Background and Objectives
Rotigotine is a dopamine receptor agonist with activity across the D1 through to D5 receptors as well as select serotonergic and adrenergic sites; continuous transdermal delivery of rotigotine with replacement of the patch once daily maintains stable plasma concentrations over 24 h. Rotigotine is indicated for the treatment of early and advanced-stage Parkinson’s disease and moderate-to-severe idiopathic restless legs syndrome. The pharmacokinetics and pharmacodynamics of a drug may vary between subjects of different ethnic origin. This study evaluated the pharmacokinetics, safety, and tolerability of single-dose treatment with rotigotine transdermal patch in Japanese and Caucasian subjects.
In this open-label, parallel-group study, healthy male and female subjects of Japanese or Caucasian ethnic origin were matched by sex, body mass index, and age. A single transdermal patch delivering 2 mg/24 h rotigotine (patch content 4.5 mg) was applied to the ventral/lateral abdomen for 24 h. The main outcome measures were the plasma concentrations of unconjugated and total rotigotine and its desalkyl metabolites and derived pharmacokinetic parameters (area under the concentration–time curve from time zero to last quantifiable concentration [AUClast], maximum plasma concentration [C max], and body weight- and dose-normalized values).
The pharmacokinetic analysis included 48 subjects (24 Japanese, 24 Caucasian). The mean apparent dose of rotigotine was 2.0 ± 0.5 mg for Japanese subjects and 2.08 ± 0.58 mg for Caucasians. Plasma concentration–time profiles of unconjugated rotigotine and of the main metabolites were similar for both ethnic groups. Parameters of model-independent pharmacokinetics, C max, time to C max (t max), and AUClast, for unconjugated rotigotine showed no statistically significant differences between Japanese and Caucasian subjects. Values of concentration-dependent pharmacokinetic parameters were higher in female subjects; this difference was minimized after correction for body weight. A statistically significant difference between ethnic groups was observed for total rotigotine concentrations (total rotigotine = unconjugated rotigotine + conjugated rotigotine), with slightly lower values in Caucasians after correction for body weight and apparent dose. No relevant differences were observed between males and females. Inter-individual variability was high. The terminal half-life for unconjugated rotigotine was 5.3 h in Japanese subjects and 5.7 h in Caucasians; corresponding values for total rotigotine were 8.6 h and 9.6 h. Less than 0.1 % of the apparent dose was renally excreted as the parent compound. Renal elimination of total rotigotine covers 11.7 % of absorbed dose in Japanese subjects and 10.8 % of the absorbed dose in Caucasians, whereas the renal elimination via total despropyl rotigotine was 8.2 and 7.1 %, respectively. The corresponding values for total desthienylethyl rotigotine were 3.5 % in Japanese subjects and 4.2 % Caucasians. Most adverse events were mild in intensity and typical for dopamine agonists or for transdermal therapeutics.
Administration of a single patch delivering 2 mg/24 h rotigotine resulted in comparable pharmacokinetic profiles in Japanese and Caucasian subjects. The rotigotine transdermal patch was generally well-tolerated. Our findings suggest similar dose requirements for Japanese and Caucasian populations.
Parkinson’s disease (PD) is the most common neurodegenerative disease after Alzheimer’s disease . Treatment of PD is complex due to the progressive nature and array of motor and non-motor features of the disease, and the early and late side effects associated with therapeutic interventions . Levodopa is still the most potent symptomatic drug for PD ; however, guidelines recommend initial treatment with a dopamine receptor agonist (particularly in young-onset patients) to avoid the development of motor complications associated with long-term levodopa use [4, 5]. Dopamine receptor agonists are also recommended as the first-line treatment for patients with moderate-to-severe idiopathic restless legs syndrome (RLS) .
