Int. Journal of Clinical Pharmacology and Therapeutics, Volume 63 (2025) - February (77 - 86)

Skin adhesion of a newly developed, bioequivalent rotigotine patch formulation in comparison to the originator product: Results of a multi-center, randomized, crossover trial in patients with Parkinson’s disease

Wolfgang H. Jost1, Maggie Wang2, Gabriel Wauer3, Annika Dax4, Ralph-Steven Wedemeyer4, 5, Barbara Schug4, André Warnke4, Ana Leblanc6, Bjoern Schurad3
1 Parkinson-Klinik Ortenau, Wolfach, Germany, 2 Luye Pharma Switzerland AG, Basel, Switzerland, 3 Luye Pharma AG, Miesbach, 4 SocraTec R&D GmbH, Oberursel, 5 SocraMetrics GmbH, Erfurt, Germany, and 6 BlueClinical Phase 1 , Hospital de Prelada, Porto, Portugal

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DOI 10.5414/CP204672

Abstract

Objectives: To demonstrate adequate skin adhesion of a new once-daily rotigotine transdermal patch (ROT-TDS) compared to the originator product (reference) in patients with Parkinson’s disease (PD).
Materials and methods: Pharmacokinetic bioequivalence (PK BE) was assessed with the 4 mg/24h patches in healthy adults in a single-/multiple-dose, crossover trial. The trial investigating skin adhesion in PD patients (stable dose ≥ 8 mg/day rotigotine) was performed with the 8 mg/24h patches as a multiple-dose, crossover trial (4 alternating once-daily patch applications). Skin status (seborrhea, sweating) was characterized at screening. Adhesion was assessed 5 minutes after application and 5 minutes before removal of each patch. Systemic safety and skin irritation/sensitization were monitored.
Results: ROT-TDS was bioequivalent to the reference product in the PK BE trial in 48 randomized healthy subjects. In the skin adhesion trial in 43 randomized PD patients, the cumulative mean percentage of adhesion (90% CI) at the end-of-dosing interval was 92.948% (90.156 – 95.740%) for ROT-TDS and 90.471% (87.574 – 93.367%) for the reference. For ROT-TDS, 80.23% of patches were ≥ 90% adhered at the end-of-dosing interval, while this was the case for 67.44% of the reference patches. Safety and skin tolerability of both products were comparable; the most frequent treatment-related adverse event was application-site pruritus for both treatments at comparable extent.
Conclusion: ROT-TDS – with shown BE to the originator reference product – displayed similar safety and local tolerability as the reference product in patients with PD. The results show a trend to improved skin adhesion of the new patch compared to the reference in the target population.

Author Details

Authors

Departments

  • 1 Parkinson-Klinik Ortenau, Wolfach, Germany,
  • 2 Luye Pharma Switzerland AG, Basel, Switzerland,
  • 3 Luye Pharma AG, Miesbach,
  • 4 SocraTec R&D GmbH, Oberursel,
  • 5 SocraMetrics GmbH, Erfurt, Germany, and
  • 6 BlueClinical Phase
  • 1 , Hospital de Prelada, Porto, Portugal

Address

Bjoern Schurad, PhD
Luye Pharma AG
Am Windfeld 35
83714 Miesbach, Germany
Email: [email protected]

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Citation

Wolfgang H Jost, Maggie Wang, Gabriel Wauer, Annika Dax, Ralph-Steven Wedemeyer, Barbara Schug, André Warnke, Ana Leblanc, Bjoern Schurad. Skin adhesion of a newly developed, bioequivalent rotigotine patch formulation in comparison to the originator product: Results of a multi-center, randomized, crossover trial in patients with Parkinson’s disease
. Int J Clin Pharmacol Ther. 2025; 63: 77-86. doi: 10.5414/CP204672. Pubmed: https://pubmed.ncbi.nlm.nih.gov/39370808/; PMID: 39370808.

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