NCT07353931ClinicalTrials.gov
Efficacy and Safety of Eloralintide (LY3841136) in Participants With Osteoarthritis Knee Pain and Obesity or Overweight
A Master Protocol for Phase 3 Randomized, Double-Blind, Placebo-Controlled Studies to Investigate the Efficacy and Safety of Once Weekly Eloralintide in Adult Participants With Osteoarthritis Knee Pain, and Obesity or Overweight (ENLIGHTEN-4)
Kurz gefasst
The YDAN master protocol will support two independent studies, J3R-MC-YOA1 and J3R-MC-YOA2. Each study will investigate how well and safely Eloralintide (LY3841136) works in adults with obesity or overweight who have osteoarthritis (OA) of the knee with pain. Participation in…
Phase 3900 Teilnehmende gesucht152 Studienzentren14 Länder
Kategorien
In 1 Register registriert
- ClinicalTrials.govNCT07353931Diesen Eintrag bei ClinicalTrials.gov öffnenSynchronisiert vor 2 Wochen
Eine Studie kann in mehreren Registern registriert sein. Wir zeigen sie einmal und verlinken jeden Eintrag, den wir haben.
Die Studieninformationen werden so angezeigt, wie sie vom Register veröffentlicht wurden, in ihrer Originalsprache.
Interesse an dieser Studie?
Anmelden oder ein Konto erstellen um Ihr Interesse zu bekunden und diese Studie zu verfolgen.
How this study is set up
The points below are drawn from the public registry record for this study. Each one cites the field or sentence it came from. A dash (—) means the record does not state something — not that it is missing or wrong. Many well-run studies, especially small ones, leave some of these blank.
- Present: Registered before enrolment beganFirst posted 2026-01-21; recorded start 2026-02-09
- Present: Has a defined primary outcomeA primary outcome measure is listed in the record
- Present: The primary outcome states a time frameThe primary outcome measure records a time frame
- Present: Participants are randomly assignedAllocation is recorded as randomised
- Present: Has a comparison groupThe record lists a placebo or comparator arm, or more than one study arm
- Present: Uses blinding (masking)A masking level is recorded in the record
- Not stated: An ethics committee is not stated in the registry recordThis registry's ingested record has no ethics-committee field
- Not stated: Regulatory oversight (such as an IND or IDE) is not stated in the registry recordThis registry's ingested record has no regulatory-authorisation field
- Not stated: A data monitoring committee is not stated in the registry recordThis registry's ingested record has no data-monitoring-committee fieldA data monitoring committee is not required for many smaller studies, and its absence here is not unusual.
- Present: No cost to participants is mentioned in the recordChecked the summary, description and eligibility text; no cost-to-participant phrase found
- Present: Sponsor has 347 other studies in this databaseCounted from the lead sponsor named in the record (Eli Lilly and Company)
- Present: Sponsor has posted results for at least one studyBased on the sponsor’s studies in this database
- The record lists 2 conditions.
- Lead sponsor type recorded as: industry.
- Intervention regulatory context: investigational, within a phased regulatory pathway.
Trial stature
Three independent measures of this study, described from its registry record — not a recommendation about it. A rigorous study by investigators nobody has heard of is better evidence than a weak study led by a famous one. How these are scored.
A strong methodological design for a phase 3 study, judged from its ClinicalTrials.gov record.
How this score is built
- Randomised allocation20/20
Participants are randomly allocated between arms
- Blinding13/20
Double-blind
- Control arm13/15
Placebo / sham control arm
- Primary-outcome specificity10/10
Named primary outcome with a defined time frame
- Endpoint type3/10
Surrogate or intermediate endpoint (conservative default)
- Multi-centre8/8
Multi-centre: 161 sites
- Data monitoring committee7/7
A data monitoring committee is in place
- Prospective registration5/5
Registered before the study start date
- Protocol / SAP posted0/5
No protocol or SAP posted to the registry
A large study, international in scope: 900 participants (target), run at 152 sites, across 14 countries.
How this score is built
- Enrolment29/40
900 participants (target)
- Site count24/25
161 sites
- Country count12/15
15 countries
- Planned duration7/10
Planned over about 27 months
- Sponsor scale9/10
Eli Lilly and Company has led 326 trials in our corpus
We have no verifiable track record for the investigator named on this trial. That is common for early-career investigators and for records held outside ClinicalTrials.gov — it is not a negative signal.
