Efficacy and Safety Study of Aplindore in Patients With Restless Legs Syndrome

Restless Legs Syndrome Clinical Trial

Official title:

A Randomized, Double-Blind, Placebo-Controlled Four Week Study of the Efficacy and Safety of Four Doses (0.05 mg, 0.1 mg, 0.25 mg, 0.5 mg) of Aplindore MR Tablets vs. Placebo in Idiopathic Restless Legs Syndrome.

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00834327
• Other study ID #: Aplindore-250
• Status: Terminated
• Phase: Phase 2
• First received: January 30, 2009
• Last updated: October 12, 2009
• Start date: February 2009
• Est. completion date: December 2009

Study information

• Verified date: October 2009
• Source: Neurogen Corporation
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This is a clinical trial to be conducted at multiple sites in the USA. Patients diagnosed with moderate to severe Restless Legs Syndrome will be randomly allocated to one of 5 treatment arms in the study. The 5 arms include 4 arms with different doses of aplindore MR tablets and 1 placebo arm. The treatment will be taken once a day. The study is blinded and neither patients, nor the investigators, will know what treatment the patient is receiving. Patients will be assigned a dose and will be maintained at that dose for several weeks (2 treatment arms include a short titration period). The entire study will take about 6 weeks. The study will measure how effective aplindore is in decreasing symptoms of Restless Legs Syndrome, and will also assess the safety and tolerability of aplindore.

Description:

Two hundred and thirty patients will be randomly assigned to one of five treatment arms in this outpatient study. Of the four aplindore arms, two arms will be titrated over a brief period until the targeted dose is achieved, and then as with the other arms, will be maintained for several weeks. Dosing will take place over a total of about 4 weeks.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 230
• Est. completion date: December 2009
• Est. primary completion date: November 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female 18-85 years;

• Must have a score of =20 on the IRLS at Day 1 (Baseline) Visit;

• Have a history of moderate to severe RLS symptoms that disrupted sleep for at least 3 nights per week over at least a 3 month period either immediately before screening or prior to starting any RLS treatment;

• Patients must be off dopamine agonists or any other medications they are taking for RLS for a minimum of one week or 5 half lives of the RLS medication whichever is longer, prior to the Day 1 (Baseline) Visit;

• Patients must be in good general health as determined by a thorough medical history and physical examination (including vital signs), and 12-lead electrocardiogram (ECG);

• Patients must have clinical laboratory values within normal reference range or must not be clinically significantly abnormal as judged by the Investigator at screening;

• Females of childbearing potential must be using an acceptable method of contraception, have a negative serum pregnancy test at screening, and a negative urine pregnancy test at baseline. Acceptable methods of contraception include oral, intrauterine, implantable, injectable contraceptives, hormonal patch, double barrier methods or condoms impregnated with spermicide. After screening, patients using oral contraceptive methods of contraception must agree to add an additional method until 30 days following the last dose of study medication. Women on oral contraceptives must have been using them for at least one month prior to screening;

• Male patients with partners of childbearing potential must agree to use adequate contraception (use of a condom and a spermicidal) during the study and for 3 months after the study;

• Female patients who have been surgically sterilized are eligible if they have a negative pregnancy test at screening and at Baseline;

• If receiving hormone replacement therapy, patients must be on a stable regimen for minimum of 3 months prior to screening;

• Patients must be able to read, understand, and provide written/dated informed consent before enrolling in the study, and must be willing to comply with all study procedures.

