ClinicalTrials.gg
RecruitingNCT07321886ENLIGHTEN-1Updated Sep 22, 2026

A Study of Eloralintide (LY3841136) in Participants With Obesity, or Overweight Without Type 2 Diabetes

A Phase 3 interventional study of Eloralintide and Placebo in Obesity and Overweight, sponsored by Eli Lilly and Company. Recruiting at 158 sites in 15 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-22.

Sponsored by Eli Lilly and Company · Phase 3, Interventional, and Treatment

From the registry’s dates

  • Started Feb 2026; still recruiting 9 months later.

Help build ClinicalTrials.gg — short surveys, remote interviews or testing, in your language. Take part →

Phase
Phase 3
Study type
Interventional
Enrollment
1,980
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-15

Among 22 studies testing eloralintide in Obesity — 14 open to participants now, 15 under way, 8 of them phase 3. eloralintide · Obesity.

Planned enrollment
3rd of 22
1,980 · median 315
Started
2026
with 11 others
Phase 3
8 of 22
8 open now
Primary completion
2028-03
later than 8 of 14 live
Registered
11th of 22
by date
Lead sponsor
22 of 22
Eli Lilly and Company

Among the 22 studies testing eloralintide in Obesity, this one is the 3rd largest by planned enrollment, is one of 12 that started in 2026, is one of 8 in phase 3, reaches primary completion later than 8 of the 14 other live ones, and was the 11th registered.

Obesity

11,536 studies on the registry are indexed under Obesity; 2,042 are open to participants now.

Browse Obesity studies →

Open to participants now

14 of the 22 studies testing eloralintide in Obesity are open now, in 12 countries. Recruiting first, the newest first:

8 more — sign in →

By country, each count listing its studies:

All 14 open studies →

About eloralintide

No approval found in the FDA or EMA files read. How studies give it is on its page →

Who these studies take

Of the 1,339 Obesity studies recruiting now, 377 (28%) set no upper age limit and 859 (64%) stop at 75 or younger; 167 take children under 18; 490 take healthy volunteers.

This study: 18 Years and older · all sexes · no healthy volunteers.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

Was this useful?
Get alerts for this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 22 studies testing eloralintide in Obesity, or all of them as a file.
02

Study summary

The purpose of this study is to evaluate the efficacy and safety of eloralintide in adults with obesity or overweight who do not have type 2 diabetes. The study has two phases: a main phase and an extension phase.

Participation in the main phase of the study will last about 75 weeks. Participants with prediabetes will continue in the extension phase for another 2 years.

03

Conditions studied

  • Obesity
  • Overweight
04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Have (BMI) at screening of the following:

    • 30 kilogram per square meter (kg/m2) OR
    • 27 kg/m2 with at least one of the following weight-related health conditions at screening:

      • high blood pressure
      • dyslipidemia
      • obstructive sleep apnea, or
      • heart disease
  • Have a stable body weight (\<5% body weight change) for 90 days prior to screening.
  • Have a history of at least one self-reported unsuccessful dietary effort to reduce body weight

Exclusion criteria

Exclusion Criteria:

  • Have a prior or planned surgical treatment for obesity (liposuction, cryolipolysis, or abdominoplasty allowed if performed >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 or type 2 diabetes
  • 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 Functional Classification Class IV congestive heart failure
  • Have taken medications or alternative remedies intended for weight loss within 90 days of screening
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

NYHA class (heart failure)

The New York Heart Association’s four classes of how much heart failure limits physical activity.

I
No limits: ordinary activity causes no undue tiredness or breathlessness.
II
Slight limits: comfortable at rest, ordinary activity causes symptoms.
III
Marked limits: comfortable at rest, less than ordinary activity causes symptoms.
IV
Symptoms even at rest; any activity makes them worse.

Studies set their own limit — many outside heart failure leave out class III–IV, while heart failure studies may ask for a particular class. Check the class this study names.

