| Literature DB >> 26827911 |
Kelly E Dooley1, Patrick P J Phillips2, Payam Nahid3, Michael Hoelscher4.
Abstract
To tackle the global TB epidemic effectively, novel treatment strategies are critically needed to shorten the duration of TB therapy and treat drug-resistant TB. Drug development for TB, stymied for decades, has enjoyed a renaissance over the past several years. However, the development of new TB regimens is hindered by the limitations in our understanding and use of preclinical models; the paucity of accurate, early surrogate markers of cure, and challenges in untangling the individual contributions of drugs to multidrug regimens in a complex, multi-compartment disease. Lack of profit motive, advocacy, and imagination has contributed mightily to the dearth of drugs we have on the shelf to treat this ancient disease. Areas that will speed the development of new regimens for TB include novel murine and in vitro pharmacodynamics models, clinical endpoints that are not culture-based, innovative clinical trial designs, and an infusion of much-needed funding.Entities:
Keywords: Hollow fiber model; Mouse model; Pharmacokinetic/pharmacodynamic; Translational science; Trial design; Tuberculosis
Mesh:
Substances:
Year: 2016 PMID: 26827911 PMCID: PMC4903928 DOI: 10.1016/j.addr.2016.01.014
Source DB: PubMed Journal: Adv Drug Deliv Rev ISSN: 0169-409X Impact factor: 15.470