Clinical Trials Directory

Trials / Terminated

TerminatedNCT04183634

An Open, Randomised, Single Dose, 2-period, 2-sequence Crossover Adhesion Study of Two Different Transdermal Patches Containing Rotigotine.

Status
Terminated
Phase
Phase 1
Study type
Interventional
Enrollment
31 (actual)
Sponsor
Sandoz · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to evaluate the adhesion of the test product when compared to the reference product following a single transdermal application.

Detailed description

The objective of this clinical trial is to evaluate the adhesion of the test product when compared to the reference product following a single transdermal application. The following evaluations will be assessed as "yes" or "no": * Cold flow (dark ring formed around the patch) * Patch movement/displacement * Patch wrinkling * Residue formation (at patch application on the release liner and at patch removal on the skin) Safety and tolerability of a single dose application of a patch containing 18 mg rotigotine (Test) against a patch containing 18 mg rotigotine (Reference) will be evaluated in terms of vital signs and AEs. AEs and clinical tolerability will be monitored at all clinical trial visits. The safety evaluation will be based upon the review of the individual values (potentially clinically important abnormalities) and descriptive statistics (summary tables, graphics). As additional safety parameters for the clinical trial physical examination findings, clinical laboratory parameters, and 12-lead ECGs will be assessed at the screening and follow-up.

Conditions

Interventions

TypeNameDescription
DRUGRotigotine TTS (Test)Transdermal patch containing Rotigotine 18 mg to deliver 8 mg/24.
DRUGNeupro (Reference)Neupro®: transdermal patch containing Rotigotine 18 mg to deliver 8 mg/24 h.

Timeline

Start date
2019-12-03
Primary completion
2020-03-16
Completion
2020-03-16
First posted
2019-12-03
Last updated
2020-11-09

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT04183634. Inclusion in this directory is not an endorsement.