CATEGORIES: Research
pns meeting

PNS, It’s A Global Effort

by | Nov 7, 2019 | 0 comments

Where do the top CMT researchers in the world unite to share leading-edge research? The Peripheral Nerve Society (PNS) meeting!

This meeting takes place once a year in cities around the world. This year’s location was the stunning city of Genova, Italy, June 22-26 at the Centro Congressi, Porto Antico Di Genova. There is no better opportunity to connect one-on-one with international experts from multiple disciplines on the topics of Charcot-Marie-Tooth and related Inherited Neuropathies, Inflammatory Neuropathies, pain and more.

The four-day program was packed with talks, presentations, collaborative meetings, educational break-outs and poster sessions. HNF was honored to present at the annual Inherited Neuropathy Consortium (INC) meeting on our new Movement is MedicineTM program, an innovative research initiative to bring exercise modalities to all patients with CMT. These studies have the potential to be an adjunct therapy to improve functional outcomes and endpoints in future CMT patient clinical trials.

In addition, HNF is a key partner of the INC and is on the internal Diversity Core Committee to help recruit a diverse patient population for the INC research studies. We are very excited to have implemented a Voice Survey in Spanish to support the Latino community to participate in clinical trials. We launched the study on September 16th and welcome participation!

CLICK TO PARTICIPATE

Allison Moore, founder/CEO of HNF presented on three research studies spotlighting the Global Registry for Inherited Neuropathy:

  1. CMT1A and Impaired Patient Mobility: Expressions, Remedies and Impact on Quality of Life
  2. The Path To Diagnosing Charcot-Marie-Tooth Disease: The Patient Experience
  3. “Examination of Risks/Benefit Profile of Medical Cannabis In CMT and HNPP and Chronic Pain Patients” – Brian Piper, Phd.

HNF was front and center at the Pharnext Presentation, as Scientific Advisory Board Member Michael Sereda presented the biomarker results of PXT3003 and world renowned Induced Pluripotent Stem Cells (iPSC) lines researcher Mario Saporta gave a thorough overview of CMT. They highlighted results from pivotal phase III trials for the first potential drug to treat CMT1A, PXT3003.

 “I have waited years for this moment and am grateful to Pharnext for choosing CMT as their first pipeline class of drugs!” – Allison Moore, HNF Founder & CEO

A focus group was also hosted by Vitacces in collaboration with Pharnext Pharmaceuticals, for their CMT research app, CMT&Me. HNF was honored to join Mark Larkin, founder of Vitaccess and his team, the distinguished advisory board, during this collaborative discussion along with other advocacy groups from around the world: CMTA, CMT France/Europe, CMT UK, and ACMT – Rete (Italy) to ensure that patient voices are being heard and continue to align with the most vital needs of the community. To join CMT&ME: Search your app carrier.

Learn more on this topic

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Hot Off the Press – Potential Treatment for CMT1A

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Support CMT Therapeutic Alliance

HNF has entered into a joint venture – the CMT Therapeutic Alliance – with a unique non profit organization (BioPontis Alliance for Rare Diseases) that brings professional drug discovery capabilities to translate our research results into potential treatments.

Sneak Peak of Fall Newsletter: CMT Research Study Survey

My name is Elizabeth Francisco and I am a graduate student from the Genetic Counseling program at the University of North Carolina Greensboro. I am inviting you to participate in a research study. The goal of my study is to learn more about the experiences of people with Charcot-Marie-Tooth (CMT) with genetic counseling and genetic testing. Adults with CMT and parents or legal guardians of someone of any age who has a diagnosis of CMT are eligible to participate

Building Awareness on CMT and Supporting the Patient Community – HNF Announces Support from Pharnext

HNFpharnext recently entered into a partnership with the French biopharmaceutical company, Pharnext, to help raise awareness of Charcot-Marie-Tooth (CMT) disease and support the CMT patient community through several initiatives. Building awareness is key! Pharnext’s support will assist HNF in distributing HNF’s CMT Update quarterly newsletter, enhancing the Global Registry for Inherited Neuropathies (GRIN), setting up activities for CMT September Awareness Month in the US and strengthening the CMT Inspire Community.

Quality of Life and CMT Research

Did you know that 95% of clinical trials fail? There are multiple causes, most related to efficacy or safety, which obviously can be harmful and risky for patients. The risk-reward of enrolling in trials is a judgment call based on the devastating effects of disease related to quality of life (QoL) or life-threatening disease. With CMT, the risk-reward is more of a challenging question for many, as CMT in most cases is non-fatal.

Help us answer questions that your doctors and the CMT Research Community aren’t too sure about.

Did you know that you can become part of a community in therapy development and further research for all forms of CMT and inherited neuropathies? The mission of the Global Registry for Inherited neuropathies (GRIN) is to collect clinical and genetic information from patients with ALL forms of Charcot-Marie-Tooth (CMT) and other related rare and ultra rare inherited neuropathies.

Hot off the press

It seems like almost weekly there is another new publication on CMT with interesting basic biology. While an earlier “Hot off the press” highlighted the work of Cherry and co-workers at the University of Texas Southwestern Medical Center who showed show that neurons lacking a gene for rab7 result in neuropathy.

New Study on CMT Type 2B

If we are to learn more about CMT and the effectiveness of rehabilitation it is worth asking the patient and their caregiver. A recent Italian study by Padua et al recently described a survey of CMT patients and caregivers and their perspectives and perceptions of rehabilitation efficacy and needs.

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