Safety, Tolerability, Pharmacodynamic, Efficacy, and Pharmacokinetic Study of DYNE-101 in Participants With Myotonic Dystrophy Type 1

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18-65
SponsorDyne Therapeutics

About this trial

The primary purpose of the study is to evaluate the safety and tolerability of multiple intravenous (IV) doses of DYNE-101 administered to participants with Myotonic Dystrophy Type 1 (DM1).

The study consists of 4 periods: A Screening Period (up to 8 weeks), a Placebo-Controlled Period (24 weeks), a Treatment Period (24 weeks) and a Long-Term Extension (LTE) Period (168 weeks) in both multiple-ascending dose (MAD) and dose expansion cohorts.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of DM1 with trinucleotide repeat size >100.

Age of onset of DM1 muscle symptoms ≥12 years.

Clinically apparent myotonia equivalent to hand opening time of at least 2 seconds in the opinion of the Investigator.

Hand grip strength and ankle dorsiflexion strength.

Disqualifiers

History of major surgical procedure within 12 weeks prior to the start of investigative product administration or an expectation of a major surgical procedure (eg, implantation of cardiac defibrillator) during the study.

History of anaphylaxis.

Medical condition other than DM1 that would significantly impact ambulation or participation in functional assessments.

Treatment with medications that can improve myotonia within a period of 5 half-lives of the medication prior to performing screening assessments.

Trial design

Design model

Sequential

Treatments tested in this trial

  • DYNE-101

    Drug

    Administered by IV infusion

  • Placebo

    Drug

    Administered by IV infusion

Treatment groups

116 Participants
are divided into 8 treatment groups

8

Treatment groups

See each treatment group below.

Group A: MAD Cohort: Placebo-Controlled Period: DYNE-101Experimental treatment 1 intervention
Group B: MAD Cohort: Placebo-Controlled Period: PlaceboPlacebo comparator 1 intervention
Group C: MAD Cohort: Treatment Period: DYNE-101Experimental treatment 2 interventions
Group D: MAD Cohort: Long-Term Extension Period: DYNE-101Experimental treatment 1 intervention
Group E: Dose Expansion Cohort: Placebo-Controlled Period: DYNE-101Experimental treatment 1 intervention
Group F: Dose Expansion Cohort: Placebo-Controlled Period: PlaceboExperimental treatment 1 intervention
Group G: Dose Expansion Cohort: Treatment Period: DYNE-101Experimental treatment 2 interventions
Group H: Dose Expansion Cohort: Long-Term Extension Period: DYNE-101Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

MAD Cohorts: Number of Participants With Treatment-Emergent Adverse Events (TEAEs)

Time frame
Through study completion, up to Week 217
2

Dose Expansion Cohorts: Change From Baseline in Myotonia as Measured by Video Hand Opening Time (vHOT)

Time frame
Baseline up to Week 25

Secondary outcomes

1

MAD Cohorts: Change From Baseline in Composite Alternative Splicing Index (CASI) in Skeletal Muscle Tissue

Time frame
Baseline up to Week 45
2

MAD Cohorts: Change From Baseline in Dystrophia Myotonica Protein Kinase (DMPK) Ribonucleic Acid (RNA) Expression in Muscle Tissue

Time frame
Baseline up to Week 45
3

MAD Cohorts: Change From Baseline in Hand Grip Relaxation Time

Time frame
Baseline up to Week 121
4

MAD Cohorts: Change From Baseline in Myotonia as Measured by vHOT

Time frame
Baseline up to Week 193

Other outcomes

Sponsors and contacts

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