ClinicalTrials.gg
Enrolling by invitationNCT06867107Updated Oct 13, 2026

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

A Phase 2 interventional study of SAT-3247 in Duchenne Muscular Dystrophy (DMD), sponsored by Satellos Bioscience, Inc.. Enrolling by invitation at 6 sites in 2 countries. Open to male participants aged 16 Years to 40 Years. Per ClinicalTrials.gov, last updated 2026-10-13.

Sponsored by Satellos Bioscience, Inc. · Phase 2, Interventional, and Treatment

Updated Oct 13, 2026Primary outcomes revised1 site addedGo to Updates ↓
Phase
Phase 2
Study type
Interventional
Enrollment
30
Allocation
Not applicable
Ages
16 Years to 40 Years
Sex
Male
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 232 studies in Muscular Dystrophy, Duchenne with a site in United States — 36 open to participants now, 60 under way, 8 of them phase 3. Muscular Dystrophy, Duchenne · United States.

Planned enrollment
80th of 171
30 · median 25
Started
2025
with 9 others
Phase 2
57 of 232
4 open now
Primary completion
2027-09
later than 28 of 59 live
Registered
216th of 232
by date

Among the 232 studies in Muscular Dystrophy, Duchenne with a site in United States, this one is the 80th largest by planned enrollment of the 171 interventional ones that give a count, is one of 10 that started in 2025, is one of 57 in phase 2, reaches primary completion later than 28 of the 59 other live ones, and was the 216th registered.

Muscular Dystrophy, Duchenne

481 studies on the registry are indexed under Muscular Dystrophy, Duchenne; 108 are open to participants now.

Browse Muscular Dystrophy, Duchenne studies →

Open to participants now

36 of the 232 studies in Muscular Dystrophy, Duchenne with a site in United States are open now. Recruiting first, the newest first:

31 more — sign in →

All 36 open studies →

A study can be open while its sites in United States have not opened yet or have stopped. Only those recruiting at a site in United States →

Who these studies take

Of the 66 Muscular Dystrophy, Duchenne studies recruiting now, 30 (45%) set no upper age limit and 34 (52%) stop at 75 or younger; 60 take children under 18; 12 take healthy volunteers.

This study: 16 Years to 40 Years · male · no healthy volunteers.

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02

Study summary

This is an open-label long-term safety and efficacy study of orally administered SAT-3247 in patients with DMD including those who previously participated in SAT-3247-CL-101.

The study will assess the long-term safety, tolerability and potential efficacy of long-term dosing of orally administered SAT-3247 60 mg in a 5-days on/2-days off (i.e. weekday dosing) regimen in an open-label design through 11 months (Group A) or 12 months (Group B), respectively. The study will enroll up to 30 participants, including up to 5 who previously participated in the SAT-3247-CL-101 study.

03

Conditions studied

  • Duchenne Muscular Dystrophy (DMD)

Keywords

  • muscle regeneration
  • SAT-3247
04

Who can participate

Ages eligible
16 Years to 40 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Previously participated in the SAT-3247-CL-101 parent clinical trials (Group A only).
  • No previous treatment with SAT-3247 (Group B only)
  • Continued status of stable glucocorticosteroid dose or no glucocorticosteroid dose for the duration of the trial.
  • Continued stable doses of prescription medicines (excluding glucocorticosteroids) and over-the-counter medicines and/or herbal supplements for supportive care for the duration of the trial.
  • Previously received delandistrogene moxeparvovec (brand name Elevidys) either in a prior clinical trial or in the commercial setting > 18 months prior to screening whose muscle function tests have stabilized or demonstrated decline ≥ 3 months prior to Screening (Group B only)
  • Receiving a stable dose of givinostat (brand name Duvyzat) for at least 18 months or longer prior to the Screening (Group B only)
  • Have previously received an exon skipper ≥ 6 months prior to Screening whose muscle function tests have stabilized or demonstrated decline ≥ 3 months prior to Screening (Group B only)
  • Have received any medication indicated for DMD (other than , including vamorolone, gene therapy, givinostat, or an exon-skipping therapy) whose last dose was ≥ 6 months prior to Screening (Group B only)
  • have received prior treatment with an gene therapy product (other than delandistrogene moxeparvovec) ≥ 24 months prior to Screening
  • ≥ 40% at Screening (Group B only)
  • Ability to understand the nature of the trial and any hazards of participating.
  • Ability to communicate satisfactorily with the investigator and physiotherapist and to participate in and comply with the requirements of the entire trial including scheduled visits, procedures, laboratory tests, questionnaires, wearable devices, and study restrictions.
  • Willingness to give written consent or assent (if not of cognitive capacity of consent in the jurisdiction where the study is being conducted) and parent/legal guardian willing to give written consent to participate (if participant is not of cognitive capacity to consent) after reading the information and consent form, and after having the opportunity to discuss the trial with the investigator or their delegate.
  • All participants, if sexually active, agree to follow the requirements and sperm donation limitations of the trial as described in the protocol.

Exclusion criteria

Exclusion Criteria:

  • Presence of acute medical condition, chronic illness or history of chronic illness (other than DMD) sufficient to invalidate the participant's participation in the trial or make it unnecessarily hazardous in the judgment of the investigator.
  • Evidence of significant hepatic dysfunction, defined as GLDH > 2X (ULN) at Screening (Group B only)
  • Entry item score on the Performance of Upper Limb (PUL2.0) assessment > 5 (Group B only)
  • Requirement for daytime ventilator assistance (Group B only)
  • Participants expected to require spine surgeries or hospitalizations for non-acute health needs within 12 months.
  • Participants with acute gastrointestinal symptoms (e.g., nausea, vomiting, diarrhea, heartburn) or acute infection (such as influenza) or a significant infection or known inflammatory process at Screening.
  • Severe behavioral or cognitive problems that preclude participation in the study, in the opinion of the investigator.
  • Development of symptomatic cardiomyopathy since completion of the parent trial.
  • Inability to swallow tablets.

    a. Tablets can be split or crushed and stirred into flavored beverages or food (e.g., apple sauce, yogurt) followed by immediate administration.

