A Proposed Target Product Profile and Developmental Cascade for New Cryptosporidiosis Treatments

08 Oct 2015

Christopher D. Huston, Thomas Spangenberg, Jeremy Burrows, Paul Willis, Timothy N. C. Wells, Wesley van Voorhis

PLOS Neglected Tropical Diseases

DOI: 10.1371/journal.pntd.0003987

Photo: Suwit Ngaokaew/Shuttershock.com


The Global Enteric Multicenter Study (GEMS), a study of infectious diarrhea involving over 20,000 children at seven sites in sub-Saharan Africa and South Asia, recently reported that the little-studied protozoan parasite Cryptosporidium ranks second to rotavirus as a cause of lifethreatening diarrhea in infants and was also associated with growth stunting and excess mortality [1]. Cryptosporidium species, predominantly Cryptosporidium hominis and Cryptosporidium parvum, were previously well known for causing chronic diarrhea in AIDS patients, as well as for their chlorine resistance and their association with waterborne outbreaks in the developed world [2–4]. Numerous smaller studies had also demonstrated the importance of cryptosporidiosis in young children and its association with malnutrition (reviewed in [5]) [5– 19], but Cryptosporidium had not previously garnered significant attention from the pharmaceutical industry or major funding organizations such as the Bill and Melinda Gates Foundation.
The GEMS put cryptosporidiosis into context amongst more studied diarrheal pathogens and brought it to the attention of these organizations. No vaccine for cryptosporidiosis exists, and the available treatments for those most at risk are inadequate. The only licensed drug, nitazoxanide, is unreliable in severely malnourished children (~56% improvement in diarrhea at 7 days versus 26% in controls [20]), and shows no benefit relative to placebo in HIV-infected patients [20–22]. More reliable, efficacious, and faster-acting treatments are needed for these populations.
View the full article on the PLOS Neglected Tropical Diseases website.