Evidence map›Paper›PMID 17517835›Full record

Trial reportAntimicrobial agents and chemotherapy2007

Effects of rifampin and multidrug resistance gene polymorphism on concentrations of moxifloxacin.

Marc Weiner, William Burman, Chi-Cheng Luo, Charles A Peloquin, Melissa Engle, Stefan Goldberg, Vipin Agarwal, Andrew Vernon

2 registry-linked trialsOpen access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Antimicrobial agents and chemotherapy, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
4.2field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00164463 phase2completednot on this map

TBTC Study 27/28 PK: Pharmacokinetic Issues in the Use of Moxifloxacin for Treatment of Tuberculosis

TypeinterventionalSponsorCenters for Disease Control and PreventionRan2004 to 2007Enrolled72ConditionsTuberculosisArmsMoxifloxacin, Isoniazid
NCT02563327 phase3completednot on this mapstarted 2016, after this paper: background citation

TBTC Study 31 PK/PD: Population Pharmacokinetic and Pharmacodynamic Study of Efficacy and Safety of High-Dose Rifapentine and Moxifloxacin for Treatment of Tuberculosis in the Study 31 Treatment Trial: Intensive PK Sampling

TypeinterventionalSponsorCenters for Disease Control and PreventionRan2016 to 2021Enrolled2,516ConditionsTuberculosisArmsRifapentine, Moxifloxacin, Rifampin, Isoniazid, Pyrazinamide
3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 2 syntheses or guidelines pooled it, 106 citations in OpenAlex.

  1. Treatment of Drug-Resistant Tuberculosis. An Official ATS/CDC/ERS/IDSA Clinical Practice Guideline.American journal of respiratory and critical care medicine · 2019
    Guideline
  2. Pooled it
  3. Trial
  4. Elevated Plasma Moxifloxacin Concentrations andAntimicrobial agents and chemotherapy · 2018
    Trial
  5. Trial
  6. Trial
  7. Trial
  8. Review
  9. Article
  10. Therapeutic drug monitoring in tuberculosis.European journal of clinical pharmacology · 2024
    Review
  11. Role of therapeutic drug monitoring in the treatment of multi-drug resistant tuberculosis.Journal of clinical tuberculosis and other mycobacterial diseases · 2024
    Article
  12. Genetic Variations and Antibiotic-Related Adverse Events.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  13. Article
  14. MDR Tuberculosis Treatment.Medicina (Kaunas, Lithuania) · 2022
    Review
  15. Article
  16. Review
  17. Frontiers in pharmacology · 2021
    Article
  18. Pharmacogenomics of Antibiotics.International journal of molecular sciences · 2020
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Marc WeinerUniversity of Texas Health Science Center, San Antonio and South Texas Veterans Health Care System, San Antonio, TX 78229-4404, USA. weiner@uthscsa.edu
William Burman
Chi-Cheng Luo
Charles A Peloquin
Melissa Engle
Stefan Goldberg
Vipin Agarwal
Andrew Vernon
Centers for Disease Control and Prevention · USThe University of Texas Health Science Center at San Antonio · USDenver Public Health · USUniversity of Colorado Denver · US

Funding

ZOLEDRONATE VS AREDIA IN MULTIPLE MYELOMA/BREAST CANCER W /BONE DISORDERSM01RR001346 · NCRR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI FERRER, ROBERT L · 1985 to 2008
$23.1M
NCRR NIH HHS M01 RR001346NCRR NIH HHS M01 RR01346
6 · The paper itself

Abstract

Treatment regimens combining moxifloxacin and rifampin for drug-susceptible tuberculosis are being studied intensively. However, rifampin induces enzymes that transport and metabolize moxifloxacin. We evaluated the effect of rifampin and the human multidrug resistance gene (MDR1) C3435T polymorphisms (P-glycoprotein) on moxifloxacin pharmacokinetic parameters. This was a single-center, sequential design study with 16 volunteers in which sampling was performed after four daily oral doses of moxifloxacin (400 mg) and again after 10 days of combined rifampin (600 mg) and moxifloxacin. After daily coadministration of rifampin, the area under the concentration-time curve from 0 to 24 h (AUC(0-24)) for moxifloxacin decreased 27%. Average bioequivalence between moxifloxacin coadministered with rifampin and moxifloxacin alone was not demonstrated: the ratio of geometric means (RGM) of the moxifloxacin AUC(0-24) was 73.3 (90% confidence intervals [CI], 64.3, 83.5) (total P value, 0.87 for two one-sided t tests). Peak moxifloxacin concentrations, however, were equivalent: the RGM of the maximum concentration of the drug in serum was 93.6 (90% CI, 80.2, 109.3) (total P value, 0.049). Concentrations of the sulfate conjugate metabolite of moxifloxacin were increased twofold following rifampin coadministration (AUC(0-24), 1.29 versus 2.79 mug.h/ml). Concomitant rifampin administration resulted in a 27% decrease in the mean moxifloxacin AUC(0-24) and a marked increase in the AUC(0-24) of the microbiologically inactive M1 metabolite. Additional studies are required to understand the clinical significance of the moxifloxacin-rifampin interaction.

Indexed as

AdultAntitubercular AgentsArea Under CurveATP Binding Cassette Transporter, Subfamily B, Member 1Aza CompoundsDrug InteractionsDrug Therapy, CombinationFemaleFluoroquinolonesHumansMaleMoxifloxacinPolymorphism, GeneticQuinolinesRifampinTherapeutic EquivalencyAntitubercular AgentsATP Binding Cassette Transporter, Subfamily B, Member 1Aza CompoundsFluoroquinolonesMoxifloxacinQuinolinesRifampin

Identifiers

PMID17517835
PMCPMC1932492
OpenAlexW2112124041

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.