Study to Investigate Pharmacokinetics (PK) of Pramipexole in Pediatric Patients Who Are Individually Optimized to Stable Pramipexole Doses for the Treatment of Idiopathic Restless Legs Syndrome (RLS)

Restless Legs Syndrome Clinical Trial

Official title:

An Open-label Clinical Study to Investigate Pharmacokinetics (PK) of Different Doses (0.125 mg, 0.25 mg, 0.5 mg) of Pramipexole Administered Once Daily Orally in Pediatric Patients Who Are Individually Optimized to Stable Pramipexole Doses for the Treatment of Idiopathic Restless Legs Syndrome (RLS)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02231918
• Other study ID #: 248.600
• Status: Completed
• Phase: Phase 2
• First received: September 3, 2014
• Last updated: September 2, 2015
• Start date: May 2006

Study information

• Verified date: September 2015
• Source: Boehringer Ingelheim
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Study to determine the pharmacokinetics (PK) of pramipexole (PPX) after administration of a single dose orally (p.o.) in pediatric patients with the diagnosis of RLS

Recruitment information / eligibility

• Status: Completed
• Enrollment: 26
• Est. primary completion date: July 2007
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 6 Years to 16 Years

Eligibility

Inclusion Criteria:

1. Male or female patients ages 6 years to 16 years (two age groups, 6 to 11 years and 12 to 16 years, with the same number of patients if possible)

2. Diagnosis of idiopathic Restless Legs Syndrome (RLS) according to the Clinical RLS criteria of the International Restless Legs Syndrome Study Group (IRLSSG)

All 4 of the following criteria must be present:

• An urge to move the legs, usually accompanied or caused by uncomfortable and unpleasant sensations in the legs. (Sometimes the urge to move is present without the uncomfortable sensations and sometimes the arms or other body parts are involved in addition to the legs.)

• The urge to move or unpleasant sensations begin or worsen during periods of rest or inactivity such as lying or sitting

• The urge to move or unpleasant sensations are partially or totally relieved by movement, such as walking or stretching, at least as long as the activity continues

• The urge to move or unpleasant sensations are worse in the evening or night than during the day or only occur in the evening or night. (When symptoms are very severe, the worsening at night may not be noticeable but must have been previously present.)

3. Must meet all 4 of the diagnostic criteria for adult RLS (see inclusion criterion No. 2 above) and either:

1. The child must be able to describe the leg discomfort in their own words or

2. The child must have 2 or 3 of the following:

• Sleep disturbance

• Periodic Limb Movements During Sleep (PLMS) index >5 per hour of sleep, or

• A biological parent or sibling with definite RLS

4. Written informed consent consistent with International Conference on Harmonisation (ICH)/ Good Clinical Practice (GCP) and Local Institutional Review Board requirements for children obtained prior to any study procedures being performed

5. Ability and willingness to comply with the study treatment regimen and to attend study assessments

6. Must be on PPX treatment at the same evening maintenance dose for a minimum of 7 days prior to entry into this study as determined by the investigator

7. A patient who is taking PPX but not as an evening maintenance dose may return for a repeat screening if the patient can be successfully switched and re-stabilized to an evening PPX maintenance dose

Exclusion criteria:

1. Any women of childbearing potential having a positive serum pregnancy test at screening

2. Any women of childbearing potential not using a medically accepted method of contraceptive (Intra-Uterine Device, oral, implantable, injectable contraceptives and estrogen patch, double barrier method [spermicide + diaphragm], or abstinence at the discretion of the investigator)

3. Patients who have a clinically significant renal disease or serum creatinine level greater than 1.0 mg/dL at screening

4. Any of the following lab results at screening:

• Hemoglobin (Hgb) below the lower limit of normal (LLN), which is determined to be clinically significant

• Basal thyroid stimulating hormone (TSH), triiodothyronine (T3) or thyroxine (T4) clinically significantly (at the investigator's discretion) out of the normal range at screening (if not caused by substitution therapy according to the investigator's opinion)

• Patients with any clinically significant abnormalities in laboratory parameters at screening at the investigator's discretion

5. Other clinically significant metabolic-endocrine, hematological, gastrointestinal disease, pulmonary disease (such as severe asthma) which in the opinion of the investigator would preclude the patient from participating in this study

6. History or clinical signs of any neurological disease with potential to secondarily cause RLS symptoms

7. Presence of any other sleep disorder such as Rapid Eye Movement (REM) sleep behavior disorder, narcolepsy, or sleep apnea syndrome

8. History of schizophrenia or any psychotic disorder, history of mental disorders, or any present Axis I psychiatric disorder according to the Diagnostic and Statistical Manual of Mental Disorders, 4th edition (DSM-IV) requiring any medical therapy

9. History of/or clinical signs of epilepsy or seizures other than fever-related seizures in early childhood

10. History of/or clinical signs of any malignant neoplasm including suspicious undiagnosed skin lesions (which may be melanoma), melanoma, or a history of melanoma

11. Any other conditions that, in the opinion of the investigator, would interfere with the evaluation of the results or constitute a health hazard for the patient

12. Allergic response to PPX or the inactive ingredients in its tablet formulation

13. Had previous treatment with dopamine agonists other than PPX within 14 days prior to the baseline visit

14. Had any other medical treatment for RLS besides the study medication within 14 days prior to the baseline visit

15. Had withdrawal symptoms of any medication at screening or at the baseline visit

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Psychomotor Agitation
• Restless Legs Syndrome
• Syndrome

