A Study of LY2951742 in Participants With Mild to Moderat... | NCT02192190 | Trialant
NCT02192190
Sponsor
Eli Lilly and Company
Status
Terminated
Last Update Posted
Sep 10, 2019Actual
Enrollment
268Actual
Phase
Phase 2
Conditions
Osteoarthritis, Knee
Interventions
LY2951742
Placebo- oral
Placebo - SC
Celecoxib
Countries
United States
Protocol Section
Identification Module
NCT ID
NCT02192190
Obsolete or Duplicate NCT IDs
Not provided
Organization Study
15515
Secondary IDs
ID
Type
Description
Link
I5Q-MC-CGAF
Other Identifier
Eli Lilly and Company
Brief Title
A Study of LY2951742 in Participants With Mild to Moderate Osteoarthritis Knee Pain
Official Title
A Phase 2, Randomized, Double-Blind, Placebo and Active-Controlled Trial of LY2951742 in Patients With Mild to Moderate Osteoarthritis Pain of the Knee
Acronym
Not provided
Organization
Eli Lilly and CompanyINDUSTRY
Status Module
Record Verification Date
Aug 2019
Overall Recruitment Status or Expanded Access Status
Terminated
Last Known Status
Not provided
Delayed Posting
Not provided
Why Stopped
Interim assessment: Lack of efficacy
Expanded Access Info
No
Start Date
Jul 2014
Primary Completion Date
Apr 2015Actual
Completion Date
Jun 2015Actual
First Submitted Date
Jul 14, 2014
First Submission Date that Met QC Criteria
Jul 14, 2014
First Posted Date
Jul 16, 2014Estimated
Results Waived
Not provided
Results First Submitted Date
Oct 8, 2018
Results First Submitted that Met QC Criteria
Oct 8, 2018
Results First Posted Date
Nov 8, 2018Actual
Certification/Extension (aka Delayed Results) First Submitted Date
Sep 3, 2015
Certification/Extension First Submitted that Passed QC Review
Sep 3, 2015
Certification/Extension First Posted Date
Sep 18, 2015Estimated
Last Update Submitted Date
Aug 29, 2019
Last Update Posted Date
Sep 10, 2019Actual
Sponsor/Collaborators Module
Responsible Party, by Official Title
Sponsor
Lead Sponsor
Eli Lilly and CompanyINDUSTRY
Collaborators
Not provided
Oversight Module
Has Data Monitoring Committee (DMC)
Yes
Is FDA Regulated Drug
Not provided
Is FDA Regulated Device
Not provided
Is Unapproved Device
Not provided
Pediatric Postmarket Surveillance of a Device Product
Not provided
Product Exported from US
Not provided
FDAAA801 Violation
Not provided
Description Module
Brief Summary
The main purpose of this study is to test if LY2951742 relieves mild to moderate knee pain. The study drugs will be given as an injection under the skin and as an oral capsule. The study will last about 28 weeks for each participant.
Detailed Description
Not provided
Conditions Module
Conditions
Osteoarthritis, Knee
Keywords
Not provided
Design Module
Study Type
Interventional
Number of References to an Expanded Access Study
Not provided
Expanded Access Types
Not provided
Patient Registry
Not provided
Target Follow-Up Duration
Not provided
Phases
Phase 2
Interventional Study Design
Allocation
Biospecimen
No data available
No data is available for this block.
Enrollment
268Actual
Arms/Interventions Module
Arm Groups
Label
Type
Description
Intervention Names
Placebo
Placebo Comparator
Placebo capsule orally, once daily for approximately 16 weeks. Placebo subcutaneous (SC) once every 4 weeks for 16 weeks (Treatment period = 16 weeks).
Other: Placebo- oral
Other: Placebo - SC
Celecoxib + Placebo
Active Comparator
Celecoxib 200 milligram (mg) capsule orally once daily for approximately 16 weeks. Placebo SC once every 4 weeks for 16 weeks (Treatment period = 16 weeks).
Other: Placebo - SC
Drug: Celecoxib
LY2951742 5 mg + Placebo
Experimental
Placebo capsule orally, once daily for approximately 16 weeks. SC injections of 5 mg LY2951742 once every 4 weeks for 8 weeks followed by placebo SC once every 4 weeks for 8 weeks (Treatment period = 16 weeks).
Drug: LY2951742
Other: Placebo- oral
Other: Placebo - SC
LY2951742 50 mg + Placebo
Experimental
Placebo capsule orally, once daily for approximately 16 weeks. SC injections of 50 mg LY2951742 once every 4 weeks for 8 weeks followed by placebo SC once every 4 weeks for 8 weeks (Treatment period = 16 weeks).
Drug: LY2951742
Other: Placebo- oral
Other: Placebo - SC
LY2951742 120 mg + Placebo
Interventions
Name
Type
Description
Arm Group Labels
Other Names
LY2951742
Drug
Administered subcutaneously (SC)
LY2951742 120 mg + Placebo
LY2951742 300 mg + Placebo
LY2951742 5 mg + Placebo
LY2951742 50 mg + Placebo
Outcomes Module
Primary Outcomes
Measure
Description
Time Frame
Change From Baseline to 8 Weeks in the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Pain Subscale
The 24-question WOMAC Osteoarthritis Index assesses osteoarthritis (OA) symptoms using pain (5 questions), stiffness (2 questions) and physical function (17 questions) subscales. The WOMAC pain subscale was calculated for each participant at each time point for analysis as the mean score (range 0-100 millimeter [mm] VAS; 0=very good and 100=very poor) of all 5 questions related to pain. Bayesian posterior adjusted mean was calculated using a Bayesian Normal Dynamic Linear Model (NDLM) dose response model with baseline and pooled investigator site included as baseline covariates.
