Satellos Bioscience Inc. (T:MSCL)
Business Focus: Bio Therapeutic Drugs
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Company News
Apr 08, 2024 07:00 ET
Satellos to Present at the 2024 Bloom Burton & Co. Healthcare Investor Conference
Satellos Bioscience Inc. (“Satellos” or the “Company”) (TSX: MSCL) (OTCQB: MSCLF), a public biotech company developing new small molecule therapeutic approaches to improve the treatment of muscle diseases and disorders, announced today that management will present at and participate in the 2024 Bloom Burton & Co. Healthcare Investor Conference t
Mar 27, 2024 07:00 ET
Satellos Bioscience Announces 2023 Year End Financial Results and Operational Highlights
Satellos Bioscience Inc. (TSX: MSCL, OTCQB: MSCLF) (“Satellos” or the “Company”), a regenerative medicine company aimed at developing therapeutics that change the way degenerative muscle diseases are treated, announced today its financial results and operational highlights for the year ended December 31, 2023. All
Valuation Ratios
Industry
Sector
Beta
1.60
--
--
Price to Sales - TTM
--
5.19
3.75
Price to Book - most recent quarter
1.41
1.91
2.06
Price to Cash Flow per share - TTM
--
9.04
10.41
Price to Free Cash Flow per share - TTM
--
6.23
14.43
Short Report
| Date | Number of Shares Shorted | Net Change |
|---|---|---|
| Mar 31, 2024 | 10,791 | -42,333 |
| Mar 15, 2024 | 53,124 | -12,486 |
| Feb 29, 2024 | 65,610 | 40,969 |
Business Summary
| Sector: Healthcare | Industry: Biotechnology & Medical Research |
Satellos Bioscience Inc. is a Canada-based a drug discovery and development company with a focus on muscle regeneration. The Company is focused on developing medicines to treat degenerative muscle conditions. Its MyoReGenX platform is specifically designed to recreate the specialized muscle stem cell niche in vitro. MyoReGenX platform enables to map pathways which modulate muscle repair and regeneration, identify, and confirm drug targets, and test drug candidates for their ability to restore muscle stem cell repair mechanisms that have been impaired by genetic mutations, disease or injury. Its lead program is an oral, small molecule drug candidate in development as a disease-modifying treatment for Duchenne muscular dystrophy. Its iCo portfolio includes Oral Amp B Delivery System, a patented oral transport technology and Bertilimumab a human monoclonal eotaxin antibody with potential to treat a range of allergic and inflammatory conditions mediated by eotaxin-1.
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