders® (MDS) in September 2021, results presented from the Phase 1 study with ABBV-0805 supported continued development of the antibody in Phase 2 with once-monthly dosing.

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Linda Hohnholz

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