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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00744471
Other study ID # A4091014
Secondary ID P3 OA HIP
Status Completed
Phase Phase 3
First received
Last updated
Start date November 17, 2008
Est. completion date August 13, 2010

Study information

Verified date February 2021
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to test the efficacy and safety of 3 doses of tanezumab in osteoarthritis of the hip in patients


Recruitment information / eligibility

Status Completed
Enrollment 627
Est. completion date August 13, 2010
Est. primary completion date March 15, 2010
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria: - Osteoarthritis of the hip according to ACR criteria with Kellgren-Lawrence x-ray grade of 2 - Unwilling or unable to take non-opiate pain medications, for whom non-opiate pain medications have not provided adequate pain relief or are candidates for Hip injections, arthroplasty or replacement surgery - Pain level and function levels as required by the protocol at Screening and Baseline - Willing to discontinue pain medications (acetaminophen will be permitted up to a certain level) before and during the study - Must agree to the contraceptive requirements of the protocol if applicable - Must agree to the treatment plan, scheduled visits, and procedures of the protocol Exclusion Criteria: - Pregnancy - BMI greater than 39 - Other severe pain, significant cardiac, neurological or psychological conditions, or above the protocol limits for laboratory and blood pressure results

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
tanezumab
Tanezumab 10 mg IV every 8 weeks
tanezumab
Tanezumab 5mg IV every 8 weeks
tanezumab
Tanezumab 2.5 mg IV every 8 weeks.
Placebo
Placebo to match tanezumab IV every 8 weeks

Locations

Country Name City State
United States Albuquerque Clinical Trials, Inc. Albuquerque New Mexico
United States New Mexico Clinical Research & Osteoporosis Center, Incorporated Albuquerque New Mexico
United States Ann Arbor Clinical Research Ann Arbor Michigan
United States Arthritis and Rheumatology of Georgia Atlanta Georgia
United States Laureate Clinical Reseach Group Atlanta Georgia
United States Maine Research Associates Auburn Maine
United States Capital Medical Clinic Austin Texas
United States Walter Chase MD Austin Texas
United States EPIC Imaging West Beaverton Oregon
United States Comprehensive Clinical Research Berlin New Jersey
United States East Penn Rheumatology Associates, PC Bethlehem Pennsylvania
United States Sonora Clinical Research Boise Idaho
United States Arthritis and Osteoporosis Center of Brooklyn Heights Brooklyn New York
United States Providence Clinical Research Burbank California
United States Carolina Bone & Joint, P.A. Charlotte North Carolina
United States Charlottesville Medical Research Charlottesville Virginia
United States Consultants for Clinical Research/Ohio GI and Liver Institute Cincinnati Ohio
United States Hilltop Physicians Inc, Hightop Medical Research Center Cincinnati Ohio
United States Innovative Research of West Florida, Inc. Clearwater Florida
United States Tampa Bay Medical Research Inc Clearwater Florida
United States Radiant Research Dallas Texas
United States Clinical Research Center of Connecticut Danbury Connecticut
United States Avail Clinical Research DeLand Florida
United States Avail Clinical Research, LLC DeLand Florida
United States Arthritis Associates of South Florida Delray Beach Florida
United States Delray Research Associates Delray Beach Florida
United States Brandywine Clinical Research Downingtown Pennsylvania
United States Altoona Center for Clinical Research Duncansville Pennsylvania
United States MAPS Applied Research Center Edina Minnesota
United States Medical Advanced Pain Specialists Edina Minnesota
United States Arthritis Medical Clinic of North County, Inc. Escondido California
United States American Health Network of IN, LLC Fishers Indiana
United States Early Family Practice Center Fort Valley Georgia
United States The Arthritis and Osteoporosis Center of Maryland Frederick Maryland
United States Northeast Georgia Diagnostic Clinic Gainesville Georgia
United States Pharmquest Greensboro North Carolina
United States St. Joseph's Mercy Clinic Hot Springs Arkansas
United States Pioneer Research Solutions Houston Texas
United States Pioneet Research Solutions, Inc Houston Texas
