2 things here : From Antisense Therapeutics and Murdoch Children’s Research Institute enter into new R&D collaboration to further explore ATL1102 use in multiple muscle diseases
- The MCRI researchers and ANP have additionally undertaken experimental work that showed antisense inhibition of CD49d in the X chromosome-linked muscular dystrophy (mdx) mouse model of DMD reduces both the CD49d target in the muscle and muscle damage. This data is expected to be submitted for publication in 2021.
- The broader immunomodulatory effects of ATL1102 are being investigated by ANP through the analysis of blood (plasma) samples retained from the Company’s Phase II trial of ATL1102 in DMD patients. ANP is presently completing this plasma analysis and is expecting this new data to provide insights on the mode of action and broader biological activity of ATL1102. ANP is planning to file for additional patent protection with this new data ahead of its proposed presentation at an appropriate scientific conference in 2H’CY21.
Not long now....
Where others have failed will Atl1102 succeed ?, page-272
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