05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
1,980 participants (estimated)

Study arms

  • Experimental
    Eloralintide Dose 1

    Participants will receive eloralintide subcutaneously (SC)

    Drug: Eloralintide

  • Experimental
    Eloralintide Dose 2

    Participants will receive eloralintide SC

    Drug: Eloralintide

  • Experimental
    Eloralintide Dose 3

    Participants will receive eloralintide SC

    Drug: Eloralintide

  • Experimental
    Eloralintide Dose 4

    Participants will receive eloralintide SC

    Drug: Eloralintide

  • Placebo comparator
    Placebo

    Participants will receive placebo SC

    Drug: Placebo

Interventions

  • Administered SC

    Also known as: LY3841136

  • DrugPlacebo

    Administered SC

06

What researchers measure

Primary outcomes

  1. Percent Change from Baseline in Body Weight

    Time frame: Baseline, Week 64

Secondary outcomes

  1. Percent Change from Baseline in Total Body Fat Mass

    Time frame: Baseline, Week 64

  2. Change from Baseline in Waist Circumference

    Time frame: Baseline, Week 64

  3. Percent Change from Baseline in Triglycerides

    Time frame: Baseline, Week 64

  4. Change from Baseline in Systolic Blood Pressure (SBP)

    Time frame: Baseline, Week 64

  5. Time to Onset of Type 2 Diabetes (T2D)

    Time to Onset of Type 2 Diabetes (T2D) in Participants with Prediabetes at Randomization

