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Updates for the Lafora Therapy Pipeline: Requesting information from our Research Community

April 24, 2026/by Chelsea's Hope

At our 2025 Lafora Symposium, several of the Lafora patient organizations decided to work together to better support therapy development for Lafora disease.

To help us prioritize therapies to support, we are requesting periodic updates on novel and repurposed therapies in development for Lafora. If you are a clinician or researcher working on a Lafora Therapy, please complete this form so that we can educate families about your research and determine the best way to support the development of your therapy.

Submissions will be reviewed by A.I.L.A., Cel-Luz Association, Chelsea’s Hope, France Lafora,  and TempoZero.

Share an Update

 

https://chelseashope.org/wp-content/uploads/2022/02/ChelseasHope1.png 0 0 Chelsea's Hope https://chelseashope.org/wp-content/uploads/2022/02/ChelseasHope1.png Chelsea's Hope2026-04-24 12:30:402026-06-22 15:43:18Updates for the Lafora Therapy Pipeline: Requesting information from our Research Community
March 10, 2026 Statement from Fondazione Telethon

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

March 10, 2026/by Chelsea's Hope

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.

https://chelseashope.org/wp-content/uploads/2026/03/March-10-2026-ION283-Telethon-featured-image.png 628 1200 Chelsea's Hope https://chelseashope.org/wp-content/uploads/2022/02/ChelseasHope1.png Chelsea's Hope2026-03-10 13:21:262026-03-10 13:21:49Telethon’s Statement on the ION283 Clinical Trial Pathway for Lafora
2025 Chelsea's Hope Lafora Children Research Fund Annual Report info@chelseashope.org www.chelseashope.org 2025 Annual Report

2025 Annual Report

February 18, 2026/by Chelsea's Hope

Chelsea’s Hope published our 2025 Annual Report! Inside, you’ll find a message from the President of the Board of Directors, Jenifer Merriam, and a summary of our impact in 2025. We also include a financial statement, goals for 2026 and beyond, and acknowledgments.

Thank you to our generous donors, committed research network, and courageous families for supporting Chelsea’s Hope last year. We appreciate your continued partnership to reach a cure!

Download the 2025 Annual Report Right-open Right-open

Stay connected by signing up for our mailing list and following our social media for regular updates. We always welcome volunteers to support our cause and invite you to join Chelsea’s Champions with a monthly gift to support our work in 2026 and beyond.

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January 20, 2026 Update Fondazione Telethon logo

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

January 20, 2026/by Chelsea's Hope

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.

Read the statement from Telethon
https://chelseashope.org/wp-content/uploads/2026/01/January-20-2026-Telethon-Update.png 628 1200 Chelsea's Hope https://chelseashope.org/wp-content/uploads/2022/02/ChelseasHope1.png Chelsea's Hope2026-01-20 08:03:322026-01-20 08:04:00Telethon’s Update on the ION283 Clinical Trial Pathway for Lafora Disease
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About Chelsea’s Hope

Chelsea’s Hope began as a website in the fall of 2007 to share Chelsea Gerber’s story with family and friends. A 501(c)(3) organization since 2009, we have made an impact by raising awareness, connecting families worldwide, funding research, and maintaining hope.

Our mission is to improve the lives of those affected by Lafora disease and help accelerate the development of treatments. [Read More]

View Chelsea’s Hope Newsletter Archive 

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Latest News

  • New Resource: Lafora Anti-Seizure Medication Guidelines

  • Join in Lafora Body Disease Day 2026!

  • Lafora Therapy Q&A Resources

  • Student Ambassador Applications Open

  • Social Security Added Lafora to Compassionate Allowances List

  • Elpida Therapeutics’ Press Release

  • ION283 to be Developed by Elpida Therapeutics

  • Update on the ION283 Program from Telethon

  • Introducing the Lafora Clinical Network Registry

  • Meet our 2026 Summer Interns!

The mission of Chelsea’s Hope is to improve the lives of those affected by Lafora disease and help accelerate the development of treatments.

Chelsea’s Hope Lafora Children Research Fund is an IRS 501(c)3 nonprofit organization. EIN: 27-1008382

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Use ICD-10 code G40.C for Lafora.

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