Buprenorphine (CAM2038) in Subjects With a Recent History of Moderate to Severe Chronic Low Back Pain

Chronic Pain Clinical Trial

— CAM2038  

Official title:

A Phase III, Randomized, Double-Blind, Placebo-Controlled, Enriched-Enrollment Withdrawal, Multicenter Study to Evaluate the Efficacy and Safety of a Long-Acting Subcutaneous Injectable Depot of Buprenorphine (CAM2038) in Subjects With Moderate to Severe Chronic Low Back Pain Currently Treated With Daily Opioids

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02946073
• Other study ID #: HS-16-555
• Status: Completed
• Phase: Phase 3
• Start date: September 2016
• Est. completion date: February 2019

Study information

• Verified date: January 2021
• Source: Braeburn Pharmaceuticals
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a Phase III, placebo-controlled, multicenter study with an enriched-enrollment withdrawal (EEW) design to evaluate the efficacy and safety of CAM2038 in opioid-experienced subjects with moderate to severe CLBP that requires continuous, around-the-clock (ATC) opioid treatment ≥ 40 mg morphine equivalent dose (MED). The study includes 5 phases: A Screening Phase (up to 2 weeks), a Transition Phase (up to 2 weeks), an Open-Label Titration Phase (up to 10 weeks), a Double-Blind Treatment Phase including a Final Study Visit (12 weeks), and a Follow-up Phase (4 weeks). The overall duration of participation in the core phase of the study (randomized Double-Blind Phase) is up to 30 weeks, from the Screening Phase through the Follow-up Phase. Subjects who complete the Double-Blind Treatment Study Phase will be offered an opportunity to continue treatment in an open label safety extension for up to 60 weeks. Additional subjects may be recruited to open label safety extension to meet the goal of 100 subjects with 60 weeks of treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1053
• Est. completion date: February 2019
• Est. primary completion date: May 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Written informed consent provided prior to the conduct of any study-related procedures.

2. Male or non-pregnant, non-lactating female subject, greater than or equal to 18 years old.

3. Body mass index (BMI) between 18 and 38 kg/m2, inclusive.

4. Treated with daily opioids for moderate to severe CLBP for a minimum of 3 months prior to Screening.

5. On a stable dose of =40 mg/day of oral morphine or MED during the 14 days prior to Screening.

6. Systolic blood pressure =100 mmHg and diastolic blood pressure =60 mmHg.

7. Female subject of childbearing potential who is willing to use a reliable method of contraception during the entire study (Screening Visit to final Follow-up). To be considered not of childbearing potential, female subjects must be surgically sterile (hysterectomy or bilateral oophorectomy, or bilateral tubal ligation with surgery at least 6 weeks before Screening).

8. Male subject who is willing to use reliable contraception

9. Willing and able to comply with all study procedures and requirements.

Exclusion Criteria:

1. Positive for hepatitis B surface antigen, hepatitis C viral RNA, or antibodies to human immunodeficiency virus (HIV).

2. Clinically significant symptoms, medical conditions, or other circumstances which, in the opinion of the investigator, would preclude compliance with the protocol, adequate cooperation in the study, or obtaining informed consent, or may prevent the subject

from safely participating in the study, including the following:

1. Severe respiratory insufficiency, respiratory depression, airway obstruction, gastrointestinal motility disorders, biliary tract disease, severe hepatic insufficiency, or planned surgery.

2. Bipolar disorder

3. Current diagnosis of Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition-defined moderate to severe substance use disorder (including alcohol), other than caffeine or nicotine.

4. Female subject planning to become pregnant during the study.

5. Surgical procedure(s) for CLBP within 6 months prior to Screening.

6. Concomitant disease(s) that could prolong the QTcF interval, such as autonomic neuropathy (caused by diabetes or Parkinson's disease), HIV, cirrhosis, Long QT Syndrome, or family history of Long QT Syndrome.

7. QTcF >450 ms for males and >470 ms for females, or clinically significant electrocardiogram (ECG) abnormality at Screening, at the investigator's discretion.

8. Currently taking medications that have the potential to prolong the QTcF interval or may require such medications during the course of the study (Appendix 1) and has clinically significant abnormalities on screening ECG readings, as determined by the investigator.

9. A nerve or plexus block, including epidural steroid injections or facet blocks, within 1 month prior to Screening or botulinum toxin injection in the lower back region within 3 months of Screening.