United States Rheumatic Disease Clinical Research Center Houston Texas
United States Talbert Medical Group Huntington Beach California
United States Westside Center for Clinical Research Jacksonville Florida
United States Appalachian Medical Research Inc. Johnson City Tennessee
United States Rheumatology, PC Kalamazoo Michigan
United States Holston Medical Group Kingsport Tennessee
United States Clinical Research Consortium Las Vegas Nevada
United States Mirkil Medical Las Vegas Nevada
United States Office of Dr. Danka Michaels, MD Las Vegas Nevada
United States Adult Medicine Specialists Longwood Florida
United States Genesis Research International Longwood Florida
United States Mansfield Health Center Mansfield Massachusetts
United States North Georgia Clinical Research Marietta Georgia
United States International Research Associates, LLC Miami Florida
United States Southwest Rheumatology and Research Group, LLC Middleburg Heights Ohio
United States Horizon Research Group Mobile Alabama
United States Arthritis and Diabetes Clinic Monroe Louisiana
United States The Medical Research Network, LLC New York New York
United States Javed Rheumatology Associates, Inc. Newark Delaware
United States Health Research Institute Oklahoma City Oklahoma
United States Quality Clinical Research, Inc. Omaha Nebraska
United States Compass Research, LLC Orlando Florida
United States The Arthritis Center Palm Harbor Florida
United States Arizona Arthritis & Rheumatology Associates, PC Paradise Valley Arizona
United States Pivotal Research Center Peoria Arizona
United States Arizona Arthritis & Rheumatology Associates, PC Phoenix Arizona
United States Arizona Research Center, Inc. Phoenix Arizona
United States Clinical Research Advantage, Inc. /Stonecreek Medical Associates, PC Phoenix Arizona
United States Advent Clinical Research Centers Pinellas Park Florida
United States Prem C. Chatpar, MD, LLC Plainview New York
United States Clinical Investigations of Texas, LLC Plano Texas
United States Accord Clinical Research, LLC Port Orange Florida
United States Avivoclin Clinical Services Port Orange Florida
United States Covance CRU, Inc. Portland Oregon
United States EPIC Imaging East Portland Oregon
United States Health Concepts Rapid City South Dakota
United States Office of Dr. Andrew Porges Roslyn New York
United States Mercy Health Research Saint Louis Missouri
United States All Florida Orthopaedic Associates Saint Petersburg Florida
United States Optimum Clinical Research Salt Lake City Utah
United States Diagnostics Research Group San Antonio Texas
United States Radiant Research San Antonio NE San Antonio Texas
United States Texas Arthritis Research Center, PA San Antonio Texas
United States Trinity Clinical Trials Santa Ana California
United States Sushma V. Gorrela, MD Spring Texas
United States The Arthritis Center Springfield Illinois
United States Stamford Therapeutics Consortium Stamford Connecticut
United States Internal Medicine Northwest, Frank S Baker Center Tacoma Washington
United States Quality of Life Medical & Research Center, LLC Tucson Arizona
United States Quality of Life Medical and Research Center Tucson Arizona
United States Tucson Orthopaedic Institute Tucson Arizona
United States Northwest Indiana Center for Clinical Research Valparaiso Indiana
United States Palm Beach Research Center West Palm Beach Florida
United States The Center for Rheumatology and Bone Research Wheaton Maryland
United States Piedmont Medical Research Associates Winston-Salem North Carolina
United States North Georgia Clinical Research Woodstock Georgia
United States North Georgia Internal medicine Woodstock Georgia
United States Clinical Pharmacology Study Group Worcester Massachusetts
United States Clinical Trials Northwest Yakima Washington
United States Pharmacotherapy Research Associates,Inc Zanesville Ohio

Sponsors (1)

Lead Sponsor Collaborator
Pfizer

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change From Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Pain Subscale Score at Week 16: Baseline Observation Carried Forward (BOCF) WOMAC: Self-administered, disease-specific questionnaire which assesses clinically important, participant-relevant symptoms for pain, stiffness and physical function in participants with osteoarthritis. WOMAC pain subscale is a 5-item questionnaire used to assess the amount of pain experienced due to osteoarthritis in hip joint during past 48 hours. It was calculated as mean of the scores from 5 individual questions scored on a numerical rating scale (NRS) of 0 (no pain) to 10 (worst possible pain), where higher scores indicated higher pain. Total score range for WOMAC pain subscale score is 0 (no pain) to 10 (worst possible pain), where higher scores indicated higher pain. Baseline (Day 1), Week 16
