MedPath

Extension Study Of Tanezumab In Osteoarthritis

Phase 3
Terminated
Conditions
Osteoarthritis
Interventions
Biological: tanezumab
Registration Number
NCT00809783
Lead Sponsor
Pfizer
Brief Summary

Safety extension study of Phase 3 Osteoarthritis trials with Tanezumab

Detailed Description

This study was terminated on 27 October 2010 following a US FDA clinical hold for tanezumab osteoarthritis clinical studies which halted dosing and enrollment of patients on 23 June 2010 for potential safety issues.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
2147
Inclusion Criteria
  • Must have participated in previous (specific) Phase 3 trials of Tanezumab in osteoarthritis
Exclusion Criteria
  • Willing to comply with scheduled visits and treatment plan Is medically fit to participate in the trial in the judgement of the Investigator

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Tanezumab 5 mgtanezumabTanezumab 5 mg
Tanezumab 10 mgtanezumabTanezumab 10 mg
Tanezumab 2.5 mgtanezumabTanezumab 2.5 mg
Primary Outcome Measures
NameTimeMethod
Number of Participants With Treatment Emergent Adverse Events (AEs) And Serious Adverse Events (SAEs)A4091016: Baseline (Day 1) up to 112 days after last dose of study medication (up to Week 80)

AE:any untoward medical occurrence in participant who received study medication without regard to possibility of causal relationship. SAE:an AE resulting in any of 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 medication and up to 112 days after last dose that were absent before treatment in this study or that worsened relative to pretreatment state. AEs included both SAEs and all non-SAEs.

Number of Participants With Clinically Significant Abnormal Electrocardiogram (ECG) FindingsA4091016: Baseline (Day 1) up to Week 80

Following parameters were analyzed for ECG abnormality: PR interval, QRS interval, QT interval, QT interval corrected using the Fridericia's formula (QTcF), QT interval corrected using the Bazett's formula (QTcB), RR interval and VR interval. Number of participants with clinically significant abnormal ECG findings were judged by investigator and reported as adverse events were presented.

Number of Participants With Abnormal Laboratory FindingsA4091016: Day 1 up to Week 80

Hemoglobin(Hgb),hematocrit,red blood cell(RBC):less than(\<)0.8\*lower limit of normal(LLN),MCV,MCH,MCHC\<0.9\*LLN or \>1.1\*ULN,platelet:\<0.5\*LLN or \>1.75\*upper limit of normal(ULN),white blood cell(WBC):\<0.6\*LLN or \>1.5\*ULN,lymphocyte,neutrophil,total neutrophil:\<0.8\*LLN or\>1.2\*ULN,basophil,eosinophil,monocyte:\>1.2\*ULN;total,direct bilirubin\>1.5\*ULN,aspartate aminotransferase,alanine aminotransferase,gamma-glutamyl transferase,LDH,alkaline phosphatase:\> 3.0\*ULN,total protein,albumin:\<0.8\*LLN or \>1.2\*ULN;blood urea nitrogen,creatinine:\>1.3\*ULN,uric acid\>1.2\*ULN;cholesterol,triglycerides\>1.3\*ULN;sodium \<0.95\*LLN or \>1.05\*ULN,potassium,chloride,calcium,magnesium,bicarbonate:\<0.9\*LLN or \>1.1\*ULN,phosphate\<0.8\*LLN or\>1.2\*ULN;glucose \<0.6\*LLN or \>1.5\*ULN,glycosylated Hgb \>1.3\*ULN,creatine kinase\>2.0\*ULN;urine(specific gravity \<1.003or\>1.030,pH \<4.5or\>8,glucose,ketone,protein,blood/Hgb,bilirubin,leukocyte esterase,crystals\>=1,RBC,WBC \>1.5\*ULN,epithelial cell\>=6,casts,hyaline cast\>1,bacteria\>20).

Secondary Outcome Measures
NameTimeMethod
Change From Parent Study Baseline in Neuropathy Impairment Score (NIS) at Week 4, 8, 16, 24, 32, 40, 48, 56, 64 and 72Baseline of the parent study (A4091011, A4091014, A4091015, A4091018); A4091016: Week 4, 8, 16, 24, 32, 40, 48, 56, 64, 72

NIS constitutes sum of 37 standard items of neuromuscular examination used to assess muscle strength, reflexes and sensation. Each item is scored separately for left and right sides. Components of muscle weakness (24 items) scored on a scale: 0 (normal) to 4 (paralysis), with higher score=more weakness; components of reflexes and sensation (13 items) scored on a scale: 0= normal, 1= decreased or 2= absent. Total NIS score range 0 (no impairment) to 244 (maximum impairment), higher score = more impairment. Parent study baseline value calculated as average of pre-dose measurements of participants from study A4091011, A4091014, A4091015 and A4091018.