10. History of chemotherapy or confirmed malignancy (except basal cell carcinoma) within the past 2 years.

11. Any other acute or chronic pain condition that could interfere with the subject's ability to report their CLBP accurately and consistently and/or interfere with the study staff's ability to assess the subjects CLBP.

12. An active or pending workman's compensation, insurance claim, or litigation related to back pain (i.e., primary claim is back pain).

13. Clinically significant history, in the opinion of the investigator, of suicidal ideation or current evidence that the subject is actively suicidal.

14. Clinically significant history of major depressive disorder that is poorly controlled with medication, per investigator judgment.

15. Hypersensitivity or allergy to BPN, other opioids, or excipients of CAM2038.

16. Hypersensitivity or allergy to acetaminophen.

17. Use of strong inhibitors or inducers of cytochrome P450 3A4 (CYP3A4), such as some azole antifungals (e.g., ketoconazole), macrolide antibiotics (e.g., clarithromycin), or protease inhibitors (e.g., ritonavir, indinavir, and saquinavir) within the 30 days prior to Screening,

18. Use or planned use of natural supplements that can affect CYP3A4, such as St. John's Wort, throughout the study.

19. Has a major bleeding disorder, such as hemophilia, or treated with high levels of anticoagulants per the investigator's discretion.

20. Current or confirmed past diagnosis of Sphincter of Oddi dysfunction.

21. Has a significant hepatic disease, as indicated by Screening clinical laboratory assessment results (aspartate aminotransferase, alanine aminotransferase, or lactate dehydrogenase values =3 × the upper limit of normal [ULN]) or has a creatinine value =1.5 × ULN).

22. Is an employee of the investigator or the trial site, with direct involvement in the proposed trial or other studies under the direction of the investigator or trial site or is a family member of the investigator or of an employee of the investigator.

23. Has any pending legal action that could prohibit participation or compliance in the study.

Criteria for Entry into the Titration Phase:

1. After at least a 12-hour washout from the last IR morphine dose, subject must have a COWS =5 and an API pain score over the past 24 hours =5 in order to receive a test dose of Buprenex.

2. Passed all baseline criteria, including a normal QTcF, had no change in QTcF >30 ms at 1 hour after the test dose with Buprenex, and had a COWS score <5 after the test dose with Buprenex.

Note:

• Subjects on BPN at Screening are required to participate in the down titration and will undergo a washout period prior to the test dose and first on-study treatment. Subjects entering the study on BPN will not transition to IR Morphine, but will refrain from taking their BPN for 12 -24 hours prior to the test dose to achieve the desired washout period.
• Subjects on BPN at Screening are still required to follow the same Day 1 procedures (e.g., confirmation of pain scores, COWS assessment and Buprenex test dose) as non-BPN subjects.

Criteria for Randomization into the Double-Blind Phase:

1. Been on a stable dose of CAM2038 q1w for at least 2 consecutive weeks.

2. CAM2038 titrated to a dose that provides analgesia (i.e., 7-day API score of =4 and at least 2 points below the value at the start of Titration Phase) and is well tolerated for 7 days before randomization.

3. Requires no more than an average of one hydrocodone/acetaminophen 5 mg/325 mg/day during the last 7 days prior to randomization.

4. Demonstrated study medication (CAM2038) compliance =80% during the previous 14 days.

5. Demonstrated daily compliance with pain intensity scoring for =11 of the previous 14 days, including the last 3 days prior to randomization. Inclusion Criteria for Open Label Extension For Subjects Continuing from The Randomized Double-Blind Phase.

Subjects must have:

1. Completed Double Blind Phase of the study

2. Signed Informed Consent for Safety Extension Subjects completing the double-blind phase will be enrolled directly into the open label extension at their respective dose level of CAM2038. They will not be required to participate in a Buprenex treatment test dosing or participate in a titration phase. For De Novo Subjects (New Subjects Recruited Directly into The Open Label Extension) Subjects who are not participating in the Double-Blind Phase of the Study must meet all of

the following inclusion criteria in order to be eligible for participation in the study:

1. Written informed consent provided prior to the conduct of any study-related procedures.

2. Male or non-pregnant and non-lactating female subject, greater than or equal to 18 years old.

3. BMI between 18 and 38 kg/m2, inclusive.

4. Treated with daily opioids for moderate to severe chronic pain disorder such as CLBP or osteoarthritis for a minimum of 3 months prior to Screening.

