its ability to suppress the virus in vitro.
claimed that ivermectin in vitro had an inhibitory action on the novel Coronavirus, reducing the load of viral RNA by 5,000 times at 48 hours. The ivermectin dose used in this study was 5 μM.
Plasma concentration of ivermectin
The in vitro study used ivermectin at a concentration that inhibits 50% of proliferating viruses (IC50). This concentration of 2 μM is 35 times higher than the maximum plasma concentration achieved in blood on oral administration of ivermectin at the approved dose of approximately 200 μg/kg. And this refers to the total plasma concentration.
Ivermectin is bound extensively by plasma protein, to the tune of 93%, which means that the maximum concentration of unbound ivermectin in the plasma is several orders of magnitude less.
When oral ivermectin is administered in humans, it reaches the lungs in unbound form, and the final concentration also depends on the presence of specific transport proteins that can keep the drug in the lung tissue, as well as how rapidly it binds to and crosses the fatty cell membrane of the cell.
Ivermectin has a wider therapeutic margin, allowing some increase in the dose if warranted, without unduly pushing up the risk of toxicity. This has led to the evaluation of higher than usual doses of ivermectin in a phase 3 trial to assess the safety. Another phase I trial looked at doses, 10-fold the approved dose.
The results showed the drug was tolerated with the ten-fold dosing regime as well as at 60 mg three times a week.
How was the study done?
The current study was aimed at analyzing the human dose necessary to achieve the experimental IC50 in the lungs. This is crucial to planning a clinical trial.
The researchers used a population model to study the pharmacokinetics of the drug. This included the transit absorption, drug elimination, and weight of the patient. The model was based on healthy participants who took 12 mg ivermectin orally after food.
A hundred simulations of total and bound ivermectin were performed to track the total plasma concentration-time profile. Different doses were used, such as the approved dose of 200 μg/kg, 120 mg in a single weekly dose, and 60 mg three times a week (at 72-hour intervals, in healthy subjects).
What are the implications of the study?
The current approach to finding a viable therapy for the SARS-CoV-2 is to repurpose existing drugs. All over the world, ivermectin came into widespread use of off-label in response to the news of the in vitro success against the virus.
At a dose of 150 μg/kg, observation of 52 patients on mechanical ventilation appeared to show clinical benefit with the drug in contrast to over 1,900 patients on conventional treatment. Though these results need to be analyzed to rule out confounding factors and biases, on the surface, they would seem to suggest that very low lung concentrations of ivermectin are able to inhibit the virus.
In other words, even when the ivermectin concentration is not anywhere near the IC50, it appears to have antiviral activity. This could suggest that the lung distribution or accumulation of this drug is far greater in humans than in cattle.
In contrast, the concentrations of ivermectin reported inhibiting the Coronavirus in vitro were markedly higher than those achieved in human lung or plasma with the approved doses of ivermectin. As a result, say the researchers, “the likelihood of a successful clinical trial using the approved dose of ivermectin is low.”
This should be a warning to conduct in vitro studies of repurposed drugs at concentrations that are safe and tolerable in humans.
The researchers advise a dose-response study using a control group, as well as testing the possibility of inhaled ivermectin and combination therapy.
The dose-response study should begin with the addition of potentiating compounds to reduce the threshold of viral inhibition to the tune of 0.1 μM rather than the 5 μM of the original experiment. Close monitoring is required since these dosage levels and protocols have not been widely studied.
Inhaled ivermectin would allow for higher dosage and increased local lung concentrations without additional systemic exposure. However, preclinical studies of its safety and tolerability are required.
Credited to Dr. Liji Thomas