Number of Participants With Clinically Significant Abnormality in Vital SignsA4091016: Baseline (Day 1) up to Week 80

Following parameters were analyzed for examination of vital signs: body temperature, blood pressure, heart rate and respiratory rate. Number of participants with clinically significant abnormality in vital signs were judged by investigator and reported as adverse events were presented.

Change From Parent Study Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Average Score at Week 4, 8, 16, 24, 32, 40, 48, 56, 64, 72, 80, 88, 96 and 104Baseline of the parent study (A4091011, A4091014, A4091015, A4091018); A4091016: Week 4, 8, 16, 24, 32, 40, 48,56, 64, 72, 80, 88, 96, 104

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 knee or hip. WOMAC average score is the mean of WOMAC pain, physical function and stiffness subscale scores and ranges from 0 (minimum difficulty) to 10 (maximum difficulty), where higher score indicates worse response. Parent study baseline value calculated as average of pre-dose measurements of the participants from study A4091011, A4091014, A4091015 and A4091018.

Number of Participants With Anti-drug Antibodies (ADA) for TanezumabA4091016: Day 1, Week 16, 24, 40, 56, 72, 80 or Early Termination (ET: anytime till Week 80)

Human serum anti-drug antibody (ADA) samples were analyzed for the presence or absence of anti-tanezumab antibodies by using the semi-quantitative enzyme-linked immunosorbent assay (ELISA). Same participant may have positive ADA result at more than 1 time point.

Change From Parent Study Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Pain Subscale Score at Week 4, 8, 16, 24, 32, 40, 48, 56, 64, 72, 80, 88, 96 and 104Baseline of the parent study (A4091011, A4091014, A4091015, A4091018); A4091016: Week 4, 8, 16, 24, 32, 40, 48,56, 64, 72, 80, 88, 96, 104

The WOMAC pain subscale is a 5-item questionnaire used to assess the amount of pain experienced due to osteoarthritis in index knee or hip joint during past 48 hours. The WOMAC pain score is calculated as mean of the scores from 5 individual questions scored on a numerical rating scale (NRS) of 0 (minimum pain) to 10 (maximum pain), where higher scores indicate higher pain. Total score range for WOMAC pain subscale score is 0 (minimum pain) to 10 (maximum pain), where higher scores indicate higher pain. Parent study baseline value calculated as average of pre-dose measurements of the participants from study A4091011, A4091014, A4091015 and A4091018.

Change From Parent Study Baseline in Patient Global Assessment (PGA) of Osteoarthritis at Week 4, 8, 16, 24, 32, 40, 48, 56, 64, 72, 80, 88, 96 and 104Baseline of the parent study (A4091011, A4091014, A4091015, A4091018); A4091016: Week 4, 8, 16, 24, 32, 40, 48,56, 64, 72, 80, 88, 96, 104

Participants answered: "Considering all the ways your osteoarthritis in your knee/hip affects you, how are you doing today?" Participants responded by using a 5-point scale where 1 = very good and 5 = very poor. Higher scores indicate worse condition. Parent study baseline value calculated as average of pre-dose measurements of the participants from study A4091011, A4091014, A4091015 and A4091018.

Change From Parent Study Baseline For Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Pain Subscale Item: Pain When Going Up or Downstairs at Week 4, 8, 16, 24, 32, 40, 48, 56, 64, 72, 80, 88, 96 and 104Baseline of the parent study (A4091011, A4091014, A4091015, A4091018); A4091016: Week 4, 8, 16, 24, 32, 40, 48,56, 64, 72, 80, 88, 96, 104

Participants answered: "How much pain have you had going up or down the stairs?" Participants responded by using a NRS of 0 to 10, where 0 = no pain and 10 = extreme pain. Higher score indicates more pain. Parent study baseline value calculated as average of pre-dose measurements of the participants from study A4091011, A4091014, A4091015 and A4091018.