5. On a stable dose of >40 mg/day of oral morphine or MED during the 14 days prior to Screening.

6. Systolic blood pressure =100 mmHg and diastolic blood pressure =60 mmHg.

7. Female subject of childbearing potential who is willing to use a reliable method of contraception during the entire study (Screening Visit to final Follow-up). To be considered not of childbearing potential, female subjects must be surgically sterile (hysterectomy or bilateral oophorectomy, or bilateral tubal ligation with surgery at least 6 weeks before Screening).

8. Male subject who is willing to use reliable contraception

9. Willing and able to comply with all study procedures and requirements. Exclusion Criteria for Subjects Continuing from The Randomized Double-Blind Phase

1. Clinically significant symptoms, medical conditions, or other circumstances which, in the opinion of the investigator, would preclude compliance with the protocol, adequate cooperation in the study, or obtaining informed consent, or may prevent the subject from safely participating in the study. Exclusion Criteria for De Novo Subjects only: Same exclusion criteria as for subjects participating in the Randomized Double-Blind Treatment Phase.

Criteria for Entry into the Titration Phase (for De novo subjects):

1. After at least a 12-hour washout from the last IR morphine dose, subject should have a COWS =5 and an API pain score over the past 24 hours =5 in order to receive a test dose of Buprenex.

2. Passed all baseline criteria, including a normal QTcF, had no change in QTcF >30 ms at 1 hour after the test dose with Buprenex, and had a COWS score <5 after the test dose with Buprenex.

Note:

• Subjects on BPN at Screening are required to participate in the down titration and will undergo a washout period prior to the test dose and first on-study treatment. Subjects entering the study on BPN will not transition to IR Morphine, but will refrain from taking their BPN for 12 -24 hours prior to the test dose to achieve the desired washout period.
• However, subjects on BPN at Screening are still required to follow the same Day 1 procedures (e.g., confirmation of pain scores, COWS assessment and Buprenex test dose) as non-BPN subjects.

Criteria for Enrolment into the Open Label Treatment Phase (for de Novo subjects):

1. Been on a stable dose of CAM2038 q1w for at least 2 consecutive weeks.

2. CAM2038 titrated to a dose that provides analgesia (i.e., 7-day API score of =4 and at least 2 points below the value at the start of Titration Phase) and is well tolerated for 7 days before randomization.

3. Requires no more than an average of one hydrocodone/acetaminophen 5 mg/325 mg/day during the last 7 days prior to randomization