Rotigotine, the levorotatory enantiomer of racemic aminotetralin, is a novel non-ergolinic dopamine receptor agonist with preferential binding to D3, D2, and D1 receptor subtypes . Rotigotine has been incorporated into a silicone-based transdermal patch that provides continuous drug delivery and stable plasma concentrations when the patch is replaced once every 24 h . Following application, approximately half of the administered rotigotine dose (46 %) is systemically absorbed . Rotigotine is rapidly metabolized, mainly by conjugation (sulfation and glucuronidation) . The terminal elimination half-life (t ½) of unconjugated rotigotine is 5.4 h  and of conjugated rotigotine is approximately 10 h . A second pathway is the formation of inactive N-desalkyl metabolites with subsequent conjugation . Efficacy of rotigotine in the treatment of early PD [12–14], advanced PD [15–17], and RLS [18–20] has been demonstrated in randomized placebo-controlled trials and rotigotine is approved for the treatment of PD and RLS in Europe and the USA.
The efficacy and tolerability of rotigotine have mainly been investigated in Caucasian subjects. Various factors including differences in height, body weight, genetic polymorphism in drug-metabolizing enzymes such as cytochrome P450 (CYP) 2C19 and CYP2C9, and enzyme, transporter and receptor saturation, may influence pharmacokinetics and pharmacodynamics of rotigotine in subjects of different ethnic origin . The route of administration also plays a role and ethnic differences may not be relevant if the drug is applied transdermally . Many physicians prescribe medications at lower doses when treating Asian patients with PD . For example, subtherapeutic doses of the dopamine receptor agonist pergolide are commonly used in clinical practice in Japan; although doses of up to 1.25 mg/day are recommended for Japanese patients, many receive just 0.6 mg/day . It is important that potential pharmacokinetic differences are considered when determining dose adjustments for different ethnic groups. To compare the pharmacokinetics and safety of rotigotine in subjects of different ethnic origin, the administration of a single transdermal patch (delivering 2 mg/24 h) in healthy Japanese and Caucasian subjects was investigated in this open-label phase I clinical study (NCT01761526).
Subjects and Methods
Study Population and Design
This open-label, non-randomized, single-dose, parallel-group study was carried out at FOCUS Clinical Drug Development GmbH, Neuss, Germany in 2002. Healthy male and female subjects of Japanese or Caucasian ethnic origin were eligible to participate if they were aged 20–45 years, had a body mass index (BMI) of 18–28 kg/m2, were willing and able to comply with all study requirements, and were healthy according to eligibility assessments (without any clinically relevant deviations from normal). Japanese participants were required to have been born in Japan to parents of 100 % Japanese origin, and to have left Japan no more than 10 years before the start of the study.
Exclusion criteria included a clinically relevant allergy; known or suspected drug hypersensitivity (in particular to any components of the trial medication); prior or current clinically relevant medical or psychiatric conditions; a history of chronic alcohol or drug abuse; positive testing for alcohol or drugs, HIV-1/HIV-2 antibodies, hepatitis B surface antigen, or hepatitis C virus antibody; and blood donation or comparable blood loss of >350 mL within 3 months prior to patch application. In addition, no acute diseases, skin diseases, suspicious and undiagnosed skin lesions, skin tumors, history of significant hypersensitivity to adhesives or other transdermal products, or recent unresolved contact dermatitis were allowed. Individuals were also excluded if they had participated in a clinical trial of an investigational product within 3 months prior to patch application; had used any concomitant medication (excluding paracetamol) within 2 weeks prior to patch application; had used methylphenidate, amphetamines, or catechol-O-methyltransferase inhibitors within 28 days prior to patch application; or had used monoamine oxidase inhibitors, reserpine, alpha-methyldopa, antipsychotic agents, antipsychotics, clozapine, olanzapine, flunarizine, cinnarizine, metoclopramide, risperidone, or quetiapine or any other known enzyme-inducing or inhibiting agent within 3 months prior to patch application. More than 5 cigarettes/day, 600 mg caffeine/day, and/or 20 g alcohol/day, a diet deviating notably from normal daily amounts of proteins, carbohydrates or fat, or heavy physical exertion 2 days before the eligibility assessment also led to exclusion. Female subjects were excluded if they were without medically adequate contraception, were pregnant or lactating, or had taken oral contraceptives or hormone replacement within 4 weeks prior to the eligibility assessment. Caucasian and Japanese subjects were matched by sex, BMI (±10 %), and age (±5 years). The study was conducted in accordance with Good Clinical Practice and the Declaration of Helsinki. The protocol and amendments were approved by the Ethics Committee of the ‘Ärztekammer Nordrhein’, Düsseldorf, Germany. Written informed consent was obtained from all participants.