Days Per Week of Concomitant Analgesic Medication UsageWeek 1-4, 5-8, 9-16, 17-24, 25-32, 33-40, 41-48, 49-56, 57-64, 65-72, 73-80, 81-88, 89-96, 97-104, 105-112

FDA approved analgesics (over-the-counter or prescription) were permitted as concomitant medications to relieve the pain of osteoarthritis. These medications included opioids, topical analgesics, NSAIDs, capsaicin products, oral/injectable corticosteroids and viscosupplementation (hyaluronan) and were prescribed at the discretion of the investigator.

Number of Participants With Clinically Significant Changes From Baseline to Week 80 in Physical Examination FindingsBaseline (Day 1) up to Week 80

Physical examination included examination of following sites in addition to general examination: abdomen, ears, extremities, eyes, head, heart, musculoskeletal, neck, nose, skin, throat and thyroid. Clinically significant changes were judged by investigator.

Change From Parent Study Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Physical Function Subscale Score at Week 4, 8, 16, 24, 32, 40, 48, 56, 64, 72, 80, 88, 96 and 104Baseline of the parent study (A4091011, A4091014, A4091015, A4091018); A4091016: Week 4, 8, 16, 24, 32, 40, 48,56, 64, 72, 80, 88, 96, 104

The WOMAC physical function subscale is a 17-item questionnaire used to assess the degree of difficulty experienced due to osteoarthritis in index knee or hip joint during past 48 hours. The WOMAC physical function score is calculated as mean of the scores from 17 individual questions scored on a NRS of 0 (minimum difficulty) to 10 (maximum difficulty), where higher scores indicate worse function. Total score range for WOMAC physical function subscale score is 0 (minimum difficulty) to 10 (maximum difficulty), where higher scores indicate worse function. Parent study baseline value calculated as average of pre-dose measurements of the participants from study A4091011, A4091014, A4091015 and A4091018.

Change From Parent Study Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Stiffness Subscale at Week 4, 8, 16, 24, 32, 40, 48, 56, 64, 72, 80, 88, 96 and 104Baseline of the parent study (A4091011, A4091014, A4091015, A4091018); A4091016: Week 4, 8, 16, 24, 32, 40, 48,56, 64, 72, 80, 88, 96, 104

WOMAC stiffness subscale: questionnaire used to assess amount of stiffness experienced due to osteoarthritis in index joint during past 48 hours. The WOMAC stiffness score is calculated as mean of scores from 2 individual questions scored on NRS of 0 (minimum stiffness) to 10 (maximum stiffness), higher scores indicate higher stiffness. Total score range for WOMAC stiffness subscale score =0 (minimum stiffness) to 10 (maximum stiffness), higher scores indicate higher stiffness. Stiffness is defined as sensation of decreased ease in movement of knee/hip. Parent study baseline value calculated as average of pre-dose measurements of the participants from study A4091011, A4091014, A4091015 and A4091018.

Percentage of Participants Who Used Concomitant Analgesic MedicationWeek 1-4, 5-8, 9-16, 17-24, 25-32, 33-40, 41-48, 49-56, 57-64, 65-72, 73-80, 81-88, 89-96, 97-104, 105-112

United States Food and Drug Administration (FDA) approved analgesics (over-the-counter or prescription) were permitted as concomitant medications to relieve the pain of osteoarthritis. These medications included opioids, topical analgesics, non-steroidal anti inflammatory drugs (NSAIDs), capsaicin products, oral/injectable corticosteroids and viscosupplementation (hyaluronan) and were prescribed as per investigator's discretion.

Percentage of Participants With Outcome Measures in Rheumatology - Osteoarthritis Research Society International (OMERACT-OARSI) ResponseA4091016: Week 4, 8, 16, 24, 32, 40, 48, 56, 64, 72, 80, 88, 96, 104

OMERACT-OARSI response:\>=50 percent(%) improvement from parent study baseline and absolute change from parent study baseline of \>=2 units at given week in WOMAC pain or physical function subscale or \>=20% improvement from parent study baseline and absolute change from parent study baseline of \>=1 unit at given week in at least 2 of following 3 items: 1)WOMAC pain subscale, 2)WOMAC physical function subscale, 3)PGA of osteoarthritis (score: 1-5, higher score=more affected).WOMAC pain, physical function subscales assess amount of pain/difficulty experienced (score:0-10, higher score=higher pain/difficulty).

