Modalis is a Waltham MA/Tokyo based biotech company developing gene therapies for rare diseases with a novel CRISPR based epigenome editing technology.
Meeting Justin and his family was both inspiring and humbling. His curiosity, intellect, and determination strengthened our resolve to advance new treatment options for individuals and families living with LAMA2-RD. #LAMA2
https://t.co/EKEBr5VS6T
Modalis Announces Publication in Human Gene Therapy of Study Demonstrating Efficient LAMA1 Gene Activation for the Treatment of LAMA2-CMD - https://t.co/lkLmr7yEOt
We are thrilled to announce a strategic partnership with SOLVE FSHD, along with successful strategic funding dedicated to advancing our MDL-103 for the treatment of facioscapulohumeral muscular dystrophy (FSHD).
Modalis has been selected as a finalist in the XPRIZE Healthspan FSHD Bonus Prize Competition and awarded research funds. #xprize
https://t.co/2uthVL1VTx
Modalis Therapeutics has received an Orphan Drug Designation from the U.S. Food and Drug Administration for MDL-101, a treatment for congenital muscular dystrophy type 1A (LAMA2-CMD).
Modalis announced our collaboration with Ginkgo Bioworks. Epigenome editing meets Synthetic Biology and the world-leading biofoundry capabilities!
https://t.co/u6ezfOvKUH