TB Research

Clofazimine as a Treatment for Multidrug-Resistant Tuberculosis: A Review

Rhea Veda Nugraha, Vycke Yunivita, Prayudi Santoso, Rob E. Aarnoutse, Rovina Ruslami

Scientia Pharmaceutica · 2021-05

Abstract

Multidrug-resistant tuberculosis (MDR-TB) is an infectious disease caused by Mycobacterium tuberculosis which is resistant to at least isoniazid and rifampicin. This disease is a worldwide threat and complicates the control of tuberculosis (TB). Long treatment duration, a combination of several drugs, and the adverse effects of these drugs are the factors that play a role in the poor outcomes of MDR-TB patients. There have been many studies with repurposed drugs to improve MDR-TB outcomes, including clofazimine. Clofazimine recently moved from group 5 to group B of drugs that are used to treat MDR-TB. This drug belongs to the riminophenazine class, which has lipophilic characteristics and was previously discovered to treat TB and approved for leprosy. This review discusses the role of clofazimine as a treatment component in patients with MDR-TB, and the drug’s properties. In addition, we discuss the efficacy, safety, and tolerability of clofazimine for treating MDR-TB. This study concludes that the clofazimine-containing regimen has better efficacy compared with the standard one and is also well-tolerated. Clofazimine has the potential to shorten the duration of MDR-TB treatment.

MeSH terms

  • Clofazimine
  • Medicine
  • Tolerability
  • Tuberculosis
  • Rifampicin
  • Regimen
  • Bedaquiline
  • Leprosy
  • Isoniazid
  • Adverse effect
  • Multiple drug resistance
  • Mycobacterium tuberculosis
  • Pharmacology
  • Tb treatment
  • Drug resistance
  • Internal medicine