BCM Families Foundation
Blue cone monochromacy (BCM) is an ultra-rare genetic disease causing mainly blind-ness, reduced acuity of vision and nystagmus. The Italian BCM Association was promoted by the mother of two children born with this disease who had been active in the field for some years through an outreach campaign to contact other families at the international level and the private funding of some re-search projects.
Science Compass, malattia genetica, ipovisione, ridotta acuità visiva, fotofobia, nistagmo, ricerca scientifica, sostenere lo sviluppo terapeutico, blue cone monochromacy
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Blue Cone Monochromacy

BCM Families Foundation

Towards the cure

Blue cone monochromacy (BCM) is an ultra-rare genetic disease causing mainly blindness, reduced acuity of vision and nystagmus.

BCM Families Foundation

The Italian BCM Association was promoted by the mother of two children born with this disease who had been active in the field  for some years through an outreach campaign to contact other families at the international level and the private funding of some research projects.

The creation of an international patients’ association, formally founded in the United States through the assistance of ScienceCompass, led the way to the definition of a structured plan to support research, based on a therapy-driven investment strategy.

The association aims at

  • overseeing the science hotspots on BCM and supporting development of the most promising research avenues;
  • implementing standards of care for patients and building an international disease registry in preparation for future clinical trials;
  • raising awareness on the disease and triggering development and distribution of visual aids to grant patients with a better quality of life.
In order to support these activities, ScienceCompass has provided the association with accurate scenario analyses mapping global research on BCM and on the biological pathways involved in the disease.

To achieve an overall view of the state of the art and potential areas to act on, ScienceCompass integrated the study of the relevant scientific literature with direct interface with international stakeholders and the scientific community in the field.

 

This analysis was pivotal for the definition of guidelines to maximize investment impact.

The study highlighted the opportunity to pursue a co-development partnership with a US biotech interested in the gene therapy of eye diseases and owning the know-how to bring the research funded by the association to the patients’ bedside.

 

Such agreement was recently signed; a gene therapy for blue cone monochromacy is now being developed.

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