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Association Institut De Myologie

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Congenital and Hereditary Diseases in Muscle Disorders

At the Association Institut De Myologie in Paris, research in this area focuses on Duchenne Muscular Dystrophy, a serious inherited condition that weakens muscles over time. The trials are designed to explore new ways to slow disease progression and support better long-term outcomes for affected patients.

  • Testing a new gene therapy approach for boys who can still walk
  • Assessing whether treatment can improve clinical effectiveness and maintain muscle function
  • Evaluating the safety and tolerability of emerging therapies over time

This work combines genetic medicine and neuromuscular research to address the underlying cause of the disease while also monitoring how well patients respond to treatment.

Musculoskeletal Diseases and Therapy Development

Clinical research at this site also examines treatment options for Duchenne muscular dystrophy in patients with more advanced mobility loss. The main goal is to determine whether a new therapy can help reduce muscle decline and preserve remaining physical function.

  • Evaluating a treatment intended to slow muscle deterioration
  • Measuring treatment effectiveness in non-ambulant patients
  • Studying the overall safety and tolerability of the therapy

These studies reflect an ongoing effort in musculoskeletal medicine to improve care for people living with progressive inherited muscle disease.

Site Overview

assignment
13
connected trials
corporate_fare
12
sponsors
science
25
IMPs

Activity Indicator

Last 6 months

0
Trials started
-100% vs previous period.
1
Trials started 6–12 months ago
13
Total trials linked
Highly Active
trending_downDeclining-100%
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Trial Flow

How this site's trials are distributed across therapeutic areas and active substances (IMPs), and how they're positioned within their overall lifecycle status. Flow thickness represents the number of unique trials.

Therapeutic areaarrow_forwardIMParrow_forwardLifecycle status

Top 4 of 6 therapeutic areas and 15 of 25 IMPs, ranked by number of trials.

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Compounds & Molecules Timeline

The time span of clinical-trial activity for the main active substances (IMPs) studied at this site over the last 8 years. Each bar runs from the earliest trial start to the most recent end; a substance with a trial still open has no recorded end and is shown as ongoing.

Trial span Ongoing Showing last 8 years
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Sponsor & Partnership

Top sponsors by active trials, and the ones that have come back for more than one study.

Active trials
8
Sponsors (total)
12
Active sponsors
7

Sponsor Network

Top 7 by active trials.

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Partnership History

Sponsors with repeated collaboration (≥ 2 trials).

Sponsor Network Graph

How sponsors and therapeutic areas connect across this site's active trials: each link is at least one active trial shared between them, and bigger nodes mean more activity. Click a node to see its exact connections.

Country Benchmark

Compared to 978 other sites in France

description
Trial volume
13
Outperforms 76% of sites
public
Therapeutic diversity
6areas
Outperforms 76% of sites
groups
Sponsor diversity
12sponsors
Outperforms 79% of sites

Therapeutic Area Benchmark — France

Select a therapeutic area to compare against other sites in France.

Competitor Comparison

Similar sites in the same country running a comparable number of trials (within ±30%), scored on how closely their trial portfolios match this one. Higher percentages mean a more similar profile.

Country: France

Market Share

Country: France

Therapeutic Area Market Share

Select a therapeutic area to view its disease coverage breakdown.

Heat Maps & Advanced Analytics

How often specific conditions appear in trials across this site and comparable sites from the same country. Each row is a site, each column a condition, and each cell the number of trials on it — darker means more activity.

Other Trials in Association Institut De Myologie

lock Showing 1 of 13 trials — the rest is available on a paid plan.

Trial Sponsor Phase Status Start Date End Date
Dose-Escalation and Comparative Study of Eteplirsen in Duchenne Muscular Dystrophy Patients with Exon 51 Skipping MutationsSarepta Therapeutics Inc.Phase IIINot RecruitingDec 2021

IMP list

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IMP Trials Status First start Last start
Sirolimus2Unknown2021-03-012021-03-01

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