Percentage of Participants With at Least 30%, 50%, 70% and 90% Reduction From Parent Study Baseline in WOMAC Pain Subscale ScoreBaseline of the parent study (A4091011, A4091014, A4091015, A4091018); A4091016: Week 4, 8, 16, 24, 32, 40, 48,56, 64, 72, 80, 88, 96, 104

The WOMAC pain subscale is a 5-item questionnaire used to assess the amount of pain experienced due to osteoarthritis in index knee or hip joint during past 48 hours. The WOMAC pain score is calculated as mean of the scores from 5 individual questions scored on a numerical rating scale (NRS) of 0 (minimum pain) to 10 (maximum pain), where higher scores indicate higher pain. Total score range for WOMAC pain subscale score is 0 (minimum pain) to 10 (maximum pain), where higher scores indicate higher pain. Parent study baseline value calculated as average of pre-dose measurements of the participants from study A4091011, A4091014, A4091015 and A4091018.

Number of Participants With Cumulative Reduction From Parent Study Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Pain Subscale Score at Week 16, 24, 56 and 104Baseline of the parent study (A4091011, A4091014, A4091015, A4091018); A4091016: Week 16, 24, 56, 104

The WOMAC pain subscale is a 5-item questionnaire used to assess the amount of pain experienced due to osteoarthritis in index knee or hip joint during past 48 hours. The WOMAC pain score is calculated as mean of the scores from 5 individual questions scored on a numerical rating scale (NRS) of 0 (minimum pain) to 10 (maximum pain), where higher scores indicate higher pain. Total score range for WOMAC pain subscale score is 0 (minimum pain) to 10 (maximum pain), where higher scores indicate higher pain. Parent study baseline value calculated as average of pre-dose measurements of the participants from study A4091011, A4091014, A4091015 and A4091018.

Percentage of Participants With Improvement of at Least 2 Points From Parent Study Baseline in Patient Global Assessment (PGA) of OsteoarthritisBaseline of the parent study (A4091011, A4091014, A4091015, A4091018); A4091016: Week 4, 8, 16, 24, 32, 40, 48,56, 64, 72, 80, 88, 96, 104

Participants answered: "Considering all the ways your osteoarthritis in your knee/hip affects you, how are you doing today?" Participants responded by using a 5-point scale where 1 = very good and 5 = very poor. Higher scores indicated worse pain. Parent study baseline value calculated as average of pre-dose measurements of the participants from study A4091011, A4091014, A4091015 and A4091018.

Change From Parent Study Baseline For Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Pain Subscale Item: Pain When Walking on a Flat Surface at Week 4, 8, 16, 24, 32, 40, 48, 56, 64, 72, 80, 88, 96 and 104Baseline of the parent study (A4091011, A4091014, A4091015, A4091018); A4091016: Week 4, 8, 16, 24, 32, 40, 48,56, 64, 72, 80, 88, 96, 104

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 score indicates more pain. Parent study baseline value calculated as average of pre-dose measurements of the participants from study A4091011, A4091014, A4091015 and A4091018.

Trial Locations

Locations (218)

Laureate Clinical Research Group

🇺🇸

Atlanta, Georgia, United States

Arthritis and Rheumatology of Georgia

🇺🇸

Atlanta, Georgia, United States

Rehabilitation Institute of Chicago

🇺🇸

Chicago, Illinois, United States

Innovative Research of West Florida, Inc.

🇺🇸

Clearwater, Florida, United States

In Vivo Clinical Research, Inc

🇺🇸

Doral, Florida, United States

Edinger Medical Group Clinical Research

🇺🇸

Fountain Valley, California, United States

Stamford Therapeutics Consortium

🇺🇸

Stamford, Connecticut, United States

River Birch Research Alliance, LLC

🇺🇸

Blue Ridge, Georgia, United States

Clinical Research Center of Connecticut

🇺🇸

Danbury, Connecticut, United States

Valley Research

🇺🇸

Fresno, California, United States

High Desert Medical Group Research for Life

🇺🇸

Lancaster, California, United States

Probe Clinical Research, Corp.

🇺🇸

Santa Ana, California, United States

Trinity Clinical Trials

🇺🇸

Santa Ana, California, United States

HeartCare (Private Practice)

🇺🇸

Bradenton, Florida, United States

Norwalk Medical Group

🇺🇸

Norwalk, Connecticut, United States

Palm Beach Research Center

🇺🇸

West Palm Beach, Florida, United States

Jefrey D. Lieberman, MD

🇺🇸

Decatur, Georgia, United States

Asif Cochinwala, MD, PA

🇺🇸

Houston, Texas, United States

Foundation for Southwest Orthopedic Research

🇺🇸

Houston, Texas, United States

The Neurology Center

🇺🇸

Houston, Texas, United States

Pharmax Research Clinic, Inc

🇺🇸

Miami, Florida, United States

Kendall South Medical Center, Inc.

