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CHAN ZUCKERBERG INITIATIVE TO FUND 30 PATIENT GROUPS, AIMING TO BUILD A MODEL FOR TACKLING RARE DISEASES

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Excerpt:

……The funded groups include the Hermansky-Pudlak Syndrome Network, focused on a hereditary disorder that causes albinism, visual impairment, and prolonged bleeding; Project 8p, targeting a chromosomal disorder that impairs physical and mental abilities; and the NEC Society, which works to prevent an intestinal disorder in infants known as necrotizing enterocolitis.

“We realize that’s only 30 groups out of 7,000 diseases,” said Tania Simoncelli, CZI’s head of science policy who is leading Rare as One, as the funding program is called. “But if we can actually work with these groups to figure out the model, figure out what’s generalizable — then anyone can do this.”….

The Project 8p Foundation (Project 8p) was created in 2018 to:

  • Accelerate future treatments, not only for 8p, but potentially for other chromosome-wide diseases as well.
  • Lead with knowledge from patients. Currently, there is no cure for 8p disorders, nor is there a standard course of treatment.

The Project 8p Foundation (Project 8p) was created in 2018 to:

  • Raise transformative funding for pioneering scientific research into treatments for a complex, rare disease involving 250+ affected genes on the short arm of the 8 th chromosome (8p). Rearrangements of these genes causes significant abnormalities to the entire neurological system, thus all organs and functions of the body– with variance in cognitive functions, gross motor skills, social development and other challenges during infancy, and throughout life;
  • Empower a unified community of 8p patients and their families so they can have meaningful lives today; and
  • Accelerate future treatments, not only for 8p, but potentially for other chromosome-wide diseases as well.