AI Article Synopsis

  • The study investigates the use of cabotegravir long-acting intramuscular injection as an HIV preexposure prophylaxis, assessing its drug localization in the body using MRI in healthy volunteers.* -
  • Eight participants received a targeted injection of cabotegravir, with MRI scans taken on Days 1, 3, and 8 to evaluate the injection site's effectiveness and how the drug was distributed within the body.* -
  • Results showed varied injection site locations and highlighted a strong correlation between the total surface area of the drug depot on Day 1 and plasma drug concentrations at later stages, indicating effective monitoring of the drug's pharmacokinetics.*

Article Abstract

Aim: Cabotegravir long-acting (LA) intramuscular (IM) injection is being investigated for HIV preexposure prophylaxis due to its potent antiretroviral activity and infrequent dosing requirement. A subset of healthy adult volunteers participating in a Phase I study assessing cabotegravir tissue pharmacokinetics underwent serial magnetic resonance imaging (MRI) to assess drug depot localization and kinetics following a single cabotegravir LA IM targeted injection.

Methods: Eight participants (four men, four women) were administered cabotegravir LA 600 mg under ultrasonographic-guided injection targeting the gluteal muscles. MRI was performed to determine injection-site location in gluteal muscle (IM), subcutaneous (SC) adipose tissue and combined IM/SC compartments, and to quantify drug depot characteristics, including volume and surface area, on Days 1 (≤2 hours postinjection), 3 and 8. Linear regression analysis examined correlations between MRI-derived parameters and plasma cabotegravir exposure metrics, including maximum observed concentration (C ) and partial area under the concentration-time curve (AUC) through Weeks 4 and 8.

Results: Cabotegravir LA depot locations varied by participant and were identified in the IM compartment (n = 2), combined IM/SC compartments (n = 4), SC compartment (n = 1) and retroperitoneal cavity (n = 1). Although several MRI parameter and exposure metric correlations were determined, total depot surface area on Day 1 strongly correlated with plasma cabotegravir concentration at Days 3 and 8, C and partial AUC through Weeks 4 and 8.

Conclusion: MRI clearly delineated cabotegravir LA injection-site location and depot kinetics in healthy adults. Although injection-site variability was observed, drug depot surface area correlated with both plasma C and partial AUC independently of anatomical distribution.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290983PMC
http://dx.doi.org/10.1111/bcp.14977DOI Listing

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