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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)

RekrutiertNimmt laut Registereintrag derzeit Teilnehmende auf.
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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

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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.

Methodological rigourSTRONG

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

ScaleLARGE

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

Investigator standingUNKNOWN

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

Eignung
GeschlechtAlle
Alter18 YearsKein Höchstalter
Gesunde FreiwilligeNein

Eignung im Wortlaut des Registers

Inclusion Criteria: * Have a body mass index (BMI) of 27 kilograms per square meter (kg/m²) or higher at screening * Have a stable body weight (less than 5% body weight change) for 90 days prior to screening * Have tried at least once to lose weight through diet but were unsuccessful * Have osteoarthritis of the knee and at least one of the following conditions: * Be over 50 years old * Have morning knee stiffness that lasts about 30 minutes * Have a crackling or grinding sound or feeling in the knee Exclusion Criteria: * Have a prior or planned surgical treatment for obesity (liposuction, cryolipolysis, or abdominoplasty allowed if performed greater than 1 year before screening) * Have a prior or planned endoscopic procedure and/or device-based therapy for obesity (prior device-based therapy acceptable if device removal was more than 6 months prior to screening) * Have type 1 diabetes, type 2 diabetes, or any other type of diabetes * Have an active knee infection * Have had within 90 days prior to screening: * heart attack * stroke * coronary artery revascularization * unstable angina, or * hospitalization due to congestive heart failure * Have a history or diagnosis of New York Heart Association Functional Classification Class IV congestive heart failure * Have taken medications or alternative remedies intended for weight loss within 90 days of screening

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

Studiendesign
StudientypInterventionell
PhasePhase 3
ZuteilungRandomisiert
InterventionsmodellPARALLEL
Primäres ZielTREATMENT
VerblindungDOUBLE (2)
Teilnahme900 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

  1. Primärer Endpunkt

    Percent Change from Baseline in Body Weight

    Percent Change from Baseline in Body Weight

    Zeitrahmen Baseline, Week 64

  2. 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

  3. Sekundärer Endpunkt

    Change from Baseline in Systolic Blood Pressure (SBP)

    Change from Baseline in SBP

    Zeitrahmen Baseline, Week 64

  4. Sekundärer Endpunkt

    Percent Change from Baseline in Triglycerides

    Percent Change in Baseline in Triglycerides

    Zeitrahmen Baseline, Week 64

  5. 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

  6. Sekundärer Endpunkt

    Percent Change from Baseline in High Sensitivity, C-reactive Protein (hsCRP)

    Percent Change from Baseline in hsCRP

    Zeitrahmen Baseline, Week 64

  7. 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

  8. Sekundärer Endpunkt

    Change from Baseline WOMAC Pain Subscale Score

    Change from Baseline WOMAC Pain Subscale Score

    Zeitrahmen Baseline, Week 40

  9. 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

  10. Sekundärer Endpunkt

    Change from Baseline in Body Mass Index (BMI)

    Change from Baseline in BMI

    Zeitrahmen Baseline, Week 64

  11. Sekundärer Endpunkt

    Change in Medication Use

    Change in Medication Use

    Zeitrahmen Baseline, Week 64

  12. 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

  13. 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

  14. Sekundärer Endpunkt

    Percent Change from Baseline in Fasting Insulin

    Percent Change from Baseline in Fasting Insulin

    Zeitrahmen Baseline, Week 64

  15. Sekundärer Endpunkt

    Percent Change from Baseline in Total Cholesterol

    Percent Change from Baseline in Total Cholesterol

    Zeitrahmen Baseline, Week 64

  16. Sekundärer Endpunkt

    Change from Baseline in Waist Circumference

    Change from Baseline in Waist Circumference

    Zeitrahmen Baseline, Week 64

  17. Sekundärer Endpunkt

    Percent Change from Baseline in Hemoglobin A1c (HbA1c)

    Percent Change from Baseline in HbA1c

    Zeitrahmen Baseline, Week 64

  18. Sekundärer Endpunkt

    Change from Baseline in WOMAC Stiffness Subscale Score

    Change from Baseline in WOMAC Stiffness Subscale Score

    Zeitrahmen Baseline, Week 64

  19. Sekundärer Endpunkt

    Change from Baseline in WOMAC Total Score

    Change from Baseline in WOMAC Total Score

    Zeitrahmen Baseline, Week 64

  20. 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

  21. 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

  22. 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

  23. 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

  24. Sekundärer Endpunkt

    Pharmacokinetics (PK): Maximum Concentration at Steady State (Cmax, ss)

    PK: Cmax, ss

    Zeitrahmen Baseline through Week 64

  25. 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

  26. Sekundärer Endpunkt

    Number of Participants with Allowed Concomitant Pain Medication

    Number of Participants with Allowed Concomitant Pain Medication

    Zeitrahmen Baseline, Week 64

Daten

Daten
Startdatum9. Februar 2026 (tatsächlich)
Primärer Abschluss1. März 2028 (geschätzt)
Abschluss1. Mai 2028 (geschätzt)
Erstveröffentlichung21. Januar 2026 (tatsächlich)
Zuletzt aktualisiert8. September 2026
Ergebnisse veröffentlichtIm Registereintrag nicht angegeben
Status zuletzt bestätigtSeptember 2026

Tatsächlich bedeutet, dass das Ereignis eingetreten ist. Geschätzt bedeutet, dass der Sponsor es erwartet. Die beiden bedeuten Unterschiedliches.