Primary Change From Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Physical Function Subscale Score at Week 16: Baseline Observation Carried Forward (BOCF) WOMAC: Self-administered, disease-specific questionnaire which assesses clinically important, participant-relevant symptoms for pain, stiffness and physical function in participants with osteoarthritis. WOMAC physical function subscale is a 17-item questionnaire used to assess the degree of difficulty experienced due to osteoarthritis in hip joint during past 48 hours. It is calculated as mean of the scores from 17 individual questions scored on a NRS of 0 to 10, where higher scores indicate worse function. Total score range for WOMAC physical function subscale score is 0 to 10, where higher scores indicate worse function. Physical function refers to participant's ability to move around and perform usual activities of daily living. Baseline, Week 16
Primary Change From Baseline in Patient Global Assessment (PGA) of Osteoarthritis at Week 16: Baseline Observation Carried Forward (BOCF) Participants answered: "Considering all the ways your osteoarthritis in your hip joint affects you, how are you doing today?", participants responded by using a 5-point scale where 1 = very good (no symptom and limitation of normal activities) and 5 = very poor (very severe symptoms and inability to carry out normal activities), where lower scores indicates better condition. Baseline, Week 16
Secondary Change From Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) in Pain Subscale Score at Week 2, 4, 8, 12 and 24: Baseline Observation Carried Forward (BOCF) WOMAC: Self-administered, disease-specific questionnaire which assesses clinically important, participant-relevant symptoms for pain, stiffness and physical function in participants with osteoarthritis. WOMAC pain subscale is a 5-item questionnaire used to assess the amount of pain experienced due to osteoarthritis in hip joint during past 48 hours. It was calculated as mean of the scores from 5 individual questions scored on a numerical rating scale (NRS) of 0 (no pain) to 10 (worst possible pain), where higher scores indicated higher pain. Total score range for WOMAC pain subscale score is 0 (no pain) to 10 (worst possible pain), where higher scores indicated higher pain. Baseline, Week 2, 4, 8, 12, 24
Secondary Change From Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) in Pain Subscale Score at Week 2, 4, 8, 12,16 and 24: Last Observation Carried Forward (LOCF) WOMAC: Self-administered, disease-specific questionnaire which assesses clinically important, participant-relevant symptoms for pain, stiffness and physical function in participants with osteoarthritis. WOMAC pain subscale is a 5-item questionnaire used to assess the amount of pain experienced due to osteoarthritis in hip joint during past 48 hours. It was calculated as mean of the scores from 5 individual questions scored on a numerical rating scale (NRS) of 0 (no pain) to 10 (worst possible pain), where higher scores indicated higher pain. Total score range for WOMAC pain subscale score is 0 (no pain) to 10 (worst possible pain), where higher scores indicated higher pain. Baseline, Week 2, 4, 8, 12, 16, 24
Secondary Change From Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Physical Subscale Score at Week 2, 4, 8, 12 and 24: Baseline Observation Carried Forward (BOCF) WOMAC: Self-administered, disease-specific questionnaire which assesses clinically important, participant-relevant symptoms for pain, stiffness and physical function in participants with osteoarthritis. WOMAC pain subscale is a 5-item questionnaire used to assess the amount of pain experienced due to osteoarthritis in hip joint during past 48 hours. It was calculated as mean of the scores from 5 individual questions scored on a numerical rating scale (NRS) of 0 (no pain) to 10 (worst possible pain), where higher scores indicated higher pain. Total score range for WOMAC pain subscale score is 0 (no pain) to 10 (worst possible pain), where higher scores indicated higher pain. Physical function refers to participant's ability to move around and perform usual activities of daily living. Baseline, Week 2, 4, 8, 12, 24