🇺🇸

Miami, Florida, United States

Independent Clinical Researchers

🇺🇸

Las Vegas, Nevada, United States

Wolfson Medical Center

🇺🇸

Las Vegas, Nevada, United States

Clinical Research Consortium

🇺🇸

Las Vegas, Nevada, United States

Arizona Research Center

🇺🇸

Phoenix, Arizona, United States

Delaware Arthritis

🇺🇸

Lewes, Delaware, United States

Sonora Clinical Research, LLC.

🇺🇸

Boise, Idaho, United States

Odyssey Research

🇺🇸

Fargo, North Dakota, United States

University Parks Hematology/Oncology

🇺🇸

Englewood, Colorado, United States

American Clinical Research, LLC

🇺🇸

Englewood, Colorado, United States

Orthopaedic Physicians Of Colorado, P.C.

🇺🇸

Englewood, Colorado, United States

Professional Research Network of Kansas, LLC

🇺🇸

Wichita, Kansas, United States

Peak Anesthesia and Pain Management

🇺🇸

Centennial, Colorado, United States

Advanced Orthopedic and Sports Medicine

🇺🇸

Parker, Colorado, United States

Plains Medical Clinic, LLC

🇺🇸

Fargo, North Dakota, United States

Clinical Research Advantage, Inc.

🇺🇸

Phoenix, Arizona, United States

Clincial Research Advantage, Inc/Central Phoenix Medical Clinic, LLC

🇺🇸

Phoenix, Arizona, United States

Arizona Arthritis & Rheumatology Associates, P.C.

🇺🇸

Phoenix, Arizona, United States

Health Research Institute

🇺🇸

Oklahoma City, Oklahoma, United States

Greystone Medical Center

🇺🇸

Birmingham, Alabama, United States

Denver Internal Medicine Group

🇺🇸

Denver, Colorado, United States

Mountain View Clinical Research, Inc.

🇺🇸

Denver, Colorado, United States

Quality Clinical Research, Inc.

🇺🇸

Omaha, Nebraska, United States

Colorado Orthopedic Consultants, PC

🇺🇸

Aurora, Colorado, United States

Tampa Medical Group, PA

🇺🇸

Tampa, Florida, United States

Quality of Life Medical and Research Center

🇺🇸

Tucson, Arizona, United States

Pinncale Research Group, LLC

🇺🇸

Anniston, Alabama, United States

Anniston Medical Clinic, PC

🇺🇸

Anniston, Alabama, United States

Pinnacle Research Group, LLC

🇺🇸

Anniston, Alabama, United States

Saadat Ansari, MD Office

🇺🇸

Huntsville, Alabama, United States

Coastal Clinical Research, Inc.

🇺🇸

Mobile, Alabama, United States

Horizon Research Group

🇺🇸

Mobile, Alabama, United States

Novara Clinical Research

🇺🇸

Mesa, Arizona, United States

Arizona Arthritis & Rheumatology Research, PLLC

🇺🇸

Paradise Valley, Arizona, United States

Pivotal Research Center

🇺🇸

Peoria, Arizona, United States

Quality of Life Medical & Research Center, LLC

🇺🇸

Tucson, Arizona, United States

University of Arizona

🇺🇸

Tucson, Arizona, United States

Tucson Orthopaedic Institute

🇺🇸

Tucson, Arizona, United States

St. Joseph's Mercy Clinic

🇺🇸

Hot Springs, Arkansas, United States

Providence Clinical Research

🇺🇸

Burbank, California, United States

Osteoporosis Medical Center

🇺🇸

Beverly Hills, California, United States

eStudySite

🇺🇸

Chula Vista, California, United States

Colorado Hematology - Oncology

🇺🇸

Englewood, California, United States

Lakewood Orthopedic Medical & Surgical Group

🇺🇸

Lakewood, California, United States

Talbert Medical Group

🇺🇸

Huntington Beach, California, United States

Arthritis Medical Clinic of North County, Inc.