Baseline, 8 Weeks
Secondary Outcomes
Measure
Description
Time Frame
Change From Baseline to 8 Weeks in the WOMAC Physical Function Subscale
The 24-question WOMAC Osteoarthritis Index assesses osteoarthritis symptoms using pain (5 questions), stiffness (2 questions) and physical function (17 questions) subscales. The WOMAC Osteoarthritis Index version 3.1 was administered according to the study schedule. The WOMAC physical function subscale was calculated for each participant at each time point for analysis as the mean score (range 0-100 mm VAS; 0=very good and 100=very poor) of all 17 questions related to physical function. Least Square Mean (LSM) was calculated using a mixed-effects model repeated measures (MMRM) approach with treatment, visit and the interaction of treatment and visit were fitted as fixed effects in the model and baseline and pooled investigator site as baseline covariates.
Other Outcomes
Not provided
Eligibility Module
Eligibility Criteria
Inclusion Criteria:
Have osteoarthritis (OA) of the knee joint based on American College of Rheumatology (ACR) criteria and confirmed with X-rays and ACR functional class of I to III
Have been on stable dose of prescription Nonsteroidal Anti-Inflammatory Drugs (NSAIDS), celecoxib, tramadol, or acetaminophen of at least 2000 mg per day for at least 20 days in the past month
Willing to stop all analgesics for OA pain during the study
Experienced pain while walking in the target knee of 50-90 mm inclusive on 0-100 Visual Analog Scale (VAS) with an increase in pain while walking of at least 10 mm following washout of current Osteoarthritis pain medications at screening
Exclusion Criteria:
Allergic to LY2951742, celecoxib, other NSAIDS, including aspirin, and similar drugs
Arthritis of the knee from other causes
Uncontrolled hypertension
Have OA pain that requires treatment with potent opioids, systemic corticosteroids, intra-articular injections, duloxetine, or venlafaxine
Moderate to severe renal impairment
Pregnant or lactating
Accepts Healthy Volunteers
No
Sex
All
Sex/Gender Based
Not provided
Sex/Gender Description
Not provided
Minimum Age
40 Years
Maximum Age
75 Years
Standard Ages
AdultOlder Adult
Study Population
Not provided
Sampling Method
Not provided
Contacts/Locations Module
Central Contacts
Not provided
Overall Officials
Name
Affiliation
Role
Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)
Jin Y, Smith C, Monteith D, Brown R, Camporeale A, McNearney TA, Deeg MA, Raddad E, Xiao N, de la Pena A, Kivitz AJ, Schnitzer TJ. CGRP blockade by galcanezumab was not associated with reductions in signs and symptoms of knee osteoarthritis in a randomized clinical trial. Osteoarthritis Cartilage. 2018 Dec;26(12):1609-1618. doi: 10.1016/j.joca.2018.08.019. Epub 2018 Sep 18.
See Also Links
Not provided
Available IPD Information
Not provided
IPD Sharing Statement Module
Plan to Share IPD
Yes
Description
Anonymized individual patient level data will be provided in a secure access environment upon approval of a research proposal and a signed data sharing agreement.
Types
Study Protocol
Statistical Analysis Plan (SAP)
Clinical Study Report (CSR)
Time Frame
Data are available 6 months after the primary publication and approval of the indication studied in the US and EU, whichever is later. Data will be indefinitely available for requesting.
Access Criteria
A research proposal must be approved by an independent review panel and researchers must sign a data sharing agreement.
Placebo capsule orally, once daily for 16 weeks. Placebo subcutaneous (SC) once every 4 weeks for 16 weeks.
FG001
Celecoxib
Celecoxib 200 milligram (mg) capsule orally once daily for 16 weeks. Placebo SC once every 4 weeks for 16 weeks.
Periods
Title
Milestones
Reasons Not Completed
Overall Study
Type
Comment
Milestone Data
STARTED
Baseline Characteristics Module
Baseline Analysis Population Description
Outcome Measures Module
Outcome Measures
Adverse Events Module
Frequency Threshold
0
More Info Module
Limitations and Caveats
Not provided
Annotation Section
No data available
No data is available for this block.
Document Section
No data available
No data is available for this block.
Derived Section
Miscellaneous Info Module
Version Holder
Jul 10, 2026
Removed Countries
Not provided
Submission Tracking
No data available
No data is available for this block.
Condition Browse Module
MeSH Terms
Intervention Browse Module
MeSH Terms
Randomized
Intervention Model
Parallel Assignment
Intervention Model Description
Not provided
Primary Purpose
Treatment
Observational Model
Not provided
Time Perspective
Not provided
Masking Info
Masking
Double
Masking Description
Not provided
Who Masked
ParticipantInvestigator
Experimental
Placebo capsule orally, once daily for approximately 16 weeks. SC injections of 120 mg LY2951742 once every 4 weeks for 8 weeks followed by placebo SC once every 4 weeks for 8 weeks (Treatment period = 16 weeks).
Drug: LY2951742
Other: Placebo- oral
Other: Placebo - SC
LY2951742 300 mg + Placebo
Experimental
Placebo capsule orally, once daily for 16 weeks. SC injections of 300 mg LY2951742 once every 4 weeks for 8 weeks followed by placebo SC once every 4 weeks for 8 weeks (Treatment period = 16 weeks).