    Time frame: Baseline to Week 168 and Week 191

  6. Change from Baseline in Body Mass Index (BMI)

    Time frame: Baseline, Week 64

  7. Change from Baseline in Hemoglobin A1c (HbA1c)

    Time frame: Baseline, Week 64

  8. Percent Change from Baseline in Fasting Insulin

    Time frame: Baseline, Week 64

  9. Percent Change from Baseline in High-Sensitivity C-Reactive Protein (hsCRP)

    Time frame: Baseline, Week 64

  10. Change from Baseline in Estimated Glomerular Filtration Rate (eGFR)

    Time frame: Baseline, Week 64

  11. Change from Baseline in Short Form-36 Version 2 (SF-36 v2) Score

    Time frame: Baseline, Week 64

  12. Change from Baseline in EQ-5D-5L

    Time frame: Baseline, Week 64

  13. Change from Baseline in Control of Eating Questionnaire (CoEQ) Score

    Time frame: Baseline, Week 64

  14. Achievement of Improved Categorical Shift in Patient Global Improvement of Status (PGIS) Physical Function Weight

    Time frame: Baseline, Week 64

  15. Change in Medication Use

    Time frame: Baseline through Week 64

  16. Percent Change from Baseline in Body Weight in Participants with Prediabetes at Randomization

    Time frame: Baseline, Week 168

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

    Time frame: Baseline through Week 64

  18. PK: Area Under the Concentration Versus Time Curve for One Dosing Interval at Steady State (AUC(0-ᴛ)ss)

    Time frame: Baseline through Week 64

07

Study locations

128 of 158 sites recruiting
  • MFA Clinical Research
    Tuscaloosa, Alabama 35405, United States
    Recruiting
    • · Contact205-331-4963
    • Mohammad Aryanpure · Principal investigator
  • Headlands Research - Scottsdale
    Scottsdale, Arizona 85260, United States
    Recruiting
    • · Contact480-725-8708
    • Benjamin Clark · Principal investigator
  • Neighborhood Healthcare Institute of Health
    Escondido, California 92025, United States
    Recruiting
    • · Contact760-737-6984
    • James Schultz · Principal investigator
  • Ark Clinical Research - Fountain Valley
    Fountain Valley, California 92708, United States
    Recruiting
    • · Contact714-988-2021
    • Mark Leibowitz · Principal investigator
  • Desert Oasis Healthcare Medical Group
    Palm Springs, California 92262, United States
    Recruiting
    • · Contact760-320-9505
    • Michael Jardula · Principal investigator
  • Peninsula Research Associates
    Rolling Hills Estates, California 90274, United States
    Recruiting
    • · Contact310-265-1623
    • David Guzman · Principal investigator
  • Care Access - Sacramento
    Sacramento, California 95831, United States
    Recruiting
    • · Contact925-734-2331
    • Francisco Garcia · Principal investigator
  • Southern California Clinical Research
    Santa Ana, California 92701, United States
    Recruiting
    • · Contact714-474-2173
    • Wayne Ho · Principal investigator
  • University Clinical Investigators, Inc.
    Tustin, California 92780, United States
    Recruiting
    • · Contact714-734-7944
    • John Kim · Principal investigator
  • Chase Medical Research, LLC
    Waterbury, Connecticut 06708, United States
    Recruiting
    • · Contact203-437-6856
    • Jenna Langello · Principal investigator
  • JEM Research Institute
    Atlantis, Florida 33462, United States
    Recruiting
    • · Contact561-968-2933
    • David Halpert · Principal investigator
  • BioMed Research & Medical Center
    Miami, Florida 33156, United States
    Recruiting
    • · Contact786-238-7110
    • Liliam Hernandez · Principal investigator
  • Adult Medicine of Lake County, Inc.
    Mt. Dora, Florida 32757, United States
    Recruiting
    • · Contact352-383-8222
    • Shirley Nagel · Principal investigator
  • American Research Centers of Florida
    Pembroke Pines, Florida 33027, United States
    Recruiting
    • · Contact954-237-3799
    • Luis del Prado Rodriguez · Principal investigator
  • AHF Pensacola
    Pensacola, Florida 32503, United States
    Recruiting
    • · Contact850-476-3131 x53026
    • Mitchell Whitehead · Principal investigator
  • IMA Clinical Research St. Petersburg
    St. Petersburg, Florida 33704, United States
    Recruiting
    • · Contact727-521-9137
    • Howard Chipman · Principal investigator
  • Teak Research Consults - Dunwoody
    Dunwoody, Georgia 30338, United States
    Recruiting
    • · Contact470-403-4755
    • Aakar Thaker · Principal investigator
  • Teak Research Consults
    Lawrenceville, Georgia 30043, United States
    Recruiting
    • Kamar Alabi · Principal investigator
  • Clinical Research Atlanta
    Stockbridge, Georgia 30281, United States
    Recruiting
    • · Contact770-507-6867
    • Jason Agran · Principal investigator
  • East-West Medical Research Institute
    Honolulu, Hawaii 96814, United States
    Recruiting
    • · Contact808-531-6886
    • Cindy Pau · Principal investigator
  • Iowa Diabetes and Endocrinology Research Center
    West Des Moines, Iowa 50266, United States
    Recruiting
    • Amy Keller · Principal investigator
  • Cotton O'Neil Clinical Research Center
    Topeka, Kansas 66606, United States
    Recruiting
    • · Contact785-354-9591
    • Katherine Willingham · Principal investigator
  • Care Access - Lake Charles (Bayou Pines)
    Lake Charles, Louisiana 70601, United States
    Recruiting
    • · Contact337-602-6642
    • William Nabours · Principal investigator
  • MedStar Good Samaritan Hospital
    Baltimore, Maryland 21239, United States
    Recruiting
    • · Contact443-444-6275
    • Adline Ghazi · Principal investigator
  • MedStar Health Research Institute (MedStar Physician Based Research Network)
    Hyattsville, Maryland 20782, United States
    Recruiting
    • · Contact443-444-5663
    • Jean Park · Principal investigator
  • Care Access - Quincy
    Quincy, Massachusetts 02169, United States
    Recruiting
    • · Contact877-791-0656
    • Chih Chao Yang · Principal investigator
  • Arcturus Healthcare , PLC, Troy Internal Medicine Research Division
    Troy, Michigan 48098, United States
    Recruiting
    • · Contact248-312-0025
    • Neil Fraser · Principal investigator
  • AMR Clinical
    Las Vegas, Nevada 89119, United States
    Recruiting
