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Completed Phase 3 Interventional

Global Study of Del-desiran for the Treatment of DM1

ClinicalTrials.gov ID: NCT06411288

Public ClinicalTrials.gov record NCT06411288. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 4:36 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Global Study to Evaluate the Efficacy and Safety of Intravenous AOC 1001 for the Treatment of Myotonic Dystrophy Type 1

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Global Study to Evaluate the Efficacy and Safety of Intravenous Delpacibart Etedesiran (abbreviated del-desiran, formerly AOC 1001) for the Treatment of Myotonic Dystrophy Type 1

Study identification

NCT ID
NCT06411288
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Avidity Biosciences, Inc.
Industry
Enrollment
159 participants

Conditions and interventions

Eligibility (public fields only)

Age range
16 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 30, 2024 (Actual)
Primary completion
Jul 23, 2026 (Actual)
Completion
Jul 29, 2026 (Actual)
Last update posted
Sep 1, 2026

2024 – 2026

United States locations

U.S. sites
18
U.S. states
15
U.S. cities
18
Facility City State ZIP Site status
Stanford University Stanford California 94305 —
University of Colorado Denver Colorado 80045 —
University of Florida Gainesville Florida 32608 —
University Research Center of South Florida Tampa Florida 33612 —
Indiana University (IU) Indianapolis Indiana 46202 —
Kansas University Medical Center Kansas City Kansas 66205 —
Kennedy Krieger Institute Baltimore Maryland 21205 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
University of Minnesota Minneapolis Minnesota 55455 —
University of Rochester Medical Center Rochester New York 14642 —
Duke University Medical Center Durham North Carolina 27708 —
Wake Forest Winston-Salem North Carolina 27157 —
University of Cincinnati Gardner Neuroscience Institute Cincinnati Ohio 45219 —
Ohio State University Columbus Ohio 43221 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
Houston Methodist Neurological Institute Houston Texas 77030 —
Virginia Commonwealth University Richmond Virginia 23298 —
University of Washington Seattle Washington 98104 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06411288, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 1, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06411288 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →