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Eloralintide and Tirzepatide

Phase 3

Overweight | Small molecule | Metabolic |Eli Lilly and Company|Last Updated: Aug 21, 2026

Target and mechanism

Target class-Tide (Peptide)
ModalitySmall molecule

Also known as Eloralintide

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindCONTROLLEDDMC
Total Trials4
Total Enrollment2,238

FDA Designations

No designations recorded

Clinical trial landscape

Eloralintide and Tirzepatide · 4 trials · 2 indications

Phase 3 2Phase 1 2
NCT07392190A Study of Eloralintide (LY3841136) in Participants With Persistent Obesity Who Are Treated With a Weekly IncretinOverweight
RECRUITING900 Analytics
NCT07282600A Study of Eloralintide (LY3841136) in Participants With Obesity or Overweight, and Type 2 DiabetesOverweight
RECRUITING1,035 Analytics
PHASE3RECRUITING
A Study of Eloralintide (LY3841136) in Participants With Persistent Obesity Who Are Treated With a Weekly Incretin
OverweightUnlock trial analytics
PHASE3RECRUITING
A Study of Eloralintide (LY3841136) in Participants With Obesity or Overweight, and Type 2 Diabetes
OverweightUnlock trial analytics

Study Endpoints

Primary Endpoints

Percent Change from Baseline in Body Weight
Baseline, Week 64
Change From Baseline In Hyperinsulinemic Euglycemic Clamp (HEC) Predicted Clamp-Derived Insulin Sensitivity (M-value)
Baseline, Week 24
Cohorts A and B: Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of Eloralintide and Tirzepatide
Day 106 Predose to Approximately Week 26

PK: AUC of Eloralintide and Tirzepatide

Cohorts A and B: PK: Maximum Concentration (Cmax) of Eloralintide and Tirzepatide
Day 106 Predose to Approximately Week 26

PK: Cmax of Eloralintide and Tirzepatide

Cohorts C and D: PK: AUC of Eloralintide and Tirzepatide
Baseline Up to Approximately Week 11

PK: AUC of Eloralintide and Tirzepatide

Cohorts C and D: PK: Cmax of Eloralintide and Tirzepatide
Baseline Up to Approximately Week 11

PK: Cmax of Eloralintide and Tirzepatide

Cohorts E and F: PK: AUC of Eloralintide
Day 8 Predose Up to Approximately Week 12

PK: AUC of Eloralintide

Cohorts E and F: PK: Cmax of Eloralintide
Day 8 Predose Up to Approximately Week 12

PK: Cmax of Eloralintide

Number of Participants with One or More Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration
Baseline Up to Approximately Week 26

A summary of TEAEs and SAEs regardless of causality, will be reported in the Reported Adverse Events module

Secondary Endpoints

Change from Baseline in Waist Circumference
Baseline, Week 64
Percent Change in Baseline in Triglycerides
Baseline, Week 64
Change from Baseline in Systolic Blood Pressure
Baseline, Week 64
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Study Design & Arms

AllocationRANDOMIZED
MaskingDOUBLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Eloralintide Dose 1EXPERIMENTALParticipants will receive eloralintide subcutaneously (SC)
Eloralintide Dose 2EXPERIMENTALParticipants will receive eloralintide SC
Eloralintide Dose 3EXPERIMENTALParticipants will receive eloralintide SC
Eloralintide Dose 4EXPERIMENTALParticipants will receive eloralintide SC
PlaceboPLACEBO_COMPARATORParticipants will receive placebo SC
EloralintideEXPERIMENTALEloralintide administered subcutaneously (SC)
Eloralintide and Tirzepatide-Cohorts A-DEXPERIMENTALEloralintide and Tirzepatide administered subcutaneously (SC)
Eloralintide-Cohorts E and FEXPERIMENTALEloralintide administered SC

Interventions

NameTypeDescription
EloralintideDRUGAdministered SC
PlaceboDRUGAdministered SC
Eloralintide and TirzepatideDRUGAdministered SC
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites187

Inclusion Criteria: * Are on stable incretin therapy at screening * With persistent obesity or overweight defined as: * ≥30 kg/m2 OR * ≥27 kg/m2 with at least one existing obesity related complication at screening: * hypertension * dyslipidemia * obstructive sleep apnea * card...

