Skip to main content
MSLENasdaq

Satellos Bioscience Inc.

Pharmaceutical preparations·Phase 2·Toronto, ON, Canada·CEO: Mr. Francis Gleeson B.B.A. M.B.A
OncologyRare Disease

MSLE evidence brief

What we can confirm

No verified snapshot fields are available yet.

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Watch the next source-backed data update.
BioSniper AIPage evidence connected

Prepared research question

What matters most for MSLE—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · MSLE

Satellos Bioscience Inc. is a clinical-stage biotechnology company developing therapies for degenerative muscle diseases, with its lead candidate SAT-3247 targeting Duchenne muscular dystrophy and currently in Phase 2 trials.

Key risk: Clinical trial failure risk

4.4/10

BioSniper Score

Based on 3 of 6 signals

Limited data coverage

Market Cap

$183.7M

Cash Runway

2.1 mo

Lead Asset

Financial data as of Dec 31, 2025.

Tracking 3 clinical trials · 1 catalyst for Satellos Bioscience Inc..

AI OverviewAI overview is shown in English only.

Satellos Bioscience Inc. is a clinical-stage biotechnology company developing therapies for degenerative muscle diseases, with its lead candidate SAT-3247 targeting Duchenne muscular dystrophy and currently in Phase 2 trials.

  • Satellos reported cash available of $69.9M (Cdn $97.5M) as of May 15, 2026, providing runway through 2027 [news · 2026-05-15].
  • The BASECAMP study remains on track to complete enrollment in Q3 2026, with eleven clinical trial sites currently active [news · 2026-05-15].
  • The TRAILHEAD study has been initiated in the U.S. in adults aged 16-25 years [news · 2026-05-15].
  • SAT-3247 received FDA Fast Track designation for Duchenne muscular dystrophy as of June 29, 2026 [news · 2026-06-29].
  • New data from the SAT-3247 clinical program will be presented at ICNMD 2026 in July 2026 [news · 2026-06-25].

What works

  • FDA Fast Track designation for SAT-3247 may expedite development and regulatory review for Duchenne muscular dystrophy [news · 2026-06-29].
  • Cash runway through 2027 provides financial stability for ongoing clinical programs [news · 2026-05-15].
  • Multiple clinical studies (BASECAMP and TRAILHEAD) are actively enrolling, indicating progress in the pipeline [news · 2026-05-15].

What to weigh

  • The company reported a net loss of $24.9M for the year ended 2025-12-31, reflecting high cash burn typical of clinical-stage biotechs [latest reported financials].
  • As a clinical-stage company with no approved products, Satellos is dependent on successful trial outcomes and future financing [news · 2026-05-15].
  • The competitive landscape for Duchenne muscular dystrophy includes other therapies, though no direct competitor trials were identified in the provided data.

From the filings

Quoted directly from source documents.

  • Cash runway through 2027

    Current cash available of $69.9M (Cdn $97.5M) provides runway through 2027

    News · May 15, 2026

  • BASECAMP enrollment timeline

    BASECAMP remains on track to complete enrollment in Q3 2026

    News · May 15, 2026

  • FDA Fast Track designation

    Satellos Gets FDA Fast Track Status For Duchenne Drug

    News · June 29, 2026

  • TRAILHEAD study initiation

    The Company has initiated the TRAILHEAD study in the U.S. in adults aged 16-25 years.

    News · May 15, 2026

Catalyst timeline

  • 2026-12-31 · Phase2_Topline · sat-3247 — Phase 2 Readout: sat-3247Topline results from the Phase 2 study of SAT-3247 are expected, which will inform efficacy and safety for Duchenne muscular dystrophy.
Risks & what to watch (3)

Key risks

  • Clinical trial failure riskSAT-3247 is in Phase 2; negative results could halt development and impact viability [news · 2026-05-15].
  • Cash burn and dilutionNet loss of $24.9M in 2025; cash runway through 2027 may require additional financing [latest reported financials].
  • Regulatory and competitive riskDuchenne market has existing and emerging therapies; Fast Track does not guarantee approval [news · 2026-06-29].

What to watch

  • Completion of BASECAMP enrollment in Q3 2026 [news · 2026-05-15].
  • Presentation of SAT-3247 data at ICNMD 2026 in July 2026 [news · 2026-06-25].
  • Phase 2 topline results for SAT-3247 expected by end of 2026 [upcoming catalysts].
  • Activation of remaining BASECAMP trial sites in Q2 2026 [news · 2026-05-15].

Sources: Competitor trials · News · Generated August 27, 2026 · How we verify sources →

Run Satellos Bioscience Inc. through your own thesis

Use the pipeline, catalyst, financial, FDA, and market facts on this page as inputs to a protocol you control.

Your protocol can:

  • Turn available Satellos Bioscience Inc. facts into screen rules or deeper checks
  • Show cited findings, blockers, and unresolved evidence together
  • Save the logic and rerun it as the company evidence changes
Run a thesis on this company — freeRun a thesis on this company

Evidence & data

Score breakdownBased on 3 of 6 signals · derived from public data

No clinical pipeline tracked — this score reflects financial & catalyst signals only.

Cash Runway0.6

2.1 months

Financial Health9.6

D/E 0.15

Pipeline MaturityN/A

No tracked pipeline phase

Pipeline BreadthN/A

No tracked pipeline candidates

Catalyst Momentum3.0

1 upcoming, next in ~123d

Insider SignalN/A

No insider transactions in the last 180 days

Runway

Catalysts

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

26

Total value held

$27.1M

Showing top 10 of 26 institutional holders of Satellos Bioscience Inc.. Open the full 13F history after sign-in.

Short Interest

% of float
-
Days to cover
Shares short
-
Daily short volume (Jun 23, 2026)
57.8%

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

MSLE short interest

Frequently asked questions

What is the AI investment thesis for Satellos Bioscience Inc.?

Satellos Bioscience Inc. is a clinical-stage biotechnology company developing therapies for degenerative muscle diseases, with its lead candidate SAT-3247 targeting Duchenne muscular dystrophy and currently in Phase 2 trials.

What is Satellos Bioscience Inc.'s next catalyst?

Satellos Bioscience Inc.'s next tracked catalyst is a Phase2_Topline event — "Phase 2 Readout: sat-3247" — expected December 31, 2026.

Who is the CEO of Satellos Bioscience Inc.?

Mr. Francis Gleeson B.B.A. M.B.A is the chief executive officer of Satellos Bioscience Inc. (MSLE).

Where is Satellos Bioscience Inc. headquartered?

Satellos Bioscience Inc. (MSLE) is headquartered in Toronto, ON, Canada.

What therapeutic areas does Satellos Bioscience Inc. focus on?

Satellos Bioscience Inc. develops therapies across Oncology, Rare Disease.

925 companies232,681 SEC filings21,419 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.