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BioWorld - Saturday, April 4, 2026
Home » Keywords » Satellos Bioscience Inc.

Items Tagged with 'Satellos Bioscience Inc.'

ARTICLES

Neurology/psychiatric

Satellos Bioscience patents new AAK1 inhibitors

March 26, 2025
Work at Satellos Bioscience Inc. has led to the identification of new AP2-associated protein kinase 1 (AAK1) inhibitors reported to be useful for the treatment of muscular dystrophy.
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Light micrograph of skeletal muscle.
Musculoskeletal

Satellos’ AAK1 inhibitor regenerates muscle in dogs

Oct. 11, 2024
Satellos Bioscience Inc. has developed and presented data for a compound that targeted the process of muscle regeneration based on modulation of satellite stem cell polarity.
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Boy in wheelchair, scenic overlook
Musculoskeletal

SAT-3247 adds rare pediatric disease designation

Aug. 8, 2024
After receiving Orphan Drug Designation earlier this year, Satellos Bioscience Inc. announced that the FDA has granted Rare Pediatric Disease Designation to SAT-3247 for the potential treatment of Duchenne muscular dystrophy (DMD).
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Pill in immersive interface
Neurology/psychiatric

Satellos files in Australia to begin clinical testing of SAT-3247 for Duchenne muscular dystrophy

July 12, 2024
Satellos Bioscience Inc. has submitted a clinical research proposal to a Human Research Ethics Committee (HREC) in Australia seeking regulatory authorization under the Therapeutic Goods Administration (TGA)’s clinical trial notification scheme to conduct a first-in-human phase I trial of SAT-3247.
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Illustration of muscle anatomy
Neurology/Psychiatric

SAT-3247 increases muscle force in mouse models of muscle degeneration

March 8, 2024
Satellos Bioscience Inc. recently presented preclinical data for the novel oral small-molecule AP2-associated protein kinase 1 (AAK1) inhibitor SAT-3247, being developed for the treatment of Duchenne muscular dystrophy and other muscle degenerative diseases, at the Muscular Dystrophy Association conference.
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Muscular dystrophy
Neurology/Psychiatric

SAT-3247 improves skeletal muscle function in mouse model of facioscapulohumeral muscular dystrophy

Feb. 14, 2024
Satellos Bioscience Inc. has released promising preliminary data showing SAT-3247 can improve skeletal muscle function in a mouse model of...
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Neurology/Psychiatric

Satellos reveals drug target, lead candidate in Duchenne program

Nov. 15, 2023
Satellos Bioscience Inc. has disclosed further information on its lead drug program in Duchenne muscular dystrophy.
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Doctor examining child in wheelchair
Neurology/Psychiatric

Satellos’ DMD candidate awarded US orphan drug and rare pediatric disease designations

Aug. 4, 2023
Satellos Bioscience Inc. has received orphan drug designation and rare pediatric disease designation from the FDA for SAT-3153 for the potential treatment of Duchenne muscular dystrophy (DMD). The first-in-class oral small-molecule therapeutic is designed to restore the innate muscle regeneration process independent of dystrophin and regardless of exon mutation status.
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Doctor examining child in wheelchair
Neurology/Psychiatric

Satellos' studies in mouse model of Duchenne muscular dystrophy support development of SAT-3153

Feb. 7, 2023
Satellos Bioscience Inc. has reported results from preclinical studies in a disease model of Duchenne muscular dystrophy (DMD). The company's proprietary Myoregenx assay platform identified a protein kinase (K9) as a potential drug target to modulate polarity in muscle stem cells.
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Light micrograph of skeletal muscle.
Neurology/Psychiatric

Satellos designates SAT-3153 as development candidate for Duchenne muscular dystrophy

Jan. 4, 2023
Satellos Bioscience Inc. has designated SAT-3153 as a development candidate for Duchenne muscular dystrophy and will move the candidate into pre-IND-enabling studies and toward an IND filing. SAT-3153 is a small molecule designed to inhibit a particular kinase protein which the company believes controls Notch polarity within muscle stem cells.
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More Articles Tagged with 'Satellos Bioscience Inc.'

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