-
Open Access Journal of Clinical Trials
-
About Dovepress
Open access peer-reviewed scientific and medical journals.
-
Open Access
Dove Medical Press is now a member of the Open Access Initiative
-
An Author's Guide
A guide to help authors get their paper published.
-
Advocacy
Support Open Access and Dove Press
-
Reprints
Promotional Article Monitoring - further details
-
Favored Author Program
Real benefits for authors, including fast-track processing of papers.
Choice of baseline in a multiple-dose thorough QT study (TQTS) – effect on analysis of moxifloxacin-induced QTc prolongation
(2243) Views (1264) Full article downloads
Authors: B Tyl, S Azzam, E Reinbolt, et al
Published Date December 2009
Volume 2010:2 Pages 1 - 7
DOI: http://dx.doi.org/10.2147/OAJCT.S7164
B Tyl1, S Azzam2, E Reinbolt2, N Blanco1, J Olbertz3, W Wheeler1
1MDS Pharma Services, Centralized Cardiac Services, Baillet-en-France, France; 2MDS Pharma Services, Early Clinical Research, Lincoln (Nebraska), USA; 3MDS Pharma Services, Early Clinical Research, Phoenix (Arizona), USA
Background: The primary endpoint of a thorough QT study (TQTS) is the change from baseline in QT corrected (QTc) measured on electrocardiograms (ECG) tracings. It has been suggested that during a crossover study, the time-matched or predose baseline could be recorded. The choice of method for baseline ECG collection may influence the results and the cost of the TQTS.
Objective: The objective of our study was to compare the collection of a time-matched baseline before each period (TMEACH), an average of all the time-matched baseline (TMMEAN), a time-matched baseline before period 1 (TMP1) and a predose baseline (PDEACH) on QT interval prolongation induced by moxifloxacin, in a 30 subjects, 5 arm cross-over TQTS.
Results: Moxifloxacin induced a similar significant increase in QT corrected using Fridericia’s formula (QTc) (lower limit of the confidence interval excluded 5 ms) at all time-points between 0.5 hours and 12 hours with all baseline methods. TMEACH was associated with a lower within subject variability (SD 5.59 ms) than TMMEAN and TMP1 (5.90 and 6.90 ms, respectively). PDEACH was associated with the highest variability (7.41 ms).
Conclusion: The collection of ECG tracings during a full baseline day before each period was associated with the lowest variability. However, the two more cost effective designs (TMP1 and PDEACH) were sufficient, in this small TQTS, to significantly detect moxifloxacin.
Keywords: thorough QT study, QT correction, baseline, design, superimposed representative complex, moxifloxacin
Readers of this article also read:
Exacerbation rate, health status and mortality in COPD – a review of potential interventions
Information technology in pharmacovigilance: Benefits, challenges, and future directions from industry perspectives
Challenges with engaging participants in behavioral intervention research trials
Time will tell: community acceptability of HIV vaccine research before and after the “Step Study” vaccine discontinuation
Perception of risk and benefit in patient-centered communication and care
The relationship between deliberate self-harm behavior, body dissatisfaction, and suicide in adolescents: current concepts
Zinc oxide nanoparticles as selective killers of proliferating cells
Clinical trials: innovation, progress and controversy
Cumulative clinical experience from over a decade of use of levofloxacin in community-acquired pneumonia: critical appraisal and role in therapy
- Testimonials
"... I was impressed at the rapidity of publication from submission to final acceptance." Dr Edwin Thrower, PhD, Yale University
- The benefits and risks of testosterone replacement therapy: a review
- Tenofovir-associated bone density loss
- Drug design with Cdc7 kinase: a potential novel cancer therapy target
- Development of mucosal adjuvants for intranasal vaccine for H5N1 influenza viruses




