Zum Inhalt

Correction: Relative Bioavailability of Dolutegravir (DTG) and Emtricitabine/Tenofovir Alafenamide Fumarate (F/TAF) Administered as Paediatric Tablet Formulations in Healthy Volunteers

  • Open Access
  • 02.05.2024
  • Correction
Erschienen in:
download
DOWNLOAD
print
DRUCKEN
insite
SUCHEN
The original article can be found online at https://doi.org/10.1007/s40262-024-01365-4.
Correction: Clinical Pharmacokinetics https://doi.org/10.1007/s40262-024-01365-4
In Table 1 of this article, the column head “DTG + F/TAT (test C)” should have read “DTG + F/TAF (test C)” and the column head “F/TAT (reference A)” should have read “F/TAF (reference A)”. The corrected table is given below.
Table 1
PK parameters of DTG, TAF, TFV, and FTC in each treatment (test versus reference)
PK parameter
DTG + F/TAF (test C)
DTG (reference B)
GLSM ratio (90% CI)
DTG
   
AUC0–∞ (h*mg/L)
40.71 (30)
40.18 (27)
1.02 (0.94–1.10)
Cmax (mg/L)
2.69 (22)
2.35 (24)
1.16 (1.10–1.23)
Tmax (h)
0.75 (0.5–1.0)
1.0 (1.0–2.0)
 
T½ (h)
12.97 (17)
13.38 (15)
 
PK parameter
DTG + F/TAF (test C)
F/TAF (reference A)
GLSM ratio (90% CI)
TAF
   
 AUC0–∞ (h*ng/mL)
104.87 (57)
115.75 (42)
0.83 (0.62–1.11)
 Cmax (ng/mL)
180.14 (44)
204.95 (37)
0.81 (0.65–1.01)
 Tmax (h)
0.3 (0.3–0.3)
0.3 (0.2–0.3)
 
 T½ (h)
0.35 (21)
0.33 (24)
 
TFV
 AUC0–last (h*ng/mL)
89.19 (54)
98.04 (32)
0.84 (0.70–1.01)
 Cmax (ng/mL)
7.03 (29)
6.34 (24)
1.06 (0.92–1.23)
 Tmax (h)
0.75 (0.3–0.9)
0.75 (0.6–1.0)
 
 T½ (h)
32.44 (36)
36.73 (33)
 
FTC
 AUC0–∞ (h*mg/L)
7.52 (15)
7.80 (20)
0.97 (0.92–1.02)
 Cmax (mg/L)
1.49 (20)
1.44 (25)
1.05 (0.94–1.17)
 Tmax (h)
0.75 (0.5–1.0)
0.78 (0.75–1.5)
 
 T½ (h)
7.41 (22)
8.14 (34)
 
This table shows the PK parameters AUC0–∞, Cmax, Tmax, and T½ as geometric means and the percentage of variation coefficient. Tmax is shown as median plus interquartile range. For DTG, FTC and TAF, the Cmax and AUC0–∞ GLSM ratios of test treatment versus reference treatment with 90% CIs are presented; for TFV, the Cmax and AUC0-last GLSM ratios of test treatment versus reference treatment with 90% CIs are presented. The test treatment (treatment C) consisted of single-dose F/TAF 180/22.5 mg TOS and DTG 30 mg DT. Reference treatment A consisted of single-dose F/TAF 180/22.5 mg TOS; reference treatment B consisted of single-dose DTG 30 mg DT
AUC area under the curve, CI confidence interval, Cmax maximum concentration, DT dispersible tablet, DTG dolutegravir, F/TAF emtricitabine/tenofovir alafenamide fumarate, FTC emtricitabine, GLSM geometric least squares mean, PK pharmacokinetic, T½ elimination half-life, TAF tenofovir alafenamide fumarate, TFV tenofovir, Tmax time to maximum plasma concentration, TOS tablet for oral suspension
The original article has been corrected.
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.
download
DOWNLOAD
print
DRUCKEN
Titel
Correction: Relative Bioavailability of Dolutegravir (DTG) and Emtricitabine/Tenofovir Alafenamide Fumarate (F/TAF) Administered as Paediatric Tablet Formulations in Healthy Volunteers
Verfasst von
Lisanne A. H. Bevers
Anne E. M. Kamphuis
L. C. Wendy van der Wekken-Pas
Rory Leisegang
David M. Burger
Angela Colbers
Publikationsdatum
02.05.2024
Verlag
Springer International Publishing
Erschienen in
Clinical Pharmacokinetics / Ausgabe 5/2024
Print ISSN: 0312-5963
Elektronische ISSN: 1179-1926
DOI
https://doi.org/10.1007/s40262-024-01378-z