Drug: LY2951742
Other: Placebo- oral
Other: Placebo - SC
Placebo- oral
Other
Administered orally
LY2951742 120 mg + Placebo
LY2951742 300 mg + Placebo
LY2951742 5 mg + Placebo
LY2951742 50 mg + Placebo
Placebo
Placebo - SC
Other
Administered SC
Celecoxib + Placebo
LY2951742 120 mg + Placebo
LY2951742 300 mg + Placebo
LY2951742 5 mg + Placebo
LY2951742 50 mg + Placebo
Placebo
Celecoxib
Drug
Administered orally
Celecoxib + Placebo
Baseline, 8 Weeks
Change in Baseline to 8 Weeks in Patient's Global Assessment of Osteoarthritis
The PGA is a patient-rated instrument that measures their assessment of overall OA symptoms. It is based on the participant's response to the question "Considering all the ways your osteoarthritis affects you, how are you doing today?" using a 100 mm VAS (0=very good and 100=very poor). LSM mean was calculated using a mixed-effects model repeated measures (MMRM) approach with treatment, visit and the interaction of treatment and visit were fitted as fixed effects in the model and baseline and pooled investigator site as baseline covariates.
Baseline, 8 Weeks
Number of Participants With a Response Rate Measured by the Outcome Measures for Rheumatology Committee and Osteoarthritis Research Society International Standing Committee for Clinical Trials Response Criteria Initiative (OMERACT-OARSI)
The responders according to OMERACT-OARSI criteria: participants with at least 50 % improvement in pain or in function scores, along with absolute improvement of 20 mm, were considered responders. Alternatively, participants were considered responders if they showed at least 20% improvement and absolute improvement of 10 mm in at least two of the following scores: pain, function and Patients Global Assessment (PGA) scores.
8 Weeks
Change From Baseline to 8 Weeks in the WOMAC Stiffness Subscale
The 24-question WOMAC Osteoarthritis Index assesses osteoarthritis symptoms using pain (5 questions), stiffness (2 questions) and physical function (17 questions) subscales. The WOMAC stiffness subscale will be calculated for each participant at each time point for analysis as the mean score (range 0-100 mm VAS; 0=very good and 100=very poor) of 2 questions related to stiffness. LSM mean was calculated using a mixed-effects model repeated measures (MMRM) approach with treatment, visit and the interaction of treatment and visit were fitted as fixed effects in the model and baseline and pooled investigator site as baseline covariates. LSM mean was calculated using a mixed-effects model repeated measures (MMRM) approach with treatment, visit and the interaction of treatment and visit were fitted as fixed effects in the model and baseline and pooled investigator site as baseline covariates.
Baseline, 8 Weeks
Change From Baseline to 8 Weeks in the WOMAC Total Score
The 24-question WOMAC Osteoarthritis Index assesses osteoarthritis symptoms using pain (5 questions), stiffness (2 questions) and physical function (17 questions) subscales.The WOMAC total score was calculated for each participant at each time point for analysis as the mean score (range 0-100 mm VAS; 0=very good and 100=very poor) of 24 questions. LSM mean was calculated using a mixed-effects model repeated measures (MMRM) approach with treatment, visit and the interaction of treatment and visit were fitted as fixed effects in the model and baseline and pooled investigator site as baseline covariates. LSM mean was calculated using a mixed-effects model repeated measures (MMRM) approach with treatment, visit and the interaction of treatment and visit were fitted as fixed effects in the model and baseline and pooled investigator site as baseline covariates.
Baseline, 8 Weeks
Anaheim
California
92801
United States
Artemis Institute for Clinical Research
San Diego
California
92103
United States
Empire Clinical Research
Upland
California
91786
United States
Diablo Clinical Research
Walnut Creek
California
94598
United States
iM Research
West Covina
California
91760
United States
Horizons Clinical Research Center
Denver
Colorado
80220
United States
Avail Clinical Research LLC
DeLand
Florida
32720
United States
AGA Clinical Trials
Hialeah
Florida
33012
United States
Palm Springs Research Institute
Hialeah
Florida
33012
United States
Community Research Foundation Inc
Miami
Florida
33155
United States
Research Institute of South Florida, Inc.
Miami
Florida
33173
United States
M&M Medical Center
Miami
Florida
33185
United States
Renstar Medical Research
Ocala
Florida
34471
United States
Compass Research
Orlando
Florida
32806
United States
United Osteoporosis Center
Gainesville
Georgia
30501
United States
Drug Studies America
Marietta
Georgia
30060
United States
Medex Healthcare Research, Inc.
Chicago
Illinois
60602
United States
Buynak Clinical Research, P.C.
Valparaiso
Indiana
46383
United States
Beacon Clinical Research, LLC
Brockton
Massachusetts
02301
United States
ActivMed Practices & Research, Inc
Methuen
Massachusetts
01844
United States
The Center for Clinical Trials, Inc.
Biloxi
Mississippi
39531
United States
Arthritis, Rheumatic & Back Disease Associates
Voorhees Township
New Jersey
08043
United States
New Mexico Clinical Research & Osteoporosis Center
Albuquerque
New Mexico
87106
United States
Drug Trials of America
Hartsdale
New York
10530
United States
Medex Healthcare Research, Inc.
New York
New York
10016
United States
Upstate Clinical Research Associates
Williamsville
New York
14221
United States
PharmQuest
Greensboro
North Carolina
27408
United States
Family Practice Center of Wooster
Wooster
Ohio
44691
United States
Altoona Center for Clinical Research
Duncansville
Pennsylvania
16635
United States
Greater Providence Clinical Research, LLC
Warwick
Rhode Island
02888
United States
Clinical Trials of South Carolina
Charleston
South Carolina
29406
United States
PCPMG Clinical Research Unit
Greenville
South Carolina
29601
United States
Accurate Clinical Research
Nassau Bay
Texas
77058
United States
Quality Research, Inc.