🇺🇸

Escondido, California, United States

Premiere Clinical Research, LLC

🇺🇸

Long Beach, California, United States

Samaritan Center for Medical Research

🇺🇸

Los Gatos, California, United States

Office of Lawrence P McAdam, MD

🇺🇸

Thousand Oaks, California, United States

Del Carmen Medical Center

🇺🇸

Reseda, California, United States

Westlake Medical Research

🇺🇸

Westlake Village, California, United States

Tampa Bay Medical Research, Inc.

🇺🇸

Clearwater, Florida, United States

Clinical Research of South Florida

🇺🇸

Coral Gables, Florida, United States

Arthritis Associates of South Florida

🇺🇸

Delray Beach, Florida, United States

Avail Clinical Research, LLC

🇺🇸

DeLand, Florida, United States

Delray Research Associates

🇺🇸

Delray Beach, Florida, United States

S & W Clinical Research

🇺🇸

Fort Lauderdale, Florida, United States

Westside Center for Clinical Research

🇺🇸

Jacksonville, Florida, United States

Adult Medicine Specialists

🇺🇸

Longwood, Florida, United States

Genesis Research International

🇺🇸

Longwood, Florida, United States

Centre for Rheumatology, Immunology and Arthritis

🇺🇸

Fort Lauderdale, Florida, United States

Sunshine Research Center

🇺🇸

Opa-locka, Florida, United States

University Clinical Research Incorporated

🇺🇸

Pembroke Pines, Florida, United States

Advent Clinical Research Centers, Inc.

🇺🇸

Pinellas Park, Florida, United States

The Arthritis Center

🇺🇸

Springfield, Illinois, United States

HeartCare Research

🇺🇸

Sarasota, Florida, United States

Progressive Medical Research

🇺🇸

Port Orange, Florida, United States

Dale G. Bramlet, MD, P.L.

🇺🇸

Saint Petersburg, Florida, United States

West Broward Rheumatology Associates, Inc.

🇺🇸

Tamarac, Florida, United States

Early Family Practice Center

🇺🇸

Fort Valley, Georgia, United States

Northeast Georgia Diagnostic Clinic, LLC

🇺🇸

Gainesville, Georgia, United States

Marietta Rheumatology Associates

🇺🇸

Marietta, Georgia, United States

North Georgia Clinical Research

🇺🇸

Woodstock, Georgia, United States

North Georgia Internal Medicine

🇺🇸

Woodstock, Georgia, United States

Millennium Pain Center

🇺🇸

Bloomington, Illinois, United States

Illinois Bone and Joint Institute, LLC

🇺🇸

Morton Grove, Illinois, United States

Koch Family Medicine

🇺🇸

Morton, Illinois, United States

MediSphere Medical Research Center, LLC

🇺🇸

Evansville, Indiana, United States

American Health Network

🇺🇸

Fishers, Indiana, United States

Northwest Indiana Center for Clinical Research

🇺🇸

Valparaiso, Indiana, United States

Pasadena Pharmacy

🇺🇸

Lexington, Kentucky, United States

McFarland Clinic, PC

🇺🇸

Ames, Iowa, United States

Arthritis Center of Lexington

🇺🇸

Lexington, Kentucky, United States

Integrated Clinical Trial Services, Inc.

🇺🇸

West Des Moines, Iowa, United States

The Pain Treatment Center of the Bluegrass

🇺🇸

Lexington, Kentucky, United States

Bluegrass Community Research, Inc

🇺🇸

Lexington, Kentucky, United States

Stanocola Medical Center

🇺🇸

Baton Rouge, Louisiana, United States

Bone and Joint Clinic of Baton Rouge

🇺🇸

Baton Rouge, Louisiana, United States

Maine Research Associates

🇺🇸

Auburn, Maine, United States

Mid-Atlantic Medical Research Centers

🇺🇸

Hollywood, Maryland, United States

Arthritis and Diabetes Clinic

🇺🇸

Monroe, Louisiana, United States

Miray Medical Center

🇺🇸

Brockton, Massachusetts, United States

The Center for Rheumatology and Bone Research

🇺🇸

Wheaton, Maryland, United States

Mansfield Health Center

🇺🇸

Mansfield, Massachusetts, United States

Beacon Clinical Research, LLC

🇺🇸

Brockton, Massachusetts, United States

Arthritis Associates Inc.

🇺🇸

Peabody, Massachusetts, United States

Great Lakes Research Group, Incorporated

🇺🇸

Bay City, Michigan, United States

KMED Research

🇺🇸

Saint Clair Shores, Michigan, United States

MAPS Applied Research Center Inc.

