ClinicalTrials.gg
Not yet recruitingNCT07765511Updated Aug 14, 2026

A Study of Macupatide (LY3532226) in Participants With Obesity or Overweight Without Type 2 Diabetes

A Phase 1 interventional study of Macupatide and Eloralintide in Obesity and Overweight, sponsored by Eli Lilly and Company. Not yet recruiting at 3 sites in Japan. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-14.

Sponsored by Eli Lilly and Company · Phase 1, Interventional, and Basic science

Phase
Phase 1
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

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

Planned enrollment
19th of 22
60 · median 315
Started
2026
with 11 others
Phase 1
9 of 22
4 open now
Primary completion
2027-06
later than 2 of 14 live
Registered
18th 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 19th largest by planned enrollment, is one of 12 that started in 2026, is one of 9 in phase 1, reaches primary completion later than 2 of the 14 other live ones, and was the 18th registered.

Obesity

11,522 studies on the registry are indexed under Obesity; 2,033 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 1,336 Obesity studies recruiting now, 377 (28%) set no upper age limit and 856 (64%) stop at 75 or younger; 168 take children under 18; 491 take healthy volunteers.

This study: 18 Years to 65 Years · all sexes · healthy volunteers too.

The full table on the hub →

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

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Watch 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 main purpose of this study is to assess how well macupatide, when dosed alone and in combination with eloralintide, is tolerated and what side effects may occur in participants with obesity or overweight without Type 2 diabetes. Blood tests will be performed to investigate how the body processes the study drug and how the study drug affects the body. For each participant, the study will last about 4 months and will include 2 stays in the Clinical Research Unit (CRU), each lasting 3-5 nights.

03

Conditions studied

  • Obesity
  • Overweight
04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

  • Are Japanese participants assigned male at birth (AMAB) or assigned female at birth (AFAB) who agree to requirements or participants who are individuals not of (INOCBP).
  • Have a greater than or equal to (≥)25 kilograms per square meter (kg/m²)
  • Have had a stable weight for the 3 months prior to screening. Stable weight is defined as less than 5 percent (%) body weight change.

Exclusion criteria

Exclusion Criteria:

  • Have known allergies to related compounds of macupatide or eloralintide, or any components of the formulations.
  • Have a history of significant atopy, including severe allergic manifestations, or multiple or severe drug allergies, or severe posttreatment reactions.
  • Have a history or presence of psychiatric disorders, including a history of major depressive disorder or severe psychiatric disorders, within the last 3 years, that would present a safety risk or may significantly impair the participant's ability to comply with study procedures.
  • Have been diagnosed with Type 1 or Type 2 diabetes mellitus.
  • Have a history of chronic medical conditions involving the heart, liver, or kidneys.
  • Have a history of any within the past 5 years except for basal cell or squamous epithelial carcinomas of the skin that have been resected with no evidence of disease for 3 years.
  • Have a history or presence of a gastrointestinal (GI) disorder or previous surgery that impacts gastric emptying.
  • Have had or plan to have during the study, a device-based or surgical treatment use for obesity.
  • Have been treated, or plan to be treated, with prescription medications or other non approved drugs intended to promote weight loss, within 3 months prior to screening.
  • Are currently enrolled or have participated, within the last 30 days, in a clinical study involving an product. If the previous investigational product has a long half-life, 5 half-lives or 30 days, whichever is longer, should have passed.
  • Have previously completed or withdrawn from this study or have previously received macupatide or eloralintide.
  • Have evidence of acute or chronic liver disease or pancreatic disease.
Terms in these criteria, in plain language(8)

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.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

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.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

05

Study design

Phase
Phase 1
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Macupatide + placebo

    Macupatide and placebo administered subcutaneously (SC)

    Drug: Macupatide · Drug: Placebo

  • Experimental
    Eloralintide + placebo

    Eloralintide and placebo administered SC

    Drug: Eloralintide · Drug: Placebo

  • Experimental
    Macupatide Dose A + Eloralintide

    Macupatide and Eloralintide administered SC

    Drug: Macupatide · Drug: Eloralintide

  • Experimental
    Macupatide Dose B + Eloralintide

    Macupatide and Eloralintide administered SC

    Drug: Macupatide · Drug: Eloralintide

  • Placebo comparator
    Placebo

    Placebo administered SC

    Drug: Placebo

Interventions

  • Administered SC

    Also known as: LY3532226

  • Administered SC

  • DrugPlacebo

    Administered SC

06

What researchers measure

Primary outcomes

  1. Number of Participants with One or More Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration

    Time frame: End of Study (Week 25)

Secondary outcomes

  1. Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of Macupatide

    Time frame: Baseline through Week 25

  2. PK: AUC of Macupatide in Combination with Eloralintide

    Time frame: Baseline through Week 25

  3. PK: Maximum Concentration (Cmax) of Macupatide

    Time frame: Baseline through Week 25

  4. PK: Cmax of Macupatide in Combination with Eloralintide

    Time frame: Baseline through Week 25

  5. Percent Change in Body Weight

    Time frame: Baseline through Week 25

07

Study locations

3 sites
  • Souseikai Fukuoka Mirai Hospital
    Fukuoka, 813-0017, Japan
    • · Contact81120023812
    • Misato Nakagawa · Principal investigator
  • Sumida Hospital
    Sumida-ku, 130-0004, Japan
    • · Contact81120023812
    • Takuma Yonemura · Principal investigator
  • Medical Corporation Houeikai Sekino Clinical Pharmacology Clinic
    Toshima City, 171-0014, Japan
    • · Contact81120023812
    • Takashi Nakamura · Principal investigator
08

References and documents

Individual participant data

Plan to share: No

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

Start is estimated for Oct 2026; primary completion for Jun 2027, 8 months later.

Of 334 industry-sponsored phase 1 interventional studies under Obesity, half reached primary completion within 9 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 15. This study's planned 8 months is below that.

Counting every sponsor, half of 439 studies reached it within 11 months; a quarter within 6 and three quarters within 24.

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

Registered
Aug 11, 2026
First posted
Aug 14, 2026
StartEst.
Oct 2026
Primary completionEst.
Jun 2027
CompletionEst.
Jun 2027
Last update
Aug 14, 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 Aug 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07765511
Responsible party
Sponsor
First posted
Aug 14, 2026
Start date
Oct 2026 (estimated)
Primary completion
Jun 2027 (estimated)
Completion
Jun 2027 (estimated)
Last update
Aug 14, 2026

Study contacts

Trial questions 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
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

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Studies of the drugs tested here: Macupatide · Eloralintide

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