San Antonio
Texas
78209
United States
Health Research of Hampton Roads Inc
Newport News
Virginia
23606
United States
National Clinical Research - Norfolk Inc
Norfolk
Virginia
23502
United States
Clinical Research Associates of Tidewater
Norfolk
Virginia
23507
United States
FG002
LY2951742 5 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC dose of 5 mg LY2951742 once every 4 weeks for 16 weeks.
FG003
LY2951742 50 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injection of 50 mg LY2951742 once every 4 weeks for 16 weeks.
FG004
LY2951742 120 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 120 mg LY2951742 once every 4 weeks for 16 weeks.
FG005
LY2951742 300 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 300 mg LY2951742 once every 4 weeks for 16 weeks.
FG00076 subjects
FG00139 subjects
FG00238 subjects
FG00338 subjects
FG00439 subjects
FG00538 subjects
Received at Least 1 Dose of Study Drug
FG00076 subjects
FG00139 subjects
FG00238 subjects
FG00338 subjects
FG00438 subjects
FG00537 subjects
COMPLETED
FG00022 subjects
FG00110 subjects
FG00213 subjects
FG00312 subjects
FG0049 subjects
FG0059 subjects
NOT COMPLETED
FG00054 subjects
FG00129 subjects
FG00225 subjects
FG00326 subjects
FG00430 subjects
FG00529 subjects
Type
Comment
Reasons
Adverse Event
FG0001 subjects
FG0011 subjects
FG0020 subjects
FG0030 subjects
FG0040 subjects
FG0050 subjects
Lost to Follow-up
FG0003 subjects
FG0013 subjects
FG0022 subjects
FG0031 subjects
FG004
Physician Decision
FG0002 subjects
FG0010 subjects
FG0020 subjects
FG0030 subjects
FG004
Terminated by Sponsor
FG00043 subjects
FG00123 subjects
FG00220 subjects
FG00323 subjects
FG004
Withdrawal by Subject
FG0004 subjects
FG0011 subjects
FG0022 subjects
FG0031 subjects
FG004
Could not Keep Visit Schedule
FG0001 subjects
FG0010 subjects
FG0020 subjects
FG0030 subjects
FG004
Positive Drug Screen
FG0000 subjects
FG0010 subjects
FG0020 subjects
FG0031 subjects
FG004
Inadequate Pain Relief
FG0000 subjects
FG0011 subjects
FG0021 subjects
FG0030 subjects
FG004
Randomized participants who received at least 1 dose of study drug.
Type of Units Analyzed
Not provided
Arm/Group Information
ID
Title
Description
BG000
Placebo
Placebo capsule orally, once daily for 16 weeks. Placebo subcutaneous (SC) once every 4 weeks for 16 weeks.
BG001
Celecoxib
Celecoxib 200 milligram (mg) capsule orally once daily for 16 weeks. Placebo SC once every 4 weeks for 16 weeks.
BG002
LY2951742 5 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC dose of 5 mg LY2951742 once every 4 weeks for 16 weeks.
BG003
LY2951742 50 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injection of 50 mg LY2951742 once every 4 weeks for 16 weeks.
BG004
LY2951742 120 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 120 mg LY2951742 once every 4 weeks for 16 weeks.
BG005
LY2951742 300 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 300 mg LY2951742 once every 4 weeks for 16 weeks.
BG006
Total
Total of all reporting groups
Denominators
Units
Counts
Participants
BG00076
BG00139
BG00238
BG00338
BG00438
BG00537
BG006266
Baseline Measures
Title
Description
Population Description
Parameter Type
Dispersion Type
Unit of Measure
Calculate Percentage
Denominator Units Selected
Denominators
Classes
Age, Continuous
Mean
Standard Deviation
years
Title
Denominators
Categories
Title
Measurements
BG00058.7± 7.94
BG00160.8± 9.86
BG00258.0± 9.60
BG003
Sex: Female, Male
Count of Participants
Participants
Title
Denominators
Categories
Title
Measurements
Female
BG00053
BG00124
BG002
Ethnicity (NIH/OMB)
Count of Participants
Participants
Title
Denominators
Categories
Title
Measurements
Hispanic or Latino
BG00042
BG00121
BG002
Race (NIH/OMB)
Count of Participants
Participants
Title
Denominators
Categories
Title
Measurements
American Indian or Alaska Native
BG0000
BG0010
BG002
Type
Title
Description
Population Description
Reporting Status
Anticipated Posting Date
Parameter Type
Dispersion Type
Unit of Measure
Calculate Percentage
Time Frame
Units Analyzed
Denominator Units Selected
Arm/Group Information
Denominators
Classes
Analyses
Primary
Change From Baseline to 8 Weeks in the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Pain Subscale
The 24-question WOMAC Osteoarthritis Index assesses osteoarthritis (OA) symptoms using pain (5 questions), stiffness (2 questions) and physical function (17 questions) subscales. The WOMAC pain subscale was calculated for each participant at each time point for analysis as the mean score (range 0-100 millimeter [mm] VAS; 0=very good and 100=very poor) of all 5 questions related to pain. Bayesian posterior adjusted mean was calculated using a Bayesian Normal Dynamic Linear Model (NDLM) dose response model with baseline and pooled investigator site included as baseline covariates.
Full Analysis Set (FAS) is the number of randomized participants who received at least 1 dose of study drug and had at least 1 post-dose baseline efficacy assessment. N = participants in the full analysis set with an evaluable WOMAC assessment at weeks 2, 4, 6 or 8. The 95% Crl (Credible Interval) is reported, not confidence interval (CI).
Posted
Least Squares Mean
95% Confidence Interval
mm
Baseline, 8 Weeks
ID
Title
Description
OG000
Placebo
Placebo capsule orally, once daily for 16 weeks. Placebo subcutaneous (SC) once every 4 weeks for 16 weeks.
