Arenaviruses are included in the World Health Organisation R\&D Blueprint list of high priority pathogens, since this virus group includes several epidemic-prone highly pathogenic viruses for which there are inadequate diagnostic, therapeutic, and preventative interventions. Junin, Machupo, Guanarito, Sabia, Lujo, and Lassa virus can all cause a viral haemorrhagic fever with high case fatality in hospitalised cases. Lassa fever is the most common severe arenavirus disease and is endemic across many low and middle income countries in West Africa, with an estimated 37.7 million people in 14 countries living in areas at risk of Lassa virus. Despite the discovery of Lassa virus in 1972 and an estimated 300,000 cases and 5000-10,000 deaths annually, there remain gaps in our understanding of the natural history of disease and in the availability of evidence based interventions. The protocol has two components. Sites may implement one or both components. 1. Cardiovascular function in Lassa fever: Lassa fever in humans is often described in the literature as being characterized by vascular leak and shock in the terminal phase, this being the main pathway to death. Whilst animal data supports this, there are very limited data in humans. One of the main aims of this study therefore is to characterize cardiovascular function in patients with Lassa fever, with the ultimate goal of informing future trials of supportive or therapeutic strategies to improve vascular leak. 2. Ribavirin pharmacokinetics and pharmacodynamics: The recommended treatment for Lassa is ribavirin, but its efficacy has not been established in randomized controlled trials and its mechanism of action is not fully understood. There are very limited PK data on ribavirin in patients with Lassa fever and the optimal dose of ribavirin for an RCT has not been established. Furthermore, there are various hypothesized mechanisms of action of ribavirin, none of which have been investigated in humans with Lassa fever. Therefore, further aims of this study are to characterize the PK of ribavirin and ribavirin metabolites (RMP, RDP, RTP) in Lassa fever patients and to identify potential mechanisms of action ribavirin in Lassa fever. Understanding Ribavirin's mechanism of action in Lassa fever is important for the optimal design of a future RCT.
Summary of cardiovascular function study Lassa fever carries a treated mortality in hospitalized patients of up to 30%. Lassa fever is often described as being characterized by vascular leak and shock in the terminal phase, but, whilst animal data supports this, there are limited data in humans. A further aim of this study therefore is to characterize cardiovascular function in patients with Lassa fever, with the ultimate goal of informing future trials of supportive or therapeutic strategies. Summary of ribavirin pharmacokinetics and pharmacodynamics sub-study Lassa fever carries a treated mortality in hospitalized patients of up to 30% in Nigeria. Ribavirin is the current standard of care. However, the efficacy of ribavirin has not been established in RCTs. There is very limited PK data on ribavirin in patients with Lassa fever and the optimal dose of ribavirin for an RCT is unknown. The aim of this study is to characterize the PK of ribavirin in Lassa fever, and identify any associations between ribavirin PK parameters and viral load and markers of inflammatory status.
Study Type
OBSERVATIONAL
Enrollment
158
Owo Federal Medical Centre
Owo, Ondo State, Nigeria
Cardiovascular
Mean Arterial Pressure is less than 65mmHg or Systolic Blood Pressure is less than 90mmgHg or pulse pressure \< 20mmHg
Time frame: through study completion, an average of 2 weeks
Ribavirin Pharmacokinetics
Proportion of patients with ribavirin CMIN above the IC90 at \> 80% of measured CMIN during therapy
Time frame: through study completion, an average of 2 weeks
Ribavirin Pharmacodynamics
Change in Lassa virus Viral Load from baseline to day 5
Time frame: 5 days
Cardiovascular
To identify the frequency of shock
Time frame: through study completion, an average of 2 weeks
Cardiovascular
To identify the frequency of persistent shock
Time frame: through study completion, an average of 2 weeks
Cardiovascular
To identify the frequency of respiratory distress
Time frame: through study completion, an average of 2 weeks
Cardiovascular
To identify the frequency of shock and respiratory distress
Time frame: through study completion, an average of 2 weeks
Cardiovascular
To identify the frequency of Death
Time frame: through study completion, an average of 2 weeks
Ribavirin Pharmacokinetics
Proportion of patients with ribavirin CMIN above the IC50 at all measured CMIN during therapy
Time frame: through study completion, an average of 2 weeks
Ribavirin Pharmacokinetics
Duration of time that ribavirin levels are above the IC90 and IC50
Time frame: through study completion, an average of 2 weeks
Ribavirin Pharmacokinetics
Calculation of AUC \[AUC∞ and AUCLAST\] (ribavirin, ribavirin metabolites)
Time frame: through study completion, an average of 2 weeks
Ribavirin Pharmacokinetics
Calculation of CMAX (ribavirin, ribavirin metabolites)
Time frame: through study completion, an average of 2 weeks
Ribavirin Pharmacokinetics
Calculation of CMIN (ribavirin, ribavirin metabolites)
Time frame: through study completion, an average of 2 weeks
Ribavirin Pharmacokinetics
Calculation of T1/2 (ribavirin, ribavirin metabolites)
Time frame: through study completion, an average of 2 weeks
Ribavirin Pharmacokinetics
Volume of distribution (ribavirin, ribavirin metabolites)
Time frame: through study completion, an average of 2 weeks
Ribavirin Pharmacokinetics
Calculation of Clearance (ribavirin, ribavirin metabolites)
Time frame: through study completion, an average of 2 weeks
Ribavirin Pharmacodynamics
Change in Lassa virus Viral Load from baseline to day 3 and day 10
Time frame: 10 days
Ribavirin Pharmacodynamics
Change in AST, ALT concentrations from baseline to day 3, 5, 10
Time frame: 10 days
Ribavirin Pharmacodynamics
Change in eGFR from baseline to day 3, 5, 10
Time frame: 10 days
Ribavirin Pharmacodynamics
Change in Haemoglobin from baseline to day 5, 10
Time frame: 10 days
Ribavirin Pharmacodynamics
Change in ISG expression from baseline to day 3, 5
Time frame: 5 days
Ribavirin Pharmacodynamics
Time to negative blood RT-PCR for Lassa virus
Time frame: through study completion, an average of 2 weeks
Ribavirin Pharmacodynamics
Requirement for blood transfusion during hospitalisation
Time frame: through study completion, an average of 2 weeks
Ribavirin Pharmacodynamics
Reaching KDIGO stage 3 during hospitalisation
Time frame: through study completion, an average of 2 weeks
Ribavirin Pharmacodynamics
Requirement for dialysis during hospitalisation
Time frame: through study completion, an average of 2 weeks
Ribavirin Pharmacodynamics
Duration of hospitalisation
Time frame: through study completion, an average of 2 weeks
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