How this score is built
- Investigator standing0/100
No investigator recorded in the registry for this trial
These describe the registry record only, and today we hold ClinicalTrials.gov data. Absent fields lower a score, and absence often reflects registration practice rather than study quality. A high-stature trial is not necessarily safer or a better choice for you — enrolling in a large definitive trial can mean a higher chance of receiving placebo, while a small early-phase study may be the only route to a new therapy.
Zusammenfassung
The YDAN master protocol will support two independent studies, J3R-MC-YOA1 and J3R-MC-YOA2. Each study will investigate how well and safely Eloralintide (LY3841136) works in adults with obesity or overweight who have osteoarthritis (OA) of the knee with pain. Participation in the study will last about 75 weeks, including screening.
Erkrankungen
- Osteoarthritis
- Overweight or Obesity
Eignung
| Geschlecht | Alle |
|---|---|
| Alter | 18 Years – Kein Höchstalter |
| Gesunde Freiwillige | Nein |
Eignung im Wortlaut des Registers
Eignung in einfachen Aussagen
Die Kriterien dieses Eintrags wurden noch nicht in einzelne Aussagen aufgeschlüsselt. Der Registertext oben ist vollständig und ist die maßgebliche Fassung.
Studiendesign
| Studientyp | Interventionell |
|---|---|
| Phase | Phase 3 |
| Zuteilung | Randomisiert |
| Interventionsmodell | PARALLEL |
| Primäres Ziel | TREATMENT |
| Verblindung | DOUBLE (2) |
| Teilnahme | 900 Teilnehmende gesucht |
Sponsor und Mitwirkende
- Eli Lilly and Company Sponsor
Studienarme und Interventionen
- Eloralintide (YOA1)EXPERIMENTAL
Participants will receive eloralintide subcutaneously (SC)
- Placebo (YOA1)PLACEBO_COMPARATOR
Participants will receive placebo SC
- Eloralintide (YOA2)EXPERIMENTAL
Participants will receive eloralintide SC
- Placebo (YOA2)PLACEBO_COMPARATOR
Participants will receive placebo SC
Interventionen
- Arzneimittel Eloralintide
Administered SC
- Arzneimittel Placebo
Placebo administered SC
Endpunkte
Primärer Endpunkt
Percent Change from Baseline in Body Weight
Percent Change from Baseline in Body Weight
Zeitrahmen Baseline, Week 64
Primärer Endpunkt
Change from Baseline in the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Pain Subscale Score
Change from Baseline in the WOMAC Pain Subscale Score
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Change from Baseline in Systolic Blood Pressure (SBP)
Change from Baseline in SBP
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Percent Change from Baseline in Triglycerides
Percent Change in Baseline in Triglycerides
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Change from Baseline in Short Form-36 (SF-36 v2) Acute Form Physical Functioning Domain Score
Change from Baseline in SF-36 v2 Score
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Percent Change from Baseline in High Sensitivity, C-reactive Protein (hsCRP)
Percent Change from Baseline in hsCRP
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Change from Baseline in the WOMAC Physical Function Subscale Score
Change from Baseline in the WOMAC Physical Function Subscale Score
Zeitrahmen Baseline, Week 40, Week 64
Sekundärer Endpunkt
Change from Baseline WOMAC Pain Subscale Score
Change from Baseline WOMAC Pain Subscale Score
Zeitrahmen Baseline, Week 40
Sekundärer Endpunkt
Change from Baseline in Distance Walked During the 6-Minute Walk Test
Change from Baseline in Distance Walked During the 6-Minute Walk Test
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Change from Baseline in Body Mass Index (BMI)
Change from Baseline in BMI
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Change in Medication Use
Change in Medication Use
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Change from Baseline in SF-36v2 Acute Form Domain Scores With Exception of the Physical Functioning Domain Score