  • Receipt of an product (including prescription medicines and investigational devices) as part of another clinical trial since completion of the parent trial or in the follow-up period of another clinical trial at the time of Screening for this study.

    a. Use of deflazacort or vamorolone in jurisdictions where these are considered investigational as they have not received health authority marketing authorization will not be exclusionary.

  • Current or expected use during the study of any medications that are known strong or moderate inhibitors of (Group B only)
  • Consumption of grapefruit, grapefruit juice, and grapefruit-containing products within 30 days of the first dose of investigational product and for the duration of the study (Group B only)
  • Possibility that the participant will not cooperate with the requirements of the protocol or is unable or unwilling to comply with the study requirements according to investigator's decision.
  • Employee, contractors, or consultants of the Sponsor, the CRO, and/or study site or their relatives.
Terms in these criteria, in plain language(6)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

LVEF (left ventricular ejection fraction)

The share of blood the heart’s main pumping chamber (the left ventricle) pushes out with each beat, measured by an echocardiogram (heart ultrasound) or a MUGA scan. About 50–70% is normal.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

CYP3A (CYP3A4) inhibitors and inducers

CYP3A is a group of enzymes, mainly CYP3A4, in the liver and gut that break down many medicines. Some medicines, supplements and foods (grapefruit, St John’s wort) slow them down or speed them up, which changes how much of a study drug stays in the body.

Studies list them so they can be avoided or switched; bring a list of everything you take, including supplements.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Treatment Arm

    SAT-3247 60 mg administered orally in a 5-days on/2-days off (weekday) dosing regimen

    Drug: SAT-3247

Interventions

06

What researchers measure

Primary outcomes

  1. Treatment emergent adverse events

    Incidence, temporal profile, and severity of treatment emergent adverse events (TEAEs)

    Time frame: 12 months

  2. SAT-3247 effect on fat fraction in biceps brachii

    Changes from baseline in intramuscular fat fraction in muscle quantitative magnetic resonance (qMR) in biceps brachii following treatment with SAT-3247.

    Time frame: 12 months

Secondary outcomes

  1. SAT-3247 effects on muscle force

    Changes from baseline in muscle force measurements as determined by dynamometry following treatment.

    Time frame: 12 months

  2. Potential for improvement in muscle function with treatment of SAT-3247

    Changes from baseline in Performance of Upper Limb (PUL2.0) assessment following SAT-3247 treatment.

    Time frame: 12 months

  3. PK measurement of SAT-3247

    Evaluate PK of SAT-3247 concentrations in non-ambulatory participants

    Time frame: 12 months

  4. Long-term effects of SAT-3247 on muscle quantitative magnetic resonance (qMR)

    Evaluate change in proton muscle transverse relaxation time (T2) in biceps brachii

    Time frame: 12 months

07

Study locations

6 sites
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

2 registry updates since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Aug 2025 (actual). Primary completion is estimated for Sep 2027, 25 months after the start.

Of 40 industry-sponsored phase 2 interventional studies under Muscular Dystrophy, Duchenne, half reached primary completion within 31 months of starting (the median), counting those still running; a quarter within 20 and three quarters within 42. This study's planned 25 months is below that.

Counting every sponsor, half of 47 studies reached it within 31 months; a quarter within 20 and three quarters within 42.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 4, 2025
First posted
Mar 10, 2025
StartActual
Aug 20, 2025
Primary completionEst.
Sep 30, 2027
CompletionEst.
Sep 30, 2027
Last update
Oct 13, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Sites
1 site added
Show site
  • Washington University School of Medicine · St Louis, United States
Oct 13, 2026
Primary outcomes
2 time frame changed
What changed in the outcomes
  • Time frameTreatment emergent adverse events24 months → 12 months
  • Time frameSAT-3247 effect on fat fraction in biceps brachii24 months → 12 months
Oct 6, 2026
Secondary outcomes
4 time frame changed
What changed in the outcomes
  • Time frameSAT-3247 effects on muscle force24 months → 12 months
  • Time framePotential for improvement in muscle function with treatment of SAT-324724 months → 12 months
  • Time framePK measurement of SAT-324724 months → 12 months
  • Time frameLong-term effects of SAT-3247 on muscle quantitative magnetic resonance (qMR)24 months → 12 months
Oct 6, 2026
Show all 2 updates
  1. Oct 13, 2026
    1 site added
    Show site
    • Washington University School of Medicine · St Louis, United States
  2. Oct 6, 2026
    Primary outcomes 2 time frame changed
    What changed in the outcomes
    • Time frameTreatment emergent adverse events24 months → 12 months
    • Time frameSAT-3247 effect on fat fraction in biceps brachii24 months → 12 months
    Secondary outcomes 4 time frame changed
    What changed in the outcomes
    • Time frameSAT-3247 effects on muscle force24 months → 12 months
    • Time framePotential for improvement in muscle function with treatment of SAT-324724 months → 12 months
    • Time framePK measurement of SAT-324724 months → 12 months
    • Time frameLong-term effects of SAT-3247 on muscle quantitative magnetic resonance (qMR)24 months → 12 months
    + 2 other changes: verification date and description

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT06867107
Lead sponsor
Satellos Bioscience, Inc.
Responsible party
Sponsor
First posted
Mar 10, 2025
Start date
Aug 20, 2025
Primary completion
Sep 30, 2027 (estimated)
Completion
Sep 30, 2027 (estimated)
Last update
Oct 13, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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