Eligibility assessments (medical history, complete physical examination, 12-lead ECG, vital signs and laboratory screening, alcohol/drug screening and serology, and pregnancy test) were conducted within 21 days before patch application. Eligibility was confirmed on Day −1 (day before patch application) with a repeat of the physical examination, vital signs, ECG, pregnancy test, and alcohol/drug screening. Eligible subjects were hospitalized on the day of patch application for a period of 60 h. One 10 cm2 patch containing 4.5 mg rotigotine (2 mg/24 h delivery) (UCB Pharma, Monheim am Rhein, Germany) was applied to the ventral/lateral abdomen in the morning and removed after 24 h. Subjects stayed in bed for at least 2 h after patch application. A follow-up visit was conducted within 5–10 days.
Sample Collection and Analytical Methods
Blood samples for the pharmacokinetic assessment of rotigotine and metabolites in plasma were collected into lithium-heparinized monovettes prior to patch application (0 h) and at 1, 2, 4, 8, 12, 16, 24, 25, 26, 28, 30, 33, 36, 48, and 60 h after patch application. Assessments included both unconjugated and total rotigotine (total rotigotine = unconjugated rotigotine + conjugated rotigotine), and the metabolites despropyl and desthienylethyl rotigotine. Samples were assayed untreated and after pre-incubation with glucuronidase to convert glucuronide and sulfate conjugates back into the unconjugated moiety for total rotigotine determination. Concentrations of rotigotine and metabolites in plasma were determined by liquid chromatography with tandem mass spectrometry (LC–MS/MS) using Positive Electrospray Ionization (ESI) and Selected Reaction Monitoring (SRM) with the following lower limits of quantification (LLQ): 0.01 ng/mL for unconjugated rotigotine, 0.01 ng/mL for total rotigotine, 0.1 ng/mL for total despropyl rotigotine, and 0.1 ng/mL for total desthienylethyl rotigotine. Internal standards were fentanyl citrate (Promochem, Wesel, Germany) for assay of unconjugated and total rotigotine and N-despropyl-propafenone oxalate for assay of the desalkyl metabolites. Standard curves were linear within the calibration range 0.01–2.0 ng/mL for unconjugated and total rotigotine, and 0.1–10 ng/mL for the metabolites. Overall accuracy and precision for calibration standards and quality controls were well within 10 % at all concentrations.
For the evaluation of renal excretion of rotigotine and its metabolites, urine was collected pre-dose and 0–24, 24–48, and 48–60 h after patch application. Urine samples were analyzed by LC–MS/MS with the following LLQs: 0.05 ng/mL for unconjugated rotigotine, 0.1 ng/mL for unconjugated despropyl rotigotine, 0.25 ng/mL for unconjugated desthienylethyl rotigotine, and 0.5 ng/mL for total despropyl rotigotine, total desthienylethyl rotigotine, and total rotigotine. Standard curves were linear within the calibration range of 0.05–2.0 ng/mL for unconjugated rotigotine, 0.1–10 ng/mL for unconjugated desthienylethyl rotigotine, and 0.5–30 ng/mL for total rotigotine and total despropyl and desthienylethyl rotigotine. In order to evaluate the apparent dose, the patches were analyzed for residual drug content after the 24-h patch-on period.
