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FFB Congratulates RPE65 Gene Therapy Researchers for Champalimaud Award

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More than two decades ago, the Foundation Fighting Blindness (FFB) began funding RPE65 gene therapy research that led in late 2017 to LUXTURNA™, the first FDA-approved gene therapy for the eye or an inherited condition. Ultimately, the Foundation provided more than $10 million in funding for the groundbreaking effort.

On September 4, 2018, seven researchers, including six previously funded by the Foundation, were recognized with the prestigious 2018 Antonio Champalimaud Vision Award for their contributions to the advancement of blindness-reversing RPE65 gene therapies. The investigators received a prize of one million euros ($1.15 million).

Mutations in the RPE65 gene cause Leber congenital amaurosis and retinitis pigmentosa, both of which lead to devastating, progressive vision loss.

The awardees included:

  • Jean Bennett, MD, PhD, Scheie Eye Institute, University of Pennsylvania School of Medicine, and Albert M. Maguire, MD, Children’s Hospital of Philadelphia. Their RPE65 gene-therapy research and human studies led to the development of LUXTURNA™.
  • Robin Ali, PhD, and James Bainbridge,MD, PhD, Institute of Ophthalmology of the University College London and Moorfields Eye Hospital, who led an RPE65 gene therapy clinical trial.
  • Samuel G. Jacobson, MD, PhD, Scheie Eye Institute, University of Pennsylvania School of Medicine, and William W. Hauswirth, PhD, University of Florida College of Medicine, who conducted extensive RPE65 gene therapy research and development, and ultimately, a clinical study.
  • Michael Redmond, PhD, National Eye Institute, who identified the role of the RPE65 gene in vitamin A processing in the retina.

“We congratulate the Champalimaud Award recipients for their groundbreaking advancements in gene therapy research, and the impact their breakthroughs in retinal-disease gene-therapy development,” says Stephen Rose, PhD, FFB’s chief scientific officer. “Thanks in part to their success, people with LCA or RP caused by biallelic mutations in the RPE65 gene could be eligible to receive this FDA-approved vision-restoring treatment. In addition, this advancement has led the way for development of many more retinal gene therapies. There are now approximately 20 clinical trials underway for retinal gene therapies including those for Stargardt disease, Usher syndrome, and retinitis pigmentosa.”

The António Champalimaud Vision Award is given alternately between contributions to overall vision research (even numbered years) and contributions to the alleviation of visual problems, primarily in developing countries (odd numbered years).

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14 Responses to 'FFB Congratulates RPE65 Gene Therapy Researchers for Champalimaud Award'

  1. douglas says:

    Hello, I noticed that comments are screened before being posted so this message is to whoever from FFB read this.

    First, I and probably many folks with retinal diseases applaud FFB generous funding to get this gene therapy off the ground onto getting FDA approval of the rpe65 gene therapy to the public.

    Folks with this rpe65 probably prayed and prayed for a miracle to happen and when it did finally arrived, their hopes are shattered due to its outrageous price tag! Maybe a handful of them would be able to afford it but what about the majority who are on SSI with Medicaid or Medicare that don’t cover this therapy.

    It is unfair that Spark is price gouging the needy. And since when did miracle comes with a price?

    What does Gordon Gund think about this?

    Douglas

    • EyeOnTheCure says:

      Hi Douglas, Spark Therapeutics has worked very closely with payers to allow commercially insured patients, who seek treatment within network, to be treated at no or near no patient out-of-pocket expense. If you want to learn more about Spark’s support services or have any questions, please feel free to visit their Patient Support Services website at http://www.mysparkgeneration.com or call their patient inquiry number at 1 833 SPARK PS (833 772 7577).

  2. Zach says:

    I have RP. How do I sign up for a clinical trial?

  3. Connie and Anthony Dovi says:

    We are so proud of Dr.Jacobson for receiving such a prestigious award and for being recognized for hisr hard work and dedication. We have been patients of Dr. Jacobson for over twenty years and consider ourselves extremely fortunate. His dedication, passion and relentless drive give us hope that a cure for RP is in our future. Congratulation to Dr. Jacobson at his staff on receiving this well deserved award. With admiration, Connie and Anthony

  4. Gladys orrantia says:

    I would like to see a treatment for retinitis pigmentosa for my Mom. She es 72 years old. 40 years with the condition and almos lost her visión. We are in mexico. Could you help us?

  5. Sivaprakash says:

    Hi.i am an RP patient from india for the last 13 years .I lost my vision 75%.is it possible to recover my vision with the help of Gene mutation RPE65. How can i proceed from India

    • EyeOnTheCure says:

      Hello, we are aware of the following clinics in India, which may be helpful:

      Shankara Netralaya, Chennai
      L. V. Prasad Eye Institute, Hyderabad – They have branches in different states
      Aravind Eye Hospital, Madhurai
      All India Institute of Medical Sciences- New Delhi

      If you are interested in a clinic in a different location, contact one of these clinics and ask them for a suggested clinic in your region.

  6. Ian says:

    Hello, will this treatment become available in the UK?

  7. Swati Verma says:

    I really like this post. love it

  8. Salman Muhammad says:

    Hi dear what is the progress of cure in retinitis pigmentosa and what will be the expected cost for the cure. please give me reply i am a food technologist and very much concerned about my cure please guide me about it.

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