Kidney Function as a Key Driver of the Pharmacokinetic Response to High‐Dose L‐Carnitine in Septic Shock

Abstract Study Objective Levocarnitine (L‐carnitine) has shown promise as a metabolic‐therapeutic for septic shock, where mortality approaches 40%. However, high‐dose (≥ 6 grams) intravenous supplementation results in a broad range of serum concentrations. We sought to describe the population pharmacokinetics (PK) of high‐dose L‐carnitine, test various estimates of kidney function, and assess the correlation of PK parameters with pre‐treatment metabolites in describing drug response for patients with septic shock. Design Population PK analysis was done with baseline normalized concentrations using nonlinear mixed effect models in the modeling platform Monolix. Various estimates of kidney function, patient demographics, dose received, and organ dysfunction were tested as population covariates. Data Source We leveraged serum samples and metabolomics data from a phase II trial of L‐carnitine in vasopressor‐dependent septic shock. Serum was collected at baseline (T0); end‐of‐infusion (T12); and 24, 48, and 72 h after treatment initiation. Patients and Intervention Patients were adaptively randomized to receive intravenous L‐carnitine (6 grams, 12 grams, or 18 grams) or placebo. Measurements and Main Results The final dataset included 542 serum samples from 130 patients randomized to L‐carnitine. A two‐compartment model with linear elimination and a fixed volume of distribution (17.1 liters) best described the data and served as a base structural model. Kidney function estimates as a covariate on the elimination rate constant (k) reliably improved model fit. Estimated glomerular filtration rate (eGFR), based on the 2021 Chronic Kidney Disease Epidemiology collaboration (CKD‐EPI) equation with creatinine and cystatin C, outperformed creatinine clearance (Cockcroft‐Gault) and older CKD‐EPI equations that use an adjustment for self‐identified race. Conclusions High‐dose L‐carnitine supplementation is well‐described by a two‐compartment population PK model in patients with septic shock. Kidney function estimates that leverage cystatin C provided superior model fit. Future investigations into high‐dose L‐carnitine supplementation should consider baseline metabolic status and dose adjustments based on renal function over a fixed or weight‐based dosing paradigm.