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Randomized, double-blind, two-way crossover bioequivalence and adhesion study, in healthy women, of a transdermal contraceptive patch with a newly sourced adhesive component at the end of shelf life vs. the EVRA patch at the beginning of shelf life
- Source :
- International Journal of Clinical Pharmacology and Therapeutics
- Publication Year :
- 2021
- Publisher :
- Dustri-Verlag Dr. Karl Feistle, 2021.
-
Abstract
- Objective Evaluate bioequivalence, based on norelgestromin (NGMN) and ethinyl estradiol (EE) plasma concentrations, and adhesion of a transdermal contraceptive patch containing a newly sourced adhesive component (test) at end of shelf life (EOSL) vs. the marketed EVRA patch (reference) at beginning of shelf life (BOSL). Materials and methods In this randomized, double-blind, two-way crossover study, healthy women received a single, 7-day application of test and reference patches in 4 sequences: two 11-day treatment periods separated by a 21-day washout. Assessments included NGMN and EE pharmacokinetics (PK), adhesion (per European Medicines Agency (EMA) 5-point scale), irritation potential and application-site reactions, and tolerability. Patches were bioequivalent if 90% CIs of geometric mean ratios (GMRs) of test/reference for Cmax, AUC168h, AUC0-tlast, and AUC∞ were 80 - 125%. Patch adhesion was comparable if ratios of geometric mean cumulative adhesion percentages were ≥ 90%. Results 68 women were randomized, and 62 completed both treatments. 55 and 59 participants in the reference and test group, respectively, had patch adhesion ≥ 80% (EMA score 0 - 1) at end of treatment. Bioequivalence was demonstrated: GMRs for pharmacokinetic (PK) parameters ranged from 102.76 - 105.57% for NGMN and 93.78 - 94.80% for EE, and associated 90% CIs were fully within the bioequivalence acceptance range (80 - 125%) for both. The patches had comparable adhesion properties (GMR, 101.4% (90% CI: 99.2 - 103.6)) and incidences of treatment-emergent adverse events. Conclusion NGMN-EE transdermal test patch at EOSL was bioequivalent to the marketed patch at BOSL, supporting widening the product's shelf-life specification. Adhesive properties and safety profiles were comparable between patches.
- Subjects :
- medicine.medical_specialty
Cmax
Urology
Transdermal Patch
Bioequivalence
Ethinyl Estradiol
Pharmacokinetics
Contraceptive Agents
contraceptive transdermal patch
Adhesives
Medicine
Norelgestromin
Humans
Pharmacology (medical)
Transdermal
Pharmacology
bioequivalence
Cross-Over Studies
business.industry
Norgestrel
Patch test
Crossover study
adhesion
Drug Combinations
Tolerability
Therapeutic Equivalency
randomized controlled trial
Female
business
pharmacokinetics
medicine.drug
Research Article
Subjects
Details
- Language :
- English
- ISSN :
- 09461965
- Volume :
- 60
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- International Journal of Clinical Pharmacology and Therapeutics
- Accession number :
- edsair.doi.dedup.....3240a933f84c5f0b53c09957fdccb94f