    • · Contact702-597-9825
    • Michael Jacobs · Principal investigator
  • IMA Clinical Research Warren
    Warren Township, New Jersey 07059, United States
    Recruiting
    • Nancy Phillips · Principal investigator
  • Albuquerque Clinical Trials, Inc.
    Albuquerque, New Mexico 87102, United States
    Recruiting
    • · Contact505-224-7407
    • Satkirin Khalsa · Principal investigator
  • Rochester Clinical Research, LLC
    Rochester, New York 14609, United States
    Recruiting
    • · Contact585-288-0890
    • Leigh Schirmer · Principal investigator
  • Monroe Biomedical Research
    Monroe, North Carolina 28112, United States
    Recruiting
    • · Contact704-283-7359
    • Awawu Igbinadolor · Principal investigator
  • Preferred Primary Care Physicians
    Uniontown, Pennsylvania 15401, United States
    Recruiting
    • · Contact724-912-0033
    • Paul Hartley · Principal investigator
  • Tribe Clinical Research, LLC
    Greenville, South Carolina 29607, United States
    Recruiting
    • · Contact864-334-0141
    • Ronald Mayfield · Principal investigator
  • Accellacare - Mt Pleasant
    Mt. Pleasant, South Carolina 29464, United States
    Recruiting
    • · Contact843-849-1880
    • Richard Mills · Principal investigator
  • AMR Clinical
    Nashville, Tennessee 37203, United States
    Recruiting
    • · Contact630-491-1900
    • Harvey Bowles · Principal investigator
  • The University of Texas Health Science Center at Houston
    Bellaire, Texas 77401, United States
    Recruiting
    • · Contact713-486-1350
    • Deborah Horn · Principal investigator
  • Velocity Clinical Research, Dallas
    Dallas, Texas 75230, United States
    Recruiting
    • Dan Lender · Principal investigator
  • UT Southwestern Medical Center
    Dallas, Texas 75390-9302, United States
    Recruiting
    • Amy Shah · Principal investigator
  • IMA Clinical Research San Antonio
    San Antonio, Texas 78229, United States
    Recruiting
    • · Contact210-692-7157
    • Priscilla Thomas · Principal investigator
  • AMR Clinical
    Norfolk, Virginia 23502, United States
    Recruiting
    • · Contact757-627-7446
    • Mary Bailey · Principal investigator
  • CONEXA Investigacion Clinica S.A.
    Buenos Aires, 1012, Argentina
    Not yet recruiting
    • · Contact5491169680411
    • María Scioscia · Principal investigator
  • Cicemo Srl
    Buenos Aires, 1424, Argentina
    Not yet recruiting
    • · Contact5491157417654
    • Pablo Costanzo · Principal investigator
  • Cardiología Palermo
    Buenos Aires, 1425, Argentina
    Not yet recruiting
    • · Contact5491140306347
    • Paula Perez Terns · Principal investigator
  • Glenny Corp. S.A.
    Buenos Aires, 1430, Argentina
    Not yet recruiting
    • · Contact01145445522
    • Martin Koretzky · Principal investigator
  • CARDIAMET Investigaciones Médicas
    Buenos Aires, C1014ACP, Argentina
    Not yet recruiting
    • · Contact5491165496764
    • Angela Romero Zarante · Principal investigator
  • Centro Médico Viamonte
    Buenos Aires, C1120AAC, Argentina
    Not yet recruiting
    • · Contact54 1149635650
    • Diego Aizenberg · Principal investigator
  • Fundación Respirar
    Buenos Aires, C1426ABP, Argentina
    Not yet recruiting
    • · Contact5411 7078 1548
    • Marina Uhrig · Principal investigator
  • Instituto de Investigaciones Clínicas Córdoba
    Córdoba, 5000, Argentina
    Not yet recruiting
    • · Contact03515102154
    • Mauro Pautasso · Principal investigator
  • INECO Neurociencias Oroño
    Rosario, 2000, Argentina
    Not yet recruiting
    • · Contact(0341) 425 8695
    • María Cappiello · Principal investigator
  • Centro Modelo de Cardiología
    San Miguel de Tucumán, 4000, Argentina
    Not yet recruiting
    • · Contact3814444500
    • GUILLERMO MERCAU · Principal investigator
  • Emeritus Research
    Botany, 2019, Australia
    Recruiting
    • Paul Bird · Principal investigator
  • Core Research Group
    Brisbane, 4064, Australia
    Recruiting
    • · Contact61738765688
    • David Colquhoun · Principal investigator
  • Emeritus Research
    Camberwell, 3124, Australia
    Recruiting
    • Sam Francis · Principal investigator
  • Life Clinical Research
    Ipswich, 4305, Australia
    Recruiting
    • · Contact0734490036
    • Cameron Booth · Principal investigator
  • Paratus Clinical Research Central Coast
    Kanwal, 2259, Australia
    Recruiting
    • Ian Forsyth · Principal investigator
  • University of the Sunshine Coast (UniSC) Clinical Trials - Meadowbrook
    Meadowbrook, 4131, Australia
    Recruiting
    • Ivan Lim · Principal investigator
  • Momentum Sunshine
    Melbourne, 3021, Australia
    Recruiting
    • · Contact0395096166
    • King Cheung · Principal investigator
  • Paratus Clinical Research - Melbourne
    Melbourne, 3070, Australia
    Recruiting
    • Kianoosh Noori Samie · Principal investigator
  • AIM Research
    Merewether, 2291, Australia
    Recruiting
    • · Contact+61 2 4963 2323
    • Claire Morbey · Principal investigator
  • Fusion Clinical Research
    Norwood, 5067, Australia
    Recruiting
    • Thomas Polasek · Principal investigator
  • USC Clinical Trials Sunshine Coast
    Sippy Downs, 4556, Australia
    Recruiting
    • Robert Scott · Principal investigator
  • ANIMA Research
    Diepenbeek, 3590, Belgium
    Recruiting
    • · Contact+32 11 94 91 15
    • Hilde Bollen · Principal investigator
  • Jessa Ziekenhuis
    Hasselt, 3500, Belgium
    Recruiting
    • · Contact011337030
    • Guido Claessen · Principal investigator
  • Kormont
    Kluisbergen, 9690, Belgium
    Recruiting
    • · Contact32 496 376259
    • Klaas Vercruysse · Principal investigator
  • Gezondheidshuis De Gloed
    Machelen, 9870, Belgium
    Recruiting
    • · Contact32 496 376259
    • Klaas Vercruysse · Principal investigator
  • Chronos Pesquisa Clínica
    Brasília, 72145-450, Brazil
    Not yet recruiting
    • Maira Polcheira · Principal investigator
  • Instituto de Pesquisa clinica de Campinas
    Campinas, 13060-080, Brazil
    Not yet recruiting
    • · Contact55 19 3267 0023
    • Sylka Rodovalho · Principal investigator
  • Private Practice - Dr.Miguel N. Hissa
    Fortaleza, 60430-350, Brazil
    Suspended