Primary pharmacokinetic variables were the plasma concentrations of unconjugated and total rotigotine and its desalkyl metabolites and derived pharmacokinetic parameters [area under the concentration–time curve (AUC) from time zero to last quantifiable concentration (AUClast), maximum plasma concentration (C max), and body weight- and dose-normalized values]. AUClast was calculated using the log/linear trapezoidal rule (linear up to C max and log thereafter).
Secondary parameters included time to C max (t max), t ½, AUC from time zero to infinity (AUC∞), total body clearance (CL), and apparent volume of distribution (V d). Urine concentrations of rotigotine (unconjugated and total) and its despropyl and desthienylethyl metabolites (unconjugated and total) were also determined. Derived parameters included amount excreted into urine (A e), fraction excreted into urine (% of applied and apparent dose; f e), and renal clearance (CLR). AUC∞ was calculated as AUClast + C last/λ z, where C last is the last quantifiable concentration and λ z the terminal rate constant. λ z was estimated by log-linear regression analysis on data points visually assessed to be in the terminal log-linear phase. t ½ was calculated as t ½ = 0.693/λ z. All concentration-dependent pharmacokinetic parameters were normalized by body weight as well as by apparent dose.
Safety and Tolerability
Vital signs and ECG measurements were performed repeatedly. A complete physical examination and safety laboratory assessments were carried out during the study and at follow-up. Adverse events (AEs) were monitored and recorded continuously. Skin tolerability was assessed pre-dose, directly after patch removal, and 3 and 24 h after patch removal according to classification scores for erythema [no reddening (0), slight reddening (1), evident reddening (2), papular reaction (3), vesiculation (4)] and for edema at the application site [no visible reaction (0), edema marginal (1), slight (2), evident (3), severe (4)]. Patch adhesiveness was assessed immediately prior to removing the patch using a score from 0 (no lift) to 5 (80–100 % lift).
Pharmacokinetic analyses were performed using the per-protocol population, which included subjects who completed the study without any important protocol deviations and for whom primary parameter data were available. Descriptive statistics were displayed for the primary parameters AUClast, C max, and normalized values by ethnic group, sex, and overall. Data points below LLQ were substituted by zero for the calculation of mean values. The log-transformed primary parameters were submitted to an analysis of variance (ANOVA) with ethnic group and sex as fixed effects. The ANOVA was calculated utilizing general linear models (PROC GLM). The resulting estimated differences and corresponding 90 % confidence intervals (CIs) were back-transformed to the original scale to calculate ratios (Japanese vs. Caucasian) and corresponding CIs. Lack of difference between ethnic groups was concluded if the 90 % CIs for the ratios were fully contained within the acceptance ranges for AUClast (80–125) and for C max (70–143), preferably with unity (100 %) included. Descriptive statistics were displayed for the secondary pharmacokinetic parameters without a formal statistical comparison between groups. All statistical evaluations were performed using SAS® software (version 8.2; SAS Institute, Cary, NC, USA).
All subjects were included in the safety analysis. AEs were coded using the dictionaries WHO Adverse Reactions Terminology (Schwarz Biosciences, version 1993) and MedDRA® (Medical Dictionary for Regulatory Activities; version 5.1). A recurrent AE (e.g., headache for a couple of hours every day) was counted as multiple AEs. Safety and tolerability data were summarized descriptively.
Fifty subjects were enrolled and received study medication. Two female Caucasian subjects were withdrawn due to AEs, leaving 48 subjects for the pharmacokinetic analysis, with 12 males and 12 females in each ethnic group. Demographic characteristics of the per-protocol population were similar for both ethnic groups, with mean body weight among Caucasians 10 % higher than among Japanese subjects (Table 1). All subjects were judged to be healthy based on their medical histories, physical examination, and laboratory results.