Secondary Change From Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Physical Subscale at Week 2, 4, 8, 12, 16 and 24: Last Observation Carried Forward (LOCF) WOMAC: Self-administered, disease-specific questionnaire which assesses clinically important, participant-relevant symptoms for pain, stiffness and physical function in participants with osteoarthritis. WOMAC physical function subscale is a 17-item questionnaire used to assess the degree of difficulty experienced due to osteoarthritis in hip joint during past 48 hours. It is calculated as mean of the scores from 17 individual questions scored on a NRS of 0 to 10, where higher scores indicate worse function. Total score range for WOMAC physical function subscale score is 0 to 10, where higher scores indicate worse function. Physical function refers to participant's ability to move around and perform usual activities of daily living. Baseline, Week 2, 4, 8, 12, 16, 24
Secondary Change From Baseline in Patient Global Assessment (PGA) of Osteoarthritis at Week 2, 4, 8, 12 and 24: Baseline Observation Carried Forward (BOCF) Participants answered: "Considering all the ways your osteoarthritis in your hip joint affects you, how are you doing today?", participants responded by using a 5-point scale where 1 = very good (no symptom and limitation of normal activities) and 5 = very poor (very severe symptoms and inability to carry out normal activities), where lower scores indicates better condition. Baseline, Week 2, 4, 8, 12, 24
Secondary Change From Baseline in Patient Global Assessment (PGA) of Osteoarthritis at Week 2, 4, 8, 12, 16 and 24: Last Observation Carried Forward (LOCF) Participants answered: "Considering all the ways your osteoarthritis in your hip joint affects you, how are you doing today?", participants responded by using a 5-point scale where 1 = very good (no symptom and limitation of normal activities) and 5 = very poor (very severe symptoms and inability to carry out normal activities), where lower scores indicates better condition. Baseline, Week 2, 4, 8, 12, 16, 24
Secondary Percentage of Participants With Outcome Measures in Rheumatology-Osteoarthritis Research Society International (OMERACT-OARSI) Response: Baseline Observation Carried Forward (BOCF) A participant was considered as an OMERACT-OARSI responder if at least one of the following criteria were met: Improvement in WOMAC pain or physical function subscale from baseline to week of interest was greater than or equal to (>=) 50 percent (%)and absolute change of >=2 units from baseline at the week of interest, or at least 2 of the following 3 being true: >=20% improvement from baseline and absolute change from baseline of >=1 unit at the week of interest in 1) WOMAC pain subscale, 2) WOMAC physical function subscale, 3) PGA of osteoarthritis. Score range for PGA: 1 = very good to 5 = very poor, where higher scores=more affected). WOMAC pain, physical function subscales assess amount of pain/difficulty experienced (score: 0 [no pain] to 10 [worst possible pain], higher score=higher pain/difficulty). Week 2, 4, 8, 12, 16, 24
Secondary Percentage of Participants With Outcome Measures in Rheumatology-Osteoarthritis Research Society International (OMERACT-OARSI) Response: Last Observation Carried Forward (LOCF) A participant was considered as an OMERACT-OARSI responder if at least one of the following criteria were met: Improvement in WOMAC pain or physical function subscale from baseline to week of interest was greater than or equal to (>=) 50 percent (%)and absolute change of >=2 units from baseline at the week of interest, or at least 2 of the following 3 being true: >=20% improvement from baseline and absolute change from baseline of >=1 unit at the week of interest in 1) WOMAC pain subscale, 2) WOMAC physical function subscale, 3) PGA of osteoarthritis. Score range for PGA: 1 = very good to 5 = very poor, where higher scores=more affected). WOMAC pain, physical function subscales assess amount of pain/difficulty experienced (score: 0 [no pain] to 10 [worst possible pain], higher score=higher pain/difficulty). Week 2, 4, 8, 12 ,16, 24
