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BioWorld - Saturday, May 9, 2026
Home » facioscapulohumeral muscular dystrophy

Articles Tagged with ''facioscapulohumeral muscular dystrophy''

RNA illustration
Neurology/Psychiatric

Mirecule and Sanofi collaborate on antibody-RNA conjugate for facioscapulohumeral muscular dystrophy

Oct. 5, 2022
Mirecule Inc. has entered into a strategic collaboration and exclusive license agreement with Sanofi SA to develop and commercialize a best-in-class antibody-RNA conjugate (ARC) for the treatment of facioscapulohumeral muscular dystrophy (FSHD).
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Gene editing illustration
Newco news

CRISPR co-inventor’s Epic Bio launches with $55M series A

July 15, 2022
By Lee Landenberger
Controlling the epigenetics of a patient, figuring out what genes are expressed and understanding their level of expression, is at the center of Epic Bio, a new company founded by Stanley Qi, co-inventor on the CRISPR patent held by the University of California.
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Pills and bottle

Fulcrum set to pivot in FSHD? No DUX4 score but secondary goals extolled

June 25, 2021
By Randy Osborne
Fulcrum Therapeutics Inc.’s phase IIb data with losmapimod in facioscapulohumeral muscular dystrophy (FSHD) brought renewed hope for patients in what historically has proved a challenging therapeutic space. Though the firm’s oral p38 mitogen-activated protein kinase inhibitor missed its primary biomarker endpoint – changes in DUX4-driven gene expression – other indicators of benefit in the study called ReDUX4 painted a bright picture.
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Boy in wheelchair, scenic overlook

Fulcrum looks for balance in its phase II FSHD study

Aug. 11, 2020
By Lee Landenberger
An interim analysis from Fulcrum Therapeutics Inc.’s phase II study of losmapimod for treating facioscapulohumeral muscular dystrophy (FSHD) produced data that pleased the CEO and displeased investors.
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Archimedes entreaties: Needful FSHD world to move via Fulcrum bid with losmapimod?

March 10, 2020
By Randy Osborne
With a phase IIb readout coming in the third quarter of 2020, Cambridge, Mass.-based Fulcrum Therapeutics Inc. might be set up for a win in facioscapulohumeral muscular dystrophy (FSHD), a genetic muscle disorder for which there’s no treatment.
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