Pharmacokinetics of Unconjugated Rotigotine
The mean apparent dose of rotigotine was 2.0 ± 0.5 mg for Japanese and 2.08 ± 0.58 mg for Caucasian subjects (accounting for approximately 44 and 46 % of the total drug content of the patch, respectively). A large inter-individual variability (overall range 0.94–3.46 mg) was observed, with a tendency towards slightly higher absorption in female subjects (Table 2).
Mean plasma concentration–time profiles of unconjugated rotigotine were similar in Japanese and Caucasian subjects following application of a single 4.5 mg patch (Fig. 1). In both ethnic groups, values were higher in female than in male subjects. After a lag-time of 2–4 h, plasma concentrations increased and reached a plateau after 8 h that was maintained until patch removal. C max was reached after approximately 16 h among male and female subjects in both ethnic groups. Following patch removal, plasma concentrations declined rapidly with a t ½ of approximately 5–6 h, and were below LLQ 12 h after patch removal.
Table 2 summarizes the pharmacokinetic parameters for unconjugated rotigotine. Variability between subjects was high in both ethnic groups. Among the Caucasian subjects, very high C max values were observed in one female (5 times the mean value) and one male (4 times the mean value); these individuals also had the highest apparent dose values. Statistical comparison for C max and AUClast for unconjugated rotigotine indicated no significant differences between the two ethnic groups with unity (1) included in the CI ranges (Table 3). Ratios were 1.14 for C max and 1.10 for AUClast without normalization. For both parameters, the differences between groups were minimized by normalization for body weight and increased by normalization for apparent dose (Table 3). Normalization for both factors resulted in a ratio for Japanese versus Caucasians of 1.08 (95 % CI 0.88–1.32) for C max and of 1.05 (95 % CI 0.85–1.28) for AUClast (Table 3). In both ethnic groups, females showed higher AUClast and C max values than males. This difference was minimized after normalization by body weight and apparent dose (Tables 2, 3).
Terminal t ½ values of unconjugated rotigotine were similar between ethnic groups and between subjects of each sex. The renal elimination of unconjugated rotigotine was ~1 μg for all subgroups. The V d was higher in Caucasians (4,243 L ± 54.3 %) than in Japanese subjects (3,283 L ± 43.1 %).
Pharmacokinetics of Total Rotigotine
Mean plasma concentrations of total rotigotine were lower in Caucasians than Japanese subjects, and were slightly higher in female subjects than in male subjects (Fig. 2). High inter-individual variability was observed. In both ethnic groups, plasma concentrations of total rotigotine reached mean maximum values after 16 h without developing a clear plateau phase. C max and AUClast were higher in Japanese subjects (Table 3); lower geometric means of C max (27 % lower) and of AUClast (24 % lower) were observed in Caucasian subjects. These differences were reduced following corrections for body weight and apparent dose (C max 23 %, AUClast 20 %) and for body weight alone (C max 20 %, AUClast 17 %). Statistical comparison between the two ethnic groups for these parameters indicated a difference as the 90 % CIs did not include unity. Normalization by body weight reduced the ratios for both parameters and included unity for AUClast, whereas normalization by apparent dose had no effect on the ratios. Statistical analysis showed no relevant differences in AUClast and C max values between male and female subjects (Table 3).
Pharmacokinetics of Despropyl and Desthienylethyl Rotigotine and its Conjugates
Mean values of parameters for model-independent pharmacokinetics of the metabolites total despropyl rotigotine and total desthienylethyl rotigotine are shown in Table 4. Terminal t ½ could not be calculated owing to an insufficient number of samples above LLQ. Plasma concentration–time curves are shown for Japanese and Caucasian subjects in Fig. 3.