Secondary Percentage of Participants With at Least 30 Percent (%), and 50 % Reduction From Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Pain Subscale Score at Week 2, 4, 8, 12, 16, 24: Baseline Observation Carried Forward WOMAC: Self-administered, disease-specific questionnaire which assesses clinically important, participant-relevant symptoms for pain, stiffness and physical function in participants with osteoarthritis. WOMAC pain subscale is a 5-item questionnaire used to assess the amount of pain experienced due to osteoarthritis in hip joint during past 48 hours. It was calculated as mean of the scores from 5 individual questions scored on a numerical rating scale (NRS) of 0 (no pain) to 10 (worst possible pain), where higher scores indicated higher pain. Total score range for WOMAC pain subscale score is 0 (no pain) to 10 (worst possible pain), where higher scores indicated higher pain. Percentage of participants with >=30% or >=50% reduction in WOMAC pain subscale score from baseline to specified weeks were reported. Baseline, Week 2, 4, 8, 12, 16, 24
Secondary Percentage of Participants With at Least 30 Percent (%), and 50% Reduction From Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Pain Subscale Score: Last Observation Carried Forward (LOCF) WOMAC: Self-administered, disease-specific questionnaire which assesses clinically important, participant-relevant symptoms for pain, stiffness and physical function in participants with osteoarthritis. WOMAC pain subscale is a 5-item questionnaire used to assess the amount of pain experienced due to osteoarthritis in hip joint during past 48 hours. It is calculated as mean of the scores from 5 individual questions scored on a NRS of 0 to 10, where higher scores indicate higher pain. Total score range for WOMAC pain subscale score is 0 to 10, where higher scores indicate higher pain. Percentage of participants with >=30% or >=50% reduction in WOMAC pain subscale score from baseline to specified weeks were reported. Baseline, Week 2, 4, 8, 12, 16, 24
Secondary Percentage of Participants With at Least 2 Points Improvement From Baseline in Patient Global Assessment (PGA) of Osteoarthritis at Week 2, 4, 8, 12 ,16 and 24: Baseline Observation Carried Forward (BOCF) Participants answered: "Considering all the ways your osteoarthritis in your knee affects you, how are you doing today?", participants responded by using a 5-point scale where 1 = very good and 5 = very poor where lower scores indicating better condition. Percentage of participants with an improvement of greater than or equal to 2 points from baseline at specified weeks were reported. Baseline, Week 2, 4, 8, 12 ,16, 24
Secondary Percentage of Participants With at Least 2 Points Improvement From Baseline in Patient Global Assessment (PGA) of Osteoarthritis at Week 2, 4, 8, 12, 16, 24: Last Observation Carried Forward (LOCF) Participants answered: "Considering all the ways your osteoarthritis in your knee affects you, how are you doing today?", participants responded by using a 5-point scale where 1 = very good and 5 = very poor where lower scores indicating better condition. Percentage of participants with an improvement of greater than or equal to 2 points from baseline at specified weeks were reported. Baseline, Week 2, 4, 8, 12, 16, 24
Secondary Percentage of Participants With Cumulative Reduction From Baseline in Western Ontario and McMaster Osteoarthritis Index (WOMAC) Pain Subscale Score at Week 16: Baseline Observation Carried Forward (BOCF) WOMAC: Self-administered, disease-specific questionnaire which assesses clinically important, participant-relevant symptoms for pain, stiffness and physical function in participants with osteoarthritis. WOMAC pain subscale is a 5-item questionnaire used to assess the amount of pain experienced due to osteoarthritis in hip joint during past 48 hours. It is calculated as mean of the scores from 5 individual questions scored on a NRS of 0 to 10, where higher scores indicate higher pain. Total score range for WOMAC pain subscale score is 0 to 10, where higher scores indicate higher pain. Participants with specified reduction (as percent) from baseline at Week 16 were reported. Baseline, Week 16