OG001
Celecoxib
Celecoxib 200 milligram (mg) capsule orally once daily for 16 weeks. Placebo SC once every 4 weeks for 16 weeks.
OG002
LY2951742 5 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC dose of 5 mg LY2951742 once every 4 weeks for 16 weeks.
OG003
LY2951742 50 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injection of 50 mg LY2951742 once every 4 weeks for 16 weeks.
OG004
LY2951742 120 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 120 mg LY2951742 once every 4 weeks for 16 weeks.
OG005
LY2951742 300 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 300 mg LY2951742 once every 4 weeks for 16 weeks.
Units
Counts
Participants
OG00065
OG00132
OG00231
OG003
Title
Denominators
Categories
Title
Measurements
OG000-19.2(-24.7 to -13.4)
OG001-31.3(-40.1 to -22.5)
OG002-16.4(-23.9 to -8.6)
OG003
Secondary
Change From Baseline to 8 Weeks in the WOMAC Physical Function Subscale
The 24-question WOMAC Osteoarthritis Index assesses osteoarthritis symptoms using pain (5 questions), stiffness (2 questions) and physical function (17 questions) subscales. The WOMAC Osteoarthritis Index version 3.1 was administered according to the study schedule. The WOMAC physical function subscale was calculated for each participant at each time point for analysis as the mean score (range 0-100 mm VAS; 0=very good and 100=very poor) of all 17 questions related to physical function. Least Square Mean (LSM) was calculated using a mixed-effects model repeated measures (MMRM) approach with treatment, visit and the interaction of treatment and visit were fitted as fixed effects in the model and baseline and pooled investigator site as baseline covariates.
FAS: Randomized participants who received at least 1 dose of study drug and had at least 1 post-dose baseline efficacy assessment. N = participants in the full analysis set with an evaluable WOMAC assessment at weeks 2, 4, 6 or 8.
Posted
Least Squares Mean
95% Confidence Interval
mm
Baseline, 8 Weeks
ID
Title
Description
OG000
Placebo
Placebo capsule orally, once daily for 16 weeks. Placebo subcutaneous (SC) once every 4 weeks for 16 weeks.
OG001
Celecoxib
Celecoxib 200 milligram (mg) capsule orally once daily for 16 weeks. Placebo SC once every 4 weeks for 16 weeks.
Secondary
Change in Baseline to 8 Weeks in Patient's Global Assessment of Osteoarthritis
The PGA is a patient-rated instrument that measures their assessment of overall OA symptoms. It is based on the participant's response to the question "Considering all the ways your osteoarthritis affects you, how are you doing today?" using a 100 mm VAS (0=very good and 100=very poor). LSM mean was calculated using a mixed-effects model repeated measures (MMRM) approach with treatment, visit and the interaction of treatment and visit were fitted as fixed effects in the model and baseline and pooled investigator site as baseline covariates.
FAS: Randomized participants who received at least 1 dose of study drug and had at least 1 post-dose baseline efficacy assessment. N = participants in the full analysis set with an evaluable PGA assessment at weeks 2, 4, 6 or 8.
Posted
Least Squares Mean
95% Confidence Interval
mm
Baseline, 8 Weeks
ID
Title
Description
OG000
Placebo
Placebo capsule orally, once daily for 16 weeks. Placebo subcutaneous (SC) once every 4 weeks for 16 weeks
OG001
Celecoxib
Celecoxib 200 milligram (mg) capsule orally once daily for 16 weeks. Placebo SC once every 4 weeks for 16 weeks.
OG002
LY2951742 5 mg + Placebo
Secondary
Number of Participants With a Response Rate Measured by the Outcome Measures for Rheumatology Committee and Osteoarthritis Research Society International Standing Committee for Clinical Trials Response Criteria Initiative (OMERACT-OARSI)
The responders according to OMERACT-OARSI criteria: participants with at least 50 % improvement in pain or in function scores, along with absolute improvement of 20 mm, were considered responders. Alternatively, participants were considered responders if they showed at least 20% improvement and absolute improvement of 10 mm in at least two of the following scores: pain, function and Patients Global Assessment (PGA) scores.
FAS: Randomized participants who received at least 1 dose of study drug and had at least one post-dose efficacy assessment. N= participants analyzed in the full analysis set with an evaluable response rate at week 8.
Posted
Number
participants
8 Weeks
ID
Title
Description
OG000
Placebo
Placebo capsule orally, once daily for 16 weeks. Placebo subcutaneous (SC) once every 4 weeks for 16 weeks.
OG001
Celecoxib
Celecoxib 200 milligram (mg) capsule orally once daily for 16 weeks. Placebo SC once every 4 weeks for 16 weeks.
OG002
LY2951742 5 mg + Placebo
Secondary
Change From Baseline to 8 Weeks in the WOMAC Stiffness Subscale
The 24-question WOMAC Osteoarthritis Index assesses osteoarthritis symptoms using pain (5 questions), stiffness (2 questions) and physical function (17 questions) subscales. The WOMAC stiffness subscale will be calculated for each participant at each time point for analysis as the mean score (range 0-100 mm VAS; 0=very good and 100=very poor) of 2 questions related to stiffness. LSM mean was calculated using a mixed-effects model repeated measures (MMRM) approach with treatment, visit and the interaction of treatment and visit were fitted as fixed effects in the model and baseline and pooled investigator site as baseline covariates. LSM mean was calculated using a mixed-effects model repeated measures (MMRM) approach with treatment, visit and the interaction of treatment and visit were fitted as fixed effects in the model and baseline and pooled investigator site as baseline covariates.
