Evidence map›Paper›PMID 39379403›Full record

Trial reportScientific reports2024

Safety and efficacy of viltolarsen in ambulatory and nonambulatory males with Duchenne muscular dystrophy.

Amy D Harper, Haluk Topaloglu, Eugenio Mercuri, Vasiliy Suslov, Liwen Wu, Cigdem Y Ayanoglu, Michael Tansey, Michelle L Previtera, Robert A Crozier, Leslie Magnus and 1 more

Registry-linked trialAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04956289 (A Phase 2 Open-label Study to Assess the Safety, Tolerability, and Efficacy of Viltolarsen in Ambulant and Non-Ambulant Boys With Duchenne Muscular Dystrophy), which is not on this map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04956289 phase2completednot on this map

A Phase 2 Open-label Study to Assess the Safety, Tolerability, and Efficacy of Viltolarsen in Ambulant and Non-Ambulant Boys With Duchenne Muscular Dystrophy (DMD) Compared to Natural History Controls

TypeinterventionalSponsorNS Pharma, Inc.Ran2021 to 2023Enrolled20ConditionsDuchenne Muscular DystrophyArmsViltolarsen
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Amy D HarperChildren's Hospital of Richmond at Virginia Commonwealth University, Richmond, VA, USA.
Haluk TopalogluDepartment of Pediatrics, Yeditepe University, Istanbul, Turkey.
Eugenio MercuriGemelli Hospital Catholic University Foundation, Rome, Italy.
Vasiliy SuslovSaint Petersburg State Paediatric Medical University, St Petersburg, Russia.
Liwen WuHunan Children's Hospital, Hunan, China.
Cigdem Y AyanogluDepartment of Pediatrics, Yeditepe University, Istanbul, Turkey.
Michael TanseyNS Pharma, Inc., Paramus, NJ, USA.
Michelle L PreviteraNS Pharma, Inc., Paramus, NJ, USA.
Robert A CrozierNS Pharma, Inc., Paramus, NJ, USA.
Leslie MagnusNS Pharma, Inc., Paramus, NJ, USA.
Paula R ClemensDepartment of Neurology, University of Pittsburgh School of Medicine, 3550 Terrace St, Pittsburgh, PA, 15261, USA. clempr@upmc.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Duchenne muscular dystrophy (DMD) is an X-linked recessive disease characterized by mutations in the dystrophin gene, causing motor and pulmonary function decline. Viltolarsen is indicated for patients with dystrophin gene mutations amenable to exon 53 skipping. Here, we report safety, motor function, and the first pulmonary function results from the open-label, phase II Galactic53 trial of viltolarsen (NCT04956289). Male participants aged ≥ 8 years with DMD received 80 mg/kg intravenous viltolarsen once weekly for 48 weeks. Results from participants receiving viltolarsen were compared with an external control cohort group-matched for multiple variables. All treatment-emergent adverse events were mild or moderate, 4 were considered treatment-related, and no participants discontinued. Participants receiving viltolarsen experienced clinically meaningful benefits in pulmonary function with higher percent predicted forced vital capacity and higher peak cough flow at Week 49 compared with the control cohort for both ambulatory and nonambulatory participants. Viltolarsen also stabilized upper limb motor function over the Treatment Period. These results support viltolarsen as an important part of the treatment armamentarium for both ambulatory as well as nonambulatory patients with DMD.

Indexed as

Muscular Dystrophy, DuchenneAdolescentChildDystrophinHumansMaleTreatment OutcomeYoung AdultDystrophinNeuromuscular diseasePediatric research

Identifiers

PMID39379403
PMCPMC11461856

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.