🇺🇸

Edina, Minnesota, United States

Medical Advanced Pain Specialists

🇺🇸

Edina, Minnesota, United States

Planters Clinic

🇺🇸

Port Gibson, Mississippi, United States

Medex Healthcare Research

🇺🇸

New York, New York, United States

Mercy Health Research

🇺🇸

Saint Louis, Missouri, United States

St. John's Clinic - Neurology

🇺🇸

Springfield, Missouri, United States

St. John's Medical Research Institute, Inc.

🇺🇸

Springfield, Missouri, United States

Diagnostic Center of Medicine

🇺🇸

Henderson, Nevada, United States

Midwest Minor Medical

🇺🇸

Omaha, Nebraska, United States

Comprehensive Clinical Research

🇺🇸

Berlin, New Jersey, United States

Office of Dr. Danka Michaels, MD

🇺🇸

Las Vegas, Nevada, United States

Mirkil Medical

🇺🇸

Las Vegas, Nevada, United States

SPRI Bronx LLC

🇺🇸

Bronx, New York, United States

G. Timothy Kelly, MD

🇺🇸

Las Vegas, Nevada, United States

Albuquerque Clinical Trials

🇺🇸

Albuquerque, New Mexico, United States

New Mexico Clinical Research & Osteoporosis Center, Incorporated

🇺🇸

Albuquerque, New Mexico, United States

Arthritis and Osteoporosis Medical Associates

🇺🇸

Brooklyn, New York, United States

Prem C. Chatpar, MD, LLC

🇺🇸

Plainview, New York, United States

AAIR Research Center

🇺🇸

Rochester, New York, United States

Carolina Bone & Joint, PA

🇺🇸

Charlotte, North Carolina, United States

The Medical Research Network, LLC

🇺🇸

New York, New York, United States

Pharmquest

🇺🇸

Greensboro, North Carolina, United States

Arthritis and Osteoporosis Consultants of the Carolinas

🇺🇸

Charlotte, North Carolina, United States

Office of Dr. Andrew Porges

🇺🇸

Roslyn, New York, United States

Consultants for Clinical Research Incorporated

🇺🇸

Cincinnati, Ohio, United States

Ohio GI and Liver Institute

🇺🇸

Cincinnati, Ohio, United States

Hilltop Medical Research Center

🇺🇸

Cincinnati, Ohio, United States

Columbus Clinical Research, Inc.

🇺🇸

Columbus, Ohio, United States

Paramount Medical Research and Consulting, LLC

🇺🇸

Middleburg Heights, Ohio, United States

PHP Center for Clinical Research

🇺🇸

Dayton, Ohio, United States

Physicians' Research, Inc

🇺🇸

Zanesville, Ohio, United States

Orthopaedic & Sports Medicine Consultants

🇺🇸

Middletown, Ohio, United States

Pharmacotherapy Research Associates,Inc

🇺🇸

Zanesville, Ohio, United States

Primecare of Southeastern Ohio, Inc

🇺🇸

Zanesville, Ohio, United States

Signal Point Clinical Research Center

🇺🇸

Middletown, Ohio, United States

East Penn Rheumatology Associates, PC

🇺🇸

Bethlehem, Pennsylvania, United States

Cor Clinical Research, LLC

🇺🇸

Oklahoma City, Oklahoma, United States

Altoona Center for Clinical Research

🇺🇸

Duncansville, Pennsylvania, United States

Clinical Research Center of Reading, LLP

🇺🇸

Wyomissing, Pennsylvania, United States

Brandywine Clinical Research

🇺🇸

Downingtown, Pennsylvania, United States

The Family Healthcare Center, PA

🇺🇸

Clinton, South Carolina, United States

Southern Orthopaedic Sports Medicine

🇺🇸

Columbia, South Carolina, United States

Coastal Carolina Research Center

🇺🇸

Mount Pleasant, South Carolina, United States

The Carolina Center for Rheumatology and Arthritis Care, PA

🇺🇸

Rock Hill, South Carolina, United States

State of Franklin Healthcare Associates, PLLC

🇺🇸

Johnson City, Tennessee, United States

Health Concepts

🇺🇸

Rapid City, South Dakota, United States

Holston Medical Group

🇺🇸

Kingsport, Tennessee, United States

Crown Imaging

🇺🇸

Dallas, Texas, United States

North Texas Joint Care, PA

🇺🇸

Dallas, Texas, United States

Metroplex Clinical Research Center

🇺🇸

Dallas, Texas, United States

One Step Diagnostic

🇺🇸

Houston, Texas, United States

Southwest Orthopedic Group

🇺🇸

Houston, Texas, United States

O. David Taunton, Jr, MD

🇺🇸

Grapevine, Texas, United States

Pioneer Research Solutions, Inc.