FAS: Randomized participants who received at least 1 dose of study drug and had at least 1 post-dose baseline efficacy assessment. N = participants in the full analysis set with an evaluable WOMAC assessment at weeks 2, 4, 6 or 8.
Posted
Least Squares Mean
95% Confidence Interval
mm
Baseline, 8 Weeks
ID
Title
Description
OG000
Placebo
Placebo capsule orally, once daily for 16 weeks. Placebo subcutaneous (SC) once every 4 weeks for 16 weeks.
OG001
Celecoxib
Celecoxib 200 milligram (mg) capsule orally once daily for 16 weeks. Placebo SC once every 4 weeks for 16 weeks.
Secondary
Change From Baseline to 8 Weeks in the WOMAC Total Score
The 24-question WOMAC Osteoarthritis Index assesses osteoarthritis symptoms using pain (5 questions), stiffness (2 questions) and physical function (17 questions) subscales.The WOMAC total score was calculated for each participant at each time point for analysis as the mean score (range 0-100 mm VAS; 0=very good and 100=very poor) of 24 questions. LSM mean was calculated using a mixed-effects model repeated measures (MMRM) approach with treatment, visit and the interaction of treatment and visit were fitted as fixed effects in the model and baseline and pooled investigator site as baseline covariates. LSM mean was calculated using a mixed-effects model repeated measures (MMRM) approach with treatment, visit and the interaction of treatment and visit were fitted as fixed effects in the model and baseline and pooled investigator site as baseline covariates.
FAS: Randomized participants who received at least 1 dose of study drug and had at least 1 post-dose baseline efficacy assessment. N = participants in the full analysis set with an evaluable WOMAC assessment at weeks 2, 4, 6 or 8.
Posted
Least Squares Mean
95% Confidence Interval
mm
Baseline, 8 Weeks
ID
Title
Description
OG000
Placebo
Placebo capsule orally, once daily for 16 weeks. Placebo subcutaneous (SC) once every 4 weeks for 16 weeks.
OG001
Celecoxib
Celecoxib 200 milligram (mg) capsule orally once daily for 16 weeks. Placebo SC once every 4 weeks for 16 weeks.
Time Frame
Not provided
Description
All randomized participants who received at least 1 dose of study drug.
All-Cause Mortality Comment
Not provided
Arm/Groups
ID
Title
Description
Deaths (Affected)
Deaths (At Risk)
Serious Events (Affected)
Serious Events (At Risk)
Other Events (Affected)
Other Events (At Risk)
EG000
Placebo
Placebo capsule orally, once daily for 16 weeks. Placebo subcutaneous (SC) once every 4 weeks for 16 weeks.
1
76
27
76
EG001
Celecoxib
Celecoxib 200 milligram (mg) capsule orally once daily for 16 weeks. Placebo SC once every 4 weeks for 16 weeks.
0
39
13
39
EG002
LY2951742 5 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC dose of 5 mg LY2951742 once every 4 weeks for 16 weeks.
0
38
8
38
EG003
LY2951742 50 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injection of 50 mg LY2951742 once every 4 weeks for 16 weeks.
0
38
8
38
EG004
LY2951742 120 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 120 mg LY2951742 once every 4 weeks for 16 weeks.
0
38
13
38
EG005
LY2951742 300 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 300 mg LY2951742 once every 4 weeks for 16 weeks.
1
37
9
37
Serious Adverse Events
Term
Organ System
Source Vocabulary
Assessment Type
Notes
Statistical Information
Angina pectoris
Cardiac disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG0030 events0 affected38 at risk
EG0040 events0 affected38 at risk
EG0051 events1 affected37 at risk
Myocardial infarction
Cardiac disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Small intestinal obstruction
Gastrointestinal disorders
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Catheter site infection
Infections and infestations
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Other Adverse Events
Term
Organ System
Source Vocabulary
Assessment Type
Notes
Statistical Information
Atrial fibrillation
Cardiac disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG0030 events0 affected38 at risk
EG0041 events1 affected38 at risk
EG0050 events0 affected37 at risk
Atrioventricular block
Cardiac disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Left ventricular hypertrophy
Cardiac disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Abdominal discomfort
Gastrointestinal disorders
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Abdominal pain
Gastrointestinal disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0013 events2 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Constipation
Gastrointestinal disorders
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0011 events1 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Diarrhoea
Gastrointestinal disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Flatulence
Gastrointestinal disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Food poisoning
Gastrointestinal disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Large intestine polyp
Gastrointestinal disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0011 events1 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Nausea
Gastrointestinal disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0021 events1 affected38 at risk
EG003
Toothache
Gastrointestinal disorders
MedDRA 17.1
Systematic Assessment
EG0002 events1 affected76 at risk
EG0011 events1 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Vomiting
Gastrointestinal disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Chest pain
General disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Fatigue
General disorders
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0021 events1 affected38 at risk
EG003
Injection site reaction
General disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Local swelling
General disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0021 events1 affected38 at risk
EG003
Nodule
General disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Oedema peripheral
General disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0011 events1 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Pain
General disorders
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0022 events2 affected38 at risk
EG003
Pyrexia
General disorders
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Drug hypersensitivity
Immune system disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Food allergy
Immune system disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Seasonal allergy
Immune system disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0011 events1 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Bronchitis
Infections and infestations
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0011 events1 affected39 at risk
EG0021 events1 affected38 at risk
EG003
Ear infection
Infections and infestations
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Gastroenteritis viral
Infections and infestations
MedDRA 17.1
Systematic Assessment
EG0003 events3 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Influenza
Infections and infestations