    Not enrolling at this site — choose another above.

  • Centro de Pesquisa Clínica de Marília - CPCLIM
    Marília, 17504-072, Brazil
    Not yet recruiting
    • · Contact55 14 21051477
    • José Sgarbi · Principal investigator
  • Núcleo de Pesquisa Clínica do Rio Grande do Sul
    Porto Alegre, 90430-001, Brazil
    Not yet recruiting
    • · Contact555137796400
    • Luis Henrique Canani · Principal investigator
  • IBPClin - Instituto Brasil de Pesquisa Clínica
    Rio de Janeiro, 20241-180, Brazil
    Not yet recruiting
    • · Contact552125277979
    • Renata Alexandra Pinheiro · Principal investigator
  • Ruschel Medicina e Pesquisa Clínica
    Rio de Janeiro, 22270-060, Brazil
    Not yet recruiting
    • · Contact552135979708
    • Luiza Siffert · Principal investigator
  • CEPIC - Centro Paulista de Investigação Clínica
    São Paulo, 04266-010, Brazil
    Not yet recruiting
    • · Contact551122713450
    • Breno Balabem Alves · Principal investigator
  • Aggarwal and Associates Limited
    Brampton, L6T 0G1, Canada
    Recruiting
    • · Contact9054589033
    • Naresh Aggarwal · Principal investigator
  • Med Trust Research
    Courtice, L1E 2J5, Canada
    Recruiting
    • · Contact905-728-7915 ext. 5
    • Anojan Kathirkamanayagan · Principal investigator
  • Dawson Clinical Research Inc.
    Guelph, N1H 1B1, Canada
    Recruiting
    • · Contact519-222-8251
    • Garry Wallace · Principal investigator
  • The Wharton Medical Clinic Clinical Trials Inc
    Hamilton, L8L 5G8, Canada
    Recruiting
    • · Contact9055238134 x 274
    • Mateen Akhtar · Principal investigator
  • Alpha Recherche Clinique
    Québec, G2J 0C4, Canada
    Recruiting
    • · Contact418-704-1112
    • Anne-Marie Beaulieu · Principal investigator
  • ALPHA Recherche Clinique
    Québec, G3K 2P8, Canada
    Recruiting
    • · Contact418-847-1112
    • Maggie Lévesque · Principal investigator
  • Bluewater Clinical Research Group Inc.
    Sarnia, N7T 4X3, Canada
    Recruiting
    • · Contact1 (519) 344-6612
    • John O'Mahony · Principal investigator
  • Winterberry Research Inc.
    Stoney Creek, L8J 0B6, Canada
    Recruiting
    • · Contact365-366-6267
    • Steven Zizzo · Principal investigator
  • Diex Recherche Inc. Division Trois-Rivieres
    Trois-Rivières, G9A 4P3, Canada
    Recruiting
    • Jean-francois Naud · Principal investigator
  • Luhe Hospital
    Beijing, 1001199, China
    Recruiting
    • Dong Zhao · Principal investigator
  • Beijing Pinggu District Hospital
    Beijing, 101200, China
    Recruiting
    • · Contact13911080328
    • yufeng li · Principal investigator
  • Sichuan Provincial People's Hospital
    Chengdu, 610072, China
    Recruiting
    • Limin Tian · Principal investigator
  • West China Hospital Sichuan University
    Chengdu, 610041, China
    Recruiting
    • · Contact18980601658
    • zhenmei an · Principal investigator
  • Zhujiang Hospital
    Guangzhou, 510280, China
    Recruiting
    • Jia Sun · Principal investigator
  • The Second People's Hospital of Hefei
    Hefei, 230011, China
    Recruiting
    • · Contact86-13956099720
    • Jun Ye · Principal investigator
  • Jinan Central Hospital
    Jinan, 250013, China
    Recruiting
    • · Contact15318816218
    • Xiaolin Dong · Principal investigator
  • The First Affiliated Hospital of Henan University of Science &Technology
    Luoyang Shi, 471003, China
    Recruiting
    • · Contact13653880139
    • Hongwei Jiang · Principal investigator
  • Jiangxi Provincial People's Hospital
    Nanchang, 330038, China
    Recruiting
    • · Contact13767035719
    • Zongyou Cheng · Principal investigator
  • Nanjing First Hospital
    Nanjing, 210000, China
    Recruiting
    • Qian Li · Principal investigator
  • Jiangsu Province Official Hospital
    Nanjing, 210008, China
    Recruiting
    • Wei Tang · Principal investigator
  • Zhongda Hospital Southeast University
    Nanjing, 210009, China
    Recruiting
    • Ling Li · Principal investigator
  • The Second Affiliated Hospital of Nanjing Medical University
    Nanjing, 210011, China
    Recruiting
    • · Contact18951762960
    • Yibing Lu · Principal investigator
  • Shanghai Sixth People's Hospital
    Shanghai, China
    Recruiting
    • Jian Zhou · Principal investigator
  • Zentrum fur klinische Forschung - Köln
    Cologne, 51069, Germany
    Active, not recruiting