🇺🇸

Houston, Texas, United States

Texas Arthritis Research Center, PA

🇺🇸

San Antonio, Texas, United States

Diagnostics Research Group

🇺🇸

San Antonio, Texas, United States

Gill Orthopedic Center

🇺🇸

Lubbock, Texas, United States

Radiant Research San Antonio Northeast

🇺🇸

San Antonio, Texas, United States

Robert R. King, M.D.

🇺🇸

Lubbock, Texas, United States

Clinical Investigations of Texas, LLC

🇺🇸

Plano, Texas, United States

Spring Family Practice Associates PA

🇺🇸

Spring, Texas, United States

Sugar Land Med-Ped, P.A.

🇺🇸

Sugar Land, Texas, United States

Aspen Clinical Research

🇺🇸

Orem, Utah, United States

Grayline Clinical Drug Trials

🇺🇸

Wichita Falls, Texas, United States

AZ Clinical Research

🇺🇸

Sugar Land, Texas, United States

Spring Clinical Research

🇺🇸

Sugar Land, Texas, United States

J. Lewis Research, Incorporated/Foothill Family Clinic South

🇺🇸

Salt Lake City, Utah, United States

Foothill Family Clinic

🇺🇸

Salt Lake City, Utah, United States

IntegraTrials, LLC

🇺🇸

Arlington, Virginia, United States

Commonwealth Orthopaedics and Rehabilitation, PC

🇺🇸

Arlington, Virginia, United States

Virginia Hospital Center

🇺🇸

Arlington, Virginia, United States

Charlottesville Medical Research

🇺🇸

Charlottesville, Virginia, United States

National Clinical Research - Norfolk, Inc.

🇺🇸

Norfolk, Virginia, United States

Office of Doris M. Rice, MD, FACR

🇺🇸

Portsmouth, Virginia, United States

HhypotheTest, LLC

🇺🇸

Roanoke, Virginia, United States

Empirical Clinical Trials

🇺🇸

Selah, Washington, United States

Arthritis Northwest

🇺🇸

Spokane, Washington, United States

Clinical Trials Northwest

🇺🇸

Yakima, Washington, United States

Masters of Clinical Research, Inc.

🇺🇸

Augusta, Georgia, United States

Memorial Medical Group Clinical Research Institute

🇺🇸

South Bend, Indiana, United States

Javed Rheumatology Associates, Inc.

🇺🇸

Newark, Delaware, United States

Gulf Coast Research, LLC

🇺🇸

Baton Rouge, Louisiana, United States

The Baton Rouge Clinic

🇺🇸

Baton Rouge, Louisiana, United States

Clinical Pharmacology Study Group

🇺🇸

Worcester, Massachusetts, United States

Clinical Research Advantage, Inc./Mesa Family Medical Center, PC

🇺🇸

Mesa, Arizona, United States

Clinical Research Advantage, Inc./Central Arizona Medical Associates, PC

🇺🇸

Mesa, Arizona, United States

Paradigm Clinical, Inc.

🇺🇸

Tucson, Arizona, United States

L-Marc Research Center

🇺🇸

Louisville, Kentucky, United States

Low Country Rheumatology, PA

🇺🇸

Charleston, South Carolina, United States

Compass Research, LLC

🇺🇸

Orlando, Florida, United States

Rheumatology Associates of Central Florida

🇺🇸

Orlando, Florida, United States

David H. Neustadt, MD

🇺🇸

Louisville, Kentucky, United States

Ann Arbor Clinical Research

🇺🇸

Ann Arbor, Michigan, United States

PMG Research of Winston-Salem

🇺🇸

Winston-Salem, North Carolina, United States

Capitol Medical Clinic

🇺🇸

Austin, Texas, United States

Walter F. Chase, MD, PA

🇺🇸

Austin, Texas, United States

Tekton Research, Inc.

🇺🇸

Austin, Texas, United States

Arthritis Treatment Center

🇺🇸

Frederick, Maryland, United States

Radiant Research

🇺🇸

Dallas, Texas, United States

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