Related Conditions & MeSH terms

• Back Pain
• Chronic Lower Back Pain
• Chronic Pain
• Low Back Pain

Intervention

Drug:
• buprenorphine

Other:
• Placebo

Locations

Country	Name	City	State
United States	Hassman Research Institute	Berlin	New Jersey
United States	Parkway Medical Center	Birmingham	Alabama
United States	Millennium Pain Center	Bloomington	Illinois
United States	River Birch Research Alliance LLC	Blue Ridge	Georgia
United States	Injury Care Research, LLC	Boise	Idaho
United States	Tampa Pain Relief Center-Brandon	Brandon	Florida
United States	Coastal Carolina Research Center	Charleston	South Carolina
United States	Medical Research South, LLC	Charleston	South Carolina
United States	Aventiv Research, Inc.	Columbus	Ohio
United States	Frost Medical Group, LLC	Conshohocken	Pennsylvania
United States	FutureSearch Trials of Dallas, LP	Dallas	Texas
United States	Renaissance Clinical Research and Hypertension Clinic	Dallas	Texas
United States	Dayton Outpatient Center (DOC) Clinical Research	Dayton	Ohio
United States	Providence Health Partners-Center for Clinical Research	Dayton	Ohio
United States	International Research Partners	Doral	Florida
United States	The SMART Clinic/Physicians Research Options LLC	Draper	Utah
United States	Otrimed	Edgewood	Kentucky
United States	Medisphere Medical Research Center	Evansville	Indiana
United States	Rapha Institute for Clinical Research	Fayetteville	North Carolina
United States	Amicis Trials	Festus	Missouri
United States	MD Studies, Inc.	Fountain Valley	California
United States	Neuro-Pain Medical Center	Fresno	California
United States	Clinical Investigation Specialists, Inc.-Gurnee	Gurnee	Illinois
United States	Boyett Health Services Inc	Hamilton	Alabama
United States	OnSite Clinical Solutions, LLC-Hickory	Hickory	North Carolina
United States	Pioneer Research Solutions Inc.	Houston	Texas
United States	Research Concepts GP, LLC-Houstion	Houston	Texas
United States	Dr. Vijapura and Associates	Jacksonville	Florida
United States	Florida Institute of Medical Research	Jacksonville	Florida
United States	Columbus Regional Research Institute	Knoxville	Georgia
United States	New Phase Research & Development	Knoxville	Tennessee
United States	Alliance Research Centers	Laguna Hills	California
United States	Clinical Trials Research	Lincoln	California
United States	Lake Howell Health Center	Maitland	Florida
United States	Drug Studies America	Marietta	Georgia
United States	Non-Surgical Orthopedics, P.C.	Marietta	Georgia
United States	Suburban Research Associates	Media	Pennsylvania
United States	Ocean Blue Medical Research Center, Inc.	Miami Springs	Florida
United States	Catalina Research Institute, LLC	Montclair	California
United States	EPIC Medical Research	Murray	Utah
United States	MedEx Healthcare Research, Inc-NY	New York	New York
United States	New York Clinical Trials, Inc	New York	New York
United States	Scientific Clinical Research, Inc.	North Miami	Florida
United States	Medical Research Internationl	Oklahoma City	Oklahoma
United States	SP Research, PLLC	Oklahoma City	Oklahoma
United States	Aspen Clinical Research	Orem	Utah
United States	International Clinical Research Institute Inc.	Overland Park	Kansas
United States	Arizona Research Center	Phoenix	Arizona
United States	Elite Clinical Studies	Phoenix	Arizona
United States	Noesis Pharma	Phoenix	Arizona
United States	Phoenix Clinical	Phoenix	Arizona
United States	The Pain Relief Center	Plano	Texas
United States	Gold Coast Research, LLC	Plantation	Florida
United States	Phoenix Medical Research	Prairie Village	Kansas
United States	Mid Columbia Research	Richland	Washington
United States	Allied Clinical Research, LLC	Sacramento	California
United States	FMPM Research	Saint Petersburg	Florida
United States	Care Practice	San Francisco	California
United States	Syrentis Clinical Research	Santa Ana	California
United States	River Cities Clinical Research Center	Shreveport	Louisiana
United States	Clinical Research of West Florida-Tampa	Tampa	Florida
United States	Tampa Pain Relief Centers-Hillsborough	Tampa	Florida
United States	Universal Pain Management Group	Valencia	California
United States	National Centers for Pain Management and Research	Vestavia Hills	Alabama
United States	Boston Paincare	Waltham	Massachusetts
United States	MedVadis Research Corporation	Watertown	Massachusetts
United States	Palm Beach Research Center	West Palm Beach	Florida
United States	Upstate Clinical Research Associates	Williamsville	New York
United States	Center for Clinical Research, LLC-Winston-Salem	Winston-Salem	North Carolina

Sponsors (3)

