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Optimized Eltrombopag Treatment of Hepatitis C virus-related thrombocytopenia
Proposal
951
Title of Proposed Research
Optimized Eltrombopag Treatment of Hepatitis C virus-related thrombocytopenia
Lead Researcher
Mohammad Saleh
Affiliation
The University of JordanAmman, JO
Funding Source
None
Potential Conflicts of Interest
Data Sharing Agreement Date
22 April 2014
Lay Summary
Globally, Hepatitis C virus (HCV) infection has an estimated prevalence of 2.35 per cent in 2011 (160 million chronically infected individuals). Thrombocytopenia is one of the most frequent hematological alterations in patients with chronic HCV. The usual protocol to treat HCV-related thrombocytopenia is to reduce the interferon dose if platelet count falls to < 30 × 109/L. Interferon therapy should be discontinued if platelet count falls to < 20 × 109/L. Recently, eltrombopag has been found to be effective mean to raise platelet counts in thrombocytopenic patients with chronic HCV infection allowing otherwise ineligible or marginal patients to begin and maintain antiviral therapy.
The objective of the present project is to develop an optimal dosing algorithm of eltrombopag. We will identify the pharmacokinetic/pharmacodynamic (PK/PD) and physiologic factors important in predicting and maximizing eltrombopag's effect in the treatment of Hepatitis C virus-related thrombocytopenia. Hence, the identified factors can be used to develop a dosing algorithm of eltrombopag.
This project is expected to improve patient care by identifying proper treatment strategies and (sub)populations that may (or may not) benefit from eltrompobag, and hence avoid antiviral therapy discontinuation.
The experimental design involves two studies that are: multicentre two-part study, consisting of an open-label (OL), Pre-Antiviral Treatment Phase (Part 1) and a randomised, double-blind (DB), placebo controlled, Antiviral Treatment Phase (Part 2). The collected data will be used to build a model that describes the relation between the administered eltrombopag dose and the change in platelets count. The main finding will be communicated in the form of an eltrombopag dosing algorithm.
Study Data Provided
[{ "PostingID": 24, "Title": "GSK-TPL103922", "Description": "Medicine: eltrombopag, Condition: Hepatitis C, Chronic, Phase: 3, GSK Clinical Study ID: TPL103922, Sponsor: GSK." },{ "PostingID": 26, "Title": "GSK-TPL108390", "Description": "Medicine: eltrombopag, Condition: Hepatitis C, Chronic, Phase: 3, GSK Clinical Study ID: TPL108390, Sponsor: GSK." }]
Statistical Analysis Plan
A nonlinear mixed effects model will be used to describe the relation between eltrombopag dose and platelet production. In pharmaceutical research, the analysis methodology is usually denoted as population pharmacokinetic/pharmacodynamic (PK/PD) modeling approach. The model will be used to the study of the sources and correlates of variability in eltrombopag doses, platelet counts, and patients' responsiveness to eltrombopag. PK/PD model evaluation will be done using standard diagnostics such as goodness of fit plots, visual predictive check, and using a part of the data as validation dataset. Screening for potential covariates that affect eltrombopag ability to stimulate platelet production will be assessed based on the ability of the covariates to explain the variability observed in eltrombopag dose.Further details will be added after the research is published.
Publication Citation
M.I.Saleh, S.Bani Melhim, H.M. Al-Ramadhani, S.Alzubiedi. Eur J Drug Metab Pharmacokinet 2019 Feb;44(1):31-42. Bayesian Population Pharmacokinetic Modeling of Eltrombopag in Chronic Hepatitis C Patients.
DOI: 10.1007/s13318-018-0490-x
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