A comparison of the pharmacokinetics of Aspen Ceftriaxone and Rocephin in community-acquired meningitis

BACKGROUND: Community-acquired bacterial meningitis (CABM) is a life-threatening condition that is common among immunocompromised individuals. Intravenous ceftriaxone, of which Rocephin (ROC) is the originator brand, is recommended as first-line therapy in South Africa. Despite concerns regarding therapeutic equivalence with generic agents, this is the first study that has been conducted comparing clinical pharmacokinetics (PK) of a generic ceftriaxone formulation with the originator. OBJECTIVE: To compare the PK and safety of Aspen Ceftriaxone (AC) and ROC in the treatment of adult CABM. METHODS: A total of 63 eligible patients were randomised 1:1 to receive 2 g of either medication twice daily for a duration based on the identity of the causative organism and their physician's clinical judgment. The primary endpoint of this study was the comparison of clinical PK, specifically the concentrations of each drug in the cerebrospinal fluid with corresponding paired plasma samples. While this study was underpowered to assess efficacy, safety could be evaluated on the basis of reported adverse events. RESULTS: The two patient groups were epidemiologically similar. There were no statistically significant differences in PK between either agent, nor any difference with regard to safety. CONCLUSION: AC can be considered as equivalent to ROC with regard to PK and safety in patients with CABM.

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Main Authors: Richards,G A, Elliott,E, Shaddock,E J, Mushi,D, Mzileni,M, Ray,R, Rulisa,S, Seolwane,F, Stacey,S L, Stolz,A, Venturas,J P, Schoeman,H
Format: Digital revista
Language:English
Published: South African Medical Association 2013
Online Access:http://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S0256-95742013001200020
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spelling oai:scielo:S0256-957420130012000202014-02-19A comparison of the pharmacokinetics of Aspen Ceftriaxone and Rocephin in community-acquired meningitisRichards,G AElliott,EShaddock,E JMushi,DMzileni,MRay,RRulisa,SSeolwane,FStacey,S LStolz,AVenturas,J PSchoeman,HBACKGROUND: Community-acquired bacterial meningitis (CABM) is a life-threatening condition that is common among immunocompromised individuals. Intravenous ceftriaxone, of which Rocephin (ROC) is the originator brand, is recommended as first-line therapy in South Africa. Despite concerns regarding therapeutic equivalence with generic agents, this is the first study that has been conducted comparing clinical pharmacokinetics (PK) of a generic ceftriaxone formulation with the originator. OBJECTIVE: To compare the PK and safety of Aspen Ceftriaxone (AC) and ROC in the treatment of adult CABM. METHODS: A total of 63 eligible patients were randomised 1:1 to receive 2 g of either medication twice daily for a duration based on the identity of the causative organism and their physician's clinical judgment. The primary endpoint of this study was the comparison of clinical PK, specifically the concentrations of each drug in the cerebrospinal fluid with corresponding paired plasma samples. While this study was underpowered to assess efficacy, safety could be evaluated on the basis of reported adverse events. RESULTS: The two patient groups were epidemiologically similar. There were no statistically significant differences in PK between either agent, nor any difference with regard to safety. CONCLUSION: AC can be considered as equivalent to ROC with regard to PK and safety in patients with CABM.South African Medical AssociationSAMJ: South African Medical Journal v.103 n.12 20132013-12-01journal articletext/htmlhttp://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S0256-95742013001200020en
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author Richards,G A
Elliott,E
Shaddock,E J
Mushi,D
Mzileni,M
Ray,R
Rulisa,S
Seolwane,F
Stacey,S L
Stolz,A
Venturas,J P
Schoeman,H
spellingShingle Richards,G A
Elliott,E
Shaddock,E J
Mushi,D
Mzileni,M
Ray,R
Rulisa,S
Seolwane,F
Stacey,S L
Stolz,A
Venturas,J P
Schoeman,H
A comparison of the pharmacokinetics of Aspen Ceftriaxone and Rocephin in community-acquired meningitis
author_facet Richards,G A
Elliott,E
Shaddock,E J
Mushi,D
Mzileni,M
Ray,R
Rulisa,S
Seolwane,F
Stacey,S L
Stolz,A
Venturas,J P
Schoeman,H
author_sort Richards,G A
title A comparison of the pharmacokinetics of Aspen Ceftriaxone and Rocephin in community-acquired meningitis
title_short A comparison of the pharmacokinetics of Aspen Ceftriaxone and Rocephin in community-acquired meningitis
title_full A comparison of the pharmacokinetics of Aspen Ceftriaxone and Rocephin in community-acquired meningitis
title_fullStr A comparison of the pharmacokinetics of Aspen Ceftriaxone and Rocephin in community-acquired meningitis
title_full_unstemmed A comparison of the pharmacokinetics of Aspen Ceftriaxone and Rocephin in community-acquired meningitis
title_sort comparison of the pharmacokinetics of aspen ceftriaxone and rocephin in community-acquired meningitis
description BACKGROUND: Community-acquired bacterial meningitis (CABM) is a life-threatening condition that is common among immunocompromised individuals. Intravenous ceftriaxone, of which Rocephin (ROC) is the originator brand, is recommended as first-line therapy in South Africa. Despite concerns regarding therapeutic equivalence with generic agents, this is the first study that has been conducted comparing clinical pharmacokinetics (PK) of a generic ceftriaxone formulation with the originator. OBJECTIVE: To compare the PK and safety of Aspen Ceftriaxone (AC) and ROC in the treatment of adult CABM. METHODS: A total of 63 eligible patients were randomised 1:1 to receive 2 g of either medication twice daily for a duration based on the identity of the causative organism and their physician's clinical judgment. The primary endpoint of this study was the comparison of clinical PK, specifically the concentrations of each drug in the cerebrospinal fluid with corresponding paired plasma samples. While this study was underpowered to assess efficacy, safety could be evaluated on the basis of reported adverse events. RESULTS: The two patient groups were epidemiologically similar. There were no statistically significant differences in PK between either agent, nor any difference with regard to safety. CONCLUSION: AC can be considered as equivalent to ROC with regard to PK and safety in patients with CABM.
publisher South African Medical Association
publishDate 2013
url http://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S0256-95742013001200020
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