Tag Archive for: lafora treatment

Telethon’s Statement on the ION283 Clinical Trial Pathway for Lafora

Fondazione Telethon Logo

Fondazione Telethon has kindly provided Chelsea’s Hope and the other advocacy organizations with a statement for the Lafora patient community. At their request, we are sharing the communication below:

Dear Members of the International Lafora Patient Community,

Fondazione Telethon remains open to contributing to the development of ION283 and to collaborating with partners in Europe and in the United States, provided that the highest ethical and scientific standards are upheld and that any decision is taken exclusively in the best interest of patients.

Fondazione Telethon acknowledges the complexity of the ION283 case, also from the perspective of Ionis, which currently holds the license for the compound.

The essential authorizations required to set up a clinical study in Italy fall within Ionis’ decision-making space. Therefore, at this stage, Fondazione Telethon cannot serve as the reference point or source of information regarding a possible future development path for ION283. The decision concerning the continuation, redesign, or activation of a clinical program is not under our direct control. Should concrete and reliable updates become available, we will share them promptly.

We are aware that several research groups, in different Countries, are actively conducting studies on Lafora disease: this reflects the commitment of the international scientific community to advancing knowledge and identifying potential therapeutic strategies.

While dealing with the hard work to ensure progresses in identifying therapeutic solutions, we respectfully invite families, associations, and researchers to bear in mind that the scientific pathway required to transform science in therapies does not allow for shortcuts. The timelines necessary to ensure safety, efficacy and compliance with regulatory standards cannot be compressed beyond what scientific rigor and ethical standards allow.

We are aware that this message may sound demanding. However, clarity is necessary to preserve families who are already facing extraordinary challenges and a sense of unpostponable urgency every day.

Our commitment remains firm: to pursue research with responsibility, scientific soundness, transparency, and deep respect for patients and their loved ones.

As a reminder, please email your questions or concerns to ion283@chelseashope.org.

Telethon’s Update on the ION283 Clinical Trial Pathway for Lafora Disease

Fondazione Telethon Logo

Fondazione Telethon has kindly provided Lafora patient organizations with a statement that includes some clarifications about ION283.

As they note, Telethon does not currently have a contract with IONIS. Until they have a contract for the license, they have no authority to submit a protocol to the EMA/FDA for a trial. If they are successful in gaining the license for ION283, they plan to:

  • Start a clinical trial as soon as possible
  • Cover all the clinical costs of the trial
  • Allow European patients currently in the Safety Study to complete their visits in Italy and continue receiving the drug after the study concludes

We appreciate the clarifications from Telethon! We will continue to update the Lafora community as we learn of developments for ION283.

As a reminder, please email your questions or concerns to ion283@chelseashope.org, and we will advocate on your behalf.

Announcing Lafora Therapy Town Hall

Lafora Therapy Town Hall Join us to discuss future treatment options and plan as a community. 28 october 2025 tuesday Register online to attend the Zoom meeting.

 

Questions about what therapies are next for the Lafora community? We are hosting a Lafora Therapy Town Hall to discuss what treatments the community can rally behind to bring from pre-clinical studies to clinical trials for our children.

Join us next Tuesday, October 28th, at 11 am PDT via Zoom.

As Lafora patient organizations – Chelsea’s Hope, Cel-luz, France Lafora, A.I.L.A. – we want to be united in our message and pursuit of treatment.

It’s been a worldwide effort to fund the safety study / phase 1 trial for ION283 at UTSW. We’ve been working towards it for years. If our patient community is going to bring another therapy forward, we must be unified in our next steps.

Families and caregivers, we hope you will be able to attend this event. Your voice matters!

Invitation to Join Listening Sessions

Families and caregivers, you might have seen in our July newsletter that we need your help to establish criteria for Centers of Excellence for treating Lafora disease.

As an ultra-rare disease, most hospitals do not know what resources are needed in order to provide the best possible care for our children with Lafora. By establishing guidelines for Centers of Excellence, we can provide a set of recommendations for treating Lafora patients and recognize hospitals that provide exemplary care for our children with Lafora.

We invite you to join us at one of the listening sessions in August to share your advice on what support you receive (or need) from your care facility. There are currently four sessions scheduled; please sign up for the session with the time and language that works best for you.

Listening Sessions

August 1: English (but all languages welcome)
Join Jenifer at 10 AM Pacific Daylight Time. >

August 8: Hindi/English
Join Vaishali at 7:30 PM India Standard Time. >

August 15: Spanish
Join Nancy at 10 AM Eastern Daylight Time. >

August 25: Italian
Join Giuseppe at 7 PM Central European Summer Time. >

Together, we can advocate for better care. By recognizing locations with expertise, we can learn from their practices and improve worldwide treatment options for Lafora patients.