Lead Sponsor	Collaborator
Braeburn Pharmaceuticals	Camurus AB, Medpace, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change From Baseline in Weekly Average of (Daily) Average Pain Intensity (WAAPI) and the Primary Timepoint Will be Week 12 of the Double-Blind Phase.	Change from baseline in Weekly Average of (Daily) Average Pain Intensity (WAAPI) and the primary timepoint will be Week 12 of the Double-Blind Phase based on the 11-Point numerical rating scale with 0 being no pain and 10 being the worst pain.	12 weeks- from randomization baseline to 12 weeks after randomization
Primary	Change From Baseline in Weekly Average of (Daily) Average Pain Intensity (WAAPI) of the Open Label Phase.	Change from baseline in Weekly Average of (Daily) Average Pain Intensity (WAAPI) of the Open Label Phase based on the 11-Point numerical rating scale with 10 being the worst pain. Baseline is defined as the last week prior to Visit 14 (Randomization Visit) for the roll-over subjects and the last week prior to Visit 14 (Enrollment Visit) for de novo subjects.	48 weeks -From baseline to 48 weeks after baseline (Baseline is defined as the last week prior to Visit 14 (Randomization Visit) for the roll-over subjects and the last week prior to Visit 14 (Enrollment Visit) for de novo subjects).
Secondary	Change From Baseline in the Weekly Average of (Daily) Worst Pain Intensity Scores at Week 12 of the Double-Blind Phase Based on 11-Point Numerical Rating Scale With 10 Being the Worst Pain.	Change from baseline in Weekly Average of (Daily) Worst Pain Intensity (WAWPI) and the primary timepoint will be Week 12 of the Double-Blind Phase based on the 11-Point numerical rating scale with 0 being no pain and 10 being the worst pain.	12 weeks- from randomization baseline to 12 weeks after randomization
Secondary	Number of Subjects With a 30% and 50% Reduction in WAAPI From Baseline to Week 12 of the Double-Blind Phase.	Number of Responders With a 30% and 50% Reduction in WAAPI from the Open-Label Titration Period Baseline to Week 12 of the Double-Blind Treatment Period (mITT Population)	12 weeks- from randomization baseline to 12 weeks after randomization
Secondary	Summary of Rescue Medication Usage- Double-Blind Phase.	Rescue medication usage (number of days used) during the Double-Blind Phase.	12 weeks- from randomization baseline to 12 weeks after randomization
Secondary	Change From Open Label Titration Baseline to Week 12 of the Double-Blind Phase in EuroQol Group 5-dimension 5-level Self-report Questionnaire Score.	Change from Open Label Titration baseline to Week 12 of the Double-Blind Phase in EuroQol Group 5-dimension 5-level self-report questionnaire score. The EuroQoL Group 5-Dimension 5-Level Self-Report Questionnaire (EQ-5D-5L) descriptive system is a generic, multidimensional, health-related, quality-of-life instrument. The profile allows subjects to rate their health state in 5 health domains: mobility, self-care, usual activities, pain/discomfort, and mood, using a 5-level scale. These combinations of attributes were converted into a weighted health-state index score, according to the US population-based algorithm, with higher scores indicating better quality of life. The score ranges from 0-100 with 0 as the worst health and 100 as the best health.	12 weeks- from randomization baseline to 12 weeks after randomization
Secondary	Change From Baseline to Week 12 of the Double-Blind Phase in Work Productivity and Activity Impairment Score	Change from baseline to Week 12 of the Double-Blind Phase in Work Productivity and Activity Impairment score. The Work Productivity and Activity Impairment (WPAI) is a self-administered instrument used to measure the effect of general health and symptom severity on work productivity and regular activities, and yields 4 types of scores (higher scores indicate greater impairment): Absenteeism (work time missed),Presenteeism (impairment at work/reduced on-the-job effectiveness), Work Productivity Loss (overall work impairment/absenteeism plus presenteeism),and Activity Impairment. Scores range from 0-100 for each of the four types with higher scores indicating greater impairment.	23 weeks- from baseline to 12 weeks after randomization
Secondary	Number of Subjects Discontinued Due to Loss of Efficacy	Number of Subjects Discontinued due to loss of efficacy, defined as discontinuation of study drug for lack of efficacy.	12 weeks- from randomization baseline to 12 weeks after randomization
Secondary	Change From Baseline to Week 12 of the Double-Blind Phase in Patient Global Impression of Improvement (PGI-I) Scale	Change from baseline to Week 12 of the Double-Blind Phase in Patient global Impression of Improvement (PGI-I) Scale. PGI-I)Scale is a single question 7-point likert scale that required the subject to assess how much his/her pain had improved or worsened relative to the start of the study at the beginning of the intervention . Ratings were: 1, much worse; 2, worse; 3, a little worse; 4, no change; 5, a little better; 6, better; or 7, much better	12 weeks- from baseline (randomization) to 12 weeks after randomization
