Published online Feb 17, 2023. doi: 10.5497/wjp.v12.i1.1
Peer-review started: September 16, 2022
First decision: October 31, 2022
Revised: November 11, 2022
Accepted: February 7, 2023
Article in press: February 7, 2023
Published online: February 17, 2023
Processing time: 153 Days and 18.3 Hours
Itraconazole is a broad-spectrum triazole antifungal. It inhibits fungal growth. It exhibits a nonlinear pharmacokinetic profile due to its varied oral bioavailability.
The test product Fixtral SB is a new formulation that has been manufactured via APSG™ (Advanced Polymeric Spray Granulation), a breakthrough innovative proprietary technology for enhancing solubility and maximizing the bioavailability of poorly soluble drug itraconazole. The new formulation is able to restrict the drug release in an acidic environment which minimizes the precipitation potential of itraconazole in the intestine thus maximizing bioavailability.
To compare the oral bioavailability and bioequivalence of Fixtral supra bioavailable itraconazole (SB) with reference product R2 (supra bioavailable 50 mg itraconazole × tablets).
The comparison of Fixtral SB (supra bioavailable itraconazole) 100 mg with Lozanoc capsules 50 mg administered as two capsules was performed, revealing that Fixtral SB is expected to have therapeutically comparable efficacy at half the equivalent dose. In terms of area under the concentration-time curve (AUC) / minimum inhibitory concentration (MIC), the pharmacodynamic activity of the test product at 100 mg dose and the marketed itraconazole 200 mg is comparable. All of the formulations tested were found to be safe and well tolerated, with manageable side effects.
Based on the results, Fixtral SB is expected to have therapeutically similar efficacy at half-equivalent doses. All the tested formulations were found to be safe and well tolerated with resolvable side effects.
The peak concentration levels of itraconazole were achieved at 10 h (T) and 8.5 h (R2), respectively. Pharmacodynamic parameter assessment shows that AUC/MIC for R1 is comparable to Fixtral SB 100 mg for MIC levels up to 16 μg /mL.
The study population consisted of 54 healthy male and female volunteers, aged between 18-45 years. Subjects were randomized to receive a single oral dose of either test product (T) or reference product (R1 and R2). Blood samples were taken pre-dose and post-dose for up to 96 h to evaluate the bioequivalence. Adverse events assessments were performed in each study period and post-study evaluation.