Renal Elimination of All Measured Compounds
In both ethnic groups, approximately 20 % of the absorbed rotigotine dose was excreted into urine over 60 h after application of patch. Rotigotine was excreted as unconjugated rotigotine (<1 %; Table 2), total rotigotine (11.7 and 10.8 % for Japanese and Caucasian subjects; Table 2), total despropyl rotigotine (8.2 and 7.1 %; Table 4), and total desthienylethyl rotigotine (3.5 and 4.2 %; Table 4). Unconjugated metabolites were not present or were below LLQ. The CLR of unconjugated rotigotine was similar in both groups, with a trend towards lower renal elimination of total rotigotine in Japanese subjects than in Caucasians (Table 2). The profile of renal elimination is shown in Fig. 4.
A total of 185 AEs were reported, of which 96 (52 %) occurred in Caucasians and 89 (48 %) occurred in Japanese subjects [women 108 (58 %), men 77 (42 %)]. No AEs were considered serious. The majority of AEs were mild in intensity. Moderate ratings were documented for nausea (six cases), vomiting (four cases), fatigue (three cases), pruritus at the application site (three cases), headache (two cases), dizziness (one case), and insomnia (one case). One case of nausea was rated as severe. All AEs were resolved by the end of the study. Application-site reactions were the most frequently reported AEs and were experienced by 85 % of Caucasian subjects and by all of the Japanese subjects. Erythema was the most common application-site reaction, and occurred in 73 % of Caucasian and 96 % of Japanese subjects. Assessment of skin tolerability showed reddening was generally slight. Evident reddening occurred in two Caucasians and one Japanese subject and marginal (i.e., barely recognizable) application-site edema was observed in 11 subjects in each ethnic group. One male Caucasian subject showed a slight application-site edema. Other common AEs included headache [Caucasian 13/26 subjects (50 %) vs. Japanese 6/24 subjects (25 %)], fatigue [9/26 (35 %) vs. 5/24 (21 %)], and nausea [7/26 (27 %) vs. 8/24 (33 %)]. Vomiting occurred in two subjects in each ethnic group; the two female Caucasian subjects discontinued the study due to nausea and vomiting. All application-site reactions were judged to be highly probably or probably related to the study medication. Other AEs were generally assessed as probably or possibly related. Patch adhesiveness was good; six Caucasian subjects and one Japanese subject showed a detachment of <20 % and one subject in each ethnic group showed a detachment between 20 and 49 %.
No clinically relevant changes were observed in laboratory parameters, physical examination, vital signs, and ECG recordings. Two Caucasian subjects had unusually high plasma concentrations of unconjugated rotigotine; there was, however, no indication of a higher incidence or intensity of AEs.
This study provides a detailed description of the pharmacokinetics of the transdermally applied dopamine agonist rotigotine in healthy Japanese and Caucasian subjects. Mean apparent doses and plasma concentration–time curves for unconjugated rotigotine were comparable between individuals from each ethnic group. No relevant differences in t max and t ½ were observed. Bioavailabilities of unconjugated rotigotine following administration of a single dose were similar in each ethnic group. Point estimates for AUClast and C max included unity, indicating a similar exposure to the active substance. Individual concentration levels for unconjugated rotigotine in plasma showed a high variability between subjects. The variability of the resulting pharmacokinetic parameters AUClast and C max was reduced after normalization by body weight and by apparent dose. Sex differences in C max and AUClast for unconjugated rotigotine were also minimized after body weight normalization.
Plasma concentrations of total rotigotine differed between ethnic groups. AUClast and C max values were ≥20 % higher in Japanese subjects than in Caucasians. Point estimates indicated a statistical difference that was minimized by normalization for body weight, but not by normalization for apparent dose. The very high CL of unchanged rotigotine (~500 L/h in both ethnic groups) indicates extensive metabolism as the main route of elimination. This is in line with an extremely high V d of about 4,000 L. Differences between V d values in Japanese and Caucasian subjects may reflect differences in body weight. No differences in the pharmacokinetics of rotigotine, especially elimination via metabolism, can be concluded. Total rotigotine concentrations do not play a role in treatment efficacy but may affect the safety and tolerability of the medication. However, the overall incidence of AEs was similar in both ethnic groups and the high plasma concentrations observed in two Caucasian subjects were not associated with a higher incidence or intensity of AEs.