Exclusion Criteria:

• Clinically significant unstable medical illness;

• Clinically significant allergic, hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, or neurological disease;

• History of non-basal cell cancer or squamous cell cancers or carcinoma in situ of the cervix within 2 years before the screening visit are excluded; for all other cancer diagnoses, patients with a history within 5 years before the screening visit are excluded;

• Patients with plasma ferritin levels less than 10 ng/mL at screening;

• A supine blood pressure > 140/90 mm/Hg at screening or baseline;

• Patients taking OTC or prescription medications that can, in the judgment of the investigator, exacerbate or are the cause of their RLS symptoms will be excluded from the study;

• Patients taking prescription drug therapy or over the counter (OTC) medication for chronic medical conditions other then RLS who are not on stable doses for at least two months prior to screening; patients who are not off any investigational drug for at least 30 days prior to screening;

• History of chronic use of dopamine antagonists for more than 6 months within the past 2 years;

• History or presence of chronic pain other than that associated with RLS. Patients should be excluded if the preponderance of the patient's complaints is related to pain and not associated with the urge to move;

• Clinically significant narcolepsy, parasomnia as an adult, significant circadian rhythm disorder, or secondary causes of RLS, (e.g., uremia or neuropathy);

• Any condition that may affect oral drug absorption;

• Travel across more than three time zones, have an expected change in sleep schedules of 6 hours or more, or have involvement in night shift work within seven days prior to screening through to study completion;

• Any clinically significant abnormal finding at the Screening Visit on physical examination, vital signs, or ECG, as determined by the Investigator; (The QTcF interval must be = 450 msec for males and = 470 msec for females);

• History of allergies, or known sensitivity, hypersensitivity, or adverse reaction to aplindore or structurally similar compounds such as flesinomax, ropinirole or ziprasadone;

• Pregnant or lactating females;

• Recent history (= one year) of alcohol or drug abuse, or current evidence of substance dependence or abuse as defined by DSM-IV criteria;

• Regular consumption of large amounts of xanthine-containing substances (i.e. more than 10 cups of coffee or equivalent amounts of xanthine-containing substances per day);

• Prior exposure to aplindore;

• Patients deemed to be in the high risk category for sleep apnea as determined by the Modified Berlin Questionnaire;

• Patients who failed prior treatment with dopamine agonists as evidenced by lack of efficacy at the maximum tolerated dose;

• Patients who test positive at Screening for hepatitis B surface antigen or hepatitis C antiboby or has a history of a positive result

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Psychomotor Agitation
• Restless Legs Syndrome
• Syndrome

Intervention

Drug:
• aplindore MR tablets or Placebo
aplindore MR tablets administered QD for about 4 weeks

Locations

Country	Name	City	State
United States	Neurotrials Research, Inc.	Atlanta	Georgia
United States	Quest Research Institute	Bingham Farms	Michigan
United States	Sleep Medicine and Research Center - St Luke's Hospital	Chesterfield	Missouri
United States	Comunity Reasearch	Cincinnati	Ohio
United States	Tri-State Sleep Disorders Center	Cincinnati	Ohio
United States	Tampa Bay Medical Research	Clearwater	Florida
United States	Community Research & Sleep Management Institute	Crestview Hills	Kentucky
United States	Sleep Medicine Associates of Texas, P.A.	Dallas	Texas
United States	University Clinical Research Deland, LLC	Deland	Florida
United States	MD Clinical	Hallandale Beach	Florida
United States	North Star Medical Research, LLC	Middleburg Heights	Ohio
United States	Coastal Carolina Research Center	Mt. Pleasant	South Carolina
United States	Excell Research, Inc.	Oceanside	California
United States	Lynn Health Science Institute	Oklahoma City	Oklahoma
United States	Broward Research Group	Pembroke Pines	Florida
United States	University Clinical Research	Pembroke Pines	Florida
United States	HOPE Research Institute	Phoenix	Arizona
United States	Lynn Institute of Pueblo	Pueblo	Colorado
United States	Wake Research Associates	Raleigh	North Carolina
United States	Paragon Research Center	San Antonio	Texas
United States	Miami Research Associates	South Miami	Florida
United States	Genova Clinical Research	Tuscon	Arizona
United States	Sleep & Behavior Medicine Institute	Vernon Hills	Illinois
United States	Gaylord Sleep Medicine	Wallingford	Connecticut

Sponsors (1)

Lead Sponsor	Collaborator
Neurogen Corporation

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The change from baseline (Day 1) to final (Day 28) on the International Restless Legs Scale (IRLS).		Day 1, Day 14, and Day 28	No