Secondary Percentage of Participants With Cumulative Reduction From Baseline in Western Ontario and McMaster Osteoarthritis Index (WOMAC) Pain Subscale Score at Week 16: Last Observation Carried Forward (LOCF) WOMAC: Self-administered, disease-specific questionnaire which assesses clinically important, participant-relevant symptoms for pain, stiffness and physical function in participants with osteoarthritis. WOMAC pain subscale is a 5-item questionnaire used to assess the amount of pain experienced due to osteoarthritis in hip joint during past 48 hours. It is calculated as mean of the scores from 5 individual questions scored on a NRS of 0 to 10, where higher scores indicate higher pain. Total score range for WOMAC pain subscale score is 0 to 10, where higher scores indicate higher pain. Participants with specified reduction (as percent) from baseline at Week 16 were reported. Baseline, Week 16
Secondary Change From Baseline in Average Daily Pain Score in the Hip Joint at Week 2, 4, 8, 12, 16 and 24: Baseline Observation Carried Forward (BOCF) Participants assessed daily average hip joint pain during the past 24 hours on an 11-point NRS ranging from 0 (no pain) to 10 (worst pain). Post baseline weekly scores were calculated as the mean of the scores over the last 7 days prior to each assessment time point. Baseline, Week 2, 4, 8, 12, 16, 24
Secondary Change From Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Stiffness Subscale Score at Week 2, 4, 8, 12, 16 and 24: Baseline Observation Carried Forward (BOCF) WOMAC: Self-administered, disease-specific questionnaire which assesses clinically important, participant-relevant symptoms for pain, stiffness and physical function in participants with osteoarthritis. WOMAC stiffness subscale is a 2-item questionnaire used to assess the amount of stiffness experienced due to osteoarthritis in hip joint during past 48 hours. It is calculated as mean of the scores from 2 individual questions each scored on numerical rating scale of 0 (minimum stiffness) to 10 (maximum stiffness), giving an overall possible mean score range of 0 (minimum stiffness) to 10 (maximum stiffness). Higher scores indicate higher stiffness. Stiffness is defined as a sensation of decreased ease in movement of hip joint. Baseline, Week 2, 4, 8, 12 ,16, 24
Secondary Change From Baseline in Western Ontario and McMaster Universities Osteoarthritis Index(WOMAC) Average Score at Week 2, 4, 8, 12,16 and 24: Baseline Observation Carried Forward (BOCF) WOMAC: Self-administered, disease-specific questionnaire which assesses clinically important, participant-relevant symptoms for pain, stiffness and physical function in participants with osteoarthritis. WOMAC: self-administered, disease-specific 24-item questionnaire which assesses clinically important, participant-relevant symptoms for pain (5 items), stiffness (2 items) and physical function (17 items) in participants with osteoarthritis of hip joint. Each item is scored on a 0 (no pain) to 10 (worst possible pain) NRS scale, where higher scores indicate higher pain/stiffness or worse function. WOMAC average score is the mean of WOMAC pain, physical function and stiffness subscale scores and ranges from 0 (no pain) to 10 (worst possible pain), where higher score indicates worse response. Baseline, Week 2, 4, 8, 12, 16, 24
Secondary Change From Baseline in Western Ontario and McMaster Universities Osteoarthritis Index(WOMAC) Pain Subscale Item (Pain When Walking on Flat Surface) Score at Week 2, 4, 8, 12, 16 and 24 : Baseline Observation Carried Forward (BOCF) WOMAC: Self-administered, disease-specific questionnaire which assesses clinically important, participant-relevant symptoms for pain, stiffness and physical function in participants with osteoarthritis. Participants answered "How much pain have you had when walking on a flat surface?". Participants responded by using a NRS of 0 to 10, where 0 = no pain and 10 =extreme pain. Higher scores indicated more pain. Baseline, Week 2, 4, 8, 12, 16, 24
Secondary Change From Baseline of Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Pain Subscale (Pain When Going up or Down Stairs) Score at Week 2, 4, 8, 12, 16 and 24: Baseline Observation Carried Forward (BOCF) WOMAC: Self-administered, disease-specific questionnaire which assesses clinically important, participant-relevant symptoms for pain, stiffness and physical function in participants with osteoarthritis. Participants answered "How much pain have you had when going up or down the stairs?". Participants responded by using a NRS of 0 to 10, where 0 = no pain and 10 = worst possible pain, where higher scores indicating higher pain. Baseline, Week 2, 4, 8, 12, 16, 24