Standorte

126 Studienzentren rekrutieren

Argentina

Argentina
EinrichtungStadtBundesland oder RegionStatus
Centro Privado de Medicina Familiar / Mindout ResearchBuenos AiresRekrutierung noch nicht begonnen
Centro Médico ArsemaBuenos AiresRekrutierung noch nicht begonnen
Stat Research S.A.Buenos AiresRekrutierung noch nicht begonnen
Organizacion Medica de InvestigacionBuenos AiresRekrutierung noch nicht begonnen
CARDIAMET Investigaciones MédicasBuenos AiresRekrutierung noch nicht begonnen
Centro de Investigaciones Clínicas BaigorriaGranadero BaigorriaRekrutierung noch nicht begonnen
INECO Neurociencias OroñoRosarioRekrutierung noch nicht begonnen
Instituto Especialidades de la Salud RosarioRosarioRekrutierung noch nicht begonnen
Centro de Investigaciones Médicas TucumanSAN M. de TucumanRekrutierung noch nicht begonnen
Medicina ReumatológicaSan FernandoRekrutierung noch nicht begonnen
Instituto de Alta Complejidad San IsidroSan IsidroRekrutierung noch nicht begonnen
Centro Polivalente de Asistencia e Investigacion Clinica - CER San JuanSan JuanRekrutierung noch nicht begonnen
Centro de Investigaciones ReumatológicasSan Miguel de TucumánRekrutierung noch nicht begonnen
Go Centro Medico San NicolásSan NicolásRekrutierung noch nicht begonnen

Belgium

Belgium
EinrichtungStadtBundesland oder RegionStatus
Antwerp University HospitalEdegemRekrutiert
Reuma Clinic, Locatie JaarbeurslaanGenkRekrutiert
UZ GentGhentRekrutiert
KormontKluisbergenRekrutiert
UZ LeuvenLeuvenRekrutiert
MeclinasMechelenRekrutiert
ZNA Jan PalfijnMerksemRekrutierung noch nicht begonnen
Medisch Centrum Latem (Hip Clinic) - Algemeen Ziekenhuis Maria Middelares LocationSint-Martens-LatemRekrutierung noch nicht begonnen

Brazil

Brazil
EinrichtungStadtBundesland oder RegionStatus
Centro de Pesquisa Sao LucasCampinasAusgesetzt
IBPClin - Instituto Brasil de Pesquisa ClínicaRio de JaneiroAusgesetzt
CPHosp Medicina, Ensino e Pesquisa (CPQuali)São PauloAusgesetzt
INTEGRA - Pesquisa Clínica e InfusõesSão PauloAusgesetzt
CEPIC - Centro Paulista de Investigação ClínicaSão PauloAusgesetzt
Hospital das Clinicas FMUSPSão PauloAusgesetzt

Canada

Canada
EinrichtungStadtBundesland oder RegionStatus
Apex TrialsGuelphRekrutiert
G.R.M.O. (Groupe de recherche en maladies osseuses) Inc.QuébecRekrutierung noch nicht begonnen
Diex Recherche Inc. Division QuebecQuébecRekrutiert
Stouffville Medical Research Institute Inc.StouffvilleRekrutiert
Maple Leaf ResearchTorontoRekrutiert
Dr. Anil K. Gupta Medicine Professional CorporationTorontoRekrutiert
Diex Recherche Inc. Division VictoriavilleVictoriavilleRekrutiert

China

China
EinrichtungStadtBundesland oder RegionStatus
Beijing Ji Shui Tan HospitalBeijingRekrutiert
The First Afflilated Hospital of Bengbu Medical CollegeBengbuRekrutiert
Jilin Province People's HospitalChangchunRekrutiert
The Second Hospital of Jilin UniversityChangchunRekrutierung noch nicht begonnen
Xiangya Hospital Central South UniversityChangshaRekrutiert
2nd Affiliated Hospital Chongqing Medical UniversiChongqingRekrutiert
The Second Affiliated hospital of Zhejiang University school of medicineHangzhouRekrutiert
The Second People's Hospital of HefeiHefeiRekrutiert
Jinan Central HospitalJinanRekrutiert
The First Affiliated Hospital of Henan University of Science &TechnologyLuoyangRekrutiert
Nanjing First HospitalNanjingRekrutiert
Zhongda Hospital Southeast UniversityNanjingRekrutiert
The Second Affiliated Hospital of Nanjing Medical UniversityNanjingRekrutiert
Jiangsu Province HospitalNanjingRekrutiert
The first affiliated hospital of Ningbo universityNingboRekrutiert

102 weitere Studienzentren sind im Registereintrag aufgeführt.

Studiendokumente

In diesem Registereintrag sind keine Dokumente verlinkt.

Änderungen im Zeitverlauf

  1. 6. August 2026

    Studienzentrum entfernt

    9 sites removed (152 total)

    161152