Change from Baseline in SF-36v2 Acute Form Domain Scores With Exception of the Physical Functioning Domain Score
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Change from Baseline in Health Status EQ-5D-5L Health State Utility
Change from Baseline in Health Status EQ-5D-5L Health State Utility
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Percent Change from Baseline in Fasting Insulin
Percent Change from Baseline in Fasting Insulin
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Percent Change from Baseline in Total Cholesterol
Percent Change from Baseline in Total Cholesterol
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Change from Baseline in Waist Circumference
Change from Baseline in Waist Circumference
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Percent Change from Baseline in Hemoglobin A1c (HbA1c)
Percent Change from Baseline in HbA1c
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Change from Baseline in WOMAC Stiffness Subscale Score
Change from Baseline in WOMAC Stiffness Subscale Score
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Change from Baseline in WOMAC Total Score
Change from Baseline in WOMAC Total Score
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Achievement of Improved Categorical Shift in Patient Global Impression of Severity (PGIS) - Target Knee Pain
Achievement of Improved Categorical Shift in PGIS - Target Knee Pain
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Achievement of Improved Categorical Shift in Patient Global Impression of Severity (PGIS) - Target Knee Function
Achievement of Improved Categorical Shift in PGIS - Target Knee Function
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Change from Baseline in Average Pain Intensity Numeric Rating Scale (API-NRS) Score
Change from Baseline in API-NRS Score
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Change from Baseline in Worst Pain Intensity Numeric Rating Scale (WPI-NRS) Score
Change from Baseline in WPI-NRS Score
Zeitrahmen Baseline, Week 64
Sekundärer Endpunkt
Pharmacokinetics (PK): Maximum Concentration at Steady State (Cmax, ss)
PK: Cmax, ss
Zeitrahmen Baseline through Week 64
Sekundärer Endpunkt
PK: Area Under the Concentration Versus Time Curve for One Dosing Interval at Steady State (AUC(0-T)ss)
PK: AUC(0-T)ss
Zeitrahmen Baseline through Week 64
Sekundärer Endpunkt
Number of Participants with Allowed Concomitant Pain Medication
Number of Participants with Allowed Concomitant Pain Medication
Zeitrahmen Baseline, Week 64
Daten
| Startdatum | 9. Februar 2026 (tatsächlich) |
|---|---|
| Primärer Abschluss | 1. März 2028 (geschätzt) |
| Abschluss | 1. Mai 2028 (geschätzt) |
| Erstveröffentlichung | 21. Januar 2026 (tatsächlich) |
| Zuletzt aktualisiert | 8. September 2026 |
| Ergebnisse veröffentlicht | Im Registereintrag nicht angegeben |
| Status zuletzt bestätigt | September 2026 |
Tatsächlich bedeutet, dass das Ereignis eingetreten ist. Geschätzt bedeutet, dass der Sponsor es erwartet. Die beiden bedeuten Unterschiedliches.
Standorte
126 Studienzentren rekrutieren
Argentina
| Einrichtung | Stadt | Bundesland oder Region | Status |
|---|---|---|---|
| Centro Privado de Medicina Familiar / Mindout Research | Buenos Aires | Rekrutierung noch nicht begonnen | |
| Centro Médico Arsema | Buenos Aires | Rekrutierung noch nicht begonnen | |
| Stat Research S.A. | Buenos Aires | Rekrutierung noch nicht begonnen | |
| Organizacion Medica de Investigacion | Buenos Aires | Rekrutierung noch nicht begonnen | |
| CARDIAMET Investigaciones Médicas | Buenos Aires | Rekrutierung noch nicht begonnen | |
| Centro de Investigaciones Clínicas Baigorria | Granadero Baigorria | Rekrutierung noch nicht begonnen | |