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Nasopharyngitis
Infections and infestations
MedDRA 17.1
Systematic Assessment
EG0004 events4 affected76 at risk
EG0012 events2 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Oral herpes
Infections and infestations
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Otitis externa
Infections and infestations
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0021 events1 affected38 at risk
EG003
Otitis media
Infections and infestations
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Pharyngitis streptococcal
Infections and infestations
MedDRA 17.1
Systematic Assessment
EG0002 events2 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Tonsillitis
Infections and infestations
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0021 events1 affected38 at risk
EG003
Tooth infection
Infections and infestations
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Upper respiratory tract infection
Infections and infestations
MedDRA 17.1
Systematic Assessment
EG0002 events1 affected76 at risk
EG0011 events1 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Urinary tract infection
Infections and infestations
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0011 events1 affected39 at risk
EG0021 events1 affected38 at risk
EG003
Arthropod bite
Injury, poisoning and procedural complications
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Contusion
Injury, poisoning and procedural complications
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Fall
Injury, poisoning and procedural complications
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Joint injury
Injury, poisoning and procedural complications
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0011 events1 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Limb injury
Injury, poisoning and procedural complications
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Tooth fracture
Injury, poisoning and procedural complications
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0021 events1 affected38 at risk
EG003
Blood creatine phosphokinase increased
Investigations
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Blood creatinine increased
Investigations
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Blood glucose increased
Investigations
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Computerised tomogram abnormal
Investigations
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0021 events1 affected38 at risk
EG003
Electrocardiogram qt prolonged
Investigations
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Glomerular filtration rate decreased
Investigations
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0021 events1 affected38 at risk
EG003
Hepatic enzyme increased
Investigations
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Hypercholesterolaemia
Metabolism and nutrition disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0011 events1 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Type 2 diabetes mellitus
Metabolism and nutrition disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Arthralgia
Musculoskeletal and connective tissue disorders
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Back pain
Musculoskeletal and connective tissue disorders
MedDRA 17.1
Systematic Assessment
EG0002 events2 affected76 at risk
EG0011 events1 affected39 at risk
EG0021 events1 affected38 at risk
EG003
Bursitis
Musculoskeletal and connective tissue disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Muscle spasms
Musculoskeletal and connective tissue disorders
MedDRA 17.1
Systematic Assessment
EG0002 events2 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Musculoskeletal pain
Musculoskeletal and connective tissue disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Neck pain
Musculoskeletal and connective tissue disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Pain in extremity
Musculoskeletal and connective tissue disorders
MedDRA 17.1
Systematic Assessment
EG0003 events2 affected76 at risk
EG0013 events3 affected39 at risk
EG0021 events1 affected38 at risk
EG003
Rotator cuff syndrome
Musculoskeletal and connective tissue disorders
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Synovial cyst
Musculoskeletal and connective tissue disorders
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Basal cell carcinoma
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Benign breast neoplasm
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Burning sensation
Nervous system disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Convulsion
Nervous system disorders
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Dizziness
Nervous system disorders
MedDRA 17.1
Systematic Assessment
EG0002 events2 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Headache
Nervous system disorders
MedDRA 17.1
Systematic Assessment
EG0005 events2 affected76 at risk
EG0013 events1 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Depressed mood
Psychiatric disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0012 events1 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Seasonal affective disorder
Psychiatric disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0021 events1 affected38 at risk
EG003
Polyuria
Renal and urinary disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Cough
Respiratory, thoracic and mediastinal disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Oropharyngeal pain
Respiratory, thoracic and mediastinal disorders
MedDRA 17.1
Systematic Assessment
EG0002 events2 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Respiratory tract congestion
Respiratory, thoracic and mediastinal disorders
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Upper respiratory tract congestion
Respiratory, thoracic and mediastinal disorders
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Alopecia
Skin and subcutaneous tissue disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0021 events1 affected38 at risk
EG003
Erythema
Skin and subcutaneous tissue disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Pruritus
Skin and subcutaneous tissue disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0011 events1 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Rash
Skin and subcutaneous tissue disorders
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Urticaria
Skin and subcutaneous tissue disorders
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Tooth extraction
Surgical and medical procedures
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Hypertension
Vascular disorders
MedDRA 17.1
Systematic Assessment
EG0001 events1 affected76 at risk
EG0011 events1 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Peripheral arterial occlusive disease
Vascular disorders
MedDRA 17.1
Systematic Assessment
EG0000 events0 affected76 at risk
EG0010 events0 affected39 at risk
EG0020 events0 affected38 at risk
EG003
Certain Agreements
Are all PI(s) employees of the sponsor?
No
Restriction Type
GT60
Results Disclosure Restriction on PI(s)?