Secondary Change From Baseline in 36-Item Short-Form Health Survey Version 2 (SF-36v2) Domain Scores at Week 12 and 24: Baseline Observation Carried Forward (BOCF) The SF-36 health survey was a self-administered questionnaire that measures each of the following 8 health domains: domain 1= general health, domain 2= physical function, domain 3= role physical, domain 4= bodily pain, domain 5= vitality, domain 6= social function, domain 7= role emotional, domain 8= mental health. Total score for each domain are scaled 0 (minimum) to 100 (maximum), where higher score indicates highest level of functioning. Baseline, Week 12, 24
Secondary Change From Baseline in 36-Item Short-Form Health Survey Version 2 (SF-36v2) Physical and Mental Component Scores at Week 12 and 24: Baseline Observation Carried Forward (BOCF) The SF-36 health survey was a self-administered questionnaire that measures each of the following 8 health domains: domain 1= general health, domain 2= physical function, domain 3= role physical, domain 4= bodily pain, domain 5= vitality, domain 6= social function, domain 7= role emotional, domain 8= mental health. Total score for each domain are scaled 0 (minimum) to 100 (maximum), where higher score indicates highest level of functioning. These 8 domains were also summarized as summary scores: mental component aggregate (MCA) and physical component aggregate (PCA). Total score range for the each summary scores =0 to 100, where higher scores represented higher level of functioning. Higher summary scores indicated a better health related quality of life. Baseline, Week 12, 24
Secondary Time to Discontinuation Due to Lack of Efficacy Median time to discontinuation due to lack of efficacy was estimated using Kaplan-Meier method. Baseline up to Week 16
Secondary Percentage of Participants Who Used Rescue Medication In case of inadequate pain relief for osteoarthritis, acetaminophen up to 4000 mg per day up to 3 days per week could be taken as rescue medication. Percentage of participants with any use of rescue medication during the particular study week were summarized. Week 2, 4, 8, 12 ,16, 24
Secondary Duration of Rescue Medication Use In case of inadequate pain relief for osteoarthritis, acetaminophen up to 4000 mg per day up to 3 days per week could be taken as rescue medication. Number of days participant used any of the rescue medication, during the specified week were summarized. Week 2, 4, 8, 12, 16, 24
Secondary Amount of Rescue Medication Taken In case of inadequate pain relief for osteoarthritis, acetaminophen up to 4000 mg per day up to 3 days per week could be taken as rescue medication. The total dosage of acetaminophen in mg used during the specified week were summarized. Week 2, 4, 8, 12, 16, 24
Secondary Number of Participants With Treatment-Emergent Adverse Events (AEs) and Serious Adverse Events (SAEs) An AE was any untoward medical occurrence in a participant who received study drug without regard to possibility of causal relationship. An SAE was an AE resulting in any of the following outcomes or deemed significant for any other reason: death; initial or prolonged inpatient hospitalization; life-threatening experience (immediate risk of dying); persistent or significant disability/incapacity; congenital anomaly. Treatment-emergent are events between first dose of study drug and up to Week 32 that were absent before treatment or that worsened relative to pretreatment state. Adverse events included both serious and all non-serious adverse events. Baseline up to Week 32
Secondary Change From Baseline in Neuropathy Impairment Score (NIS) at Week 2, 4, 6, 8, 12, 16 and 24 The NIS is a standardized instrument used to evaluate participant for signs of peripheral neuropathy. Neurologic examination assessed strength of groups of muscles of the head and neck, upper limbs and lower limbs, deep tendon reflexes and sensation (tactile, vibration, joint position sense and pin prick) of index fingers and great toes in order to complete the NIS. The NIS is the sum of scores of over all 37 items (24 scored 0-4; 13 scored 0-2), made separately for left and right sides, giving a possible overall score range of 0 (no impairment) to 122 (severe impairment). NIS Total score range (total of both left and right sides) was 0 (no impairment) to 244 (severe impairment), where higher scores indicated increased impairment. Baseline, Week 2, 4, 6, 8, 12, 16, 24
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