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BioWorld - Wednesday, March 25, 2026
Home » Topics » Disease categories and therapies » Musculoskeletal

Musculoskeletal
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Child in wheelchair with parent, doctor

Scholar Rock’s phase III Sapphire gleams; bright new bid in SMA

Oct. 7, 2024
By Randy Osborne
Shares of Scholar Rock Holding Corp. (NASDAQ:SRRK) soared $26.86, or 362%, to close Oct. 7 at $34.28, after the Cambridge, Mass.-based firm disclosed positive top-line data from the phase III Sapphire study testing apitegromab in patients with spinal muscular atrophy (SMA). Apitegromab, which Wainwright analyst Andres Maldonado said will “transform SMA” therapy, met the primary endpoint with statistically significant and clinically meaningful improvement in motor function as measured by the Hammersmith Functional Motor Scale Expanded.
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Musculoskeletal

Petragen discovers new ENPP1 inhibitors

Oct. 1, 2024
Petragen Inc. has described ectonucleotide pyrophosphatase/phosphodiesterase family member 1 (ENPP1) inhibitors reported to be useful for the treatment of cancer, gingivitis, musculoskeletal and connective disorders, hematological diseases, bone, cardiovascular, immunological and neurological disorders, among others.
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BioWorld Insider podcast: Capricor’s CEO pursues a BLA and talks rare disease

Sep. 27, 2024
By Lee Landenberger
Capricor Therapeutics Inc. just wrapped up a visit with the U.S. FDA and is prepping to file a BLA in October for its Duchenne muscular dystrophy treatment. Linda Marbán, the company’s CEO, is the guest on the newest BioWorld Insider podcast and she talks about deramiocel (CAP-1002), the company’s allogeneic cardiac-derived cell therapy, for treating the rare disease and how the FDA has made strong efforts in helping lay the groundwork for deramiocel.
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Doctor examining child's leg

Wave Life soars on WVE-N531 phase II Duchenne data

Sep. 24, 2024
By Karen Carey
Interim phase II data of Wave Life Sciences Ltd.’s oligonucleotide, WVE-N531, revealed “impressive” dystrophin expression, solid safety and the potential for once-monthly dosing for boys with Duchenne muscular dystrophy who are amenable to exon 53 skipping. The findings drove Wave Life’s stock (NASDAQ:WVE) up by 53.4%, or $2.85, to close Sept. 24 at $8.19, after peaking earlier in the day at $8.35, its 52-week high.
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Illustration of motor neuron connecting to muscle fiber
Neurology/psychiatric

ARGX-119 prevents early postnatal lethality and reverses disease relapse in model of congenital myasthenia

Sep. 23, 2024
Argenx SE’s ARGX-119 is a monoclonal antibody (MAb) targeting the muscle-specific kinase (MuSK) Frizzled (Fz)-like domain, and has entered early clinical development for the treatment of neuromuscular diseases.
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Juleen Zierath on stage at EASD 2024
Endocrine/metabolic

Studies on exercise and health win EASD prize

Sep. 19, 2024
By Mar de Miguel
How do exercise and insulin collaborate in metabolism? The European Association for the Study of Diabetes (EASD) and the Novo Nordisk Foundation recognized the work of Juleen Zierath in this topic with the Diabetes Prize for Excellence at their recent annual meeting.
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Juleen Zierath on stage at EASD 2024
Endocrine/metabolic

Studies on exercise and health win EASD prize

Sep. 18, 2024
By Mar de Miguel
How do exercise and insulin collaborate in metabolism? The European Association for the Study of Diabetes (EASD) and the Novo Nordisk Foundation recognized the work of Juleen Zierath in this topic with the Diabetes Prize for Excellence at their recent annual meeting.
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Capricor and Nippon Shinyaku add Europe to DMD deal

Sep. 17, 2024
By Lee Landenberger
Capricor Therapeutics Inc. has expanded its commercialization and distribution deal with Nippon Shinyaku Co. Ltd. to include the EU and the U.K. for deramiocel, Capricor’s lead asset, in treating Duchenne muscular dystrophy (DMD). In the new agreement, Capricor will receive an up-front payment of $20 million. Capricor will handle development and manufacturing duties for deramiocel while Nippon Shinyaku will be responsible for the sales and distribution.
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Illustration of muscle anatomy
Musculoskeletal

LMK-235 prevents diabetic muscle atrophy in vivo

Sep. 17, 2024
Researchers from Ajou University presented data from a preclinical study that aimed to assess the potential of using the histone deacetylase (HDAC) inhibitor LMK-235 for the prevention of diabetic muscle atrophy.
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Daily grind: Ascendis achondroplasia win not grate for Biomarin

Sep. 16, 2024
By Randy Osborne
Predictably, weekly vs. daily subcutaneous injections made a big difference in the achondroplasia space, where shares of Copenhagen, Denmark-based Ascendis Pharma A/S (NASDAQ:ASND) closed Sept. 16 at $139.57, up $20.35, or 17%, on favorable, pivotal top-line data with Transcon CNP (navepegritide), as competitor Biomarin Pharmaceutical Inc.’s stock (NASDAQ:BMRN) ended the day at $69.86, down $15.04, or 17.7%.
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