Yes
Other Details
Not provided
Point of Contact
Title
Organization
Phone
Extension
Email
Chief Medical Officer
Eli Lilly and Company
800-545-5979
ID
Term
D020370
Osteoarthritis, Knee
Ancestor Terms
ID
Term
D010003
Osteoarthritis
D001168
Arthritis
D007592
Joint Diseases
D009140
Musculoskeletal Diseases
D012216
Rheumatic Diseases
Browse Leaves
Not provided
Browse Branches
Not provided
ID
Term
C000628360
galcanezumab
D000068579
Celecoxib
Ancestor Terms
ID
Term
D000096926
Benzenesulfonamides
D013449
Sulfonamides
D000577
Amides
D009930
Organic Chemicals
D001555
Benzene Derivatives
D006841
Hydrocarbons, Aromatic
D006844
Hydrocarbons, Cyclic
D006838
Hydrocarbons
D013450
Sulfones
D013457
Sulfur Compounds
D011720
Pyrazoles
D001393
Azoles
D006573
Heterocyclic Compounds, 1-Ring
D006571
Heterocyclic Compounds
Browse Leaves
Not provided
Browse Branches
Not provided
4 subjects
FG0053 subjects
0 subjects
FG0050 subjects
21 subjects
FG00523 subjects
5 subjects
FG0053 subjects
0 subjects
FG0050 subjects
0 subjects
FG0050 subjects
0 subjects
FG0050 subjects
56.7
± 7.95
BG00458± 9.29
BG00556.4± 9.38
BG00658.2± 8.91
23
BG00322
BG00423
BG00519
BG006164
Male
BG00023
BG00115
BG00215
BG00316
BG00415
BG00518
BG006102
17
BG00319
BG00419
BG00517
BG006135
Not Hispanic or Latino
BG00034
BG00118
BG00221
BG00319
BG00418
BG00520
BG006130
Unknown or Not Reported
BG0000
BG0010
BG0020
BG0030
BG0041
BG0050
BG0061
0
BG0030
BG0040
BG0050
BG0060
Asian
BG0002
BG0011
BG0022
BG0030
BG0040
BG0050
BG0065
Native Hawaiian or Other Pacific Islander
BG0000
BG0010
BG0020
BG0030
BG0040
BG0050
BG0060
Black or African American
BG00019
BG0017
BG00211
BG00313
BG00412
BG00513
BG00675
White
BG00054
BG00131
BG00225
BG00325
BG00423
BG00523
BG006181
More than one race
BG0000
BG0010
BG0020
BG0030
BG0040
BG0050
BG0060
Unknown or Not Reported
BG0001
BG0010
BG0020
BG0030
BG0043
BG0051
BG0065
31
OG00430
OG00530
-24.2
(-31.0 to -17.2)
OG004-21.8(-29.3 to -14.2)
OG005-17.7(-25.2 to -10.0)
OG002
LY2951742 5 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC dose of 5 mg LY2951742 once every 4 weeks for 16 weeks.
OG003
LY2951742 50 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injection of 50 mg LY2951742 once every 4 weeks for 16 weeks.
OG004
LY2951742 120 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 120 mg LY2951742 once every 4 weeks for 16 weeks.
OG005
LY2951742 300 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 300 mg LY2951742 once every 4 weeks for 16 weeks.
Units
Counts
Participants
OG00065
OG00132
OG00231
OG00331
OG00430
OG00530
Title
Denominators
Categories
Title
Measurements
OG000-16.5(-22.3 to -10.8)
OG001-30.6(-38.8 to -22.4)
OG002-15.4(-23.7 to -7.12)
OG003-23.5(-31.4 to -15.6)
OG004-19.5(-28.2 to -10.9)
OG005-18.4(-26.8 to -9.9)
Placebo capsule orally, once daily for 16 weeks. SC dose of 5 mg LY2951742 once every 4 weeks for 16 weeks.
OG003
LY2951742 50 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injection of 50 mg LY2951742 once every 4 weeks for 16 weeks.
OG004
LY2951742 120 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 120 mg LY2951742 once every 4 weeks for 16 weeks.
OG005
LY2951742 300 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 300 mg LY2951742 once every 4 weeks for 16 weeks.
Units
Counts
Participants
OG00062
OG00131
OG00229
OG00330
OG00428
OG00528
Title
Denominators
Categories
Title
Measurements
OG000-22.5(-28.8 to -16.2)
OG001-36.7(-45.7 to -27.6)
OG002-18.5(-27.9 to -9.1)
OG003-19.4(-28.0 to -10.8)
OG004-21.2(-31.2 to -11.1)
OG005-20.4(-30.0 to -10.9)
Placebo capsule orally, once daily for 16 weeks. SC dose of 5 mg LY2951742 once every 4 weeks for 16 weeks.
OG003
LY2951742 50 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injection of 50 mg LY2951742 once every 4 weeks for 16 weeks.
OG004
LY2951742 120 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 120 mg LY2951742 once every 4 weeks for 16 weeks.
OG005
LY2951742 300 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 300 mg LY2951742 once every 4 weeks for 16 weeks.
Units
Counts
Participants
OG00041
OG00120
OG00229
OG00322
OG00416
OG00519
Title
Denominators
Categories
Title
Measurements
OG00021
OG00114
OG0027
OG00315
OG00410
OG00510
OG002
LY2951742 5 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC dose of 5 mg LY2951742 once every 4 weeks for 16 weeks.
OG003
LY2951742 50 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injection of 50 mg LY2951742 once every 4 weeks for 16 weeks.
OG004
LY2951742 120 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 120 mg LY2951742 once every 4 weeks for 16 weeks.
OG005
LY2951742 300 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 300 mg LY2951742 once every 4 weeks for 16 weeks.
Units
Counts
Participants
OG00065
OG00132
OG00231
OG00331
OG00430
OG00530
Title
Denominators
Categories
Title
Measurements
OG000-18.5(-24.6 to -12.4)
OG001-31.4(-40.1 to -22.7)
OG002-15.1(-24.0 to -6.3)
OG003-23.7(-32.1 to -15.4)
OG004-21.3(-30.7 to -12.0)
OG005-17.3(-26.2 to -8.3)
OG002
LY2951742 5 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC dose of 5 mg LY2951742 once every 4 weeks for 16 weeks.
OG003
LY2951742 50 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injection of 50 mg LY2951742 once every 4 weeks for 16 weeks.
OG004
LY2951742 120 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 120 mg LY2951742 once every 4 weeks for 16 weeks.
OG005
LY2951742 300 mg + Placebo
Placebo capsule orally, once daily for 16 weeks. SC injections of 300 mg LY2951742 once every 4 weeks for 16 weeks.