Countries:United StatesAustraliaBelgiumBrazilChinaCzechiaIndiaIsraelJapanMexicoPuerto RicoRomaniaSpainTaiwanArgentinaGermanyPolandSlovakiaSouth KoreaSweden
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Recent Changes (Last 90 Days)

LOWAug 21, 2026NCT07282600lastUpdatePostDate: changed
LOWAug 21, 2026NCT07392190lastUpdatePostDate: changed
LOWAug 21, 2026NCT07282600lastUpdatePostDate: changed
LOWAug 21, 2026NCT07392190lastUpdatePostDate: changed
LOWAug 6, 2026NCT07282600lastUpdatePostDate: changed
LOWAug 6, 2026NCT07392190lastUpdatePostDate: changed
LOWAug 6, 2026NCT07282600lastUpdatePostDate: changed
LOWAug 6, 2026NCT07392190lastUpdatePostDate: changed
LOWJul 17, 2026NCT07665879Status: NOT_YET_RECRUITING → RECRUITING
LOWJul 17, 2026NCT07282600lastUpdatePostDate: changed
LOWJul 17, 2026NCT07392190lastUpdatePostDate: changed
LOWJul 17, 2026NCT07665879Status: NOT_YET_RECRUITING → RECRUITING
LOWJul 17, 2026NCT07282600lastUpdatePostDate: changed
LOWJul 17, 2026NCT07392190lastUpdatePostDate: changed
LOWJul 17, 2026NCT07665879Status: NOT_YET_RECRUITING → RECRUITING
LOWJul 7, 2026NCT07282600lastUpdatePostDate: changed
LOWJul 7, 2026NCT07392190lastUpdatePostDate: changed
LOWJul 7, 2026NCT07282600lastUpdatePostDate: changed
LOWJul 7, 2026NCT07392190lastUpdatePostDate: changed
LOWJun 24, 2026NCT07665879NEW_TRIAL: changed

Frequently asked questions about Eloralintide and Tirzepatide

What is Eloralintide used for?

Eloralintide is an investigational small molecule being studied for obesity, overweight, osteoarthritis knee pain, and obstructive sleep apnea in people with obesity or overweight. It is also being evaluated in healthy volunteers. The drug is in clinical development by Eli Lilly and Company and is not yet approved.

What does Eloralintide target?

Eloralintide is a peptide-based small molecule, classified under the -tide (peptide) target class. Its specific molecular target is not disclosed in available clinical trial information. The drug is being studied for its effects on body weight and related conditions such as osteoarthritis and sleep apnea.

Who is developing Eloralintide?

Eloralintide is being developed by Eli Lilly and Company, a pharmaceutical company traded on the NYSE under the ticker LLY. The company is conducting clinical trials of Eloralintide across multiple countries, including the United States, China, and several European and Asian nations.

What phase is Eloralintide in?

Eloralintide is in Phase 1 and Phase 3 clinical trials. Phase 1 studies are evaluating safety and tolerability in healthy participants and in Chinese participants with obesity or overweight. Phase 3 trials are recruiting participants with osteoarthritis knee pain or obstructive sleep apnea who also have obesity or overweight.

What clinical trials is Eloralintide in?

Eloralintide has four registered clinical trials. NCT06916091 is a completed Phase 1 study in Chinese participants with obesity or overweight. NCT07353931 is a recruiting Phase 3 trial for osteoarthritis knee pain. NCT07369011 is a recruiting Phase 3 trial for obstructive sleep apnea. NCT07701083 is a recruiting Phase 1 study in healthy participants.

Is Eloralintide the same as LY3841136?

Yes, Eloralintide is also known as LY3841136. Clinical trial records use both names interchangeably, with LY3841136 appearing in study titles and Eloralintide as the drug name. Patients and researchers searching for either name will find the same investigational drug being developed by Eli Lilly.