Secondary	Change From Baseline in Weekly Average of (Daily) Worst Pain Intensity (WAWPI) of the Open Label Phase.	Change from baseline in Weekly Average of (Daily) Worst Pain Intensity (WAWPI) and the primary timepoint will be Week 52 of the Open Label Phase based on the 11-Point numerical rating scale with 10 being the worst pain. Baseline is defined as the last week prior to Visit 14 (Randomization Visit) for the roll-over subjects and the last week prior to Visit 14 (Enrollment Visit) for de novo subjects.	48 weeks -From baseline to 48 weeks after baseline (Baseline is defined as the last week prior to Visit 14 (Randomization Visit) for the roll-over subjects and the last week prior to Visit 14 (Enrollment Visit) for de novo subjects).
Secondary	Subject Discontinued Due to Loss of Efficacy, Defined as Discontinuation of Study Drug for Lack of Efficacy.	Subject Discontinued Due to Loss of Efficacy, Defined as Discontinuation of Study Drug for Lack of Efficacy Open Label Phase.	48 weeks -From baseline to 48 weeks after baseline (Baseline is defined as the last week prior to Visit 14 (Randomization Visit) for the roll-over subjects and the last week prior to Visit 14 (Enrollment Visit) for de novo subjects).
Secondary	Summary of Rescue Medication Usage-Open Label Phase	Rescue medication usage (number of days used) during the Open Label Phase.	48 weeks -From baseline to 48 weeks after baseline (Baseline is defined as the last week prior to Visit 14 (Randomization Visit) for the roll-over subjects and the last week prior to Visit 14 (Enrollment Visit) for de novo subjects).
Secondary	Summary of Change From Baseline in EuroQoL Group EQ-5D-5L Scores Over Time-Open Label Phase	Change from Open Label Titration baseline in EuroQol Group 5-dimension 5-level self-report questionnaire score in the Open Label Phase. The EuroQoL Group 5-Dimension 5-Level Self-Report Questionnaire (EQ-5D-5L) descriptive system is a generic, multidimensional, health-related, quality-of-life instrument. The profile allows subjects to rate their health state in 5 health domains: mobility, self-care, usual activities, pain/discomfort, and mood, using a 5-level scale. These combinations of attributes were converted into a weighted health-state index score, according to the US population-based algorithm, with higher scores indicating better quality of life. The score ranges from 0-100 with 0 as the worst health and 100 as the best health.	48 weeks -From baseline to 48 weeks after baseline (Baseline is defined as the last week prior to Visit 14 (Randomization Visit) for the roll-over subjects and the last week prior to Visit 14 (Enrollment Visit) for de novo subjects).
Secondary	Summary of Change From Baseline in Clinical Global Impression of Improvement (CGI-I) Scale-Open Label	Summary of Change from Baseline in Clinical Global Impression of Improvement (CGI-I) scale. The Clinician Global Impression of Improvement (CGI-I) Scale is a 7-point scale that required the clinician to assess how much the subject's Pain had improved or worsened relative to the start of the study. Assessments were rated as: 1, very much improved; 2, much improved; 3, minimally improved; 4, no change; 5, minimally worse; 6, much worse; or 7, very much worse	48 weeks -From baseline to 48 weeks after baseline (Baseline is defined as the last week prior to Visit 14 (Randomization Visit) for the roll-over subjects and the last week prior to Visit 14 (Enrollment Visit) for de novo subjects).
Secondary	Summary of Change From Baseline in Patient Global Impression of Improvement (PGI-I) Scale	Change from baseline in the Open Label Phase in Patient global Impression of Improvement (PGI-I) Scale. PGI-I Scale is a single question 7-point likert scale that required the subject to assess how much his/her pain had improved or worsened relative to the start of the study. Ratings were: 1, much worse; 2, worse; 3, a little worse; 4, no change; 5, a little better; 6, better; or 7, much better	48 weeks -From baseline to 48 weeks after baseline (Baseline is defined as the last week prior to Visit 14 (Randomization Visit) for the roll-over subjects and the last week prior to Visit 14 (Enrollment Visit) for de novo subjects).
Secondary	Summary of Change From Baseline in Work Productivity and Activity Impairment Questionnaire (WPAI) Open Label Phase	Change from baseline in the Open Label Phase in Work Productivity and Activity Impairment score with a range of 0-100 for 4 types of scores with higher scores indicating greater impairment. The Work Productivity and Activity Impairment (WPAI) is a self-administered instrument used to measure the effect of general health and symptom severity on work productivity and regular activities, and yields 4 types of scores (higher scores indicate greater impairment): Absenteeism (work time missed),Presenteeism (impairment at work/reduced on-the-job effectiveness), Work Productivity Loss (overall work impairment/absenteeism plus presenteeism),and Activity Impairment. Scores range from 0-100 for each of the four types with higher scores indicating greater impairment.	48 weeks -From baseline to 48 weeks after baseline (Baseline is defined as the last week prior to Visit 14 (Randomization Visit) for the roll-over subjects and the last week prior to Visit 14 (Enrollment Visit) for de novo subjects).
Secondary	Number of Subjects Discontinued Due to Loss of Efficacy	Number of Subjects Discontinued due to loss of efficacy, defined as discontinuation of study drug for lack of efficacy.	48 weeks -From baseline to 48 weeks after baseline (Baseline is defined as the last week prior to Visit 14 (Randomization Visit) for the roll-over subjects and the last week prior to Visit 14 (Enrollment Visit) for de novo subjects).