DMD Research News

Each year at La Force Foundation, we select the most interesting and promising research for Duchenne muscular dystrophy (DMD) to support.

We live in an era of ultra-fast change, where science and technology are working together more than they ever have. This is especially true for DMD, which has seen significant strides in genetic research.

Before we fund projects, it’s important to ensure that the research protocols are ethical and that the preliminary results of the research are auspicious. With the help of the Duchenne Alliance, we consult experts in the field of genetics to ensure that projects have real potential to advance the treatment of DMD.

This year, La Force is participating in three research projects that we believe are extremely promising.

DMD Research Funded in 2016 – 2017 – 2018

How can I find out about clinical trials?

Enlisting in a DMD registry can guide the medical researchers who plan clinical trials of new therapies to you. A registry can help these scientists to identify children with DMD who live near a particular research centre and contact them about upcoming clinical trials.

Registries

Learn more about registries here.

Learn more about:

CRISPR/CAS9 UNDERSTANDING CRISPR/CAS9 WITH JACQUES P. TREMBLAY

EDASALONEXENT POSITIVE RESULTS AND NO SIDE EFFECTS

EDASALONEXENT  THE POTENTIAL TO MODIFY DMD

DEFLAZACORT DEFLAZACORT OVER PREDNISONE/PREDNISOLONE?

EXONDYS® NEGATIVE OPINION FOR EXONDYS® IN EUROPE

GENE TRANSFER SGT-001 SOLID BIOSCIENCES ANNOUNCES NEW PRECLINICAL DATA ABOUT GENE TRANSFER

GENE TRANSFER SGT-001 SOLID BIOSCIENCES INITIATES CLINICAL TRIAL FOR GENE TRANSFER

TRANSLARNA™ (ATALUREN) POSITIVE NEWS FOR TRANSLARNA™ (ATALUREN)

TRANSLARNA™ (ATALUREN)A PROMISING TREATMENT FOR DMD

STAT3 A NEW RESEARCH TO TREAT DMD

CAP-1002 CAPRICOR INITIATES HOPE-2 CLINICAL TRIAL

GOLODIRSEN NEW DMD EXON-SKIPPING THERAPY ON THE WAY