Plasma concentrations of total rotigotine desalkyl metabolites were similar in both ethnic groups; however, they were near or below the LLQ. The low concentrations of metabolites in plasma and the high variability of the values in all subgroups confounded interpretation of the pharmacokinetic parameters. The CLR of the active substance was similar in both groups. The A e was slightly higher for Japanese subjects but accounted for <1 % of the dose absorbed, indicating a very small contribution of renal excretion to the CL of unconjugated rotigotine. Comparable amounts of total rotigotine and total desalkyl metabolites were excreted into urine. The proportion of total despropyl metabolite was more than double that of the desthienylethyl metabolite for both ethnic groups. The metabolic profile of rotigotine observed in our study is in agreement with the results of a pharmacokinetic study in Caucasian subjects .
The major isoenzyme involved in rotigotine N-desalkylation, CYP2C19, is known to be differentially expressed in different ethnic groups; around 25 % of Asian individuals and 3–5 % of Caucasians have a poor metabolizer phenotype . However, a study in healthy Caucasian subjects has shown that selective inhibition of CYP2C19 does not affect the steady-state pharmacokinetic profile of rotigotine . Rotigotine dose adjustment may not be necessary in patients who are poor CYP2C19 metabolizers.
Application of a single rotigotine patch was safe and generally well-tolerated. Most AEs were mild in intensity and typical of dopamine agonists (e.g., nausea) or transdermal therapeutics (e.g., mild and transient erythema). Japanese subjects reported a higher incidence of application-site reactions (100 vs. 85 %) and a lower incidence of headache (25 vs. 50 %) than Caucasians. In the current study, the higher incidence of AEs observed in women than in men (58 vs. 42 %) may be due to sex-related differences in pharmacodynamic response. Patch adhesiveness was good for both ethnic groups; it was, however, better in Japanese than Caucasian subjects.
The administration of a single patch delivering 2 mg/24 h rotigotine resulted in comparable pharmacokinetic profiles in Japanese and Caucasian subjects. The extent of rotigotine exposure was affected by body weight, but did not appear to be affected by sex. Transdermal rotigotine was safe and generally well-tolerated by both ethnic groups. These findings suggest similar dose requirements for Japanese and Caucasian populations.
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This study was funded by UCB Pharma, Monheim am Rhein, Germany. Willi Cawello, Marina Braun, and Jan-Peer Elshoff are employees of UCB Pharma, Monheim am Rhein, Germany. Seong R. Kim, Junji Ikeda, and Tomoo Funaki are employees of Otsuka Pharmaceutical Co., Ltd., Tokyo, Japan. The authors acknowledge the participation of FOCUS Clinical Drug Development GmbH (Neuss, Germany), which conducted the study. AAI Deutschland GmbH & Co. KG, Neu-Ulm, Germany performed all bioanalytical work to quantify rotigotine and metabolites in plasma and urine samples. Editorial support was provided by Hannah Carney (Evidence Scientific Solutions, Horsham, UK) and was contracted by UCB Pharma, Brussels, Belgium. The authors also acknowledge Ging-Ging Li, CMPP (Global Publications Manager, Movement & Sleep Disorders, UCB Pharma, Brussels, Belgium) for publication coordination. All costs associated with the development and the publishing of the present manuscript were met by the sponsor.
ClinicalTrials.gov registration number: NCT01761526.
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Cawello, W., Kim, S.R., Braun, M. et al. Pharmacokinetics, Safety and Tolerability of Rotigotine Transdermal Patch in Healthy Japanese and Caucasian Subjects. Clin Drug Investig 34, 95–105 (2014). https://doi.org/10.1007/s40261-013-0150-5
- Japanese Subject
- Caucasian Subject
- Dopamine Receptor Agonist
- Patch Application