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Satellos Bioscience Inc. (MSLE)

Satellos Bioscience Inc., a biotechnology company, develops medicines to treat degenerative muscle diseases primarily in Canada and Australia. The company uses its proprietary platform MyoReGenX, an automated microscopy system that recapitulates the muscle stem cell environment ex-vivo. It develops SAT-3247 an oral, small-molecule drug candidate for the treatment of Duchenne muscular dystrophy disease. The company has a license agreement the with Ottawa Hospital Research Institute (OHRI); and an option agreement with the University of British Columbia. Satellos Bioscience Inc. was founded in 2018 and is headquartered in Toronto, Canada.

Sector: Pharmaceutical Preparations

Industry: Biotechnology

Satellos Bioscience Inc. Common Stock logo

Satellos Bioscience Inc. Common Stock

NASDAQ:MSLEHealthcare
-1.69%$6.70
Mkt Cap$142.15M
Float18.81M
O/S21.22M
Vol
$ Vol
RVOL
Inst Own36.2%
SI0.5%
Earnings
Dilution
Phase Distribution
5 lead-sponsored trials·2 active·2 completed
Early Phase 11
Phase 11
Phase 23
(1 more as collaborator)
Status Overview
Not yet recruiting1
Recruiting1
Active, not recruiting1
Completed2

Trials need funding. See this company's dilution risk and cash position.

Clinical Trials
Sponsor role
Status
Phase
  • Phase 2
    Enrolling by invitation

    An Open-label Long-term Follow-up Study of SAT-3247 for Participants With Duchenne Muscular Dystrophy Including Those Who Participated in SAT-3247-CL-101

    SAT-3247

    Duchenne Muscular Dystrophy (DMD)

    Enrollment
    30
    Start
    Aug 2025
    Primary Completion
    Sep 2027est.
    Completion
    Sep 2027est.
    NCT06867107
  • Phase 2
    Active, not recruiting

    Phase 2 Study of SAT-3247 in Pediatric Ambulatory Patients

    SAT-3247, Placebo

    Duchenne Muscular Dystrophy, Duchenne +3

    Enrollment
    51
    Start
    Dec 2025
    Primary Completion
    Mar 2027est.
    Completion
    Feb 2028est.
    NCT07287189
  • Phase 2
    Not yet recruiting

    A Study of SAT-3247 to Evaluate the Safety, Tolerability, and Efficacy in Participants With Facioscapulohumeral Muscular Dystrophy (FSHD)

    forazapadin, Placebo Comparator

    Facioscapulohumeral Muscular Dystrophy (FSHD)

    Enrollment
    51
    Start
    Dec 2026est.
    Primary Completion
    Dec 2028est.
    Completion
    Jun 2029est.
    NCT07872306
  • Phase 1
    Completed

    Safety Study of iCo-007 Intravitreal Injection to Treat Diabetic Macular Edema

    iCo-007 Intravitreal Injection

    Diffuse Diabetic Macular Edema

    Enrollment
    15
    Start
    Feb 2008
    Primary Completion
    May 2010
    Completion
    Jun 2010
    NCT00886808
  • Early Phase 1
    Completed

    First in Human SAD/MAD Safety and PK Study With Adult DMD Safety and PK Cohort

    SAT-3247, matched placebo

    Duchenne Muscular Dystrophy

    Enrollment
    77
    Start
    Aug 2024
    Primary Completion
    Apr 2025
    Completion
    Apr 2025
    NCT06565208