Intervention

Drug:
• MIRAPEX® - low

• MIRAPEX® - medium

• MIRAPEX® - high

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Boehringer Ingelheim

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cmax,ss	Maximum concentration of the Pramipexole (PPX) in plasma at steady state over a uniform dosing interval (Cmax,ss).	0.25h before the drug administration on day1 and 0.5 h, 1 h, 2 h, 3 h, 5 h, 7h, 12h and 24h after the last drug administration on day 1.	No
Primary	Cmin,ss	Minimum measured concentration of the analyte in plasma at steady state over a uniform dosing interval (Cmin,ss).	0.25h before the drug administration on day1 and 0.5 h, 1 h, 2 h, 3 h, 5 h, 7h, 12h and 24h after the last drug administration on day 1.	No
Primary	Cpre,N	Predose concentration of the analyte in plasma at steady state immediately before administration of the next dose N (Cpre,N).	0.25h before the drug administration on day1 and 0.5 h, 1 h, 2 h, 3 h, 5 h, 7h, 12h and 24h after the last drug administration on day 1.	No
Primary	Cavg	Average concentration of the analyte in plasma at steady state (Cavg).	0.25h before the drug administration on day1 and 0.5 h, 1 h, 2 h, 3 h, 5 h, 7h, 12h and 24h after the last drug administration on day 1.	No
Primary	Tmax,ss	Time from dosing to maximum concentration at steady state (Tmax,ss).	0.25h before the drug administration on day1 and 0.5 h, 1 h, 2 h, 3 h, 5 h, 7h, 12h and 24h after the last drug administration on day 1.	No
Primary	Tmin,ss	Time from dosing to minimum concentration at steady state (Tmin,ss ).	0.25h before the drug administration on day1 and 0.5 h, 1 h, 2 h, 3 h, 5 h, 7h, 12h and 24h after the last drug administration on day 1.	No
Primary	AUCt,ss	Area under the concentration-time curve of the analyte in plasma at steady state over a uniform dosing interval (AUCt,ss ).	0.25h before the drug administration on day 1 and 0.5 h, 1 h, 2 h, 3 h, 5 h, 7h, 12h and 24h after the last drug administration on Day 1.	No
Primary	?z,ss	Terminal rate constant in plasma at steady state (?z,ss ).	0.25h before the drug administration on day1 and 0.5 h, 1 h, 2 h, 3 h, 5 h, 7h, 12h and 24h after the last drug administration on day 1.	No
Primary	t1/2,ss	Terminal half-life of the analyte in plasma at steady state (t1/2,ss ).	0.25h before the drug administration on day1 and 0.5 h, 1 h, 2 h, 3 h, 5 h, 7h, 12h and 24h after the last drug administration on day 1.	No
Primary	MRTpo,ss	Mean residence time of the analyte in the body at steady state (MRTpo,ss).	0.25h before the drug administration on day1 and 0.5 h, 1 h, 2 h, 3 h, 5 h, 7h, 12h and 24h after the last drug administration on day 1.	No
Primary	CL/F,ss	Apparent clearance of the analyte in the plasma after extravascular administration at steady state; F = absolute bioavailability factor (CL/F,ss ).	0.25h before the drug administration on day1 and 0.5 h, 1 h, 2 h, 3 h, 5 h, 7h, 12h and 24h after the last drug administration on day 1.	No
Primary	Vz/F,ss	Apparent volume of distribution during the terminal phase ?z following an extravascular dose at steady state (Vz/F,ss ).	0.25h before the drug administration on day1 and 0.5 h, 1 h, 2 h, 3 h, 5 h, 7h, 12h and 24h after the last drug administration on day 1.	No
Primary	Ae 0-12,ss	Amount of analyte that is eliminated in urine at steady state over a time interval t1to t2 (0-12h).	12 hours after last study drug administration on day 1	No
Primary	fe 0-12,ss	Fraction of administered drug excreted unchanged in urine at steady state over a time interval t1 to t2 (fe 0-12,ss ).	12 hours after last study drug administration on day 1.	No
Primary	CLR,ss	Renal clearance of the analyte at steady state (CLR(0-12),ss ).	12h after last study drug administration on day 1	No
Primary	PTF	Peak-trough fluctuation (PTF) is defined as the difference between Cmax and Cmin divided by Cavg and multiplied with 100% at steady-state.	0.25h before the drug administration on day1 and 0.5 h, 1 h, 2 h, 3 h, 5 h, 7h, 12h and 24h after the last drug administration on day 1.	No
Secondary	Number of Patients With Drug Related Adverse Events	Number of patients with adverse events due to study drug.	From first drug administration until 24 hours after last study drug administration, upto 48 days	No
Secondary	Vital Signs (Systolic and Diastolic Blood Pressure)	Vital signs (Systolic and diastolic blood pressure (both supine and after standing for 1 minute)).	-0:15h(hours) pre-dose, and 0:30h, 1:00h, 2:00h, 3:00h, 5:00h, 7:00h, 12:00h, 24:00h post-dose.	No
Secondary	Vital Signs (Pulse Rate)	Vital signs (Pulse rate (both supine and after standing for 1 minute)).	-0:15h(hours) pre-dose, and 0:30h, 1:00h, 2:00h, 3:00h, 5:00h, 7:00h, 12:00h, 24:00h	No

External Links

•   Link