    Not enrolling at this site — choose another above.

  • Universitaetsklinikum Carl Gustav Carus Dresden
    Dresden, 01307, Germany
    Active, not recruiting

    Not enrolling at this site — choose another above.

  • StudyPoint Duisburg
    Duisburg, 47269, Germany
    Active, not recruiting

    Not enrolling at this site — choose another above.

Showing the first 100 of 158 sites across 15 countries. Choose a country and city above to see the rest.

08

References and documents

Individual participant data

Plan to share: Yes — 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.

Supporting information: Study protocol, Statistical analysis plan, Clinical study report

Time frame: Data are available 6 months after the primary publication or 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 should be approved by an independent review panel and researchers should sign a data sharing agreement.

Data sharing details ↗ · vivli.org

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Feb 2026 (actual). Primary completion is estimated for Mar 2028, 25 months after the start.

Of 199 industry-sponsored phase 3 interventional studies under Obesity, half reached primary completion within 21 months of starting (the median), counting those still running; a quarter within 18 and three quarters within 27. This study's planned 25 months is above that.

Counting every sponsor, half of 262 studies reached it within 24 months; a quarter within 18 and three quarters within 34.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 5, 2026
First posted
Jan 7, 2026
StartActual
Feb 6, 2026
Primary completionEst.
Mar 2028
CompletionEst.
Jul 2030
Last update
Sep 22, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07321886
Responsible party
Sponsor
First posted
Jan 7, 2026
Start date
Feb 6, 2026
Primary completion
Mar 2028 (estimated)
Completion
Jul 2030 (estimated)
Last update
Sep 22, 2026

Study contacts

Trial question or participation questions: 1-877-CTLILLY (1-877-285-4559) or
Contact
LillyTrials@Lilly.com
1-317-615-4559
Physicians interested in becoming principal investigators please contact
Contact
clinical_inquiry_hub@lilly.com
Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 8 AM - 8 PM Eastern time (UTC/GMT - 5 hours, EST)
study director · Eli Lilly and Company

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Discussion

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Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Studies of the drug tested here: Eloralintide

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