Abstract
Drug resistance in Mycobacterium tuberculosis arises from the man-made selection of mutants that result from spontaneous chromosomal alterations. Preventing the development of drug-resistant TB through a good control program based on directly observed treatment, short-course, is of paramount importance. Established multidrug-resistant (MDR)-TB requires alternative specific chemotherapy, comprising drugs with higher cost and greater toxicity delivered on a programmatic basis. The development of new anti-TB drugs would help to prevent and treat MDR-TB. Notably, moxifloxacin and gatifloxacin are being tested for shortening treatment in Phase III trials, while three novel compounds, TMC-207, OPC-67683 and PA-824 are in Phase II studies for both drug-susceptible and drug-resistant disease. The roles of surgery and immunotherapy in the management of MDR-TB require further evaluation. The recent emergence of extensively drug-resistant TB poses a serious challenge to the global control of TB. In order to combat extensively drug-resistant TB, strengthening of directly observed treatment, short-course and drug-resistance programs, alongside other strategies, including the development of newer diagnostics and drugs, is mandatory.
Original language | English |
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Pages (from-to) | 405-421 |
Number of pages | 17 |
Journal | Expert Review of Clinical Pharmacology |
Volume | 2 |
Issue number | 4 |
DOIs | |
Publication status | Published - 2009 |
Externally published | Yes |
ASJC Scopus Subject Areas
- General Pharmacology, Toxicology and Pharmaceutics
- Pharmacology (medical)
Keywords
- Drug resistant
- Fluoroquinolone
- New drugs
- Treatment
- Tuberculosis