Cited by 44Hormonal and reproductive studiesAdvancements in Transdermal Drug DeliveryAdrenal Hormones and Disorders

Comparison of the steady-state pharmacokinetics, metabolism, and variability of a transdermal testosterone patch versus a transdermal testosterone gel in hypogonadal men

Mazer, Norman, Bell, Damon, Wu, Jingyang, Fischer, Jerome, Cosgrove, Michael, Eilers, Barbara·2005·The Journal of Sexual Medicine

Abstract

Aim: To compare the pharmacokinetics (PK), metabolism, intra- and inter-subject variability of a permeation-enhanced testosterone patch versus a topical testosterone gel. Methods: 28 hypogonadal men were treated with a testosterone patch (5 mg/day applied at 2200 h) and a 1% testosterone gel (5 g/day applied at 0800 h; nominal delivery 5 mg/day), each for 14 days, in an open-label crossover design. PK profiles of total testosterone (TT) and calculated free testosterone (cFT) were measured on day 7 and day 14 of each treatment, with patches or gel applied to the abdomen; dihydrotestosterone (DHT) and estradiol (E2) profiles were measured on day 14. The time-average (Cavg), maximum (Cmax), time of maximum (Tmax) and minimum concentrations (Cmin) were derived from each profile. The intra- and inter-subject coefficients of variation (CVintra and CVinter) of the TT and cFT parameters were computed by ANOVA. Results: Nightly applications of the patch produced a mean TT profile that mimicked the circadian pattern of healthy men. Morning applications of the gel produced a flatter mean profile; though individual subjects exhibited significant peaks at variable times. For TT, the mean and 90% confidence intervals of the patch/gel ratio of Cavg (1.030; 0.936–1.133; P > 0.05) and Cmax (1.086; 0.974–1.211; P > 0.05) met the criteria for bioequivalence. Cmin was lower for the patch. DHT levels and DHT/T ratios were 2 to 3-fold higher for the gel (P < 0.0001). E2 levels and E2/T ratios were comparable. CVintra and CVinter for Tmax approached 100% for the gel and were 23% and 42%, respectively, for the patch (P < 0.0001). Other variability parameters were generally comparable. Both products were well tolerated, and the patches adhered well. Conclusions: These findings reflect the different mechanisms of transdermal absorption from the patch and gel and provide new considerations for selecting testosterone replacement therapies in hypogonadal men.

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Crossref · 10.1111/j.1743-6109.2005.20231.x

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Authors
Mazer, N., Bell, D., Wu, J., Fischer, J., Cosgrove, M., & Eilers, B.
Affiliations
  • University of Utah (US)
  • Watson Laboratories, Inc., Clinical R&D,   Salt Lake City,
  • Diabetes & Glandular Disease Clinic (US)
  • Clinical Research Services (DE)
Corresponding author
Mazer, Norman
Venue
The Journal of Sexual Medicine
Published
2005-03-01
Volume
2
Issue
2
Pages
213-226
ISSN
  • 1743-6095 (ISSN-L)
  • 1743-6109
OpenAlex
W2168964163
Cited by
44
References
23
Citations by year
2026: 2 · 2025: 1 · 2024: 1 · 2023: 1 · 2021: 1 · 2020: 1 · 2019: 1 · 2018: 2 · 2017: 2 · 2016: 3 · 2015: 2 · 2014: 5 · 2013: 1 · 2012: 1
FWCI
3.10
Type
journal article
Language
en
Open access
closed
Locations
  • The Journal of Sexual Medicine (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advancements in Transdermal Drug Delivery
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
Keywords
testosterone gel, testosterone replacement therapy, hypogonadism, steady-state pharmacokinetics, free testosterone, dihydrotestosterone, estradiol, bioequivalence, percutaneous absorption, interindividual variability, crossover comparison
MeSH terms
Administration, Cutaneous, Adult, Aged, Androgens, Estradiol, Gels, Humans, Hypogonadism, Male, Middle Aged, Dihydrotestosterone, Testosterone, Therapeutic Equivalency, Cross-Over Studies

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