| INECO Neurociencias Oroño | Rosario | Rekrutierung noch nicht begonnen | |
| Instituto Especialidades de la Salud Rosario | Rosario | Rekrutierung noch nicht begonnen | |
| Centro de Investigaciones Médicas Tucuman | SAN M. de Tucuman | Rekrutierung noch nicht begonnen | |
| Medicina Reumatológica | San Fernando | Rekrutierung noch nicht begonnen | |
| Instituto de Alta Complejidad San Isidro | San Isidro | Rekrutierung noch nicht begonnen | |
| Centro Polivalente de Asistencia e Investigacion Clinica - CER San Juan | San Juan | Rekrutierung noch nicht begonnen | |
| Centro de Investigaciones Reumatológicas | San Miguel de Tucumán | Rekrutierung noch nicht begonnen | |
| Go Centro Medico San Nicolás | San Nicolás | Rekrutierung noch nicht begonnen |
Belgium
| Einrichtung | Stadt | Bundesland oder Region | Status |
|---|---|---|---|
| Antwerp University Hospital | Edegem | Rekrutiert | |
| Reuma Clinic, Locatie Jaarbeurslaan | Genk | Rekrutiert | |
| UZ Gent | Ghent | Rekrutiert | |
| Kormont | Kluisbergen | Rekrutiert | |
| UZ Leuven | Leuven | Rekrutiert | |
| Meclinas | Mechelen | Rekrutiert | |
| ZNA Jan Palfijn | Merksem | Rekrutierung noch nicht begonnen | |
| Medisch Centrum Latem (Hip Clinic) - Algemeen Ziekenhuis Maria Middelares Location | Sint-Martens-Latem | Rekrutierung noch nicht begonnen |
Brazil
| Einrichtung | Stadt | Bundesland oder Region | Status |
|---|---|---|---|
| Centro de Pesquisa Sao Lucas | Campinas | Ausgesetzt | |
| IBPClin - Instituto Brasil de Pesquisa Clínica | Rio de Janeiro | Ausgesetzt | |
| CPHosp Medicina, Ensino e Pesquisa (CPQuali) | São Paulo | Ausgesetzt | |
| INTEGRA - Pesquisa Clínica e Infusões | São Paulo | Ausgesetzt | |
| CEPIC - Centro Paulista de Investigação Clínica | São Paulo | Ausgesetzt | |
| Hospital das Clinicas FMUSP | São Paulo | Ausgesetzt |
Canada
| Einrichtung | Stadt | Bundesland oder Region | Status |
|---|---|---|---|
| Apex Trials | Guelph | Rekrutiert | |
| G.R.M.O. (Groupe de recherche en maladies osseuses) Inc. | Québec | Rekrutierung noch nicht begonnen | |
| Diex Recherche Inc. Division Quebec | Québec | Rekrutiert | |
| Stouffville Medical Research Institute Inc. | Stouffville | Rekrutiert | |
| Maple Leaf Research | Toronto | Rekrutiert | |
| Dr. Anil K. Gupta Medicine Professional Corporation | Toronto | Rekrutiert | |
| Diex Recherche Inc. Division Victoriaville | Victoriaville | Rekrutiert |
China
| Einrichtung | Stadt | Bundesland oder Region | Status |
|---|---|---|---|
| Beijing Ji Shui Tan Hospital | Beijing | Rekrutiert | |
| The First Afflilated Hospital of Bengbu Medical College | Bengbu | Rekrutiert | |
| Jilin Province People's Hospital | Changchun | Rekrutiert | |
| The Second Hospital of Jilin University | Changchun | Rekrutierung noch nicht begonnen | |
| Xiangya Hospital Central South University | Changsha | Rekrutiert | |
| 2nd Affiliated Hospital Chongqing Medical Universi | Chongqing | Rekrutiert | |
| The Second Affiliated hospital of Zhejiang University school of medicine | Hangzhou | Rekrutiert | |
| The Second People's Hospital of Hefei | Hefei | Rekrutiert | |
| Jinan Central Hospital | Jinan | Rekrutiert | |
| The First Affiliated Hospital of Henan University of Science &Technology | Luoyang | Rekrutiert | |
| Nanjing First Hospital | Nanjing | Rekrutiert | |
| Zhongda Hospital Southeast University | Nanjing | Rekrutiert | |
| The Second Affiliated Hospital of Nanjing Medical University | Nanjing | Rekrutiert | |
| Jiangsu Province Hospital | Nanjing | Rekrutiert | |
| The first affiliated hospital of Ningbo university | Ningbo | Rekrutiert |
102 weitere Studienzentren sind im Registereintrag aufgeführt.
Studiendokumente
In diesem Registereintrag sind keine Dokumente verlinkt.
Änderungen im Zeitverlauf
- 6. August 2026
Studienzentrum entfernt
9 sites removed (152 total)
161152