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Innovations in the ability to probe more enhanced understand biologic systems in the past 30 years1-3 have enabled the medical community to develop new therapeutic agents and change the course of many life-shortening diseases. 4, 5 Despite this success, bridging the gap between promising laboratory observations and the development of effective therapies remains risky and expensive, with fewer than 1 in 10, 500 early translational programs successfully obtaining Food and Drug Administration (FDA) approval, at an expense of almost $1 billion. 6 Most therapeutic development fails in the preclinical phase, which is sometimes described as the "valley of loss of life. "7
For this reason and because therapies for a few conditions will have a restricted eventual market value, the pharmaceutical industry has already been hesitant to initiate early-stage programs to take care of so-called orphan diseases. In recognition of a critical need, federal companies have developed programs to catalyze innovation and minimize limitations to early progress new therapies. 8 During the past two decades, disease-focused foundations likewise have developed a new method to bridging this preclinical gap. In a process known as venture philanthropy, such foundations have formed relationships with industry and federal agencies to share the financial risk of therapeutic development, shorten the early translational pipeline, and advance research with "a give attention to human, not financial, return. "9 In addition, foundations and their academic partners have accelerated early development by providing access to patient populations for clinical tests and assistance from disease-specific experts in study design, which has helped in bridging the gap in therapeutic development.
In this review, we will give attention to about three diseases -- cystic fibrosis, multiple myeloma, and type 1 diabetes mellitus -- to illustrate how aide among academic institutions, footings, and industry partners have evolved to address the therapeutic challenges of these conditions.
CYSTIC FIBROSIS
Within 1989, the discovery of the gene that causes cystic fibrosis and the cystic fibrosis transmembrane conductance regulator (CFTR) protein10, eleven greatly increased interest within the scientific community in this life-shortening genetic disease, which influences approximately 75, 000 patients worldwide. Together with support from the Cystic Fibrosis Foundation (CFF) and the National Institutes of Health (NIH), researchers quickly expanded knowledge about the biogenesis, maturation, and functionality of CFTR, a controlled epithelial anion channel12; such knowledge provided the necessary scientific framework for the development of therapeutic targets. In addition, an international consortium13 determined more than 1700 mutations and identified genotype-phenotype correlations with standard case definitions, 14 which enabled a precision-medicine strategy to therapeutic development. In the 1990s, attempts were made to treat cystic fibrosis by gene-replacement remedy shipped to airway epithelia. Although early in vitro15 and in vivo studies16 provided proof of concept, many barriers, including a strong host immune response, were encountered. 17 These obstacles ended such initial clinical development programs.
In the decade after the discovery of the cystic fibrosis gene, scientific knowledge expanded but did not lead to a remedy that corrected CFTR function. In 1999, the CFF launched the Healing Development Program (TDP) to attract both academic and industry partners and get started high-throughput screening for CFTR modulators. 18, 19 The CFF embraced the concept of venture philanthropy9, 20 to improve the interest of industry in an orphan disease. However, the success of the TDP was dependent on far more than financial support. 21 The program created a cultural change that allowed the CFF, academic clinicians and experts, federal agencies (the NIH and FDA), and industry to create a strong partnership with common goals and timelines.

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