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Avidity Biosciences clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine and the EU Clinical Trials Information System (CTIS) — current trials in our UK, USA and EU (CTIS) registers with Avidity Biosciences as lead sponsor. Synced 26 Sep 2026
6Current trials
2Recruiting now
2Drugs in these trials
3Trial registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 — Top 14 finalist
Compiled from ClinicalTrials.gov and CTIS registry records · Last verified · Editorial standards
At a glance

Avidity Biosciences is the lead sponsor of 6 current clinical trials in our UK, USA and EU (CTIS) registers. 2 are recruiting patients now. The most common phase is Phase 3. The drugs named most often in its trials are AOC 1044 and Del-brax. The most-studied condition is FSHD.

ClinicalTrials.gov trials by status

  • Recruiting240%
  • Active, closed240%
  • By invitation120%

Trials by phase

  • Phase 3360%
  • Phase 2240%
01

Clinical trials sponsored by Avidity Biosciences

5 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
A Study to Evaluate Del-brax (Also Referred to as AOC 1020) in Participants With FSHD
NCT07038200 · ClinicalTrials.gov ↗ · Facioscapulohumeral Muscular Dystrophy, FSHD, FSHD - Facioscapulohumeral Muscular Dystrophy
Drug: Del-brax
Phase 3 Recruiting 2025-06 UK, USA
A Phase 3 Study to Evaluate the Safety and Efficacy of AOC 1044 (Also Referred to as Delpacibart Zotadirsen) in Participants With DMD With Gene Mutations Amenable to Exon 44 Skipping
NCT07587242 · ClinicalTrials.gov ↗ · Muscular Dystrophies, Muscular Dystrophies (Duchenne, Becker, Myotonic Dystrophy), Muscular Disorders, Atrophic
Drug: AOC 1044
Phase 3 Recruiting 2026-09 UK
Global Open-Label Extension Study of Del-desiran for the Treatment of DM1
NCT07008469 · Myotonic Dystrophy Type 1, DM1, Myotonic Dystrophy
Phase 3 By invitation 2025-06 UK, USA
Phase 2 Open-label Extension Study of AOC 1020 in Participants With Facioscapulohumeral Muscular Dystrophy (FSHD)
NCT06547216 · FSHD, FSHD1, FSHD2
Drug: Del-brax
Phase 2 Active, closed 2024-07 UK, USA
Ph2 Open-label Study of AOC 1044 in Duchenne Muscular Dystrophy Participants With Mutations Amenable to Exon44 Skipping
NCT06244082 · DMD, Duchenne Muscular Dystrophy, Duchenne
Drug: AOC 1044
Phase 2 Active, closed 2024-01 USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Titles and statuses are copied from the registry as published.

02

Avidity Biosciences in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System with Avidity Biosciences as sponsor. Some are the same study as a ClinicalTrials.gov record above; the two registries share no common ID. Trials with a site in Ireland are listed first.

StudyPhaseStatusCountries
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Global Study with an Open-Label Extension to Evaluate the Efficacy and Safety of Intravenous AOC 1044 (delpacibart zotadirsen) for the Treatment of DMD with Gene Mutations Amenable to Exon 44 Skipping
2025-523087-20-00 · CTIS ↗ · Musculoskeletal Diseases
Drug: AOC 1044
Phase 3 Ongoing Italy, Germany, France + 4 more
03

Drugs in Avidity Biosciences trials

2 compounds

Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.

04

Conditions in Avidity Biosciences trials

18 conditions
FSHD2FSHD12FSHD21FMD1Myotonic Dystrophy Type 11DM11Myotonic Dystrophy1Myotonia1Facioscapulohumeral Muscular Dystrophy1FSHD - Facioscapulohumeral Muscular Dystrophy1Muscular Dystrophies1Muscular Dystrophies (Duchenne, Becker, Myotonic Dystrophy)1Muscular Disorders, Atrophic1Muscular Disease1DMD1Duchenne Muscular Dystrophy1Duchenne1Exon 441
05

By trial register

RegisterTrialsRecruiting
Clinical trials in UK42
Clinical trials in USA41
EU register (CTIS)1—

A trial with sites in more than one country appears in each of those registers.

06

Questions about Avidity Biosciences trials

How many clinical trials does Avidity Biosciences sponsor?

Avidity Biosciences is the lead sponsor of 5 current trials on ClinicalTrials.gov in our UK and USA registers, and 1 authorised or ongoing trial in the EU register (CTIS), as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Avidity Biosciences trials recruiting?

Yes. 2 of its 5 ClinicalTrials.gov trials are recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Which drugs is Avidity Biosciences testing?

Its current trials name 2 drugs and biologicals as interventions. The most frequent are AOC 1044 (3) and Del-brax (2). The number in brackets is how many of its trials name each drug.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The the registries data on this page was last retrieved on 26 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.